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PMID: 11773130 Published · ppublish English Evaluation Study Journal Article Research Support, Non-U.S. Gov't

Direct detection and characterization of Shiga toxigenic Escherichia coli by multiplex PCR for stx1, stx2, eae, ehxA, and saa.

Journal of clinical microbiology ·Vol. 40 ·No. 1 ·2002-01-00 ·Pages 271-4

Paton AW, Paton JC

Abstract

We recently described a novel megaplasmid-encoded adhesin produced by certain Shiga toxigenic Escherichia coli (STEC) strains that lack the locus for enterocyte effacement (LEE) pathogenicity island. This adhesin, designated Saa (STEC autoagglutinating adhesin), may be a marker for a subset of LEE-negative STEC strains capable of causing severe gastrointestinal and systemic diseases in humans. In this study, we developed a pentavalent PCR assay for the detection of saa as well as other proven and putative STEC virulence genes (stx1, stx2, eae, and ehxA). The five primer pairs used in the assay do not interfere with each other and generate amplification products of 119, 180, 255, 384, and 534 bp.

MeSH Terms
Adhesins, Bacterial/genetics DNA Primers Escherichia coli/genetics,metabolism,pathogenicity Escherichia coli Infections/diagnosis,microbiology Escherichia coli Proteins/genetics Feces/microbiology Humans Polymerase Chain Reaction/methods Sensitivity and Specificity Shiga Toxins/genetics,metabolism Virulence/genetics
Chemicals
Adhesins, Bacterial DNA Primers Escherichia coli Proteins SAA protein, E coli Shiga Toxins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Paton Adrienne W
Department of Molecular Biosciences, Adelaide University, Adelaide, South Australia 5005, Australia.
Paton James C
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Article Info
Journal
Journal of clinical microbiology
Abbr.
J Clin Microbiol
ISSN
0095-1137
Published
2002-01-00
Pages
271-4
Language
English
Region
United States
NLM ID
7505564
PMCID
PMC120136
Subset
IM
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