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Infection and Immunity, March 1999, p. 1116-1124, Vol. 67, No. 3
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Evolutionary Relationships of Pathogenic Clones of Vibrio
cholerae by Sequence Analysis of Four Housekeeping
Genes
Roy
Byun,
Liam D. H.
Elbourne,
Ruiting
Lan, and
Peter R.
Reeves*
Department of Microbiology, The University of
Sydney, Sydney, New South Wales 2006, Australia
Received 17 July 1998/Returned for modification 6 October
1998/Accepted 10 December 1998
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.
*
Corresponding author. Mailing address: Department of
Microbiology (GO8), The University of Sydney, Sydney, New South Wales 2006, Australia. Phone: (61)(2) 9351 2536. Fax: (61)(2) 9351 4571. E-mail: reeves{at}angis.usyd.edu.au.
Infection and Immunity, March 1999, p. 1116-1124, Vol. 67, No. 3
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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