The prevalence of verocytotoxin-producing Escherichia coli (VTEC) and E-coli O157 : H7 in beef in Sweden determined by PCR assays and an immuno-magnetic separation (IMS) method

Citation
R. Lindqvist et al., The prevalence of verocytotoxin-producing Escherichia coli (VTEC) and E-coli O157 : H7 in beef in Sweden determined by PCR assays and an immuno-magnetic separation (IMS) method, FOOD MICROB, 15(6), 1998, pp. 591-601
Citations number
31
Categorie Soggetti
Food Science/Nutrition
Journal title
FOOD MICROBIOLOGY
ISSN journal
07400020 → ACNP
Volume
15
Issue
6
Year of publication
1998
Pages
591 - 601
Database
ISI
SICI code
0740-0020(199812)15:6<591:TPOVEC>2.0.ZU;2-I
Abstract
The number of cases of enterohaemorrhagic Escherichia coli (EHEC) in Sweden has increased dramatically since 1995 but no source of the infections has been identified. The prevalence of verocytotoxin-producing E. coli (VTEC), including E, coli O157:H7 in imported and domestic raw beef in Sweden, was determined by PCR assays and immune-magnetic separation (IMS, Dynal). VTEC was detected by a multiplex PCR directed at sequences on the vt1 and vt2 ge nes, and the prevalence of E. coli O157:H7 was estimated by the IMS assay a nd a SZ-PCR which detects E. coli O157:H7 land some strains of O157:NM, O55 :H7 and O55:NM). VTEC was detected in 15.5% (57/368) and 1.1% (6/543) of th e imported and domestic beef samples, respectively, by the multiplex PCR. E . coli O157:H7 was detected in 0.3% and 2.4% of the imported beef samples b y the IMs and SZ-PCR assays, respectively. in domestic beef E. coli O157:H7 was not detected by either method, indicating that the occurrence in Swedi sh beef was less than 0.6% with a 95% certainty. The overall prevalence of VTEC was estimated to be 4.0%, by adjusting for the relative proportion of imported and domestic beef in Sweden and, similarly, the overall prevalence of E. coli O157:H7 was 0.06% (IMS) or 0.5% (SZ-PCR). We propose that a use ful strategy to analyse a large number of food samples for VTEC and E. coli O157:H7 is an initial screening of samples using the multiplex VT-PCR in c onjunction with enrichment and buoyant density centrifugation, followed by further analyses on the fraction of VT-positive samples using either the IM S method or SZ-PCR. (C) 1998 Academic Press.