Affiliation:
1. Department of Microbiology, The University of Sydney, Sydney, New South Wales 2006, Australia
Abstract
ABSTRACT
Studies of the
Vibrio cholerae
population, using molecular typing techniques, have shown the existence of several pathogenic clones, mainly sixth-pandemic, seventh-pandemic, and U.S. Gulf Coast clones. However, the relationship of the pathogenic clones to environmental
V. cholerae
isolates remains unclear. A previous study to determine the phylogeny of
V. cholerae
by sequencing the
asd
(aspartate semialdehyde dehydrogenase) gene of
V. cholerae
showed that the sixth-pandemic, seventh-pandemic, and U.S. Gulf Coast clones had very different
asd
sequences which fell into separate lineages in the
V. cholerae
population. As gene trees drawn from a single gene may not reflect the true topology of the population, we sequenced the
mdh
(malate dehydrogenase) and
hlyA
(hemolysin A) genes from representatives of environmental and clinical isolates of
V. cholerae
and found that the
mdh
and
hlyA
sequences from the three pathogenic clones were identical, except for the previously reported 11-bp deletion in
hlyA
in the sixth-pandemic clone. Identical sequences were obtained, despite average nucleotide differences in the
mdh
and
hlyA
genes of 1.52 and 3.25%, respectively, among all the isolates, suggesting that the three pathogenic clones are closely related. To extend these observations, segments of the
recA
and
dnaE
genes were sequenced from a selection of the pathogenic isolates, where the sequences were either identical or substantially different between the clones. The results show that the three pathogenic clones are very closely related and that there has been a high level of recombination in their evolution.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
79 articles.
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