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PMID: 2902187 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Toxin, toxin-coregulated pili, and the toxR regulon are essential for Vibrio cholerae pathogenesis in humans.

The Journal of experimental medicine ·Vol. 168 ·No. 4 ·1988-10-01 ·Pages 1487-92

Herrington DA, Hall RH, Losonsky G, Mekalanos JJ, Taylor RK, Levine MM

Abstract

Isogenic mutant strains of V. cholerae O1 lacking elements of a genetic regulon controlled by toxR and implicated in virulence were tested in volunteers. A deletion mutation in ctxA, the gene encoding the A subunit of cholera toxin, markedly attenuated disease symptoms without affecting intestinal colonization. Deletion of toxR, the gene encoding the cholera toxin-positive regulatory protein resulted in a diminution in colonizing capacity. A deletion mutation in tcpA, encoding the major subunit of the toxin coregulated pilus (regulated by toxR), abolished the colonizing capacity of this strain. These results show for the first time the role of a specific pilus structure in colonization of the human intestine by V. cholerae O1 and exemplify the significance of a genetic regulon in pathogenesis.

MeSH Terms
Adult Antibodies, Bacterial/biosynthesis Cholera/immunology,microbiology,prevention & control Cholera Toxin/genetics Double-Blind Method Fimbriae, Bacterial/physiology Genes, Bacterial Genes, Regulator Humans Immunization Microscopy, Electron Mutation Vibrio cholerae/genetics,immunology,pathogenicity,ultrastructure Virulence
Chemicals
Antibodies, Bacterial Cholera Toxin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Herrington D A
Department of Medicine, University of Maryland School of Medicine, Baltimore 21201.
Hall R H
Losonsky G
Mekalanos J J
Taylor R K
Levine M M
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14 references, click to expand
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1988-10-01
Pages
1487-92
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2189073
Subset
IM
Grants
NIAID NIH HHS · AI-02524995 · United States
NIAID NIH HHS · AI-18045 · United States
NIAID NIH HHS · AI-25096 · United States
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