Affiliation:
1. Department of Biology, Haverford College, Haverford, Pennsylvania 19041
Abstract
ABSTRACT
Heat-resistant agglutinin 1 (Hra1) is an accessory colonization factor of enteroaggregative
Escherichia coli
(EAEC) strain 042. Tia, a close homolog of Hra1, is an invasin and adhesin that has been described in enterotoxigenic
E. coli
. We devised a PCR-restriction fragment length polymorphism screen for the associated genes and found that they occur among 55 (36.7%) of the enteroaggregative
E. coli
isolates screened, as well as lower proportions of enterotoxigenic, enteropathogenic, enterohemorrhagic, and commensal
E. coli
isolates. Overall, 25%, 8%, and 3% of 150 EAEC strains harbored
hra1
alone,
tia
alone, or both genes, respectively. One EAEC isolate, 60A, produced an amplicon with a unique restriction profile, distinct from those of
hra1
and
tia
. We cloned and sequenced the full-length agglutinin gene from strain 60A and have designated it
hra2
. The
hra2
gene was not detected in any of 257 diarrheagenic
E. coli
isolates in our collection but is present in the genome of
Salmonella enterica
serovar Heidelberg strain SL476. The cloned
hra2
gene from strain 60A, which encodes a predicted amino acid sequence that is 64% identical to that of Hra1 and 68% identical to that of Tia, was sufficient to confer adherence on
E. coli
K-12. We constructed an
hra2
deletion mutant of EAEC strain 60A. The mutant was deficient in adherence but not autoaggregation or invasion, pointing to a functional distinction from the autoagglutinin Hra1 and the Tia invasin. Hra1, Tia, and the novel accessory adhesin Hra2 are members of a family of integral outer membrane proteins that confer different colonization-associated phenotypes.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
23 articles.
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