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Validation of a commercially available indirect ELISA using a nucleocapside recombinant protein for detection of Schmallenberg virus antibodies.

Bréard, Emmanuel
Lara, Estelle
Comtet, Loïc
Viarouge, Cyril
Doceul, Virginie
Desprat, Alexandra
Vitour, Damien
Pozzi, Nathalie
Cay, Ann Brigitte
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Abstract

A newly developed Enzym Like Immuno Sorbant Assay (ELISA) based on the recombinant nucleocapsid protein (N) of Schmallenberg virus (SBV) was evaluated and validated for the detection of SBV-specific IgG antibodies in ruminant sera by three European Reference Laboratories. Validation data sets derived from sheep, goat and bovine sera collected in France and Germany (n = 1515) in 2011 and 2012 were categorized according to the results of a virus neutralization test (VNT) or an indirect immuno-fluorescence assay (IFA). The specificity was evaluated with 1364 sera from sheep, goat and bovine collected in France and Belgium before 2009. Overall agreement between VNT and ELISA was 98.9% and 98.3% between VNT and IFA, indicating a very good concordance between the different techniques. Although cross-reactions with other Orthobunyavirus from the Simbu serogroup viruses might occur, it is a highly sensitive, specific and robust ELISA-test validated to detect anti-SBV antibodies. This test can be applied for SBV sero-diagnostics and disease-surveillance studies in ruminant species in Europe.

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2013-07-01
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Peer reviewed scientific article
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Animals, Antibodies, Neutralizing, Antibodies, Viral, Bunyaviridae Infections, Cattle, Enzyme-Linked Immunosorbent Assay, Europe, Fluorescent Antibody Technique, Indirect, Gene Expression, Neutralization Tests, Nucleocapsid Proteins, Orthobunyavirus, Reagent Kits, Diagnostic, Recombinant Proteins, Reproducibility of Results, Roc Curve, Sheep
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