Affiliation:
1. Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138
Abstract
ABSTRACT
We studied the ancestry of virulence-associated genes in
Escherichia coli
by examining chromosomal regions specific to pathogenic isolates. The four virulence determinants examined were the alpha-hemolysin (
hly
) loci
hlyI
and
hlyII
, the type II capsule gene cluster
kps
, and the P (
pap
) and S (
sfa
) fimbria gene clusters. All four loci were shown previously to be associated with pathogenicity islands of uropathogenic
E. coli
isolates. The
hly
,
kps
,
sfa
, and
pap
regions each have an unexpected clustered distribution among the
E. coli
collection of reference (ECOR) strains, but all these regions were absent from a collection of diarrheagenic
E. coli
isolates. Strains in the ECOR subgroup B2 typically had a combination of at least three of the four loci, and all strains in subgroup D had a copy of the
kps
and
pap
clusters. In contrast, only four strains in subgroup A had either
hly
,
kps
,
sfa
, or
pap
, and no subgroup A strains had all four together. Strains of subgroup B1 were devoid of all four virulence regions, with the exception of one isolate that had a copy of the
sfa
gene cluster. This phylogenetic distribution of strain-specific sequences corresponds to the ECOR groups with the largest genome size, namely, B2 and D. We propose that the pathogenicity islands are ancestral to subgroups B2 and D and were acquired after speciation, with subsequent horizontal transfer into some group A, B1, and E lineages. These results suggest that the
hly
,
kps
,
sfa
, and
pap
pathogenicity determinants may play a role in the evolution of enteric bacteria quite apart from, and perhaps with precedence over, their ability to cause disease.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
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