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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