Affiliation:
1. Division of Infectious Diseases, Department of Medicine, Vanderbilt University School of Medicine and VA Medical Center, Nashville, Tennessee,1 and
2. First Department of Internal Medicine, Nagoya University School of Medicine, Nagoya, Japan2
Abstract
ABSTRACT
Helicobacter pylori
is naturally competent for DNA transformation, but the mechanism by which transformation occurs is not known. For
Haemophilus influenzae
,
dprA
is required for transformation by chromosomal but not plasmid DNA, and the complete genomic sequence of
H. pylori
26695 revealed a
dprA
homolog (HP0333). Examination of genetic databases indicates that DprA homologs are present in a wide variety of bacterial species. To examine whether HP0333 has a function similar to
dprA
of
H. influenzae
, HP0333, present in each of 11 strains studied, was disrupted in two
H. pylori
isolates. For both mutants, the frequency of transformation by
H. pylori
chromosomal DNA was markedly reduced, but not eliminated, compared to their wild-type parental strains. Mutation of HP0333 also resulted in a marked decrease in transformation frequency by a shuttle plasmid (pHP1), which differs from the phenotype described in
H. influenzae
. Complementation of the mutant with HP0333 inserted in
trans
in the chromosomal
ureAB
locus completely restored the frequency of transformation to that of the wild-type strain. Thus, while
dprA
is required for high-frequency transformation, transformation also may occur independently of DprA. The presence of DprA homologs in bacteria known not to be naturally competent suggests a broad function in DNA processing.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
86 articles.
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