Inter-laboratory comparison of 2 ELISA kits used for foot-and-mouth disease virus nonstructural protein serology

Author:

Browning Clare F. J.1,Di Nardo Antonello1,Henry Lissie1,Pollard Tim2,Hendry Lynne2,Romey Aurore3,Relmy Anthony3,Eble Phaedra4,Brocchi Emiliana5,Grazioli Santina5,King Donald P.1,Ludi Anna B.1ORCID

Affiliation:

1. The Pirbright Institute, Pirbright, Surrey, United Kingdom

2. Animal and Plant Health Agency, New Haw, United Kingdom

3. ANSES, Laboratoire de Santé Animale de Maisons-Alfort, INRA, École Nationale Vétérinaire d’Alfort, ANSES, Université Paris-Est, Maisons-Alfort, France

4. Wageningen Bioveterinary Research (WBVR), Lelystad, The Netherlands

5. Istituto Zooprofilattico Sperimentale della Lombardia e dell’Emilia-Romagna, Brescia, Italy

Abstract

Serologic assays used to detect antibodies to nonstructural proteins (NSPs) of foot-and-mouth disease virus (FMDV) are used for disease surveillance in endemic countries, and are essential to providing evidence for freedom of the disease with or without vaccination and to recover the free status of a country after an outbreak. In a 5-site inter-laboratory study, we compared the performance of 2 commercial NSP ELISA kits (ID Screen FMD NSP ELISA single day [short] and overnight protocols, ID.Vet; PrioCHECK FMDV NS antibody ELISA, Thermo Fisher Scientific). The overall concordance between the PrioCHECK and ID Screen test was 93.8% (95% CI: 92.0–95.2%) and 94.8% (95% CI: 93.1–96.1%) for the overnight and short ID Screen incubation protocols, respectively. Our results indicate that the assays (including the 2 different formats of the ID Screen test) can be used interchangeably in post-outbreak serosurveillance.

Funder

Biotechnology and Biological Sciences Research Council

department for environment, food and rural affairs, uk government

Publisher

SAGE Publications

Subject

General Veterinary

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