Abstract

Bovine leukaemia virus (BLV) is the causative agent of enzootic bovine leucosis, which has been reported worldwide. BLV has been found recently in human tissue and it could have a significant impact on human health. A possible hypothesis regarding viral entry to humans is through the consumption of infected foodstuffs. This study was aimed at detecting the presence of BLV DNA in raw beef and fresh milk for human consumption. Nested PCR directed at the BLV gag gene (272 bp) was used as a diagnostic test. PCR products were confirmed by Sanger sequencing. Forty-nine per cent of the samples proved positive for the presence of proviral DNA. This is the first study highlighting the presence of the BLV gag gene in meat products for human consumption and confirms the presence of the viral DNA in raw milk, as in previous reports. The presence of viral DNA in food products could suggest that viral particles may also be found. Further studies are needed to confirm the presence of infected viral particles, even though the present findings could represent a first approach to BLV transmission to humans through foodstuff consumption.

Highlights

  • Fifty beef samples weighing around 15 g each were obtained from butchers in Bogotá whilst the 50 samples of milk were obtained from farms specialising in dairy production located in different parts of Colombia

  • The second hypothesis concerns possible Bovine leukaemia virus (BLV) transmission through vaccine production processes involving the use of BLV-contaminated foetal bovine sera, even though no experimental evidence has been published regarding this issue

  • The third hypothesis proposes that the virus might infect humans through the consumption of bovine-derived products from BLV-infected cattle [10, 23], leading to the idea of evaluating meat and milk products for human consumption as a possible pathway for viral entry

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Summary

Objectives

This study was aimed at detecting the presence of BLV DNA in raw beef and fresh milk for human consumption

Methods
Results
Conclusion

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