Volume 11 - 2024 | https://doi.org/10.3389/fvets.2024.1371495 This article is part of the Research TopicWildlife-Domestic Animal Interface: Threat or Sentinel?View all 9 articles Schmallenberg virus (SBV) is an arthropod-borne virus that emerged recently in northwestern Europe in 2011 that affects domestic and wild ruminants and induces abortion SBV has spread very rapidly to too many countries in the world The overall serological investigation of SBV is needed to improve modeling predictions and assess the overall impact on ruminant animals which helps to design interventions for control and prevention strategies this study aimed to estimate the overall serological assay of SBV in both domestic and wild ruminants around the world This systematic review was conducted as per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines International databases were employed To search for relevant articles The pooled prevalence with a 95% confidence interval was calculated with a random effects model and I2 were used to assess the sources of heterogeneity The overall pooled proportion of SBV in domestic and wild ruminants was 49 and 26% Substantial heterogeneity was observed in studies on domestic ruminants (I2 = 99.7%; p < 0.01) and studies on wild ruminants (I2 = 97.9%; p < 0.01) The pooled prevalence of SBV was significantly associated with publication time the highest pooled prevalence of SBV was reported in cattle (59%) In addition to the subgroup analysis based on publication year the pooled prevalence of SBV infection has become endemic since 2013 (49%) among domestic animals in the world the highest anti-SBV antibodies (66%) were detected by a virus neutralization test the major wild animals that were infected by SBV were red deer The highest sub-pooled prevalence of SBV was found in roe deer (46%) the prevalence of SBV was high in cattle among domestic ruminants and in roe deer among wild animals According to the current information provided by this meta-analysis evidence-based risk management measures should be established to restrict SBV spread in both domestic and wild ruminants The diagnosis of SBV infection in living adult animals is difficult for veterinarians A protocol targeting the S segment was later developed and showed higher sensitivity the detection of anti-SBV antibodies present in the serum of infected animals can be performed by the indirect method of SBV infection diagnosis The virus neutralization test (VNT) and enzyme-linked immunosorbent assay (ELISA) have been developed as tools for serological diagnosis According to the European Food Safety Authority (EFSA) SBV infection had also been confirmed in approximately 9,000 ruminant herds across Europe and nearly half of them were reported in France especially when virus shedding is only transient and the time frame is unknown since antibodies remain detectable for longer periods This investigation was important for scientific evidence for the researchers and baseline survey collectors regarding the dairy herd reproductive infectious diseases it supports intervention regarding the prevention and control of the virus this systematic review and meta-analysis aimed to provide an overall estimate of the seroprevalence of SBV in both domestic and wild animals around the globe The literature search was conducted from 12 August to 20 September 2023. A systematic assessment of published articles reporting the overall proportion of SBV was performed based on the PRISMA checklist (33) (Supplementary material 1) The major working protocol was performed in seven key steps: study eligibility criteria A comprehensive search strategy was made to identify all relevant studies snowball searching from retrieved articles and other manual methods were used for literature searches to select included studies by two authors (MD and AS) independently The research question was “What is the pooled prevalence of SBV in domestic and wild ruminants in the world?” The following Mesh terms were used in electronic database search: “Schmallenbergvirus,” “SBV,” “PrevalenceofSchmallenberg virus” “epidemiology of Schmallenberg virus,” “Schmallenberg virus in cattle,” “Schmallenberg virus in sheep,” “Schmallenberg virus in goat,” “Schmallenberg virus in domestic ruminants,” Schmallenberg virus in wild ruminants “Schmallenberg virus in wild animals,” “Schmallenberg virus in red deer,” “Schmallenberg virus in roe deer,” “Schmallenberg virus in wild goat,” Schmallenberg virus in wild boar,” Schmallenberg virus in bison “Schmallenberg virus in buffalo,” “Schmallenberg virus in fallow deer,” and “Schmallenberg virus in mouflon.” Even we have searched articles based on the combination of these words with specific continents and countries as the context All identified studies were imported to Medley software to remove duplicates and scientific citations from the references The search was performed by three field experts (Microbiology and Veterinary Clinical Medicine) to avoid authors’ bias This meta-analysis includes all of the primary descriptive studies that have been published in the English language that document the occurrence of SBV in domestic and wild ruminants The inclusion criteria included articles with a clear estimation of the prevalence of SBV Study animals became domestic and wild ruminants around the globe at any year Samples had to be collected from animals that had not been experimentally infected Studies that do not have clear and detailed estimates of the proportion of SBV in the affected host were also excluded Intervention studies that lacked baseline data on the association between animal exposure and disease were excluded from the meta-analysis The literature search was conducted from August to September 2023 The included studies were reported from continents in any study year The relevant data were extracted independently by two investigators (MD and AS) Quantitative and qualitative data extraction from the included studies was performed and presented in the form of a table in an Excel spreadsheet The extracted components encompassed the name of the primary author along with the year of publication and all domestic and wild species of ruminants the number of seropositive animals (primary outcome interest) Disagreements were resolved by discussion and consultation with a third author Quality assessment was performed to verify the methodological quality of this systematic review (MD and BD). The quality assessment of the included studies was assessed by the Appraisal tool for Cross-Sectional Studies (AXIS) quality tool (34) This quality assessment tool includes different items including study design In a logistic-normal random-effect regression model the logit transformation was utilized to estimate the pooled proportions and a mixed-effect logistic regression model was employed for the subgroup analysis The Cochran’s Q test (reported as the p-value), τ2 (between-study variance), and inverse variance index (I2) were used to assess the sources of heterogeneity, which describes the percentage of observed total variation between studies that is due to heterogeneity rather than chance. As explained by Higgins and Thompson (37) the I2 index was estimated to represent low Heterogeneity was deemed to be statistically significant if the I2 value exceeded 50% and the Q test revealed a p-value of less than 0.10 The degree of study heterogeneity has been evaluated using a forest plot diagram The forest plot diagram displayed the weights and 95% confidence intervals for each study To determine specific between-study variability a subgroup analysis of the proportion of the SBV in ruminants was performed based on study year Publication bias is usually evaluated through a funnel plot in which asymmetry can be assessed visually publication bias was assessed using funnel plot diagrams and Egger’s regression test Sensitivity analysis of studies was performed to evaluate the effect of each study on the pooled result The results showed that the studies were the prime determinants of the pooled result As shown in the PRISMA 2020 flowchart (Figure 1) a total of 929 articles in various electronic databases and other methods were searched from which 8 were excluded after article duplication assessment (n = 8) 30 records were marked as ineligible by automation tools (n = 30) and 41 records were removed for other reasons (n = 41) 534 articles were excluded by article title and abstract screening 316 studies were reports searched for retrieval and 233 articles were reports not retrieved A total of 82 (n = 82) articles were reports being evaluated for eligibility and 41 (n = 41) of them were excluded for various reasons 41 (n = 41) studies were included for meta-analysis A PRISMA flowchart for searched relevant articles The characteristics of the studies about SBV are intricately described in a step-by-step manner The study animals comprised of cattle which are of all ages A total of 41 independent articles (domestic n = 17) were considered for the analysis of all pooled prevalence SBV in wild and domestic ruminants A meta-analysis was carried out separately for the prevalence of SBV in domestic and wild ruminants the included studies for this meta-analysis were conducted and published in different parts of the world between 2011 and 2022 We noticed that the same article was used multiple times due to different species of animals and the types of samples were serum (blood) and brain tissue it helps to reduce the variability between studies In the meta-analysis of studies regarding SBV a total of 41 independent articles were incorporated in both domestic and wild ruminants (domestic it should be noted that certain articles were utilized multiple times due to their relevance in similar years but in different animal species a total of 40 dependent and independent articles were included in the case of domestic ruminants while 42 articles were included in wild ruminants Forest plot plots with random-effects meta-analysis of SBV infection in domestic ruminants Funnel plot plots the standard error by log odds of the proportion of SBV domestic ruminants The regression test for funnel plot asymmetry was done using a mixed-effects meta-regression model and standard error as a predictor (Eger’s test b = −0.2035 (CI: −0.6588 The test for funnel plot asymmetry was also performed via rank correlation test for funnel plot asymmetry (Kendall’s tau = −0.0073 heterogeneity was explored through a subgroup analysis Subgroup analyses were conducted based on study year All of the subgroup analyses of exploratory outcomes showed considerable heterogeneity (I2 > 98) Significant statistical heterogeneity in the subgroup analysis reveals a likely interaction among exploratory variables Based on the species of ruminant animals, the included studies were categorized into three groups: cattle (n = 22), sheep (n = 11), and goat (n = 6). Significant discrepancies were found in the subgroup analysis of the most SBV prevalence by animal type. As shown in Figure 4 the subgroup analysis revealed that the pooled prevalence of SBV in cattle was 59% (95% CI: 43–74%) and (I2 = 100%: τ2 = 2.5168=; p = 0) followed by sheep at 37% (95% CI: 20–58%) and (I2 = 100%: τ2 = 1.9884; p = 0.0) and goat at 18% (95% CI: 4–52%) and (I2 = 99%: τ2 = 4.0281; p < 0.01) Pooled prevalence of SBV by domestic ruminant species In terms of the year of publication, as shown in Figure 5 the subgroup analysis found that the pooled prevalence of SBV virus in domestic ruminants was 27% (95% CI: 25–56%) with 99% degree of heterogeneity (I2) and (τ2 = 3.1833: p < 0.01) in the up to or before 2013 group 49% (95% CI: 25–56%) in the 2013 or later group with 98% degree of heterogeneity (I2) Sub-pooled prevalence of SBV in domestic ruminants by publication year In terms of the method of diagnosis, subgroup analysis of the method of diagnosis was carried out. The method of diagnosis was categorized into VNT, ELISA, and RT-qPCR. In this case, we also encountered considerable heterogeneity (I2 > 50) in each group. The highest study heterogeneity (I2 = 100) was revealed in the diagnosis of SBV by ELISA methods. The sub-pooled prevalence (66%, Figure 6) of SBV was highest in the diagnosis method of VNT The subgroup difference test suggested that there was a statistically significant group effect (Q = 23.49; DF = 2; p < 0.0001) and rank correlation test revealed that there was no asymmetrical distribution of studies indicating that smaller studies were not likely to be overlooked Funnel plot plots the standard error by log odds of the proportion of SBV wild ruminants a high level of variability was observed in studies focusing on fallow deer with an I2 value of 98 and a p-value of <0.01 this is the first meta-analysis of the global prevalence of SBV infection in wild and domestic ruminants although many investigations regarding the prevalence of SBV infection in ruminants in different countries have been conducted The overall serological investigations of SBV are needed to improve modeling predictions and assess the overall impact of SBV in ruminant animals Wildlife animals may be susceptible to multiple infectious agents of public health or veterinary relevance thereby potentially forming a reservoir that bears the constant risk of re-introduction into the human or livestock population A meta-analysis was performed to estimate the pooled prevalence of SBV infection in domestic and wild ruminants in the world The current meta-analysis includes 34 articles and it found that the overall pooled prevalence of SBV was 54 and 26% in domestic and wild ruminants These differences may be related to the availability of vaccination the clinical stage of the virus during sampling and the density of the vector (culicoides) environmental characteristics such as humidity and variation in temperature during the night and day affect the density of the vector influencing the possible transmission and consequently the prevalence of SBV in both domestic and wild ruminants This investigation presents compelling evidence of SBV infection in both domestic and wild ruminants worldwide The findings of the present study appear to suggest an increase in the spread of SBV after the year 2013 our research also indicated a high distribution of SBV in both domestic and wild ruminants while other countries have recently discovered the presence of the virus where the SBV was detected around the year 2018 the current study revealed a lack of comprehensive information regarding the propagation of SBV in wild animals the seroprevalence of SBV is significantly high particularly about dairy cattle in African countries This research also aids in enhancing our comprehension of the range of species susceptible to the virus and evaluating the effectiveness of current SBV serological assays in both wild and domestic ruminants further investigation is required concerning the spread of the virus in wild animals as well as the implementation of preventive and control measures There are several limitations in our meta-analysis and included articles our systematic review only includes published articles the subgroup analysis was limited to only publication year or detection method as moderators for investigation of the source of heterogeneity between studies and the included studies did not cover all wild ruminants the articles we found did not cover all regions of the world as some countries had no published articles The final limitation was that our review was not registered in the PROSPERO database The current meta-analysis demonstrates the significant rate at which the overall prevalence of SBV was higher in domestic ruminants (49%) compared with wild ruminants (26%) the present study reveals that the overall serological assay was greater in cattle in comparison with small ruminants the roe deer exhibited the highest seropositivity This investigation includes a substantial number of European studies indicating a better comprehension or possibly a high distribution of the intermediate host (vectors) Based on the available evidence regarding its emergence in 2011 we presume that the global coverage of the virus is extensive this virus will exert a significant impact on dairy industries it is imperative to pay close attention to this disease to counteract its rapid dissemination worldwide certain countries should prioritize early diagnosis for both domestic and wild ruminants The original contributions presented in the study are included in the article/Supplementary material further inquiries can be directed to the corresponding author The author(s) declare that no financial support was received for the research We gratefully acknowledge the University of Gondar for providing some of the materials and important pieces of training The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets.2024.1371495/full#supplementary-material First detection of Schmallenberg virus RNA in bovine semen Crossref Full Text | Google Scholar Schmallenberg virus infection among Red Deer 3. 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This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) distribution or reproduction in other forums is permitted provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited in accordance with accepted academic practice distribution or reproduction is permitted which does not comply with these terms *Correspondence: Melkie Dagnaw, bWVsa2llZGFnbmF3MzUyOEBnbWFpbC5jb20= Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher 94% of researchers rate our articles as excellent or goodLearn more about the work of our research integrity team to safeguard the quality of each article we publish First identified in Ireland in October 2012 Schmallenberg still remains a threat to Irish sheep flocks and cattle herds As part of a recent Let’s Talk Sheep Webinar, Audrey Jenkinson, a Superintending Veterinary Inspector with the National Disease Control Centre at the Department of Agriculture, Food and the Marine, provided an insight into Bluetongue and Schmallenberg disease Presenting information provided by her colleagues in the Regional Veterinary Laboratories, Audrey Jenkinson noted that there was evidence that the Schmallenberg virus was circulating in Ireland in mid to late 2024 as the population’s immunity generally wanes after 5-7 years and no vaccine is currently available “The trouble with Schmallenberg is that it can cause birth deformities but by the time those lambs or calves are then born the detectable traces of the virus could be long gone,” she noted it is known to cause abortion and deformed lambs The congenital deformities which occur include: twisted neck maybe also ‘locked’; limbs bent and locked; shortened lower jaws; and abnormalities with excess fluid in the brain On the likelihood of the disease occurring this spring Audrey Jenkinson said: “Our lab colleagues expect that there could well be significant Schmallenberg related losses on some farms this spring.” she noted that estimates of up to 15% losses have been reported in the past The Superintending Veterinary Inspector urged farmers to vigilant for birth abnormalities Extra care is also required in terms cleanliness as evidence from France and the Netherlands suggests that some calves and lambs can be born perfectly normal She added: “Don’t assume an abnormality or abortion issue is Schmallenberg because there is so many other diseases that can cause these things.” And she urged farmers to continue to submit samples to their local Regional Veterinary Lab ideally fresh carcasses with afterbirths and maternal bloods in order to have the best chance of getting a diagnosis the full recording of the Let’s Talk Sheep Webinar is available to view below: Early lambing flocks across the UK have been impacted by Schmallenberg virus with reports of deformities in newborn lambs and higher abortion rates with some regions seeing cases for the first time National Sheep Association (NSA) chief executive Phil Stocker confirmed that the virus has been present for about a month with “some fairly serious reports” coming in from affected areas See also: Several bluetongue restrictions lifted but zones to remain He noted that Schmallenberg typically fades as the lambing season progresses with early lambing flocks typically most vulnerable Mr Stocker suggested that shifting towards later lambing could help because the first part of the pregnancy cycle for early lambers (in the autumn) coincides with peak midge activity Schmallenberg virus poses a significant risk to the sheep sector due to the lack of a vaccine in the UK Mr Stocker stressed the importance of testing to distinguish Schmallenberg from bluetongue The Animal and Plant Health Agency (Apha) is offering free Schmallenberg testing in England and Wales and the NFU has confirmed the virus remains a regional issue for now A farm in Dumfries and Galloway was particularly hard-hit with many born alive but severely deformed said Schmallenberg was just one of the pathological agents that can cause high barren rates “It is also important to remember that we do not yet know the full extent of the effects that bluetongue virus has had on fertility and calves and lambs that are being born around now,” he said “This is why it is very important to report poorer than expected fertility results as well as the arrival of deformed or neurologically affected neonates to your vet so that testing may be carried out.” NFU chief livestock adviser John Royle added that the situation may worsen with bluetongue virus potentially contributing to higher barren rates and deformed calves and lambs “This may be the tip of the iceberg as we see the virus overwinter resulting in emergence much earlier,” he warned Visit our Know How centre for practical farming advice A total of 63 cases of the Schmallenberg virus (SBV) were identified in the UK last winter This page provides key information on the virus including useful guidance and advice if you spot cases on farm The Schmallenberg virus (SBV) is an insect borne viral disease It can affect all ruminants (such as sheep goats and deer) and camelids (such as llama and alpaca) and can also be the cause of late abortion or birth defects in new born cattle It does not affect humans or food safety; meat and milk from infected animals are also safe to eat and drink The virus often spreads very quickly – disease can last between 2-7 days There is no vaccine available for SBV and no plans for production of a new vaccine Farmers should remain vigilant for signs of disease and report any suspicions to APHA or their private vet The last wave of Schmallenberg occurred between 2016-17 where over 200 cases were confirmed by APHA across sheep and cattle holdings in Great Britain Return to top Cases of Schmallenberg rose across the UK in autumn 2023 a total of 63 cases were confirmed to APHA The majority of cases were found in stillborn lambs meaning that positive cases do not need to be reported to Defra Therefore it is difficult to say with accuracy the total number of cases seen across the autumn and winter There are no plans for Defra to compensate farms that are affected by SBV As SBV often presents itself in late abortion or birth defects infection often goes unnoticed until the gestation period has passed The acute disease usually lasts between 2-7 days in adult animals before they begin to develop robust immunity herd milk is found to drop on average between 0.3 and 1kg per cow clinical signs of SPV are often mild or absent Not all birth defects are due to SBV – for example Some bulls can persistently intermittently excrete SBV in semen for up to 3 months post infection SBV can cause deformities as the virus crosses the placenta and replicates in the central nervous system tissue It also causes the maternal recognition of pregnancy Often birthing ruminants infected with SBV require a caesarean or fetotomy to deliver to avoid trauma to the dam meaning that its circulation is very much weather dependent so we tend to see midge numbers peaking in the summer Flocks or herds that are mating in the summer or early autumn are the worst affected The length of gestation is also important; we expect to see clinical signs in sheep first It is likely that SBV last circulated during the 2017/18 mating season we are on the edge of the SPV endemic zone where we tend to see explosive outbreaks every couple of years reflecting a cycle of every 3-5 years when we have naïve animals exposed to circulating virus there were no plans to cull infected animals as SBV is likely to be transmitted by insects such as midges making culling an ineffective means of stopping disease spread There is also evidence that once an animal is infected with SBV they quickly develop immunity and are not likely to remain infectious There were no movement restrictions in place for the 2023-2024 winter and is it unlikely for Defra to take future restrictive action against the disease This is because SBV cases that are being detected in new born animals are likely to be as a result of infection in the summer/autumn movement restrictions would likely be ineffective as SBV may already have been transmitted by insects across the country If you are in need of help or support in the aftermath of a Schmallenberg infection on farm there are a number of farming organisations that can help NFU CallFirst is also available for help and advice on farming, legal or technical issues on 0370 845 8458 This page was first published on 31 January 2024 Once you have submitted your query someone from NFU CallFirst will contact you your query will then be passed to the appropriate NFU policy team The information you provide will be used for the purpose of recording and responding to your query. 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Read our cookie policy to learn more Strictly necessary: Strictly necessary cookies serve critical purposes While you have the option to adjust your browser settings to disable these cookies keep in mind that doing so might impact the website’s functionality Functionality cookies: Functionality cookies are cookies that help enhance a website’s performance and functionality functionality cookies can be used to allow video playback or remember a user’s region Analytical/performance cookies: All data gathered through analytical cookies is anonymous and used solely to improve our website’s performance and your user experience Analytical cookies help us understand how you use our website They tell us which pages you visit most frequently They help us create a better user experience for you and all our NFU members Your cookie preferences can be managed in your browser settings disabling analytical cookies may limit your ability to access certain features or receive personalised content Targeting cookies: Our targeting cookies monitor your interactions with websites Horse breeding from planning through foal care Prevention and treatment for problems of the equine foot Discussions about the welfare of our equine friends How to care for the basic health needs of horses All aspects of caring for performance horses Design and maintain a healthy horse operation News and issues for equine health professionals What does it take to optimize the equine immune response and fight off disease EDCC Health Watch 2024 AAEP Convention 2024 EquiSUMMIT 2024 Olympics Our animal behavior experts field your questions about why your horse does XYZ Equine nutritionists respond to queries about forage Veterinarians and researchers tackle questions about equine athletes The Horse’s experts answer your questions during a monthly live audio event Join us as we interview leading equine researchers from the University of Kentucky Checklists and identification forms for horse owners Please login to access None of the antibody-positive horses showed clinical signs of disease Rasehk said it’s possible that the disease had run its course by the time the horses were tested and the antibodies were still present in the system or it’s feasible that horses just don’t develop clinical disease despite infection A recently discovered virus known to infect ruminants in parts of Europe might infect horses as well: Researchers have just identified antibodies to the Schmallenberg virus They are the first horses worldwide to test positive for these antibodies TheHorse.com is home to thousands of free articles about horse health care In order to access some of our exclusive free content Stay on top of the most recent Horse Health news with Seek the advice of a qualified veterinarian before proceeding with any diagnosis Don’t have an account? Register for a FREE account here This website uses cookies so that we can provide you with the best user experience possible Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful Strictly Necessary Cookie should be enabled at all times so that we can save your preferences for cookie settings we will not be able to save your preferences This means that every time you visit this website you will need to enable or disable cookies again Metrics details recurrent epizootics of bluetongue virus and Schmallenberg virus have been reported in the western Palearctic region goats and wild ruminants and are transmitted by native hematophagous midges of the genus Culicoides (Diptera: Ceratopogonidae) Culicoides dispersal is known to be stratified due to a combination of dispersal processes occurring actively at short distances and passively or semi-actively at long distances allowing individuals to jump hundreds of kilometers we aim to identify the environmental factors that promote or limit gene flow of Culicoides obsoletus an abundant and widespread vector species in Europe using an innovative framework integrating spatial population genetics and statistical approaches A total of 348 individuals were sampled in 46 sites in France and were genotyped using 13 newly designed microsatellite markers We found low genetic differentiation and a weak population structure for C Using three complementary inter-individual genetic distances we did not detect any significant isolation by distance but did detect significant anisotropic isolation by distance on a north-south axis We employed a multiple regression on distance matrices approach to investigate the correlation between genetic and environmental distances Among all the environmental factors that were tested only cattle density seems to have an impact on C obsoletus over land found in the present study calls for a re-evaluation of the impact of Culicoides on virus dispersal and highlights the urgent need to better integrate molecular spatial and statistical information to guide vector-borne disease control and little attempt has been made to link the former to environmental factors Given the high dispersal capacity and the stratified dispersal pattern of Culicoides it is crucial to determine inland connectivity among populations and to identify the potential environmental factors that promote or limit gene flows between them Mapping averaged pairwise information (MAPI) allows the visual comparison of genetic dissimilarity with some environmental factors and also the development of working hypotheses it is also necessary to use statistical analyses of genetic and environmental distances as a complement to MAPI The aims of the present study are to determine the inland connectivity of populations of a main vector species at large geographical scales and to identify the environmental factors that promote or limit gene flows between Culicoides populations in France we characterized 13 microsatellite markers dedicated to C We propose a complementary framework integrating multiple approaches which can be applied more generally to the study of gene flow and its links with environmental factors In order to estimate unbiased gene flow of C only individuals identified as such were used for further analyses we selected 3135 primer pairs flanking dinucleotide SSR motifs with a minimum of 12 repeats and amplifying fragments between 150 and 300 bp in length and a half-denaturation temperature close to 55 °C We screened a set of 30 primer pairs and optimized both polymerase chain reaction (PCR) and multiplex PCR conditions followed by a final elongation of 5 min at 72 °C Fragments were separated on an Applied Biosystems 3500xL Genetic Analyzer Allelic size allocations for all individuals and microsatellite markers were performed using the program GeneMapper version 5 (Applied Biosystems Life Technologies) with double blind reading to limit the potential interpretation bias from the reader This ∆K value is a way to determine the inflection in the [ln P(D)] curve The clustering resulting from the Bayesian inference was transposed into percentages of assignment of each individual to the K inferred clusters and plotted on a map GENELAND also uses a Bayesian algorithm to infer population genetic clusters while taking into account the spatial position of individuals making it a spatially explicit clustering method The most probable number of clusters was also determined by running the algorithm with K ranging from 1 to 10 The analysis was based on 1,000,000 MCMC iterations with a thinning of 1000 maximum rate of the Poisson process fixed to 100 maximum number of nuclei in the Poisson-Voronoi tessellation fixed to 300 and a burn-in of 100 We used the R package graphics to produce a distribution map of genetic structure resulting from STRUCTURE and GENELAND analyses geo-referenced grids of environmental values) either treated as potential resistance (R) or conductance (C) factors: The projected distance matrix was calculated for each angle between all sampling sites When calculating the projected geographical distance as a function of the angle between populations dAB is the geographical distance between population A and B and aAB is the angle between populations A and B.  Genetic clustering and genetic differentiation of Culicoides obsoletus Results of the genetic clustering analyses performed with GENELAND (a) and STRUCTURE (b) as well as smoothing of pairwise measures performed with mapping averaged pairwise information (MAPI) and based on (c) Rousset’s (aR) and (d) factorial correspondence analysis (FCA) inter-individual genetic distances A specific color has been assigned to each genetic cluster in a and b d Genetic dissimilarity is represented by a color scale ranging from red (lower genetic dissimilarity) to blue (higher genetic dissimilarity) The black circles indicate the sampling sites no significant association was found between LKC genetic distance and the environmental distances (Q values always < 0) Although our method of analysis seems complementary and coherent for the detection of genetic structure obsoletus is not genetically or geographically structured at the scale of France The most genetically dissimilar individuals were mainly from the southernmost populations of the sampling area Multiple non-exclusive lines of argument might explain the significant anisotropic isolation by distance observed on a north–south axis in France Population sampling at the same scale could allow comparison and estimation of genetic diversity anisotropic isolation by distance may be due to an artifact of the sampling methods used if the extent of the sampling varies depending on direction the distances projected from the angles may represent different distance distributions and lead to the over-representation of the values of strong genetic metrics in the direction of the scatter plot and the hit of positive correlation signals the absence of correlation does not necessarily mean more gene flow but an absence of isolation by distance which can also result from a strong drift and thus less gene flow; a drift which depends on both dispersion and population sizes It is therefore essential to use as a complement—as we have done here and with which we have achieved a similar result—an approach that weights the geographical distances between populations according to their orientation with respect to a given angle axis passing through the barycenter This type of study would make it possible to estimate the effective size of the populations the use of high-throughput sequencing approaches using markers such as double-digest restriction-site associated DNA sequencing can provide greater resolution in view of the large number of single nucleotide polymorphisms (SNPs) revealed at a local scale and improve our understanding of the active and passive dispersal of Culicoides It could also be relevant to include more microsatellite markers or SNPs to improve genetic resolution and observe the matching and assignment of each individual this study provides the first complete landscape genetic analysis of C a major vector species of animal viruses in Europe This study shows that the genetic structure of populations at the scale of a country can become homogeneous through large-scale dispersion a very high inland dispersal and vectorization capacity which has to be taken into consideration in further work on vector competence and epidemiological modeling of disease transmission Wind direction could be a key factor in the dispersal of many insect vector species Futures studies should increase their geographical extent to cover the entire area of species distribution and enable a better understanding of the limits of Culicoides gene flow In addition to the biological information presented here this study highlights several important areas for the improvement of methodologies that may currently limit the inclusion of wind direction in landscape genetic analyses All data generated or analyzed during this study are included in this article and its additional files The newly generated sequences have been submitted to the GenBank database under accession numbers MT828832-MT828844 All the cytochrome c oxidase subunit 1 sequences are available on request A new individual-based spatial approach for identifying genetic discontinuities in natural populations Bluetongue and Douglas virus activity in New South Wales in 1989: further evidence for long-distance dispersal of the biting midge Culicoides brevitarsis Culicoides and the emergence of bluetongue virus in northern Europe Real-time quantitative reverse transcription-PCR assays specifically detecting bluetongue virus serotypes 1 First occurrence of Culicoides obsoletus-transmitted bluetongue 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Ceratopogonidae) in the southeastern United States compared with sequences from Ontario Relative performance of Bayesian clustering software for inferring population substructure and individual assignment at low levels of population differentiation FLOCK provides reliable solutions to the “number of populations” problem Optimizing the trade-off between spatial and genetic sampling efforts in patchy populations: towards a better assessment of functional connectivity using an individual-based sampling scheme Environmental factors influencing the velocity of bluetongue virus serotype 8 epizootic wave in France Host preferences of Palaearctic Culicoides biting midges: implications for transmission of orbiviruses Field observations during the bluetongue serotype 8 epidemic in 2006 case fatality and clinical recovery in sheep and cattle in the Netherlands Re-emergence of bluetongue virus serotype 8 in France Biotic and abiotic factors shape the microbiota of wild-caught populations of the arbovirus vector Culicoides imicola Culicoides (Diptera: Ceratopogonidae) host preferences and biting rates in the Netherlands: comparing cattle (Diptera: Ceratopogonidae) on cattle and sheep in northeast Germany Culicoides chiopterus as a potential vector of bluetongue virus in Europe A new algorithm quantifies the roles of wind and midge flight activity in the bluetongue epizootic in northwest Europe Characteristics of wind-infective farms of the 2006 bluetongue serotype 8 epidemic in northern Europe Founding events in species invasions: genetic variation Comparison of four species-delimitation methods applied to a DNA barcode data set of insect larvae for use in routine bioassessment What we still don’t know about invasion genetics Inferring population decline and expansion from microsatellite data: a simulation-based evaluation of the Msvar method Download references SD and MG are supported by the Fonds National de la Recherche Scientifique (Belgium) AM and MJ have been awarded fellowships from the H2020-727393 PALE-Blu project funded by the EU Ronan Rivallan and Xavier Argout at the Grand plateau technique regional de génotypage in Montpellier France for their help in the development of the microsatellite markers and Aurore Manez for her help in the genotyping Karine Berthier and Marie-Pierre Chapuis for constructive exchanges which helped to improve the relevance of our conclusions The authors are grateful to all the partners who assisted in the Culicoides sampling and shipping We thank William Wint (University of Oxford PALE-Blu partner) for his continued support in extracting and preparing meteorological data This study was partially funded by EU grant H2020-727393 PALE-Blu and by the VectorNet project (OC/EFSA/AHAW/2013/02-FWC1) funded by the European Centre for Disease Prevention and Control (ECDC) and the European Food Safety Authority (EFSA) The contents of this publication are the sole responsibility of the authors and do not necessarily reflect the views of the European Commission Ignace Rakotoarivony & Maïa de Wavrechin Institut Agronomique et Vétérinaire Hassan II TB contributed to the collection of Culicoides samples and IR and MD contributed to the identification of Culicoides and MW performed the molecular biology manipulations SD and MJ developed the techniques and workflow for the landscape genetics analysis the first draft of which was written by AM All the authors read and approved the final manuscript The authors declare that they have no competing interests Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations Sampling sites and associated genetic diversity Reference sequences used for specific assignation Origin and numbers of individuals used to build up the DNA library necessary for the development of the microsatellite markers Primers of the 13 microsatellite markers used to genotype C TFm half denaturation temperature in degrees Environmental variables tested as potential factors that could impact inter-individual genetic differentiation of C obsoletus in France (raster cell resolution: 0.04 arcmin) Map of wind direction averaged from 2000 to 2010 Sampling sites are represented by black points The color scale represents the wind direction from 0 to 360 ° from north The arrowheads indicate the exact wind direction of each raster pixel Isolation by distance analyses: density plots Mantel tests and linear regressions performed with each inter-individual genetic distance considered in this study Identification of the optimal number of genetic clusters (K) inferred by STRUCTURE using the δ(K) and L’(K) methods Population genetic structure results by clustering analyses performed STRUCTURE A specific color has been assigned to each inferred genetic cluster Results of univariate analyses: determination coefficients (R2) estimated from univariate regressions between genetic and environmental distances [C] indicates that the considered environmental raster was treated as a conductance factor for the computation of environmental distances with circuit theory [R] indicates that the considered environmental raster was treated as a resistance factor for the computation of environmental distances with circuit theory Q Difference between environmental multiple regression on distance matrices (MRDM) R2 and null raster MRDM R2 The results for K = 10 are not shown as they were non-significant Bar plots of population genetic structure results by clustering analyses performed by STRUCTURE for K = 2 and K = 4 unless otherwise stated in a credit line to the data Download citation DOI: https://doi.org/10.1186/s13071-020-04522-3 Anyone you share the following link with will be able to read this content: a shareable link is not currently available for this article Testing undertaken by the Regional Veterinary Laboratories (RVLs) and prompted after the receipt of a number of reports of milk drop syndrome in dairy herds this summer has confirmed the circulation of Schmallenberg virus (SBV) in some herds A statement released by the National Disease Control Centre of the Department of Agriculture Food and the Marine on September 25 read: “The RVLs have received a number of reports of milk drop syndrome in dairy herds this summer A high rate of seropositivity to Schmallenberg virus (SBV) has been found in the samples submitted from some of these herds.” it notes that some of the clinical signs included milk drop pyrexia (raised temperature) and apparent pregnancy loss although not all clinical signs were present in all affected animals The National Disease Control Centre also confirmed that many of the positive animals had been born since 2018 which is when the virus is thought to have most recently circulated in Ireland and indicates more recent re-emergence of the virus It urged care when interpreting single serology (blood test) results the virus itself has been detected or very recent infection has been diagnosed using paired serology tests around the same time the clinical signs occurred suggesting that SBV was responsible” the National Disease Control Centre offered the following: “Animal keepers should be vigilant for the clinical signs described and consult their veterinary practitioner for advice if they are seen.” Metrics details Schmallenberg virus (SBV) is transmitted by insect vectors and therefore vaccination is one of the most important tools of disease control novel subunit vaccines on the basis of an amino-terminal domain of SBV Gc of 234 amino acids (“Gc Amino”) first were tested and selected using a lethal small animal challenge model and then the best performing formulations also were tested in cattle coli expressed nor the reduced form of “Gc Amino” protected from SBV infection immunization with “Gc Amino”-encoding DNA plasmids and “Gc-amino” expressed in a mammalian system conferred protection in up to 66% of the animals the best performance was achieved with a multivalent antigen containing the covalently linked Gc domains of both All vaccinated cattle and mice were fully protected against SBV challenge infection in the absence of antibodies against the viral N-protein differentiation between vaccinated and field-infected animals allows an SBV marker vaccination concept the presented vaccine design also could be tested for other members of the Simbu serogroup and might allow the inclusion of additional immunogenic domains This has been discussed as a possible basis of effective vaccines against SBV as well as against related orthobunyaviruses by using the corresponding genomic regions such a domain further represents a promising subunit marker vaccine candidate since antibodies against the N protein would be induced by an SBV field infection and not by vaccination with the Gc domain and several validated commercial N-based ELISA tests are available which could be used as companion test system until now it is not known how the domain must be presented or expressed in order to correctly present the key immunogenic domains different approaches were selected: (I) DNA immunization; (II) protein expression in E coli and a mammalian expression system to examine the influence of glycosylation and other posttranslational modifications; (III) immunization with the non-reduced and the reduced form of the protein to evaluate the influence of disulfide bonds; and (IV) the influence of additionally attached domains and thereby potential use as multivalent vaccines The Phusion HF DNA polymerase used for the PCR and the enzymes applied for cloning were obtained from New England Biolabs (Frankfurt am Main A PCR product using the plasmid encoding for SBV-Gc Amino as template was generated with the oligonucleotides AATTATTCCATGGGTATCAACTGCAAGAACATCCAGAGCACC (restriction sites in bold) and TAATAACTCGAGAATCAGGCTCAGGGTGGTCAGGGTC and subsequently digested with NcoI and XhoI and ligated to the plasmid pGRS-79_Ulm (Roman-Sosa unpublished) which was also treated with these enzymes The plasmid was checked by sequencing with the oligonucleotides T7 promoter (TAATACGACTCACTATAGGG) and T7 terminator (GCTAGTTATTGCTCAGCGG) SBV-Gc Amino was used without affinity tag A PCR product was generated with the oligonucleotides AATTATTGCTAGCGCCACCATGGAGACAGACACAC and ATAAAtctagaCTAAATCAGGCTCAGGGTGGTCAG and the plasmid encoding for SBV-Gc Amino as a template Subsequently the PCR product was restriction digested with NheI/XbaI before being ligated to the pCI Mammalian Expression Vector (Promega Germany) also processed with these enzymes The plasmid was checked by sequencing with the primers pCI-fwrd (CCTTTCTCTCCACAGGTGTCCACTCC) and pCI-rev-A (AGCATTTTTT TCACTGCATT CTAGTTG) the plasmid was digested with HindIII and XbaI and the fragment was ligated to the plasmid pEXPR-IBA-103 (IBA which was also processed with the same enzymes A PCR product was generated with the oligonucleotides ttattaaCATATGGATGCTCAGGTCGGGCCGG and AATTATTTCTAGAGCCACCATGGAGACAGACACAC using the plasmid encoding for AKA-Gc Amino as template The DNA fragment was digested with NheI and XbaI and ligated to the plasmid pSignalSeq also processed with these enzymes the plasmid was digested with XbaI and KpnI and the fragment was ligated to pGRS-19 (Roman-Sosa unpublished) which also was restriction digested with these enzymes The plasmids for the constructs AKA-Gc Amino and AKA-Gc Amino-SBV-Gc Amino were controlled by sequencing with the primers pEXPR-fwrd (GAGAACCCACTGCTTACTGGC) and pEXPR-rev (TAGAAGGCACAGTCGAGG) To generate the vaccine SBV-Gc Amino red the protein SBV-Gc Amino was treated with 10 mM DTT and 0.2% Triton X-100 (v/v) in buffer W (100 mM Tris-HCl pH 8.0 and the cysteines were alkylated with 10 mg/ml iodoacetamide for 15 min at 37 °C All protein concentrations were determined using Bradford reagent (BioRad and aliquots were stored at −80 °C until use the N-terminal 234 residues of SBV Gc were ligated to the pCI Mammalian Expression Vector (Promega Germany) and used directly for immunization of mice (SBV-Gc Amino (DNA)) For immunization of mice with proteins GERBU ADJUVANT MM (GERBU Biotechnik GmbH, Heidelberg, Germany) and for immunization of cattle POLYGEN™ (MVP Technologies, Omaha, USA) were used as adjuvants. All vaccines are listed in Table 1 The results were expressed as the percentage of the sample OD relative to the positive control OD (S/P*100) Micro-neutralization tests against SBV or AKAV were performed as described previously19 Evaluation was done by assessment of the cytopathic effect after 3 days All samples were tested in quadruplicate and the antibody titers were calculated as ND50 according to Behrens and Kaerber The nitrocellulose membranes were incubated with cattle sera diluted 1/100 in PBS-Tween (0.1% Tween20) overnight at 4 °C followed by an incubation with a horseradish peroxidase-conjugated anti-bovine antibody (Dianova Germany; diluted 1/20 000 in PBS-Tween) for 1 hour at RT Beta Actin was detected using an anti-Beta Actin monoclonal antibody (1/10 000 Germany) and a peroxidase-conjugated anti-mouse antibody (1/10 000 Proteins were visualized using the Super Signal West Pico Chemiluminescent substrate (Thermo Scientific Germany) and analyzed by the Intas ChemoCam System (Intas Science Imaging Instruments GmbH The experimental protocols were reviewed by the responsible state ethics commission and were approved by the competent authority (State Office for Agriculture Food Safety and Fisheries of Mecklenburg-Vorpommern All experiments were performed in accordance with relevant guidelines and regulations This SBV strain represents the most suitable challenge material for the used small animal model since it turned out to be of very high virulence for IFNAR −/− mice the copy number per mg of the corresponding organ sample was calculated Blood samples taken at autopsy were additionally analyzed by in-house ELISAs The animals were euthanized four weeks after challenge infection rectal body temperatures were measured daily and the animals were examined for clinical signs by veterinarians Two animals each of groups C01 and C03 and three cattle of groups C02 and C04 suffered from trichophytia and were treated with TRICHOVAC LTF 130 (IDT Biologika Animal Health and 3× group C04) received antibiotics (Baxyl LA 200 [Veyx-Pharma GmbH Germany] and Metapyrin [Serumwerk Bernburg AG Sera were taken at weekly intervals throughout the study and analyzed by a microneutralization test against SBV isolate BH80/11 a commercially available N-based ELISA (ID Screen® Schmallenberg virus Competition and in-house ELISAs against the proteins used for immunization Sera from unvaccinated control animals were tested against all proteins used for immunization of the other animal groups and against AKA-Gc Amino in in-house ELISAs Sera of group C03 (AKA-Gc Animo-SBV-Gc Amino) taken on the days of vaccination and three weeks after the second immunization were analyzed additionally by a standard microneutralization test against AKAV and sera obtained 4 weeks after challenge infection from cattle of groups C01 mandibular and mesenteric lymph nodes and analyzed by real-time PCR Body weight after challenge infection of mice with SBV and real-time PCR results of blood samples taken 2 and 7 days after infection Sera taken from the control animals (pCI-vector and environmental control mice) were tested against all three antigens; with the exception of the only mouse of group M08 which survived the challenge infection, no reaction to any of the antigens was observed (Supplementary Fig. 3) All sera of group C03 (vaccine AKA-Gc Amino-SBV-Gc Amino) taken on the day of the first vaccination scored negative in the neutralization test against AKAV On the day of the second immunization two animals tested negative and two positive (neutralizing titers 1/10 and 1/7) and three weeks after the second vaccination neutralizing antibodies against AKAV were detectable in all four cattle (titers 1/17 None of the cattle showed any relevant SBV-specific clinical signs during the entire study The results of individual animals in each group are depicted in different colors; the identical colors are used in the corresponding panels of Figs 2 and 3 In all animals without detectable viraemia also the organ samples tested negative by real-time PCR whereas in every viraemic cattle SBV genome was found in at least one organ sample (Ct values ranging from 30.4 to 40.5) none of the established SBV vaccines enables differentiation of vaccinated from field-infected animals (DIVA) coli expression system was included in the present study mice vaccinated with proteins expressed in E.coli did not develop a detectable immune response and were not protected against virulent virus challenge This indicates that correct glycosylation is of vital importance for the antigenicity and immunogenicity of the SBV-Gc-Amino domain rendering E.coli an unsuitable expression system which in the present study resulted in a similar performance of the HEK-cell expressed Gc-domain and the DNA-mediated vaccine in immunized mice indicating correct presentation of the antigen in both delivery systems as demonstrated by the loss of immunogenicity upon reduction the maintenance of disulfide bonds within the Gc-Amino domain seems to be crucial for correct presentation of the antigen it must be anticipated that in the present study the key immunogens most likely the aminoterminal domain of Gc were not completely accessible using the SBV-Gn-L-Gc construct There might be a negative interaction with the Gn component of this construct the sterile protection conferred by the AKA-Gc Amino-SBV-Gc Amino construct is most likely exclusively caused by the immunogenic SBV domain Gc-Amino and its optimized presentation or stabilization by the linked AKAV domain The suitability of the IFNAR −/− mouse model for SBV vaccination studies was demonstrated in direct comparison with cattle showing equal results in both animals species partial protection by SBV-Gc-Amino and SBV-Gn-L-Gc expressed in mammalian cells and complete sterile immunity conferred by AKA-Gc Amino-SBV-Gc Amino in cattle and in mice This makes the selected mouse model a handy and versatile tool for SBV vaccine research Especially as vaccination and challenge experiments in ruminants are complicated due to the need of adequate high containment housing the mouse model facilitates direct comparison of different vaccine delivering systems and/or expression systems the double-construct AKA-Gc Amino-SBV-Gc Amino completely prevented viremia in all vaccinated cattle and mice after subsequent challenge infection with virulent SBV making it an efficient and safe candidate vaccine it enables differentiation between vaccinated and field-infected animals using the detection of the SBV-N-protein by commercial antibody ELISAs The approach of this study additionally demonstrated that novel safe and efficient vaccines can be produced very quickly without the necessity to handle the infectious virus during the production process which is an advantage compared to the currently available inactivated or live attenuated vaccines The identification of key immunogenic domains and their crucial structural 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work was in part financially supported by the Zoonoses Anticipation and Preparedness Initiative (ZAPI 115760) within the Innovative Medicines Initiative (IMI Call 11 - IMI-JU-11-2013-04) Conceived and designed the experiments: K.W. Contributed reagents/materials/analysis tools: K.W. All authors read and approved the final manuscript The authors declare no competing financial interests Download citation Sign up for the Nature Briefing: Microbiology newsletter — what matters in microbiology research Metrics details an arthropod-transmitted pathogenic bunyavirus continues to be a threat to the European livestock industry causing morbidity and mortality among young ruminant livestock based on bacterially expressed SBV nucleoprotein (SBV-N) administered with a veterinary-grade Saponin adjuvant SBV-N with Saponin induced strong non-neutralizing broadly virus-reactive antibodies Vaccination assays also suggest that this level of immune protection is cell mediated as evidenced by the lack of neutralizing antibodies as well as interferon-γ secretion observed in vitro co-administered with veterinary-grade Saponin adjuvant may serve as a promising economical alternative to current SBV vaccines and warrant further evaluation in large ruminant animal models we propose that this strategy may be applicable to other bunyaviruses where only 20% of UK livestock producers reported previously using SBV vaccines but 80% would consider doing so if SBV vaccines were priced at 1 (British) pound per dose the idea of a simpler and more cost-effective SBV subunit vaccine has yet to be explored It is with these financial constraints in mind that we propose to generate a more economical SBV vaccine based on our previous findings that SBV nucleoprotein does have immunoprotective properties based on a potent CD8+-T-cell response recombinantly expressed SBV-N can augment a cell-mediated immunological response against virulent SBV infection The ability of these vaccines to protect against virulent SBV has been evaluated using interferon α/β (IFNAR) knockout mice a small-animal model that has previously been shown to validate SBV vaccine candidates Correlates of protection can be observed through increased broadly virus-reactive titers decreased clinical signs and near undetectable levels of viremia These results suggest that a more cost-efficient subunit vaccine can be generated which would be of practical interest to livestock producers taken from IFNAR-/- A129 mice following two vaccinations Each point indicates the mean value of each group at 450 nm The one-sided error bars at each point represent the standard deviation Each of the diluition shows statistical significance as determined using a one-way ANOVA test In order to assess the degree of humoral immunity induced by the different vaccine candidates the above mentioned sera were also titered for broadly virus-reactive neutralizing antibodies no serum from any experimental group exhibited any detectable levels of neutralizing titers (data not shown) Dot plot measuring the change in weight of all six vaccinated groups following challenge with virulent SBV The histograms show the mean weight of each group with the error bar as the standard deviation from the mean and symbols (black circle triangle etc.) the individual weight measurements within each group The green horizontal line denotes the average weight of each group prior to SBV challenge (day 0) Although no statistical significance was found in weight changes after vaccination in each group three out of the four control groups experienced the death of at least one mouse Red crosses (†) denote the death of a mouse at a given timepoint Viremia of A129 mice following viral challenge with virulent SBV. Blood from each vaccinated mouse was taken at 3, 6, 10 and 13 dpi. RNA was extracted from 100 µl of blood, and eluted in the same volume using the extraction technique described in the “Materials and methods” section Values presented are the number of SBV genome copies/ml Error bars are presented as the standard deviation from the mean Cellular proliferation of splenocytes from vaccinated IFNAR-/- A129 mice. Splenocytes were extracted from mice vaccinated with one of the following: 1) SBV N; 2) SBV N + Saponin; 3) GFP, or; 4) GFP + Saponin. Splenocytes from each mouse were then incubated with CFSE (see “Materials and methods” section) and stimulated with inactivated SBV for 3 days The cells were then fixed and incubated with either CD4 (a) or CD8-specifc (b) antibodies and the proliferation index (average number of divisions of just the responding cells) quantified by flow cytometry The cell proliferation index is presented as the value of stimulated splenocytes (i.e in the presence of antigen) minus that of splenocytes under non-stimulating conditions Secreted IFN-γ from splenocytes of vaccinated IFNAR-/- A129 mice Splenocytes were extracted from mice vaccinated with one of the following: 1) SBV N; 2) SBV N + Saponin; 3) GFP The cells were then isolated and stimulated ex vivo using inactivated SBV Detection of secreted IFN-γ was measured using ELISA and measured using a spectrophotometer at 450 nm its lack of putative N-linked glycoproteins suggests that most of its biological properties could be retained when recombinantly expressed in bacteria morbidity and mortality upon BH619/12 challenge were not reliable indicators of vaccine efficacy viremia assessment offered a more accurate estimation of the protective capabilities of these vaccines since: (a) it could also be readily expressed in bacteria and; (b) it had a similar molecular weight to SBV-N we measured the presence of broadly virus-reactive antibodies from the serum of all vaccinated animals Although mice in the SBV-N group were able to induce a high-level of broadly virus-reactive antibodies the SBV-N + Saponin group was able to induce a higher level of SBV-antibody titers IgG isotyping of the vaccinated mice also showed that in SBV-N (with or without Saponin) generated primarily IgG1 immunoglobulins; these results would be consistent with a Th1 response the contribution of Saponin in increasing the immunogenicity of SBV-N was confirmed through cell-proliferation assays where the SBV-N + Saponin group displayed greater CD4 + and CD8 + T-cell proliferation relative to the SBV-N group (and the GFP negative control groups) the results were not able to reach statistical significance Other factors may have also contributed to this which include the lack of optimized in vitro cell proliferation conditions as well as the possibility that the stimulated T-cells were located outside the spleen (i.e both the SBV-N and SBV-N + Saponin were capable of inducing IFN- γ secretion; however as in the case of the cell-proliferation assay the small sample size prevented the data from being statistically significant we looked for clinical signs normally associated with SBV infection in IFNAR-/- mice (i.e we found that unprotected mice showed a decrease in weight of approximately 5% within 7 days when challenged with SBV 80/11-4 strain when using the more virulent SBV BH619/12 strain no statistically significant changes in weight loss were observed in any groups These findings were further confirmed when viremia was measured following SBV challenge Mice in the SBV-N + Saponin group showed significantly less presence of SBV with an undetectable presence of the virus at days 10 and 13 in combination with a veterinary grade Saponin can be an efficient vaccine candidate against SBV infection These findings are consistent with results from our previous study where DNA vaccines were designed based on ORFs of the SBV genome While we found two candidates (SBV-N and SBV-Gc ecto-1) we decided to pursue using SBV-N as a subunit vaccine based on its ability to be readily expressed in E where large-scale production can be used to produce a more economically practical vaccine candidate and we have determined that for our experiments in mice each experimental dose costed approximately 0.07 € were found to have CD8 + T-cells that could secrete IFN-γ years after infection (by ELISpot in response to peptide stimulation) thereby confirming the role that these cells have in the host immune response Based on our results with bacterially-expressed SBV nucleoprotein we hypothesize that other recombinant bunyaviral nucleoproteins may have immunoprotective properties when administered with an appropriate adjuvant to definitively evaluate SBV nucleoprotein’s ability to confer protection against viral challenge and to validate the efficacy of SBV nucleoprotein when co-administered with Saponin further vaccination studies are required using large ruminant animal models The Schmallenberg virus strain BH619/12 (7th culture passage) was provided by the Friedrich-Loeffler-Institute (FLI) through the European Virus Archive (EVA) and dilutions of the virus stock were used directly for all subsequent mouse experiments The mice used in the vaccination experiments were A129 IFNAR α/β-/- (B & K Universal Ltd All animal experiments using SBV were performed at the BSL3 animal facilities of NEIKER Institute (Derio Spain) or the BSL3 + animal facilities at CISA/INIA (Madrid with all proposed experiments (including containment vaccination viral challenge and euthanasia) adhering to the ethical guidelines for animal care and experimentation and having received institutional approval (see below) the GFP was excised from the aforementioned vector and the cDNA of SBV nucleoprotein (Genbank accession number H2AM13) was ligated into the vector through the AgeI/XhoI restriction sites Subunit vaccine candidates were expressed in E.coli BL21 with colonies being selected on LB-Kanamycin plates at 37 °C Individual colonies were then cultured in LB broth with Kanamycin (50 µg/mL) and induced with 1 mM IPTG for 12 h at 30 °C Each clarified cell lysate in non-denaturating and non-reducing conditions [1X phosphate-buffered saline (PBS) buffer with EDTA-free protease inhibitor cocktail] was incubated with Ni-NTA resin (ThermoFischer) in batch mode at 4 °C for two hours Then protein-bound resin was eluted with 1X PBS buffer supplemented with 500 mM imidazole (Sigma-Aldrich) Eluted proteins were then further purified through an additional step of size-exclusion gel-filtration chromatography using a HiLoad 16/60 Superdex 200 pg column (GE Healthcare) pre-equilibrated in 1 X PBS for the SBV-N and a Superdex 16/60 75 pg column (GE Healthcare) for the GFP The changes in weights (as well as all hereafter generated data) were analyzed for statistical significance using a one-way ANOVA test (see below) was added starting at a 1:1 × 103 dilution and serially diluted to 1:2048 × 103 The plates were incubated for 1 h at 37 °C The plates were washed 3 times with PBS/0.1% Tween 20 and incubated with HRP-conjugated anti-mouse IgG (Sigma Following another three washes with PBS / 0.1% Tween the plates were developed with 1-Step Ultra TMB substrate solution (Fisher Scientific then stopped with one volume of 2 M sulfuric acid and the absorbance measured at a 450 nm ELISA plates were coated for 2 h with 5 µg/mL previously purified SBV nucleoprotein at room temperature and blocked with PBS/0.1% Tween 20 2% BSA overnight at 4 °C Heat inactivated sera samples harvested two weeks after the last vaccination from mice belonging to the groups 1 2 and 6 were added on duplicates serially diluted at 1:10 and 1:100 After 1 h incubation at 20 °C the plates were washed 4 times with PBS / 0.1% Tween 20 and incubated with HRP-conjugated secondary goat anti-mouse IgG1 Following another 4 washes with PBS/0.1% Tween and one wash with PBS the reaction was stopped with one volume of 2 M sulfuric acid and the absorbance measured at a 450 nm sera collected from vaccinated mice were serially diluted The mixtures were added to BHK-21 cells in a 96-well plate and monitored for cytopathogenic effect (CPE) after 4 days control sera from both SBV-convalescing sheep as well as uninfected sheep were used as positive and negative controls respectively (with both sera being a kind gift from Dr During the SBV viral challenge 100 µl of blood was collected at 3 RNA was extracted using the Paramagnetic Beads RNA extraction kit (Life River China) according to the manufacturer’s instructions The presence of SBV RNA was detected using the SBV dtec-RT-qPCR kit (Genetic PCR Solutions Spain) using 5 µl of the extracted RNA samples Real-time PCR was performed on an Agilent 3005 P Real-time PCR system and the HEX channel to measure the internal controls provided by the manufacturer The thermal profile used was as follows: 50 °C for 10 min followed by 40 cycles of the following: 95 °C for 10 s and 60 °C for 60 s Phytohaemagglutinin (PHA) was used as a positive control at 5 µg/mL whereas the negative control used was medium without antigen The plates were incubated for 3 days at 37 °C at 5% CO2 immunostained for CD8 and CD4 (PE-anti-CD8a and APC-anti-CD4 Data were acquired using FACScalibur (BD Bioscience USA) and analyzed using FlowJo v10.6.1 software This software enables for the evaluation of the green fluorescence of the CFSE was used to determine the proportion of dividing cells within each CD4 + and CD8 + cell population Splenocytes from the cellular proliferation assay also served to quantify secreted IFN-γ inactivated SBV) used were identical to the conditions used for the cell proliferation assays 96-well High Binding Costar 3590 were coated with 2 µg/ml of anti- IFN- γ capture antibody AG-18/RA-6A2 (BD Pharmingen) the wells were washed two times with PBS/0.05% Tween 20 and blocked with PBS/0.05% Tween/0.1% BSA for 1 h at 37 °C 50 ul of supernatant was added to each well and incubated for 1 h at 37 °C The plates were then washed with PBS / 0.05% Tween and incubated with 1 mg/ml of anti- IFN- γ biotinylated mAb R46A2 (BD Pharmingen) for 1 h at 37 °C plates were washed with PBS / 0.05% Tween and 50 µl of peroxidase-labeled streptavidin at a 1/500 dilution in PBS added to each well and incubated at 37 °C for 1 h and the TMB substrate (Sigma-Aldrich) was added for 10 min followed by one volume of stopping solution (0.5 M sulfuric acid) The one-way analysis of variance (ANOVA) was used to assess whether there are any statistically significant differences between the resulting means of the different experiments when more than two groups were considered When analysis was performed across two groups only [eg SBV-N versus PBS (control)] then the unpaired t-test with Welch’s correction was used to take into account the unequal variance and possible sample sizes To this end we used GraphPad PRISM version 8.4.2 The study was approved by the Diputacíon Foral de Bizkaia 12/2018 for experiments carried out at the NEIKER-Basque Institute for Agricultural Research and Development and by the Comunidad de Madrid permit PROEX 108/15 for research performed at the Animal Health Research Center (INIA-CISA) All experiments were monitored by staff veterinarians and animals that exhibited severe signs of morbidity were euthanized by cervical dislocation Generation of recombinant oropouche viruses lacking the nonstructural protein NSm or NSs Schmallenberg virus: a novel viral disease in northern Europe Natural intrauterine infection with Schmallenberg virus in malformed newborn calves The emergence of Schmallenberg virus across Culicoides communities and ecosystems in Europe First detection of Schmallenberg virus in elk (Alces alces) indicating infection of wildlife in Bialowieza National Park in Poland Detection of the Schmallenberg virus in nulliparous Culicoides obsoletus/scoticus complex and C punctatus—the possibility of transovarial virus transmission in the midge population and of a new vector First report of Schmallenberg virus infection in cattle and midges in Poland Larska, M., Krzysiak, M. K., Kesik-Maliszewska, J. & Rola, J. Cross-sectional study of Schmallenberg virus seroprevalence in wild ruminants in Poland at the end of the vector season of 2013. BMC Vet. Res. https://doi.org/10.1186/s12917-014-0307-3 (2014) Mouchantat, S. et al. A broad spectrum screening of Schmallenberg virus antibodies in wildlife animals in Germany. Vet. Res. https://doi.org/10.1186/s13567-015-0232-x (2015) Spatial and temporal patterns of Schmallenberg virus in France in 2016 Schmallenberg virus: on its way out or due for a comeback? How is Europe positioned for a re-emergence of Schmallenberg virus? Survey to determine the farm-level impact of Schmallenberg virus during the 2016–2017 United Kingdom lambing season Viruses versus vaccines: the economics of herd immunity British Society of Immunology (BSI): Newsletter (2018) DNA vaccination regimes against Schmallenberg virus infection in IFNAR(-/-) mice suggest two targets for immunization N-terminal domain of Schmallenberg virus envelope protein Gc delivered by recombinant equine herpesvirus type 1 and modified vaccinia virus Ankara: immunogenicity and protective efficacy in cattle Crystal structure of Schmallenberg orthobunyavirus nucleoprotein-RNA complex reveals a novel RNA sequestration mechanism Structure of Schmallenberg orthobunyavirus nucleoprotein suggests a novel mechanism of genome encapsidation Nucleocapsid protein structures from orthobunyaviruses reveal insight into ribonucleoprotein architecture and RNA polymerization Elucidating the mechanisms of action of saponin-derived adjuvants Wernike, K., Eschbaumer, M., Breithaupt, A., Hoffmann, B. & Beer, M. Schmallenberg virus challenge models in cattle: infectious serum or culture-grown virus?. Vet. Res. https://doi.org/10.1186/1297-9716-43-84 (2012) Adjuvants enhancing cross-presentation by dendritic cells: the key to more effective vaccines? Rift valley fever: recent insights into pathogenesis and prevention A DNA vaccine encoding ubiquitinated Rift Valley fever virus nucleoprotein provides consistent immunity and protects IFNAR(-/-) mice upon lethal virus challenge Long-lived CD8+ T cell responses following Crimean-Congo haemorrhagic fever virus infection Comparison of SUMO fusion technology with traditional gene fusion systems: enhanced expression and solubility with SUMO Protection against lethal Rift Valley fever virus (RVFV) infection in transgenic IFNAR(-/-) mice induced by different DNA vaccination regimens Download references We would like to thank the European Virus Archive (EVAg) https://www.european-virus-archive.com/evag-portal and the laboratory of Dr Martin Beer for providing us with the FLI Schmallenberg virus strain BH 619/12 and the control sera Belén Borrego (CISA-INIA) for her assistance This work was supported by the Marie Sklodowska Curie Actions programme number MSCAIF-EF-ST-660155 (H.B Innovación y Universidades RTI2018-095700-B-I00 (N.G.A.A.) the Basque Departamento de Desarrollo Económico e Infraestructura 37-2017-00036 (N.G.A.A.) and “La Caixa” Foundation (ID 100010434) INPhINIT “La Caixa” fellowship LCF/BQ/DI19/11730041 (G.S.G MICINN is also thanked for the Severo Ochoa Excellence Accreditation to the CIC bioGUNE (SEV-2016-0644) Fundamental and Applied Research for Animals & Health (FARAH) Center for Cooperative Research in Biosciences (CIC bioGUNE) Basque Research and Technology Alliance (BRTA) NEIKER-Basque Institute for Agricultural Research and Development Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd) performed diagnostic work together with I.S. and generated purified Schmallenberg virus produced recombinant proteins with help from D.C.; G.L performed the cell proliferation and cytokine assays with help from S.M.; A.B. prepared the manuscript with contributions from all authors The authors declare no competing interests Download citation DOI: https://doi.org/10.1038/s41598-020-73424-2 Metrics details A model previously developed for the wind-borne spread by midges of bluetongue virus in NW Europe in 2006 is here modified and applied to the spread of Schmallenberg virus in 2011 The model estimates that pregnant animals were infected 113 days before producing malformed young the commonest symptom of reported infection and explains the spatial and temporal pattern of infection in 70% of the 3,487 affected farms most of which were infected by midges arriving through downwind movement (62% of explained infections) or a mixture of downwind and random movements (38% of explained infections) dusk) when these insects are known to be most active The main difference with Bluetongue is the higher rate of spread of SBV which has important implications for disease control Spatial distribution of SBV from 2011 to 2012 (a single SBV infection in southern Spain is not shown) and of BTV-8 in 2006 the data shown are for the first 121 days of both outbreaks (the full extent of the BTV epizootic in 2006) The inset shows the details of the BTV-8 area but horizontal (direct animal to animal) transmission is unknown strongly implying that midges respond to the smell of their hosts by flying upwind to find them the modal distance covered in farm-to-farm infections was no more than 1 km31 and upwind infections were associated with shorter average distances between infectious and infected farms than downwind ones Here we present a modified version of BTV-SWOTS31 to analyse understand and simulate the spread of SBV in Europe in 2011–2012 (SBV-SWOTS) The results of BTV-SWOTS and SBV-SWOTS are compared in order to detect and explain similarities and differences between these two diseases Following previous practice31 we here use the term ‘vector’ only in its mathematical sense and the term ‘midges’ to describe both the insects and their role as carriers of both BTV and SBV The term ‘midge vector’ therefore refers to a mathematical description of the distance and direction of midge flight Both BTV-SWOTS and SBV-SWOTS were implemented using a high threshold probability (a ratio > = 0.95 of the number of trajectories connecting a particular infectious farm A to a newly infected farm B over the total number of infectious trajectories reaching farm B in the same interval of time) indicating that any particular farm had been infected from one particular previously-infected farm Farms that did not reach this threshold were considered as unlikely to have been infected by any putative ‘source farm’ within the dataset This high threshold excluded very few farms in the BTV-SWOTS analysis (8%) strongly indicating that a network of (modelled and quantified) infection routes linked most farms in the dataset This relatively high certainty of the infection network probably arose because of the relatively short distances (many less than 1 km) between the BTV-infected farms in the landscape the same high probability threshold excludes 30% of SBV-infected farms probably because these farms were farther apart (the average distance between all infected farms in the dataset is 461 km with standard deviation = 255 km) and so less likely to fall within the plumes of infected midges arising from previously infected farms the SBV simulation model successfully connected 70% of all infected farms This figure rises as the threshold probability is lowered from 0.95 but reaches a maximum of 89% only when the threshold is lowered to 0.13 SBV-SWOTS is still unable to explain 11% of all infections Classification of the SBV infected farms according to the type of midge movement involved 55% of the infected farms in the dataset were predicted by the model to be ‘dead ends’ (i.e so that less than half of all farms were involved in infecting other farms There was no significant change during the post 100-day period in either the average or maximum distance between infected farms Nuances of midge behaviour that are likely to increase the chance of locally contacting the next host for a blood meal appear to be constrained by the envelope of the prevailing winds at the time of day Thus if a farm reported an SBV- malformed newborn lamb on the 14th December 2011 (the first case in our dataset) the infectious bite would have occurred on about the 24th August 2011 If SBV is similar in this respect to Akabane then cattle would be susceptible to SBV over a range of DA from 100 to 190 days: more than half of this period would therefore be covered by the SBV-SWOTS allowed maximum value of 155 days is likely to be more difficult to explain with SBV-SWOTS The present results suggest that disease events that happen a long time before their recorded outcome are amenable to the same sort of analysis as was previously applied to BTV with a much shorter time between cause and effect We stress that all values of DA between 0 and 155 days were explored by the SBV model which selected a rather precise value of 113 days as the most likely time of infection before the recorded outcome which Midge mobility revealed by the example of SBV and analysed by SBV-SWOTS suggests that Control and Protection Zones need to be considerably bigger making the control of midge borne diseases that much more difficult latitude (GPS co-ordinates) and date of the report of the infection at each farm were used in the analysis SBV was declared notifiable in Germany and the Netherlands only from the end of March 2012 but in fact Germany had been contributing SBV case Reports to the OIE since the start of the outbreak and the number of new cases reported there from the end of March shows little change from those reported before this time (thus 2% of all of the 1376 cases from Germany between December 2011 and May 2012 were reported in December 2011 seems to show a distinct effect of the notification order The Dutch reports in May 2012 (173 cases) will have contributed in only a minor way to the parameter estimates in SBV-SWOTS (which were based on all of the 3,487 case reports) and none of them was explained in the simulation part of the SBV-SWOTS analysis were not included because they occurred outside the period analysed (see above) Both databases undoubtedly suffer from missing data but there are relatively minor differences between them Thus differences between the management of the BTV-8 and SBV outbreaks (movement restrictions were never imposed for SBV) are slight and the datasets can be directly compared 11% of the data used in this analysis were of SBV cases not associated with foetal abnormalities 35% as foetal abnormalities in cattle and almost 2% as foetal abnormalities in goats (only one case was reported from deer) DT = days travelled by the midges between infectious and infected farms Unlike time-dependent differential models of epidemic spread (where identification of the location and timing of the index case is often crucial) SWOTS adopts more of a ‘mass action’ approach; estimated (averaged) parameter values apply to the entire dataset over the entire course of the outbreak and each disease report makes a more or less equal contribution to the parameter estimates The parameters and variables to be optimised by the SBV-SWOTS are the day of infection after fertilisation of the vertebrate host (see below) the number of days of midge travel from farm to farm (days travelled DT) and the time of day (TOD) associated with the largest correlation between infection and midge vectors (in nature SBV-SWOTS then simulates the outbreak by re-calculating the midge vectors according to the optimised parameters and a stochastic wind field assuming pre-defined distributions for wind angle and speed centred on their modelled mean values Sampling from distributions of both wind speed and direction is necessary because the wind can show considerable variation in these variables within a few hours Wind trajectories were recalculated 1,000 times with values of speed and direction drawn from their respective mathematical distributions Hence each infected farm in each interval in SBV-SWOTS is associated with many different possible infected midge trajectories going from it Some of these trajectories will end up on uninfected farms and eventually infect them SBV-SWOTS examines the associations between these calculated midge vectors and the calculated (farm to farm) infection vectors for the same time period and identifies the most likely (highest correlation between midge and infection vectors) source and route of infection to each susceptible farm Because the midge vectors allowed a variety of combinations of up-wind the highest correlations between midge and infection vectors also identified the most likely type of midge movement responsible for infecting one farm from another We recognise that the real parameter of interest is not DA but the day of infection after fertilisation and conception occurred at an unrecorded date before the recorded foetal abnormality and hence could not be considered directly in the models an estimate of the time of infection after conception can be made We also later estimated the intrinsic incubation period by calculating the average difference between the time when one farm was shown in the model to be infecting another farm and the time that the infecting farm had itself been first infected This is a somewhat indirect measure of IIP and will probably also include at least part of the extrinsic incubation period in the midges (EIP the time taken for the development of a transmissible infection in a newly-infected midge) Hence the incubation periods calculated by SWOTS are likely to be a measure of (EIP + IIP) rather than of EIP or IIP alone Knowing the IIP from independent studies allows the estimation of EIP from this figure A second modification of SBV-SWOTS concerned the wind-fields which had been modelled) only at the locations of infected farms BTV-SWOTS therefore had to interpolate wind speed and direction from these data for any other point of interest the wind speeds and directions were modelled on a regular 0.25 degree grid and SBV-SWOTS simply selected the wind data at the nearest grid point Establishment of a reverse genetic system for Schmallenberg virus ‘Schmallenberg virus’--a novel orthobunyavirus emerging in Europe The 2006 outbreak of bluetongue in northern Europe--the entomological perspective Financial consequences of the Dutch bluetongue serotype 8 epidemics of 2006 and 2007 Field Veterinary Survey on Clinical and Economic Impact of Schmallenberg Virus in Belgium Transbound Emerg Dis; 10.1111/tbed.12030 (2012) Epizootic spread of Schmallenberg virus among wild cervids First detection of Schmallenberg virus in elk (Alces alces) indicating infection of wildlife in Białowiez·a National Park in Poland EFSA. "Schmallenberg" virus: analysis of the epidemiological data (May 2013). EFSA Technical Report (2013)URL: http://www.efsa.europa.eu/en/supporting/doc/429e.pdf (Accessed 21/10/2013) Lack of evidence for zoonotic transmission of Schmallenberg virus Salient lesions in domestic ruminants infected with the emerging so-called Schmallenberg virus in Germany Schmallenberg virus in central nervous system of ruminants Epizootic of ovine congenital malformations associated with Schmallenberg virus infection Bluetongue Serotype 2 and 9 Modified Live Vaccine Viruses as Causative Agents of Abortion in Livestock: A Retrospective Analysis in Italy Transbound Emerg Dis; 10.1111/tbed.12004 (2012) Genetic reassortment between Sathuperi and Shamonda viruses of the genus Orthobunyavirus in nature: implications for their genetic relationship to Schmallenberg virus RNA interference targets arbovirus replication in Culicoides cells Detection of Schmallenberg virus in different Culicoides spp First report of Schmallenberg Virus Infection in Cattle and Midges in Poland Culicoids as vectors of Schmallenberg virus Preliminary estimate of Schmallenberg virus infection impact in sheep flocks - France Continued presentation of cases of Schmallenberg virus in sheep in England Schmallenberg virus antibodies detected in cattle in Wales Assessing the risk of windborne spread of bluetongue in the 2006 outbreak of disease in northern Europe Investigating Incursions of Bluetongue Virus Using a Model of Long-Distance Culicoides Biting Midge Dispersal Estimating front-wave velocity of infectious diseases: a simple Assessment of the risk of a bluetongue outbreak in Europe caused by Culicoides midges introduced through intracontinental transport and trade networks Modelling bluetongue virus transmission between farms using animal and vector movements Quantitative analysis of transmission parameters for bluetongue virus serotype 8 in Western Europe in 2006 Colostral transmission of bluetongue virus nucleic acid among newborn dairy calves in California Factors affecting Bluetongue serotype 8 spread in Northern Europe in 2006: The geographical epidemiology [Bluetongue Disease: An Analysis of the Epidemic in Germany 2006–2009] Arthropods as Vectors of Emerging Diseases (ed Mehlhorn H.) [103–135] (Springer Berlin Heidelberg Transmission of Schmallenberg Virus during Winter Endophily in Culicoides associated with BTV-infected cattle in the province of Limburg Biotic and Abiotic Factors Influencing Distribution and Abundance ofCulicoides obsoletusGroup (Diptera: Ceratopogonidae) in Central Italy Diel flight periodicity of the biting midge Culicoides impunctatus and the effects of meteorological conditions Duration of viraemia infectious to Culicoides sonorensis in bluetongue virus-infected cattle and sheep Culicoides biting midges: Their role as arbovirus vectors Large-scale cross-sectional serological survey of schmallenberg virus in belgian cattle at the end of the first vector season Distribution of Schmallenberg Virus and Seroprevalence in Belgian Sheep and Goats Transbound Emerg Dis; 10.1111/tbed.12050 (2013) Quantifying Dispersal of European Culicoides (Diptera: Ceratopogonidae) Vectors between Farms Using a Novel Mark-Release-Recapture Technique e61269; 10.1371/journal.pone.0061269 (2013) The range of attraction for light traps catching Culicoides biting midges (Diptera: Ceratopogonidae) Congenital-Abnormalities in Newborn Lambs after Infection of Pregnant Sheep with Akabane Virus Modelling the spatial distribution of Culicoides biting midges at the local scale pastures and woodlands: the fine-scale distribution of Palearctic Culicoides spp biting midges along an agro-ecological gradient A new dynamical core for the Met Office's global and regional modelling of the atmosphere Download references We thank Laura Burgin from UK Met Office for the generation of the wind data and Simon Carpenter, Simon Gubbins and Chris Sanders from the Institute of Animal Health for the useful discussions on the OIE dataset. L.S. and D.J.R. are supported by the European Union grant FP7-261504 EDENext and this paper is catalogued by the EDENext Steering Committee as EDENext188 (http://www.edenext.eu) The contents are the sole responsibility of the authors and do not necessarily reflect the views of the European Commission conceived and designed the study and wrote the manuscript performed the analysis and prepared all the figures and tables Data sources and comparison with EFSA database Modelled Schmallenberg spread in Europe 2011/2012 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ Download citation Tropical Animal Health and Production (2020) Sign up for the Nature Briefing newsletter — what matters in science has been confirmed at four sheep farms in Norfolk The Schmallenberg virus is believed to be carried by midges. It surfaced in the Netherlands and Germany in August 2011 and since then on hundreds of farms there and in Belgium Themicrobe is difficult to detect in adult animals According to the Department for Environment it is likely the disease has been here since the autumn carried via insects blown across the channel Defra anticipates more cases will appear and has asked for "enhanced surveillance" from vets and farmers The disease has now been confirmed on farms in the UK 18 JanuaryAnimals that have the virus and become pregnant have either miscarriages stillbirths or offspring with deformities such as a twisted neck There are mild symptoms of the virus in other adult animals – a few days of fever and sometimes diarrhoea – but these cannot be easily distinguished from other common illnesses It mostly affects sheep but can also enter cattle or goats Russia banned imports of sheep and goat meat as well as live animals from the Netherlands on 18 January The Dutch agriculture ministry said China had asked for more information The UK's agency said the true extent of Schmallenberg is not known. The Netherlands has been hardest hit while in Belgium it has been detected in 126 farms meaning farmers have no legal duty to report it and there are no control measures imposed on infected farms or restrictions on buying and selling animals "This may change based on forthcoming information over the coming weeks but at present it is not anticipated," said Defra allowing vets time to gather more information A Defra spokesman said it was "very much early days" in determining the course of further action; however farms already co-existed with salmonella and leptospirosis (Weil's disease) The National Farmers Union said the discovery of the virus in Britain would be a worry for all livestock keepers "This is a new virus and there is still much that we don't know about it," said NFU animal welfare adviser Catherine McLaughlin "Farmers can help by reporting any unusual symptoms If they are considering importing ruminants from the affected parts of continental Europe the NFU would strongly recommend that they discuss their plans with their vet first to reduce the risk of buying in the virus." The European Centre for Disease Prevention and Control released a human health risk assessment for Schmallenberg virus on 22 December genetically similar orthobunyaviruses have not caused disease to humans it is unlikely that this virus would cause disease in humans but it cannot be excluded at this stage." Metrics details Schmallenberg virus (SBV) is principally transmitted by Culicoides midges and affects ruminants Clinical presentation is typified by foetal abnormalities relatively few animals present with clinical signs In this paper we further develop a previously published stochastic mathematical model of SBV spread to investigate the optimal deployment of a vaccine for SBV in Scotland a country that has experienced only sporadic and isolated cases of SBV We consider the use of the vaccine under different temperatures and explore the effects of a vector preference for feeding on cattle We demonstrate that vaccine impact is optimised by targeting it at the high risk areas in the south of Scotland At higher than average temperatures and hence increased transmission potential the relative impact of vaccination is considerably enhanced Vaccine impact is also enhanced if vectors feed preferentially on cattle These findings are of considerable importance when planning control strategies for SBV and also have important implications for management of other arboviruses such as Bluetongue virus Environmental determinants and feeding preferences should be researched further to inform development of effective control strategies Schmallenberg virus (SBV) is a novel Orthobunyavirus, a member of the Simbu serogroup and is closely related to Akabane and Shamonda viruses1 That there is evidence of spread during 2011 2012 and 2013 suggests that the disease has mechanisms for overwintering through the period of low vector activity The mechanisms for overwintering are yet to be determined but could be through vertical transmission but the possibility of reintroduction into these serologically naive populations remains This finding could have implications for the likely pattern of transmission for a highly infectious disease such as SBV in mixed livestock contexts SBV is not a notifiable disease in the UK and it is likely that farmers would be given the choice of whether to vaccinate their animals Therefore guidance as to how to use the vaccine most effectively would be beneficial Given the further data that now exist on SBV transmission and the availability of vaccines To evaluate the effect of temperature on the potential for SBV spread in Scotland; To evaluate the potential for vector feeding preferences to alter the pattern of SBV transmission; To evaluate the effectiveness of different strategies for targeting vaccines for SBV; To evaluate the potential for spread in subsequent years following the introduction of SBV The proportion of farms for which the daily average temperature is greater than the baseline for the EIP of 12.35°C during the summer months This is presented for the mean temperature 2012 mean temperature and 2013 mean temperature The pattern of infections shows a focus in the south west for both cattle and sheep, this applies in years with daily mean temperatures and when the temperatures match those from 2013 (Figure 2). The parish level seroprevalence as a proportion of animals infected (averaged over 1000 model iterations) among cattle and sheep following introduction on day 45 given the mean temperature (top) and the temperatures seen during 2013 (bottom) In an epidemic with the daily mean temperatures for 1990–2006 and an introduction on day 45, it is only sheep flocks that lamb prior to February that would be at considerable risk of presenting with birth malformations. The window in which cattle would be at risk is larger, this is due to the longer window of pregnancy in which cattle are at risk (Figure 3). Given the epidemic in Figure 3A which is based upon the epidemic fitted to the mean temperature in Figure 2 graphs B and C show the number of days of pregnancy that a cow or ewe will be at risk of infection that could lead to birth abnormalities The red bars represent elevated risk (greater than 0.01% of animals infected daily) and the blue blocks lower (but still some) risk (greater than 0.001% and less than 0.001% of animals infected daily) Map of SBV seroprevalence as a proportion of animals infected (averaged over 1000 model iterations) when there is a vector preference for feeding upon cattle rather than sheep Farm level seroprevalence for cattle (black points) and sheep (red points) with and without a vector feeding preference This is fitted with mean temperatures from 2013 The numbers of infected animals resulting from disease introduction under different vaccination strategies The red points are vaccination with a vector feeding preference for cattle and blue points the vaccination strategy without feeding preference The grey centre line is the equality line – if sheep and cattle were becoming infected at equal rates relative to their population During a year of average temperatures the disease must be introduced during the month of June for there to be substantial spread This has implications for the options for control of the disease so the timing of introduction could be coupled with data on the current temperatures to give an early warning as to the threat that the introduction presents This would provide the opportunity to develop appropriate control options based upon these data the model could be further adapted to incorporate temperature and precipitation in the kernel shape Vaccination can be used by individual livestock owners with the aim of protecting their animals from infection that may cause losses (represented by the ad hoc vaccination strategy in this study) vaccination may be used more tactically to break the transmission chain and reduce overall disease spread tactical vaccination was represented by the strategies of vaccination in the south and vaccinating cattle Although ad hoc vaccination is beneficial to individual livestock keepers our study clearly shows the overall benefit of using tactical approaches The value of the cattle vaccination strategy is further enhanced if there is a cattle feeding preference the potential for spread in subsequent years decreases This is because the animals become infected and develop immunity during the first year and thus fewer susceptible animals remain may be explained by this depletion of susceptible animals These results are important for SBV management and control but also have important implications should there be another epidemic of BTV in GB incorporation of more accurate knowledge on vector feeding preferences into models for BTV may provide an opportunity to break the transmission chain by targeting vaccination at animals at greatest risk of infection such information may be very helpful in prioritising resources to limit spread the vector will survive to lay a potentially infectious bite on another animal by a probability defined by the vector mortality rate and EIP interval between blood meals and vector mortality rate are temperature dependent parameters for the EIP there is a minimum temperature below which the process will not operate The infected vector will feed on animals on the same or other farms as defined by a Gaussian spatial kernel with a mean transmission distance of 14 km35 that describes both the movement of the vector and movement of infected livestock The model assumes a season of vector activity that runs between 1st May and 31st October with two peaks in vector abundance where T0 is the observed temperature and 12.35°C is the minimum temperature at which incubation can take place25 temperatures in 2012 were 0.8°C lower than average and in 2013 were 0.92°C higher than average Among cattle 27.5% of stock is replaced; 55% of the stock is under 2 years old and 31.9% of these animals are slaughtered annually (data from the Cattle Tracing System cattle movement database) 18.4% of the animals over two years old are slaughtered and replaced from the younger stock annually In all analyses we consider two scenarios for feeding preference: The vector is equally likely to feed on a cow as a sheep The odds that a midge will feed on a sheep with odds of 0.205 relative to a cow, based upon Ayllón et al.31 The model considers four strategies for deploying the vaccine: All cattle and sheep that are being reared for breeding replacement stock are vaccinated (referred to in the results as “all”); 50% of herds and flocks (selected randomly) vaccinate all breeding cattle and sheep to represent a voluntary program with 50% uptake (“ad hoc vaccination”); All breeding cattle are vaccinated (“cattle vaccination”); Breeding cattle and sheep on herds and flocks located in the south of Scotland in the counties to the south of the Forth and Clyde are vaccinated (“south vaccination”); We analyse the protective impact of vaccination by comparing the results of model runs with vaccination against baseline scenarios in which there is no vaccination undertaken The number of animals vaccinated and percentage of animals vaccinated The percentage reduction in the number of infections Calculated as: where IB is the number infected without vaccination and IV is the number infected with vaccination The number of infections spared per vaccinated animal Calculated as: where IB is the number infected without vaccination IV is the number infected with vaccination and V the number vaccinated There are a number of assumptions that underlie this paper, some of which have previously been stated in Bessell et al.21: Farm composition is homogeneous and ages of animals on each farm are assumed to be the same across the country or hill and lowland sheep farms can be treated similarly if the spatial distribution of an epidemic were being analysed the homogeneity of farms may create more specific foci of spread That the width of the spatial kernel will not vary with temperature Given a daily Culicoides dispersal distance the transmission kernel should vary as the incubation period varies The animal is equally infectious on each day of its infectious period Once infected an animal will recover with full immunity and will not be susceptible to further infection The attractiveness of a farm for vector feeding is based on the number of livestock on the farm and is determined by distance and the number of livestock Large studies of efficacy are not yet available We do not incorporate vectors feeding on species other than cattle and sheep Other hosts include horses and wild ruminants but the distribution of these species and the vector ecology in terms of feeding is relatively poorly understood During an epidemic involving southern Scotland there is likely to be some transmission with farms in northern England as this is likely to be a two-way exchange we consider that this would have minimal effect on the epidemic Schmallenberg virus infection in small ruminants – First review of the situation and prospects in Northern Europe EFSA. “Schmallenberg” virus: analysis of the epidemiological data (May 2013). Technical Report (2013)URL: http://www.efsa.europa.eu/en/supporting/doc/429e.pdf (Date of access: 19/06/2014) Seroprevalence of Schmallenberg Virus Antibodies among Dairy Cattle The Schmallenberg Virus epidemic in Europe - 2011–2013 Modelling the continental-scale spread of Schmallenberg virus in Europe: Approaches and challenges “Schmallenberg” virus: Analysis of the Epidemiological Data and Assessment of Impact Does covering of farm-associated Culicoides larval habitat reduce adult populations in the United Kingdom Implicating Culicoides biting midges as vectors of Schmallenberg virus using semi-quantitative RT-PCR Schmallenberg virus detection in bovine semen after experimental infection of bulls Evidence of excretion of Schmallenberg virus in bull semen Schmallenberg virus in Dutch dairy herds: potential risk factors for high within-herd seroprevalence and malformations in calves and its impact on productivity Identifying environmental drivers of insect phenology across space and time: Culicoides in Scotland as a case study Transmission of Schmallenberg virus in a housed dairy herd in the UK NFUS. Schmallenberg Surveillance Results Out. URL: http://www.nfus.org.uk/news/2013/may/schmallenberg-surveillance-results-out (2013) The impact of Schmallenberg virus on British sheep farms during the 2011/2012 lambing season Prevalence of seropositive sheep within flocks where Schmallenberg virus infection was suspected or confirmed Evidence of Schmallenberg virus in Scotland in 2012 First case of Schmallenberg disease confirmed in Scotland Schmallenberg virus circulating in Scotland Inferences about the transmission of Schmallenberg virus within and between farms The influence of the wind in the Schmallenberg virus outbreak in Europe Feeding patterns of biting midges of the Culicoides obsoletus and Culicoides pulicaris groups on selected farms in Brandenburg Identification of blood meals of the Scottish biting midge by indirect enzyme-linked immunosorbent assay (ELISA) Identity and diversity of blood meal hosts of biting midges (Diptera: Ceratopogonidae: Culicoides Latreille) in Denmark R: A Language and Environment for Statistical Computing Bivand, R. & Lewin-Koh, N. maptools: Tools for reading and handling spatial objects. (2014)URL: http://CRAN.R-project.org/package=maptools (Date of access: 19/06/2014) A modeling framework to describe the transmission of bluetongue virus within and between farms in Great Britain two-vector basic reproduction ratio (R(0)) for bluetongue vector-feeding preferences and the risk of African horse sickness transmission in Great Britain Host feeding patterns of Culicoides species (Diptera: Ceratopogonidae) within the Picos de Europa National Park in northern Spain Bloodmeal analysis reveals avian Plasmodium infections and broad host preferences of Culicoides (Diptera: Ceratopogonidae) vectors The generation of monthly gridded datasets for a range of climatic variables over the UK Scottish Government. Results from the June 2012 Scottish Agricultural Census. URL: http://www.scotland.gov.uk/Publications/2012/09/1148 (2012) Responses of the biting midge Culicoides impunctatus to acetone carbon dioxide and an octenol-phenol mixture in northwestern Florida Comparing methods to estimate the reproduction ratio of Bluetongue Download references This work was undertaken as part of the Scottish Government EPIC project. KRS and BVP are partly supported by EU grant FP7-261504 EDENext and this paper is catalogued by the EDENext Steering Committee as EDENext236 (http://www.edenext.eu) The contents of this publication are the sole responsibility of the authors and don't necessarily reflect the views of the European Commission performed the analysis and drafted the manuscript contributed to aspects of arbovirus epidemiology and H.A made changes to and approved the manuscript Download citation Growing numbers of flocks are being struck by the deadly Schmallenberg virus in the south of England Vets are urging farmers with deformed lambs to send them for post-mortem so they can be tested for the virus This can be done free of charge through the Animal and Plant Health Agency (Apha) but vets are hopeful this might change if more flocks are identified as infected See also: Expert advice on assessing and managing lambing difficulties Vet Kirby Dobson from Tyndale Vets in Gloucestershire estimates that 20 of their early lambing flocks have been blighted by the virus The practice covers a 150-mile radius from the South West to Worcester and crosses the Severn Bridge into South Wales “So far it has mainly been pedigree flocks that lamb in January Most of these are Suffolk and Texel and have lost up to 50% of lambs,” she explains The last significant wave of Schmallenberg happened in 2016-17 when Apha confirmed 141 sheep farms in England Wales and Scotland had tested positive for the virus Kirby believes the sharp rise in cases this year is the result of warm and wet weather in late autumn This would have presented ideal conditions for biting midges The most susceptible stage for foetal deformities is days 25-50 of gestation in sheep with older foetuses able to clear the virus She says typical malformations to look for include fused neck and legs or the neck bent in an S-shape This makes it extremely difficult for the lambs to pass safely through the pelvic canal and any live lambs are unviable and must be euthanised Source: National Animal Disease Information Service Schmallenberg usually runs in cycles of three to five years but this latest outbreak does not fit this pattern and the midge challenge has been higher this year Farmers were still getting flystrike in November [because conditions were so mild] “There is no definite pattern to the disease spread in our area they said it was not fitting the three-to-five-year pattern of immunity.” Kirby says it is difficult to gauge if this is only the tip of the iceberg although she remains hopeful the worst is over given that later lambing flocks have seen improved scanning rates compared with earlier ones “I’m hoping the higher scanning rates indicate ewes haven’t been infected says it has had “several reports” of Schmallenberg says it is turning out to be a difficult time for many of its clients “We have been called out to a large number of farms who are suffering with Schmallenberg virus.” says he attended a farm to help lamb a triplet The ewe had two deformed lambs in one horn of the uterus and an unaffected lamb on the other side adding: “We had rams at the back end that failed Schmallenberg blood tests One flock afflicted was Pat Greaney’s early lambing flock of pedigree Suffolks The ewes were artificially inseminated on 6 August to lamb on 28 December but Schmallenberg was not identified until 29 December “I went to lamb a ewe and I could only feel one back leg “The first lamb’s bottom jaw was not fully formed and the front legs were fused backward in a lying position It died within minutes of being born,” Pat recalls “We lost both lambs and the ewe never recovered from the operation,” he adds the Greaneys have lost two ewes and six lambs – all doubles – to the disease but the hardest thing was looking at the lambs but this is gruesome – the image is etched in your mind forever.” He says he is hearing of more flocks locally that have the disease and warns others not to take shortcuts with vet intervention in case ewes require a C-section or the lambs need putting down Good aftercare of ewes birthing infected lambs is also imperative They managed to save one ewe by promptly treating her with anti-inflammatories and antibiotics although he concedes the lambs were breached and birthed easier Pat is concerned some of the later calving animals could be harbouring foetuses infected with Schmallenberg but we put it down to heat stress at the time “There’s nothing we can do apart from expect the worst and hope for the best.” Another farmer from the Worcestershire/Shropshire border has lost more than 50 lambs from his flock of 175 early lambers He estimates the virus has already cost him £10,000 says: “About 90% [of ewes] are presenting nowhere near right and can’t be lambed without assistance.” Although he has avoided having to call the vet for C-sections there are still two large groups left to lamb He adds: “A lot of farmers nearby are having similar problems Katie Ford lambs a flock of 800 mixed ewes with her parents near Newent They have lost 17 lambs and two ewes from an early lambing group of Suffolk crosses They were synchronised to lamb after Christmas Six scanned empty and 25 of the remaining 60 ewes had lambs with Schmallenberg two recipient ewes lambed healthy Dutch Spotted lambs Schmallenberg presents itself differently this time around – the lambs are more malleable and are easier to lamb.” With the next batch starting to lamb in February she hopes the remainder of the flock will be unaffected “The midges have been [active] until late last year contact the Royal Agricultural Benevolent Institution on 0800 188 4444 or the Farming Community network 03000 111 999 with the disease potentially spreading across the entire UK They blamed climate change for bringing the virus to the country and said other new viruses could follow where the illness was first detected in August 2011 in the small town that gives the virus its name There are also hundreds of infected farms in France "It is inevitable we will detect more and more cases [in the UK]," said Professor Matthew Baylis, a veterinary epidemiologist at Liverpool University The birth deformities are the end result of mothers being infected with the virus earlier in their pregnancy so with the lambing season in its early stages and calving not beginning until April further infections are certain to be revealed Scientists say there is no evidence that people are affected by the virus The virus is believed to have been brought into the UK by biting midges, blown from mainland Europe in the autumn 2011 and infecting pregnant ewes and cows There is nothing that can be done about the malformed lambs we see now," said Baylis Very little is yet known about the virus, so whether a fresh outbreak will occur in 2012 is unknown. But Professor Peter Mertens, who leads the vector-borne diseases programme at the UK's Institute for Animal Health in Surrey said: "This virus has the potential to spread across the entire country It is likely the virus will not go away in a year I think that would be almost too good to be true." Similar diseases have become endemic in other countries Mertens said the virus would be more likely to spread if midges were not the only way it infected animals "The very high prevalence of infection on some farms – up to 100% of animals – raises an interesting question: is there some other form of local spread Animals that contract Schallenberg virus while pregnant have miscarriages stillbirths or offspring with deformities such as a twisted necks The symptoms of the virus in adult animals are mild – a few days of fever loss of appetite and sometimes diarrhoea – which makes it hard to distinguish from other common illnesses Schmallenberg virus is the second midge-borne disease known to have invaded the UK, with bluetongue virus having arrived in 2007 "The spread of bluetongue virus was driven entirely by the temperature changes in Europe," he said "Our changing climate is making it more likely these things happen." Bluetongue virus was first identified in Europe in the 1920s but was confined to southern Spain and Turkey until the 1990s only reaching northern Europe in 2006 and the UK in 2007 Baylis believes other new diseases could arrive in the UK as a result of a climate change There is currently no test for Schmallenberg virus suitable for widespread use and no vaccine Work has begun on a vaccine but it will take at least 18 months to be tested and licensed though he anticipated no problems in producing an effective vaccine In the meantime little can be done to protect livestock beyond housing them inside Nets and insecticides have proven to be of little use "There is no evidence of infection in humans," added Mertens "It is a little bit of an unknown but everything we know [about these viruses] says it is not a risk." Tests on people in the Netherlands for the virus have all been negative Metrics details During 2011 Schmallenberg virus (SBV) presented as a novel disease of cattle and sheep that had apparently spread through northern Europe over a relatively short period of time This paper describes the development of a model of SBV spread applied to Scotland in the event of an incursion This model shows that SBV spread is very sensitive to the temperature with relatively little spread and few reproductive losses predicted in years with average temperatures but extensive spread (>1 million animals infected) and substantial reproductive losses in the hottest years These results indicate that it is possible for SBV to spread in Scotland however spread is limited by climatic conditions and the timing of introduction Further results show that the transmission kernel shape and extrinsic incubation period parameter have a non-linear effect on disease transmission so a greater understanding of the SBV transmission parameters is required may determine the potential for spread of SBV and other arboviruses in Scotland impunctatus dominating in bog and heathland habitats whilst other C obsoletus complex species are primarily associated with pastural livestock farming impunctatus to transmit BTV and potentially SBV Assessment of the likely extent of spread and ramifications in Scotland would aid control and deployment of resources following introduction To investigate the likely extent and impact of an SBV epidemic in Scotland To explore the effect of temperature on the risk of SBV spread in Scotland and the potential effect of climatic warming on SBV transmission To explore the importance of the parameters of SBV transmission in particular the parameters relating to the vector Stacked barplots of the number of sheep (red bars) and cattle (black bars) infected on each day of the simulated epidemic under the baseline implementation in which the mean temperature is used The dashed line represents the start of the period in which in-lamb ewes may be at risk of reproductive losses There is little disease spread if there is introduction earlier or later than day 60 Stacked barplots of the number of sheep (red bars) and cattle (black bars) infected on each day of the simulated epidemic when the maximum temperature is used The broken line represents start of the period in which in-lamb ewes may be at risk of reproductive losses. Note the different scale compared to Figure 1 The number of farms infected against the number of disease introductions under the extreme case maximum temperature scenario The solid red line represents the median and the broken red lines the 2.5 and 97.5 percentiles The points have been jittered to ease interpretation Comparison of the numbers of animals infected under the scenarios in Table 1 Red points correspond to the exponential kernel The black lines represent the range from the 10th to the 90th percentiles The distribution of parish level risk of transmission illustrated by the expected number of infectious vectors resulting from an infected animal on day 60 under the extreme case maximum temperature scenario is shown by Figure 5. There is a distinct concentration of higher risk in the south-west with some patches of higher risk in northerly areas. The expected number of infectious bites () resulting from an infected host on the 30th June (day 60) under the extreme case maximum temperature scenario this model assumed that all pregnant animals infected during the at risk period are at risk of reproductive losses but the true proportion of these animals would go on to suffer abortions or birth malformations is currently unknown so the observed number of reproductive losses in an epidemic may be lower a large number of cattle will become infected and this could manifest clinically in drops in milk production or calf birth malformations and reproductive losses Under the baseline scenario, the size of the epidemic was exponentially smaller than the maximum temperature scenario, with around one thousandth of the numbers of animals infected (Table 1, Figure 4) these analyses show that even during an average year SBV does present a risk to livestock in Scotland If average temperatures and frequency of warm periods in Scotland increase as a result of global warming then the risk of vector borne disease spread in Scotland and elsewhere in Europe will continue to increase so can be considered as credible values for SBV The sensitivity of the model to these parameters highlights the need to better understand the parameters for SBV transmission if we are to accurately predict the spread of the disease under the maximum temperature scenario the Gaussian kernel resulted in more animals on more farms being infected This is because the Gaussian kernel allows the virus to spread more rapidly to new areas where as the exponential kernel limits transmission and ensures that locally the epidemic burns-out faster However the reverse is true when the mean temperature is used This is because under the lower temperatures there are fewer areas suitable for spread The tighter exponential kernel is more effective in ensuring that infection remains within these areas whereas the wider Gaussian kernel allows more opportunity for the virus to escape these risk areas to areas that are less favourable for spread and conditions are less likely to lead to further transmission the climatic conditions in Scotland are at the lower end of the scale that is suitable for SBV transmission but are still adequate for the disease to spread given warmer than average (but still feasible) temperatures SBV could spread very quickly within Scotland with significant impacts in both the sheep and cattle populations This is upon the assumption that SBV will spread with similar parameters as BTV and is highly dependant upon the nature of vector movement with respect to a transmission kernel how the disease spreads within Scotland is very dependant upon the precise nature of the EIP of SBV The model used in this analysis is a stochastic simulation model comprising two main compartments: a) the transmission from livestock host to vector; and b) the transmission from vector to host Different introduction scenarios are simulated by seeding of infection on to farms to represent importation of infected animals or windborne virus spread A number of assumptions have been made in this model: No disease control measures will be employed The EIP for SBV will be the same as for BTV at time t the number of vectors that will feed on an infectious animal and survive sufficient time to lay an infectious bite is defined by a daily rate The actual number of infectious bites is taken from a Poisson distribution (Pois()) vt = 0.25 when t < 30 (31st May) or t > 140 (September 18th) and t is between 65 (5th July) and 100 (9th August) days vi is a term that describes the likely vector abundance given the landcover in a 1km buffer around i with the more competent species associated with pasture and less competent species associated with heathland: where and are the proportion of land within the 1 km buffer classed as pasture and heathland respectively is the number of infectious animals on i at time t σv is the probability of transmission from animal host to vector and is equal to 0.19, based upon experimental infections3 the EIP (Ve) and the interval between blood meals (vb) where T is the temperature and the daily survival probability is In order to account for a vector taking more than one potentially infectious meal the infectious bite rate of a vector is given by: This assumes that the midge will not survive to lay more than 10 infectious bites (although the probability of surviving more than two bites being very small and is almost negligible) An infected vector from farm i will infect an animal on farm j (i can be the same as j) with probability defined by: where is a spatial transmission kernel based upon the Euclidean distance between farms i and j () and describes the distances a vector will travel between infection and the laying of infectious bites describes the attractiveness of a farm to a vector and is equal to the number of susceptible hosts () on holding j is a scaling parameter that ensures that any potentially infectious bite is laid only once: The model parameters are summarised in Table 2 The model introduces infection on different start dates from the 1st June (being the first month at which temperatures are suitable for within vector incubation) with 30 day intervals between start days (up to start day = 120 (29th August)) The model is initiated by introducing disease on certain ‘seed’ farms. The seeds are assumed to be introductions from England, so a farm is more likely to be a seed if it is further south (described in the supplementary information) with seeds sampled at random (with replacement so it is possible for a seed farm to become infected twice) The seed is infected by a single random animal becoming infected The shape of the exponential kernel (red line) and Gaussian kernel (blue line) To explore the sensitivity of the model to certain parameters sensitivity analysis was conducted by altering the parameter and rerunning the model with the new values and comparing these results to those from the baseline (mean temperature) scenario Analysis was conducted to explore the effects of using the maximum mean monthly temperature of each grid cell over the period of the data (1990–2006) The parameter for EIP is taken from studies of BTV and the parameter for SBV may have a different minimum incubation temperature or a different virus replication rate Thus an equation with a minimum temperature 1°C cooler: Implicating Culicoides biting midges as vectors of Schmallenberg virus using semi- quantitative RT-PCR EFSA “Schmallenberg” virus: analysis of the epidemiological data 1 10 on Schmallenberg Virus in Northern Europe Impact of climate change and other factors on emerging arbovirus diseases Potential arbovirus emergence and implications for the United Kingdom host and landscape factors on Culicoides species in Scotland Distribution and Abundance in Scotland of Culicoides Midge Species and their Potential as Vectors of Animal Disease Oral Susceptibility to Bluetongue virus of Culicoides (Diptera: Ceratopogonidae) from the United Kingdom The vector potential of British Culicoides species for bluetongue virus Observations on biology of Culicoides impunctatus Goetgh (Diptera:Ceratopogonidae) in Southern England EFSA “Schmallenberg” virus: Analysis of the Epidemiological Data and Assessment of Impact Assessing the consequences of an incursion of a vector-borne disease I Identifying feasible incursion scenarios for bluetongue in Scotland Assessing the consequences of an incursion of a vector-borne disease Spread of bluetongue in Scotland and impact of vaccination 9 on Schmallenberg Virus in Northern Europe Temperature dependence of the extrinsic incubation period of orbiviruses in Culicoides biting midges Estimates for local and movement-based transmission of bovine tuberculosis in British cattle Representing the UK's cattle herd as static and dynamic networks Potential for transmission of infections in networks of cattle farms Sheep movement networks and the transmission of infectious diseases Mapping the basic reproduction number (R0) for vector-borne diseases: a case study on bluetongue virus Seasonal transmission of bluetongue virus by Culicoides sonorensis (Diptera: Ceratopogonidae) at a southern California dairy and evaluation of vectorial capacity as a predictor of bluetongue virus transmission Seasonal abundance and survivorship of Culicoides sonorensis (Diptera: Ceratopogonidae) at a southern California dairy with reference to potential bluetongue virus transmission and persistence Environmental effects on vector competence and virogenesis of bluetongue virus in Culicoides: interpreting laboratory data in a field context Rates of bluetongue virus transmission between Culicoides sonorensis and sheep CORINE Land Cover technical guide - Addendum 2000 Download references This work was undertaken as part of the Scottish Government EPIC project. IGH was supported through Institute Strategic Grant funding from the BBSRC. KRS and BVP are partly supported by EU grant FP7-261504 EDENext and this paper is catalogued by the EDENext Steering Committee as EDENext084 (http://www.edenext.eu) contributed to aspects of arbovirus epidemiology and HKA contributed to veterinary aspects of SBV Supplementary information for: Epidemic potential of an emerging vector borne disease in a marginal environment: Schmallenberg in Scotland Download citation Sorry, a shareable link is not currently available for this article. Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily. Notifications can be managed in browser preferences. Farmers fear livestock crisis after thousands of animals killed by Schmallenberg disease I would like to be emailed about offers, events and updates from The Independent. Read our Privacy notice Tens of thousands of lambs have been stillborn or deformed throughout Britain as a result of the deadly Schmallenberg virus, with the industry bracing itself for what could be a blighted lambing season. In infected flocks the rate of lamb loss has been between 25 and 30 per cent on average, according to the National Farmers Union livestock chief, who has lost 40 per cent of the lambs from his early breeding flock to the emerging virus. Schmallenberg has been reported on more than 1,200 farms across the country, but there are fears the disease is being under-reported and that the Government is not taking the threat seriously enough. Although there are hopes that many later-lambing ewes, which make up the majority of the national flock, have escaped infection, farmers warn that losses on a similar rate throughout the lambing season would plunge the sheep-farming industry into “crisis”. “Farmers need a good lambing season to avert a crisis,” Robin Milton, the NFU’s Uplands chairman who keeps 700 ewes on Exmoor, Devon, said. “It’s a fragile state of affairs. If there was even a five per cent loss, in some flocks, that’s the profit for the year gone.” Sheep farmers are already struggling with falling lamb prices and the after effects of last year’s poor weather. Farmgate prices for lambs have dropped by a quarter and the wholesale price is down 17 per cent, but the price for lamb on the shelf has dipped only two per cent, leaving farmers to pick up the deficit. Schmallenberg first appeared in eastern England more than a year ago, but is now believed to have spread to every county in England and Wales. The virus, which originated in Germany and is thought to have spread in infected insects blown across the Channel, causes abortions and birth defects in livestock. Cattle farmers also fear the virus could affect this year’s calves. Uncertainty over the damage Schmallenberg might cause has led to calls for the Government to accelerate development of a vaccine, which is not predicted to be released on to the market until next year. Defra is still treating Schmallenberg as a low-priority, non-notifiable disease, meaning that farmers do not have to report cases of it, which has led to fears the Government may be underestimating its true extent. The virus is spread by midges, mosquitoes and ticks and although an infection to a ewe or a ram does not necessarily mean offspring will die, early losses have raised concerns that the disease’s impact could be greater than first feared. The Government anticipates that later lambing flocks will be less vulnerable because later-breeding animals may have had time to develop natural immunity to the virus. “It would be useful if the Government did everything they could to make the vaccine available,” Mr Sercombe said. “Confidence in sheep farming is at rock bottom. The safest option is to give us the vaccine to protect our flocks.” A Defra spokesman said: “It’s extremely distressing for any farmer whose flocks have been affected by Schmallenberg – particularly those who have seen a greater impact on their sheep and cows.” Schmallenberg virus is an emerging livestock virus that originated in Germany and has been detected in Belgium, the Netherlands and now the UK. It is transmitted by vectors such as midges, mosquitoes and ticks. It is believed the disease arrived in the UK carried by midges blown across the Channel. The virus can cause late abortion or birth defects in newborn sheep, cattle and goats as well as diseases such as milk drop, pyrexia and diarrhoea in adult cattle. It is not a notifiable disease, meaning that farmers do not have to report it, but they are advised to contact a vet if they encounter symptoms in their livestock. There is a low likelihood of any risk to public health. Join thought-provoking conversations, follow other Independent readers and see their replies Data from the Animal Health and Veterinary Laboratories Agency, part of the Department for Environment, Food and Rural Affairs (Defra), showed Schmallenberg virus had been confirmed in livestock in all counties of England and Wales as well as to a more limited extent in Scotland The virus was detected in the Netherlands and Germany in late 2011 and named after the town in North Rhine-Westphalia where it first emerged it tends to cause abnormalities to skulls and limbs loss of appetite and reduced milk production It was first detected in lambs in eastern England at the start of 2012 A possible vaccine has been developed and tried out elsewhere in Europe with apparent success. Defra's Veterinary Medicines Directorate has confirmed it is considering an application for use of the Bovilis SBV vaccine The spread of the disease will be seen more vividly with the lambing season and the National Farmers Union has called on the government to make sure the vaccine is available soon warning that while the disease is still classified as low impact overall it can cause significant difficulties to individual farmers Joanne Pugh from the National Sheep Association told the BBC: "It's incredibly high impact for the flocks that have had it and had massive losses." The Schmallenberg virus first emerged in the Netherlands and Germany last year causing mild to moderate symptoms in adult cattle including reduced milk yield and diarrhoea and late abortions and birth deformities in newborn sheep It is thought the virus is spread by midges and has crossed the Channel from the continent The Animal Health and Veterinary Laboratories Agency (AHVLA) said the infection had now been identified on 74 farms Five of the positive cases have been diagnosed in cattle none of the affected farms have reported importing animals during 2011 from the affected areas in mainland Europe Positive cases have been identified on the Isle of Wight and in Wiltshire This is in addition to the counties in the east and south of England which have previously had cases identified A spokesman for the Department for Environment Food and Rural Affairs said: "As everyone connected with the livestock industry has been expecting the number of cases of Schmallenberg has increased as lambing and calving begin to gather pace "Schmallenberg has been identified in the south and we suspect livestock got the virus from infected midges blown across the Channel from affected areas in Europe and governments continue to gather information about the progress and effects of this disease it's vital that farmers continue to report any suspicions they have as soon as possible "The European Centre for Disease Prevention and Control says it is unlikely Schmallenberg virus would cause disease in humans." The Schmallenberg virus has survived the winter in the UK and because it is highly efficient at spreading quickly and infecting whole herds it could reach as far as Scotland and Wales "There is no reason why it should not spread to most of the [UK] this year," said Peter Mertens, professor at the Institute for Animal Health the susceptible animals are there – it could spread to the whole country." The first cases of the Schmallenberg virus in the UK were found early this year in farms in the south and east of England though there could be many more as yet undetected ewes and cows can give birth to offspring with severe deformities from bent limbs to animals born without a brain There is believed to be no risk to human health and the deformed animals are removed from the food chain Farmers have been warned that the signs of infection include stillbirths or major birth defects in lambs and calves reduced milk yield and loss of appetite in adult animals The risks to offspring occur only if females become infected with the virus during the early to middle stages of pregnancy This is likely to limit the damage to farmers from the virus which is markedly less devastating than the bluetongue virus which struck northern Europe in 2006 killing up to a third of infected animals but it is not as bad as that," said Martens But while the economic impact across the country is likely to be "relatively limited" according to the government's chief veterinary officer Nigel Gibbens the disease could still be "distressing for individual farmers" Farmers will not receive compensation if their herds are infected A vaccine is now in development, and veterinary experts are hopeful that it can be brought forward soon, though it is unlikely to be this year. When the bluetongue virus hit northern Europe the UK was able to vaccinate susceptible animals in early 2008 before the insects that carried it re-emerged from winter As a result there were no more infections in the UK "Bluetongue was a major success story," said Mertens The Schmallenberg virus was first isolated in December 2011 after numerous cases across Europe and named after the German town where it was identified It is related to viruses that cause cattle disease in Africa but similar insect-borne diseases have not been found before in northern Europe Mertens said it was clear that climate change was a factor in its spread assisted by increasing international trade He warned that other illnesses were likely to spread northwards as the climate warms Schmallenberg virus has continued to spread across Europe since I last wrote about it two years ago The infectious agent was named for the German town where the virus was first discovered non-fatal illness in adult sheep and cattle Clinical signs include fever and loss of appetite and weight Milk production can be substantially reduced in affected dairy cattle Jailed chicken farmer found to be in compliance for number of laying hens after EFA inspection nannies and cows that are infected for the first time while pregnant New studies have found that only a small proportion of infected pregnant cows have these severe outcomes Researchers have found Schmallenberg virus in biting midges from several European countries which supports the theory that these tiny insects play an important role in virus spread Transmission continued last winter but it is unknown whether midges were present within barns to spread the virus or if other insects were capable of transmission Schmallenberg virus is not spread by contact Infected dams can pass the virus to offspring Antibodies in infected cattle can last at least two years after infection Recovered animals are resistant to re-infection for at least a year Several tests have been developed over the last two years that use blood or tissues Vaccines have been developed but their widespread efficacy use and cost-benefit have yet to be established Researchers found no trace of it in cattle and sheep blood from the years immediately before the first cases occurred which suggests it was either circulating at low levels or came from elsewhere The European Food Safety Authority says the most significant economic impact is from trade restrictions imposed by countries where the disease is not endemic The impact at the herd level seems to vary One study of dairy cows found only small differences in milk production and slightly reduced fertility during the season when Schmallenberg virus emerged compared to the previous year some farms experienced greater than 40 percent lamb mortality The disease also took its toll on producers with one in four farmers reporting a high impact on emotional well-being An explosion of research has occurred since 2012 with more than 100 scientific papers published found that 100 percent of cattle and more than 40 percent of sheep and goats had antibodies against Schmallenberg virus It’s possible that the test used in the study could have cross-reacted with other viruses Researchers need to do further testing to confirm that Schmallenberg is indeed present in Africa laboratories and research institutions collaborated in response to this outbreak with remarkable speed and openness which bodes well for future disease emergence scenarios The Canadian Food Inspection Agency has modified importation requirements to prevent Schmallenberg virus from entering Canada Animals from which sperm or embryos are collected must test negative for the virus before entry into Canada The virus hasn’t jumped the ocean to North America yet but understanding emerging disease issues across the world is important given the speed and volume of global travel and trade Newsletter Sign Up - Receive free Western Producer newsletters Breaking ag news stories and commodities markets snapshots delivered daily right to your inbox Δdocument.getElementById( "ak_js_1" ).setAttribute( "value" Cattle markets hold value amidst uncertainty Drought preparation is better than reaction Producers must take foot-and-mouth disease seriously Farmer incorporates cattle into grain operation to boost soil health Terms and Conditions | Privacy Policy | © 2025 Western Producer Publications Limited Partnership "(Required)" indicates required fields Δdocument.getElementById( "ak_js_2" ).setAttribute( "value" A key building block in the Schmallenberg virus could be targeted by anti-viral drugs according to a new study led from the University of Leeds which causes birth defects and stillbirths in sheep was first discovered in Germany in late 2011 and has already spread to more than 5,000 farms across Europe There is currently no way of treating infected animals but a study published in Nucleic Acids Research reports that the Schmallenberg virus nucleocapsid protein A University of Leeds-led team of virologists and structural biologists used X-ray crystallography and electron microscopy to decipher the three-dimensional shape of the nucleocapsid protein and also show how it builds the inner workings of the virus itself of the University of Leeds’ Faculty of Biological Sciences and co-leader of the study said: “The protein forms a chain a bit like a necklace that wraps around and protects the RNA This chain also recruits other proteins that are vital to the virus’ ability to multiply and cause disease We have developed a very finely detailed picture of the shape of the protein and all the nooks and crannies that it needs to present to other molecules to be able to function.” The nucleocapsid proteins bind together in a ring-like structure of four identical protein units and the ring is held together by contacts between the protein units a bit like people holding hands in a circle also from Leeds’ Faculty of Biological Sciences said: “The shape of the nucleocapsid protein has shown us important details of how the individual proteins in these rings are interacting This not only tells us how the virus works but importantly we think we can block that interaction and disrupt the process of making the ring It would stop the protein wrapping up the RNA We are now designing small molecules that could block ring formation and could therefore be an effective antiviral drug.” The Schmallenberg virus appears to be spread by midges It causes a relatively mild illness in adult animals but is responsible for stillbirths and birth defects in cattle Food and Rural Affairs (DEFRA) believes the disease was probably brought into the UK from infected midges blown across the Channel causing severe losses on many holdings across the entire UK There is new evidence that the Schmallenberg virus can also spread to wild animal populations such as deer and wild boar raising the possibility that a reservoir of the disease could develop outside the control of farmers and cause problems for many years to come Developing a vaccine for the Schmallenberg virus is a possibility One already exists for the similar Akabane virus but the discovery by the Leeds-led team is the first step toward developing a treatment that could be used after an animal is infected The research was funded by The Wellcome Trust and involved researchers from The University of Leeds “Nucleocapsid protein structures from orthobunyaviruses reveal insight into ribonucleoprotein architecture and RNA polymerization,” is published in Nucleic Acids Research.Further information Dr John Barr and Dr Thomas Edwards are available for interview Copies of the paper and high-resolution computer generated images of the structure of the protein and virus are available on request Contact Chris Bunting, Press Officer, University of LeedsT: +44 (0)113 343 2049 E: c.j.bunting@leeds.ac.uk Weeks after government vets confirmed the arrival in Britain of the deadly Schmallenberg virus which causes miscarriages and birth deformities in lambs 74 farms in southern and eastern England have been found to have the disease and the number is expected to rise sharply as the lambing season peaks imports and exports are unlikely because officials do not want to further jeopardise rural economies to combat a virus that has also affected cattle and goats across Europe but is not thought to be dangerous to people Public health bodies are monitoring the health of farmers farm workers and vets who have been in contact with infected animals The National Farmers Union has warned of a "ticking time bomb" over the disease which has affected up to 20% of lambs on some farms which is thought to have been carried by midges over the North Sea or English Channel is named after a farm in Germany where it was first identified last year It was initially seen in cattle and quickly spread through the Netherlands and Belgium to northern France The virus has hit sheep on 69 farms and cattle on five since its first detection in England last month, according to the Animal Health and Veterinary Laboratories Agency (AHVLA) The midges suspected of being the virus carriers probably arrived last summer, according to the Department for Environment, Food and Rural Affairs "The midges are not around at the moment so movement restrictions are not going to have any effect," said a spokesman Such restrictions could cause huge problems for farmers without reducing the spread of the disease AHVLA says methods of infection have not been confirmed "The potential for direct transmission (ie direct from one animal to another) is therefore Symptoms of the disease have not been identified in adult sheep but it causes diarrhoea There is currently no treatment and a vaccine could take 18 months to two years to develop Farmers are calling for a more definitive method of recording cases of Schmallenberg virus as the true extent of the issue remains largely unrecorded Sheep farmers across the country have repeatedly expressed concerns as this year’s lambing season has seen the highest numbers of affected flocks within the past five years See more: Surge in cases of Schmallenberg impacting lambing chief executive of the National Sheep Association (NSA) said that the organisation has received worrying reports from farmers across the country “It seems to be at its worst through the West Midlands belt from Somerset “That’s where we’re hearing about the biggest losses.” Mr Stocker explains that Schmallenberg tends to follow a four- or five-year pattern The disease was first detected in the UK in 2012 with a large initial outbreak – an event which was followed by years of lower instances “The critical time is if in-lamb ewes are bitten from day 10 to 65 – essentially that first one-third of pregnancy – then the unborn lamb has got a high chance of being affected,” said Mr Stocker then they build up immunity and carry that for quite some time “It is causing some real stress and anxiety When you talk to the farmers going through it the first thing they will mention is anxiety While a licensed vaccine for Schmallenberg does exist it is not currently in production or available in the UK “A lot of people who have been badly hit this year have said that they would use a vaccine every year from now on “They wouldn’t run this risk again – it has just been devastating,” said Mr Stocker “The vaccine manufacturers have had their fingers burnt on this before when they’ve produced a load and not seen the uptake “But I think there would be enough demand for there to be a production of vaccines this year.” To try and build an accurate picture of the number of losses this year and to give the vaccine manufacturers hard industry evidence Mr Stocker says affected farmers should be regularly in touch with their vets “They should be talking to their vets about samples being submitted to the veterinary investigation centres for proper analysis although quite often you will just get aborted lambs or lambs that are born alive and just don’t survive and you struggle to get them going it’s going to be very difficult for us on an industry scale to see what is going on.” Shrewsbury sheep farmer Ben Lowe has lost 40% of his pedigree Texel lambs to Schmallenberg this year with devastating emotional and financial losses He says that farmers need a reliable mechanism to be able to report and quantify the losses that they have had “The biggest concern of mine at the moment is that the whole situation is massively under-reported and under-quantified,” he said  “Schmallenberg is silent and kept in lambing sheds kept quiet with farmers that are struggling with it “The only difference with something like bluetongue is that it is so much more demonstrative in the way that you have adult cattle and sheep Ben has had to keep them away from the lambing sheds this year due to the high number of traumatic losses “You get to the point where you’re snapping legs to get them out “These fused limbs are so stiff that you have to snap the legs to be in a position to get the lamb out “I can’t put either myself or my boys through what we went through again.” the industry will have a shot at getting a Schmallenberg vaccine back into production Especially from a food security point of view when we have uncertain times ahead of us and a massive potential loss in lamb production in the UK.” Zoetis has announced the launch of Zulvac SBV a new Schmallenberg vaccine licensed for use in cattle and sheep in two doses at a three week interval the second at least two weeks before mating Zulvac SBV is licensed for use in cattle and sheep in two doses at a three week interval Duration of immunity is six months in cattle and seven in sheep this covers the window of susceptibility during pregnancy; in sheep from day 28 to 56 Animals infected during these periods are at risk of malformed offspring and subsequent stillbirth The company says vaccination combined with insecticidal measures to control the midge vector remains the most effective way of protecting the population1 and ensuring a more unified level of immunity Zoetis vet Carolyn Hogan said: "Although SBV is now considered to be an enzootic pathogen in England and Wales there is plenty of evidence that seroprevalence at farm level – particularly on sheep farms - varies the proportion of herds and flocks naïve to SBV and at risk via introduction of naïve replacements increases So the risk of reinfection in assumed enzootic areas is potentially underestimated2 are widespread in Europe and move easily between farms and regions Carolyn says that whilst there have been no confirmed diagnoses of congenital abnormalities in calves or lambs from APHA in 2014 or 2015 unconfirmed anecdotal cases have been reported "We do not know whether our ruminant population is immune or susceptible and neither do we know if another SBV challenge will appear Vaccination remains the most effective way of ensuring valuable livestock are protected." PS: Whilst you're here, take a moment to see our latest job opportunities for vets Contact Us | Our Privacy Policy | Cookies | Terms & Conditions Facebook | Linkedin | Instagram | Twitter Learn more about advertising on VetSurgeon.org With numerous reports of Schmallenberg appearing in early lambing flocks this season farm vet from Cross Counties Farm Vets – part of the VetPartners group Mrs Rigby chairs the VetPartners Sheep Clinical Interest Group and runs the Cross Counties Flock Health Club She also has a small flock of sheep at home Have you seen an unusually high level of Schmallenberg in early lambing flocks so far this season I didn’t see any cases of Schmallenberg last year and only a couple of cases the year before Our earliest lambers seem to have been affected at the end of their lambing and those just starting are seeing cases now too In some parts of the country the situation has been much worse with some litters having one or more seemingly unaffected lambs Some of the affected lambs are born alive and need euthanising How is this affecting your farming clients Lambing is a high pressure time of year as it is For some it’s the anticipation of what’s to come having heard news of cases on neighbouring farms for others it’s the heartache of having to deal with increased mortalities The economic effects of poorer scanning results and fewer live lambs will be felt later in the year which obviously has a big impact on farming businesses Since Schmallenberg is spread by infected midges climate and therefore climate change undoubtedly has an effect A mild wet autumn/winter last year will have allowed midge survival later in the year meaning ewes could be bitten and infected during the critical window in pregnancy.At the moment it is thought that Schmallenberg is now endemic in our midge populations whereas previously infection occurred when infected midges were blown here from abroad This means future outbreaks are less dependent on the weather and infection levels overseas We currently seem to see the worst outbreaks of SBV in three-to-five-year cycles but also due to waning immunity in the national sheep flock meaning there is a greater number of susceptible sheep every three-to-five years The APHA are currently offering free Schmallenberg testing on brain samples from affected lambs or blood samples from ewes to look for exposure to the virus It’s really important that we continue testing even if it seems ‘obvious’ that’s its SBV to ensure we are assuming the correct diagnosis and to help us build a picture of the national situation or any other notifiable diseases on your farm Ruminant Health and Welfare has a web page dedicated to updates and information including farmer FAQs for BTV3, please visit: https://ruminanthw.org.uk/bluetongue-virus/ Read more livestock articles here Business and Rural news from the UK’s favourite monthly farming magazine We’ve now moved to our new office in Stowmarket If you wish to contact us please use our new address: Vets are urging farmers to be vigilant for Schmallenberg virus (SBV) – which can mimic other diseases including bluetongue – as a rising number of early lambing flocks are hit with deadly SBV this season Independent sheep consultant Fiona Lovatt said the UK has seen an increase in SBV “I’ve seen SBV in flocks that have been lambing since the beginning of January – a flock down in Dorset as well as a couple in the Cheshire area (22% of lambs born were affected in one of these flocks) “This is devastating for the farmers and really disheartening for everyone involved at lambing time,” she commented APHA has been offering free testing and since December 2023 has confirmed more than 25 cases in England through its scanning surveillance system However more suspect cases and samples are received daily The majority of the confirmed cases are congenital deformed lambs as a result of intra-uterine infection during pregnancy Acute clinical disease in adult cattle presents as: Adult sheep and goats generally do not show signs of clinical disease or with deformities following infection of the dam The most susceptible stages of pregnancy for foetal deformities are days 62–180 in cattle and 25–50 in sheep A recent technical webinar saw Rudolph Reichel stress the importance of ruling out other conditions which could mimic SBV – including bluetongue virus This is particularly important due to the new BTV-3 strain circulating in the UK as less is known about how this serotype presents Mr Reichel said recent cases of SBV have been confirmed in November showing signs of milk drop in dairy cattle congenital deformed lambs are being submitted which are likely to have been born end of December/early January and more recently in Oxfordshire and Gloucestershire so usually cases peak in late summer/early autumn However it’s thought that warmer weather this winter could be responsible for the unusual cases NSA chief executive Phil Stocker said: “It is extremely concerning to hear of proven (and assumed) cases of this virus in many areas of the UK These cases are from animals that were bitten by infected midges back in the autumn during their early stages of pregnancy.  “NSA would urge all working with sheep and cattle at these times to be vigilant to the signs of SBV and to contact their vets should they suspect the presence of any cases on their farms.” Dr Ami Sawran of Westpoint Farm Vets commented: “The SBV cases currently being detected are likely due to infection in late summer/early autumn Most cases confirmed by APHA are in stillborn lambs but it is worth noting that this may be seen in cattle “There are currently no plans to offer a vaccine for SBV however many different diseases can cause abortion or deformation in neonates some of which are manageable at herd or flock level so it is important to pursue diagnostics to determine the cause on your farm “If you have unfortunately been affected by poor scanning percentages abortions or issues at lambing and calving it is important to speak with your vet to determine any management changes that may serve to protect your herd or flock.” Farmers affected by SBV are encouraged to take part in a survey by the University of Nottingham to help build a picture of the extent of the problem, which can be found here For more information on free APHA SBV testing visit here Read more livestock articles here A devastating virus that causes fatal deformities in lambs has emerged again six years after killing thousands across UK farms Schmallenberg virus has been identified in 50 different flocks so far with farmers being urged to submit dead lambs with skeletal deformities for post-mortem Phil Stocker, chief executive of the National Sheep Association, told the Times that farmers have already experienced huge losses: "Some people are reporting 20% of the lamb crop lost," he said it causes severe malformations of lamb foetuses The disease spread through Western Europe in 2011 and caused a major epidemic the following lambing season It is thought the latest cases were caused by midges blown across the sea from the Netherlands or Germany largely disappeared over the following years – potentially through immunity built up by the animals with vets warning it could have a major impact - most breeding ewes have not yet given birth Ben Strugnell, from Farm Post Mortems, told Meat Trades Journal: "The possible re-emergence of Schmallenberg was predicted following a study in autumn 2015 which tested young flock replacement sheep in the south of England the results of which suggested that levels of immunity may have dropped "It is very important that if producers encounter lambs with skeletal deformities these are submitted for post-mortem examination so appropriate samples can be taken to establish whether Schmallenberg is the cause .. Younger sheep may be most at risk as older ones may be immune from previous exposure to the virus." The first case was detected in Cornwall in October experts warned that governments and farmers had become less aware of the virus because of its reduced circulation said: "Five years after its initial emergence this could shape the ideal conditions for a renewed large scale re-emergence of Schmallenberg virus that would probably be followed by a new abortion storm It seems advisable to closely monitor the situation via different surveillance techniques to allow timely warnings to veterinarians and farmers and to remind them to remain alert." the disease has been detected in the North East of England Get our news on your inbox! Suscribe x MercoPress, en Español Montevideo, May 6th 2025 - 02:55 UTC A disease that can lead to lambs and calves being stillborn or deformed has spread to every county in England and Wales Some farmers are expected to lose livestock during the lambing season Schmallenberg virus was first detected in the UK earlier this year in the south and east of England “We've seen quite rapid geographic spread,” the government's Chief Veterinary Officer “That means a lot of herds and flocks will have been exposed to the disease The likelihood is that many of them won't show disease because they weren't infected at the right time to show disease ”Some will - in those herds and flocks we expect an impact of 2-5% of their lambs and calves.“ Schmallenberg causes severe deformities in lambs and calves born to infected mothers Cases have been documented on 976 farms in England and Wales officials believe the true number of cases is higher The first sign is often when livestock give birth to deformed or dead young - which can be months after the infection has occurred the number of infected flocks and herds is likely to be ”very high“ head of endemic food-borne zoo-noses at the Animal Health Veterinary Laboratories Agencies said farmers should be vigilant for signs of infection particularly when livestock are giving birth ”The infection has been transmitted through the whole of England and Wales The new emerging livestock disease was identified late last year It is believed the virus was carried to England by midges blown across the Channel and was then spread by native midges during the summer Evidence from Europe suggests that around 6% of infected sheep flocks (and 4% of infected cattle herds) will suffer symptoms from the disease which is only dangerous when it is passed to the unborn lamb or calf Flocks that are infected should expect to lose between 2% and 5% of lambs I have no idea what this has to do with Latin America but it does and as a farmer I am worried that it will spread here The Europeans are very strict about animal health standards in South America but are very sloppy about controlling thier own research stations This latest disease “escaped” from a research station in Germany The last outbreak of foot and mouth disease in UK emanated from a research laboratory in Kent Not to mention the feeding of sheeps brains infected with scrapie to cattle which created BSE and its related human diseases which killed a number of people Well out here we dont allow those sloppy practices to kill people Commenting for this story is now closed.If you have a Facebook account, become a fan and comment on our Facebook Page 2012 4:32 PMFast-Spreading Animal Virus Leaps Europe UK BordersA newly identified disease dubbed the Schmallenberg virus is moving rapidly through livestock in Europe and it has authorities both worried and puzzled Superbug blogger Maryn McKenna reports.Save this storySaveSave this storySaveA newly identified disease is moving rapidly through livestock in Europe and has authorities both worried and puzzled dubbed Schmallenberg virus for a town in west-central Germany where one of the first outbreaks occurred kids and calves to be born dead or deformed The new virus belongs to the Bunyaviridae family Genetic characterisation has shown that the new virus is closest to the following Simbu serogroup viruses: Shamonda- which do not cause disease in humans.However at least 30 orthobunyaviruses are zoonotic and may cause disease in humans with symptoms ranging from mild to severe -- e.g Schmallenberg outbreaks in Germany as of Feb 6.The insect vector is also believed to be how the disease got to the UK The seven counties where it has been found so far -- Norfolk West Sussex and Hertfordshire -- are all in the southeast They are the first places in the UK to catch winds from the Continent and therefore the first where anything carried by the wind The international disease-warning mailing list ProMED has collected links to all the maps of outbreaks published so far: And the CDC journal Emerging Infectious Diseases has just posted ahead of print the first paper on the new disease Meanwhile, the British Veterinary Record seizes on the outbreaks to make a larger point: Finding new diseases such as Schmallenberg depends on having good disease surveillance -- but in the UK It is precisely this kind of emerging disease threat that scanning surveillance aims to detect – and it is also this kind of disease threat that might not be detected promptly if arrangements for surveillance fall short of the mark.. Schmallenberg virus is not the first new disease to be detected by scanning surveillance It was scanning surveillance that identified the emergence of BSE in the late 1980s and the early detection of pandemic H1N1 influenza in pigs antimicrobial resistance in Salmonella and virulent psoroptic mange in cattle The AHVLA has noted that the value of its surveillance programme has greatly exceeded the cost in recent years with monetised benefits having been estimated at over £200 million a year (Hat tip to constant reader Pat Gardiner.) It is the essential source of information and ideas that make sense of a world in constant transformation The WIRED conversation illuminates how technology is changing every aspect of our lives—from culture to business The breakthroughs and innovations that we uncover lead to new ways of thinking I wrote about maintaining enthusiasm for farming I have been criticised for being negative and praised for straight-talking We got away with it in the February lambers but have been badly hit by the virus in the late-March group A new symptom of the virus seems to be floppy non-viable lambs that aren’t deformed but cannot get going See also: Schmallenberg outbreak hits early lambing flocks An inability to regulate body temperature is one of the first signs We’ve had lambs that have got going but then go floppy and can’t bear their own weight This has been extremely tiring and demoralising and it looks like it’s killing about 11% – and that’s before all the other losses from stillbirths and E coli Wet conditions forced us to house everything for two weeks It’s been nice to have the option of sheds We have good grass cover on the rented ground The lambing students from Nottingham were good and understood lamb mal-presentation very quickly including a couple of caesareans in the Texels which was very fortunate given how many had died over the winter but the Baltimore Bridge collision will result in container ships being in the wrong place for at least eight weeks The trip around Africa is extremely expensive and of course the nightmare weather will peg the lamb crop down A strong hogg price will probably mean people cash in sheep on the trade On with the next job: bull preparations for the spring sale We have two great Charolais easy-calving bulls and two muscly Simmentals