Abstract

SummaryUnder‐reporting of foot‐and‐mouth disease (FMD) masks the true prevalence in parts of the world where the disease is endemic. Laboratory testing for the detection of FMD virus (FMDV) is usually reliant upon the collection of vesicular epithelium and fluid samples that can only be collected from acutely infected animals, and therefore animals with sub‐clinical infection may not be identified. Milk is a non‐invasive sample type routinely collected from dairy farms that has been utilized for surveillance of a number of other diseases. The aim of this study was to examine the application of milk as an alternative sample type for FMDV detection and typing, and to evaluate milk as a novel approach for targeted surveillance of FMD in East Africa. FMDV RNA was detected in 73/190 (38%) individual milk samples collected from naturally infected cattle in northern Tanzania. Furthermore, typing information by lineage‐specific rRT‐PCR assays was obtained for 58% of positive samples, and corresponded with the virus types identified during outbreak investigations in the study area. The VP1‐coding sequence data obtained from milk samples corresponded with the sequence data generated from paired epithelial samples collected from the same animal. This study demonstrates that milk represents a potentially valuable sample type for FMDV surveillance and might be used to overcome some of the existing biases of traditional surveillance methods. However, it is recommended that care is taken during sample collection and testing to minimize the likelihood of cross‐contamination. Such approaches could strengthen FMDV surveillance capabilities in East Africa, both at the individual animal and herd level.

Highlights

  • Foot-­and-­mouth disease (FMD) is a highly contagious disease of cloven-­hooved mammals and is of great global economic importance (Knight-­Jones & Rushton, 2013)

  • Pan-­serotypic real-­time reverse-­transcription polymerase chain reaction assays have been described for the rapid detection of FMD virus (FMDV) in typical clinical samples (Callahan et al, 2002; King et al, 2006; Reid et al, 2002; Shaw et al, 2007)

  • Alternative explanations should be considered, including the possibility that these results represent (a) contamination due to contact with materials infected with other FMDV types during sample collection in the field, transport or testing in the laboratory; or (b) cross-­reaction between the individual typing rRT-­PCR assays, no evidence of this has been observed during the validation of these tests (Bachanek-­Bankowska et al, 2016)

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Summary

SHORT COMMUNICATION

Opportunities for enhanced surveillance of foot-­and-­mouth disease in endemic settings using milk samples. Pan-­serotypic real-­time reverse-­transcription polymerase chain reaction (rRT-­PCR) assays have been described for the rapid detection of FMDV in typical clinical samples (Callahan et al, 2002; King et al, 2006; Reid et al, 2002; Shaw et al, 2007) These assays target highly conserved genomic regions that are shared among all serotypes and topotypes, but do not differentiate between them. Alternative explanations should be considered, including the possibility that these results represent (a) contamination due to contact with materials infected with other FMDV types during sample collection in the field, transport or testing in the laboratory; or (b) cross-­reaction between the individual typing rRT-­PCR assays, no evidence of this has been. In animal A, SAT 1 was detected in the vesicular lesion sample only

Vesicular fluid
Findings
SUPPORTING INFORMATION
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