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PMID: 10542181 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The Vibrio cholerae O139 Calcutta bacteriophage CTXphi is infectious and encodes a novel repressor.

Journal of bacteriology ·Vol. 181 ·No. 21 ·1999-11-00 ·Pages 6779-87

Davis BM, Kimsey HH, Chang W, Waldor MK

Abstract

CTXphi is a lysogenic, filamentous bacteriophage. Its genome includes the genes encoding cholera toxin (ctxAB), one of the principal virulence factors of Vibrio cholerae; consequently, nonpathogenic strains of V. cholerae can be converted into toxigenic strains by CTXphi infection. O139 Calcutta strains of V. cholerae, which were linked to cholera outbreaks in Calcutta, India, in 1996, are novel pathogenic strains that carry two distinct CTX prophages integrated in tandem: CTX(ET), the prophage previously characterized within El Tor strains, and a new CTX Calcutta prophage (CTX(calc)). We found that the CTX(calc) prophage gives rise to infectious virions; thus, CTX(ET)phi is no longer the only known vector for transmission of ctxAB. The most functionally significant differences between the nucleotide sequences of CTX(calc)phi and CTX(ET)phi are located within the phages' repressor genes (rstR(calc) and rstR(ET), respectively) and their RstR operators. RstR(calc) is a novel, allele-specific repressor that regulates replication of CTX(calc)phi by inhibiting the activity of the rstA(calc) promoter. RstR(calc) has no inhibitory effect upon the classical and El Tor rstA promoters, which are instead regulated by their cognate RstRs. Consequently, production of RstR(calc) renders a CTX(calc) lysogen immune to superinfection by CTX(calc)phi but susceptible (heteroimmune) to infection by CTX(ET)phi. Analysis of the prophage arrays generated by sequentially integrated CTX phages revealed that pathogenic V. cholerae O139 Calcutta probably arose via infection of an O139 CTX(ET)phi lysogen by CTX(calc)phi.

MeSH Terms
Bacterial Proteins Base Sequence DNA, Viral/analysis Inoviridae/genetics,isolation & purification,physiology Lysogeny Molecular Sequence Data Promoter Regions, Genetic Repressor Proteins/genetics,metabolism Sequence Analysis, DNA Transduction, Genetic Vibrio cholerae/growth & development,virology Viral Proteins/genetics,metabolism Virus Replication
Chemicals
Bacterial Proteins DNA, Viral Repressor Proteins RstR protein, Vibrio cholerae Viral Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Davis B M
Tufts University School of Medicine and Division of Geographic Medicine and Infectious Diseases, Tupper Research Institute, Boston, Massachusetts 02111, USA.
Kimsey H H
Chang W
Waldor M K
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Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1999-11-00
Pages
6779-87
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC94144
Subset
IM
Grants
NIAID NIH HHS · R01 AI042347 · United States
NIDDK NIH HHS · P30 DK034928 · United States
NIAID NIH HHS · AI-42347 · United States
NIDDK NIH HHS · P30DK-34928 · United States
NIAID NIH HHS · T32 AI07329 · United States
NIAID NIH HHS · T32 AI007329 · United States
NIAID NIH HHS · R37 AI042347 · United States
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