Affiliation:
1. National Laboratory for Enteric Pathogens, National Microbiology Laboratory, Winnipeg, Canada
Abstract
ABSTRACT
Strains of Shiga toxin-producing
Escherichia coli
(STEC) have been associated with outbreaks of diarrhea, hemorrhagic colitis, and hemolytic-uremic syndrome in humans. Most clinical signs of disease arise as a consequence of the production of Shiga toxin 1 (Stx1), Stx2 or combinations of these toxins. Other major virulence factors include enterohemorrhagic
E. coli
hemolysin (EHEC
hlyA
), and intimin, the product of the
eaeA
gene that is involved in the attaching and effacing adherence phenotype. In this study, a series of multiplex-PCR assays were developed to detect the eight most-important
E. coli
genes associated with virulence, two that define the serotype and therefore the identity of the organism, and a built-in gene detection control. Those genes detected were
stx
1
,
stx
2
,
stx
2c
,
stx
2d
,
stx
2e
,
stx
2f
, EHEC
hlyA
, and
eaeA
, as well as
rfbE
, which encodes the
E. coli
O157 serotype;
fliC
, which encodes the
E. coli
flagellum H7 serotype; and the
E. coli
16S rRNA, which was included as an internal control. A total of 129
E. coli
strains, including 81 that were O157:H7, 10 that were O157:non-H7, and 38 that were non-O157 isolates, were investigated. Among the 129 samples, 101 (78.3%) were
stx
positive, while 28 (21.7%) were lacked
stx
. Of these 129 isolates, 92 (71.3%) were EHEC
hlyA
positive and 96 (74.4%) were
eaeA
positive. All STEC strains were identified by this procedure. In addition, all Stx2 subtypes, which had been initially identified by PCR-restriction fragment length polymorphism, were identified by this method. A particular strength of the assay was the identification of these 11 genes without the need to use restriction enzyme digestion. The proposed method is a simple, reliable, and rapid procedure that can detect the major virulence factors of
E. coli
while differentiating O157:H7 from non-O157 isolates.
Publisher
American Society for Microbiology