Key result
Commercial NSP-ELISA kits yield ~72% lower field sensitivity than LPBE in infected cattle and pigs.
Why the study?
Do commercial NSP-ELISA kits have comparable sensitivity and specificity to LPBE for detecting FMDV antibodies?
Observational (n=670)
Do commercial NSP-ELISA kits have comparable sensitivity and specificity to LPBE for detecting FMDV antibodies?
Absolute Event Rate: 28.4% vs 100%
p-value: p=<0.01
Commercial NSP-ELISA kits have lower sensitivity than LPBE for detecting FMDV antibodies, making them unsuitable for a 'vaccination-to-live' policy in Japan.
In this study, we validated three commercial ELISA (NSP-ELISA) kits that detect antibodies to a nonstructural protein of foot-and-mouth disease virus (FMDV) in terms of their specificities and sensitivities. Although the specificities of the NSP-ELISA kits were as high as that of liquid-phase blocking ELISA (LPBE) in non-infected, non-vaccinated animals, the sensitivities of the NSP-ELISA kits were significantly lower than those of the present LPBE and did not agree with the findings of a previous report on infected animals in the field. Therefore, although countries can adopt both a "vaccination-to-kill" policy and a "vaccination-to-live" policy after emergency vaccination during an FMD epidemic, the NSP-ELISA kits do not seem to be suitable for the latter policy in Japan. These results should be useful for choosing appropriate control measures for potential future FMD epidemics in Japan and elsewhere.
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Fukai et al. (2013) conducted an observational in Foot-and-Mouth Disease (n=670). NSP-ELISA kits (PrioCHECK, SVANOVIR, IDEXX) vs. Liquid-phase blocking ELISA (LPBE) was evaluated on Diagnostic sensitivity in infected animals in the field (p=<0.01). The sensitivities of the three commercial NSP-ELISA kits in infected cattle and pigs in the field were significantly lower (21.6-28.4% and 4.0%, respectively) than that of the LPBE (100%).
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