Comparative Genomic Analyses of the Vibrio Pathogenicity Island and Cholera Toxin Prophage Regions in Nonepidemic Serogroup Strains of
Vibrio cholerae
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Published:2003-03
Issue:3
Volume:69
Page:1728-1738
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ISSN:0099-2240
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Container-title:Applied and Environmental Microbiology
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language:en
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Short-container-title:Appl Environ Microbiol
Author:
Li Manrong12, Kotetishvili Mamuka1, Chen Yuansha1, Sozhamannan Shanmuga12
Affiliation:
1. Department of Epidemiology and Preventive Medicine, University of Maryland School of Medicine 2. VA Maryland Health Care System, Baltimore, Maryland 21201
Abstract
ABSTRACT
Two major virulence factors are associated with epidemic strains (O1 and O139 serogroups) of
Vibrio cholerae
: cholera toxin encoded by the
ctxAB
genes and toxin-coregulated pilus encoded by the
tcpA
gene. The
ctx
genes reside in the genome of a filamentous phage (CTXφ), and the
tcpA
gene resides in a vibrio pathogenicity island (VPI) which has also been proposed to be a filamentous phage designated VPIφ. In order to determine the prevalence of horizontal transfer of VPI and CTXφ among nonepidemic (non-O1 and non-O139 serogroups)
V. cholerae
, 300 strains of both clinical and environmental origin were screened for the presence of
tcpA
and
ctxAB
. In this paper, we present the comparative genetic analyses of 11 nonepidemic serogroup strains which carry the VPI cluster. Seven of the 11 VPI
+
strains have also acquired the CTXφ. Multilocus sequence typing and restriction fragment length polymorphism analyses of the VPI and CTXφ prophage regions revealed that the non-O1 and non-O139 strains were genetically diverse and clustered in lineages distinct from that of the epidemic strains. The left end of the VPI in the non-O1 and non-O139 strains exhibited extensive DNA rearrangements. In addition, several CTXφ prophage types characterized by novel repressor (
rstR
) and
ctxAB
genes and VPIs with novel
tcpA
genes were found in these strains. These data suggest that the potentially pathogenic, nonepidemic, non-O1 and non-O139 strains identified in our study most likely evolved by sequential horizontal acquisition of the VPI and CTXφ independently rather than by exchange of O-antigen biosynthesis regions in an existing epidemic strain.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
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