Literature DB >> 9618534

CTXphi immunity: application in the development of cholera vaccines.

H H Kimsey1, M K Waldor.   

Abstract

CTXphi is a filamentous bacteriophage that encodes cholera toxin, the principal virulence factor of Vibrio cholerae. CTXphi is unusual among filamentous phages because it encodes a repressor and forms lysogens. CTXphi can infect the existing live-attenuated V. cholerae vaccine strains derived from either the El Tor or classical V. cholerae biotypes and result in vaccine reversion to toxinogenicity. Intraintestinal CTXphi transduction assays were used to demonstrate that El Tor biotype strains of V. cholerae are immune to infection with the El Tor-derived CTXphi, whereas classical strains are not. The El Tor CTXphi repressor, RstR, was sufficient to render classical strains immune to infection with the El Tor CTXphi. The DNA sequences of the classical and El Tor CTXphi repressors and their presumed cognate operators are highly diverged, whereas the sequences that surround this "immunity" region are nearly identical. Transcriptional fusion studies revealed that the El Tor RstR mediated repression of an El Tor rstA-lacZ fusion but did not repress a classical rstA-lacZ fusion. Likewise, the classical RstR only repressed a classical rstA-lacZ fusion. Thus, similar to the mechanistic basis for heteroimmunity among lambdoid phages, the specificity of CTXphi immunity is based on the divergence of the sequences of repressors and their operators. Expression of the El Tor rstR in either El Tor or classical live-attenuated V. cholerae vaccine strains effectively protected these vaccines from CTXphi infection. Introduction of rstR into V. cholerae vaccine strains should enhance their biosafety.

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Year:  1998        PMID: 9618534      PMCID: PMC22729          DOI: 10.1073/pnas.95.12.7035

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  18 in total

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  48 in total

1.  Formation of chromosomal tandem arrays of the SXT element and R391, two conjugative chromosomally integrating elements that share an attachment site.

Authors:  B Hochhut; J W Beaber; R Woodgate; M K Waldor
Journal:  J Bacteriol       Date:  2001-02       Impact factor: 3.490

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Authors:  B M Davis; K E Moyer; E F Boyd; M K Waldor
Journal:  J Bacteriol       Date:  2000-12       Impact factor: 3.490

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Authors:  A L Gallego-Hernandez; W H DePas; J H Park; J K Teschler; R Hartmann; H Jeckel; K Drescher; S Beyhan; D K Newman; F H Yildiz
Journal:  Proc Natl Acad Sci U S A       Date:  2020-04-30       Impact factor: 11.205

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Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-29       Impact factor: 11.205

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Authors:  Harvey H Kimsey; Matthew K Waldor
Journal:  J Bacteriol       Date:  2009-08-07       Impact factor: 3.490

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Authors:  Brigid M Davis; Harvey H Kimsey; Anne V Kane; Matthew K Waldor
Journal:  EMBO J       Date:  2002-08-15       Impact factor: 11.598

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Authors:  H H Kimsey; M K Waldor
Journal:  Infect Immun       Date:  1998-09       Impact factor: 3.441

8.  RS1 satellite phage promotes diversity of toxigenic Vibrio cholerae by driving CTX prophage loss and elimination of lysogenic immunity.

Authors:  M Kamruzzaman; William Paul Robins; S M Nayeemul Bari; Shamsun Nahar; John J Mekalanos; Shah M Faruque
Journal:  Infect Immun       Date:  2014-06-16       Impact factor: 3.441

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Authors:  Javier Campos; Eriel Martínez; Edith Suzarte; Boris L Rodríguez; Karen Marrero; Yussuan Silva; Talena Ledón; Ricardo del Sol; Rafael Fando
Journal:  J Bacteriol       Date:  2003-10       Impact factor: 3.490

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Journal:  J Clin Microbiol       Date:  2002-09       Impact factor: 5.948

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