Eight-hour PCR-based procedure for the detection of Salmonella in raw oysters.

Abstract:

:The aim of this study was to evaluate the ability of a nested PCR system to detect Salmonella senftenberg in raw oysters. The specific primers of the PCR were derived from the invA gene sequence, essential for Salmonella invasiveness into epithelial cells. First, for the extraction of DNA, four methods (guanidine isothiocyanate, E.Z.N.A. Mollusc Kit, Chelex-100, and lysis with detergents) were compared. A nested PCR method combined with 3.5 h pre-enrichment in buffered peptone water (BPW) and DNA extraction by the resin Chelex-100 is proposed for the detection of S. senftenberg in oyster samples. The detection limit of the method is less than 0.1 CFU/ml (<1 CFU/g of oyster). This procedure is shown to be an excellent tool for the sensitive detection of S. senftenberg from naturally contaminated oysters, with results being obtained within 8 h.

journal_name

FEMS Microbiol Lett

authors

Vázquez-Novelle MD,Pazos AJ,Abad M,Sánchez JL,Pérez-Parallé ML

doi

10.1016/j.femsle.2004.12.016

keywords:

subject

Has Abstract

pub_date

2005-02-01 00:00:00

pages

279-83

issue

1

eissn

0378-1097

issn

1574-6968

pii

S0378-1097(04)00905-X

journal_volume

243

pub_type

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