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Genesis of variants of Vibrio cholerae O1 biotype El Tor: role of the CTXf array and its position in the genome

IR@IICB: CSIR-Indian Institute of Chemical Biology, Kolkata

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Title Genesis of variants of Vibrio cholerae O1 biotype El Tor: role of the CTXf array and its position in the genome
 
Creator Nandi, Suvobroto
Maiti, Diganta
Saha, Arjun
Bhadra, Rupak K
 
Subject Infectious Diseases and Immunology
 
Description The gene encoding cholera toxin, the principal virulence factor of Vibrio cholerae, is encoded by a filamentous, lysogenic bacteriophage known as CTXf. The genome of V. cholerae, the host for CTXf, consists of two chromosomes, one large and one small. Here, it is shown that localization and array of CTX prophage DNA in either the large or small chromosome of V. cholerae is likely to be one of the reasons for the emergence of O1 biotype El Tor variants isolated just before and after the V. cholerae O139 cholera outbreak in 1992. Analyses of the organization of the CTX region of the genome of pre-O139 El Tor strains revealed that these strains carry two distinct CTX prophages integrated in the small chromosome in tandem: CTXET, the prophage having a conserved NotI site in its repeat sequence segment which seems to be specific for the El Tor strains so far examined, followed by CTXcalc-like genome, the prophage found in recent O139 clinical isolates from Calcutta. In sharp contrast, in post-O139 El Tor strains only one copy of the CTXET prophage was found to be integrated in the large chromosome. To the authors’ knowledge, the presence of CTX prophage in the small chromosome of O1 El Tor strains has not been reported previously.
 
Publisher American Society for Microbiology
 
Date 2003
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://www.eprints.iicb.res.in/565/1/MICROBIOLOGY%2DSGM%2C149%2C_89%2D97[95].pdf
Nandi, Suvobroto and Maiti, Diganta and Saha, Arjun and Bhadra, Rupak K (2003) Genesis of variants of Vibrio cholerae O1 biotype El Tor: role of the CTXf array and its position in the genome. Journal of Clinical Microbiology, 149. pp. 89-97.
 
Relation http://dx.doi.org/10.1099/mic.0.25599-0
http://www.eprints.iicb.res.in/565/