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Modelling the long-term seroprevalence evolution against Schmallenberg virus (SBV) is of first interest to plan vaccination strategies and to predict viral resurgence. The objectives of this study were first to estimate the duration of colostral immunity and the persistence of active immunity in a sheep flock that encountered two episodes of natural SBV infection and then to model the evolution of SBV seroprevalence by considering immune status as well as zootechnical variables. The entire sheep flock of the University of Namur composed by around 400 ewes producing 600 lambs a year and characterized by an annual 24.0% renewal rate was used for this study from January 2012 until December 2016. Antibody titers were estimated by performing Virus Neutralization Test (VNT) from blood and colostrum samples collected in lambs and adult sheep. Colostral antibodies against SBV of lambs born to seropositive ewes were detectable during four months. A significant increase of anti-SBV antibody titers was observed in lambs' serum as well as in ewes' colostrum between the time of first viral episode (2011) and the time of SBV reemergence (2012) suggesting a booster effect of viral resurgence on immune status. In naturally SBV infected adult sheep, the active immunity was estimated to last at least four years. These results combined with flock management data allowed to develop a mathematical model to predict the evolution of SBV seroprevalence at a herd scale. The accuracy of this model was assessed by VNT experiment performed at the end of the study. By applying this model to the sheep flock of the University of Namur, it was estimated that an annual 24.0% renewal rate led to total seronegativity, and so high susceptibility to viral resurgence, in 50 months after time of last natural infection. The third SBV episode detected in this research sheep flock within the expected time demonstrated huge within-flock susceptibility., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Schmallenberg virus (SBV), initially identified in Germany in 2011, spread rapidly throughout Europe causing significant economic losses in ruminant livestock. The ability to correctly detect emerging and re-emerging diseases such as SBV with reliable tests is of high importance. Firstly, we tested diagnostic performance, specificity, and sensitivity of three different assays used in SBV antibody detection using control sheep samples of determined status. After obtaining the results from the control samples, we assessed the potential of the assays to detect previously infected animals in field situations. The samples were investigated using IDEXX Schmallenberg virus Antibody Test Kit, ID Screen Schmallenberg virus Competition Multi-species ELISA and Serum Neutralisation Test (SNT). Analysis of control samples revealed that SNT was the most suitable test, which was therefore used to calculate concordance and test performance for the two other ELISA tests. To evaluate whether different assay performances had an impact under field conditions, sheep samples from two different contexts were tested: the emergence of SBV in Ireland and the re-emergence of SBV in Belgium. Comparing the results obtained from different assays to the non-reference standard assay SNT, we showed considerable differences in estimates of their sensitivity to detect SBV antibodies and to measure seroprevalence of the sheep flocks. Finally, a calculation of the number of randomly selected animals that needs to be screened from a finite flock, showed that SNT and ID.Vet are the most suitable to detect an introduction of the disease in low seroprevalence situations. The IDEXX ELISA test was only able to detect SBV antibodies in a higher seroprevalence context, which is not optimal for monitoring freedom of disease and surveillance studies.

A large sheep flock screened over a two-year period showed active spreading of Schmallenberg virus (SBV) during the summers of 2011 and 2012. Transplacental infections were observed during the two associated lambing periods (the winters of 2012 and 2013). Analysis of small (S) segment sequences of 38 SBV-positive samples, collected during periods of viral spreading and lambing revealed intra-herd sequences diversity and sub-consensus variability occurring after transplacental infections. In comparison with the nucleoprotein (N), which appeared to be conserved, the non-structural protein (NSs) showed the highest level of variability at the time of viral emergence and over the two-year analysis period.

Reemergence of Schmallenberg virus (SBV) occurred among lambs (n = 50) in a sheep flock in Belgium between mid-July and mid-October 2012. Bimonthly assessment by quantitative reverse transcription PCR and seroneutralization demonstrated that 100% of lambs were infected. Viremia duration may be longer in naturally infected than in experimentally infected animals.

Detected for the first time in 2011, Schmallenberg virus (SBV) is an orthobunyavirus of the Simbu serogroup that caused a large outbreak in European ruminants. In a tight time frame, data have been obtained on SBV epidemiology and the clinical pictures associated with this new viral infection, but little information is available on the molecular biology of SBV. In this study, SBV sequence variability was characterized from the central nervous system of two stillborn lambs in a naturally infected herd. A hypervariable region (HVR) was detected in the N-terminal region of the SBV Gc glycoprotein through sequencing and analysis of the two full-length genomes representative of intra-herd SBV dissemination. In vitro growth assays coupled with full-length genome sequencing were performed on the two isolates after successive cellular passages, showing an in vitro adaptation of SBV and mutation accumulation inside the HVR in the absence of immune selective pressure.