A multiplex PCR method for simultaneous detection of Yersinia enterocolitica and ail gene has been applied on samples from slaughtered pig carcasses. The method was effective, fast and simple, capable of detecting pathogenic Yersinia enterocolitica in 48-72 hours. It offers significant advantages over the microbiological methods of isolation, allowing shorter response times and early detection of strains carrying the pathogenicity factor.
“Applicazione di un metodo biomolecolare per la ricerca rapida di Yersinia enterocolitica patogena in carcasse di suini regolarmente macellati”
LOSCHI, Anna Rita;
2010-01-01
Abstract
A multiplex PCR method for simultaneous detection of Yersinia enterocolitica and ail gene has been applied on samples from slaughtered pig carcasses. The method was effective, fast and simple, capable of detecting pathogenic Yersinia enterocolitica in 48-72 hours. It offers significant advantages over the microbiological methods of isolation, allowing shorter response times and early detection of strains carrying the pathogenicity factor.File in questo prodotto:
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