Literature DB >> 11292584

Microbes and microbial Toxins: paradigms for microbial-mucosal toxins. V. Cholera: invasion of the intestinal epithelial barrier by a stably folded protein toxin.

W I Lencer1.   

Abstract

Cholera toxin (CT) produced by Vibrio cholerae is the virulence factor responsible for the massive secretory diarrhea seen in Asiatic cholera. To cause disease, CT enters the intestinal epithelial cell as a stably folded protein by co-opting a lipid-based membrane receptor, ganglioside G(M1). G(M1) sorts the toxin into lipid rafts and a retrograde trafficking pathway to the endoplasmic reticulum, where the toxin unfolds and transfers its enzymatic subunit to the cytosol, probably by dislocation through the translocon sec61p. The molecular determinants that drive entry of CT into this pathway are encoded entirely within the structure of the protein toxin itself.

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Year:  2001        PMID: 11292584     DOI: 10.1152/ajpgi.2001.280.5.G781

Source DB:  PubMed          Journal:  Am J Physiol Gastrointest Liver Physiol        ISSN: 0193-1857            Impact factor:   4.052


  29 in total

1.  Differential infection of polarized epithelial cell lines by sialic acid-dependent and sialic acid-independent rotavirus strains.

Authors:  M Ciarlet; S E Crawford; M K Estes
Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

2.  Transfer of the cholera toxin A1 polypeptide from the endoplasmic reticulum to the cytosol is a rapid process facilitated by the endoplasmic reticulum-associated degradation pathway.

Authors:  Ken Teter; Rebecca L Allyn; Michael G Jobling; Randall K Holmes
Journal:  Infect Immun       Date:  2002-11       Impact factor: 3.441

3.  Role of ubiquitination in retro-translocation of cholera toxin and escape of cytosolic degradation.

Authors:  Chiara Rodighiero; Billy Tsai; Tom A Rapoport; Wayne I Lencer
Journal:  EMBO Rep       Date:  2002-11-21       Impact factor: 8.807

4.  Cytolethal distending toxin-induced cell cycle arrest of lymphocytes is dependent upon recognition and binding to cholesterol.

Authors:  Kathleen Boesze-Battaglia; Angela Brown; Lisa Walker; Dave Besack; Ali Zekavat; Steve Wrenn; Claude Krummenacher; Bruce J Shenker
Journal:  J Biol Chem       Date:  2009-02-23       Impact factor: 5.157

5.  Rethinking cholera pathogenesis- No longer all in the same "camp".

Authors:  Kim E Barrett
Journal:  Virulence       Date:  2016-07-14       Impact factor: 5.882

6.  Hydrocortisone modulates cholera toxin endocytosis by regulating immature enterocyte plasma membrane phospholipids.

Authors:  Lei Lu; Yuanwu Bao; Abdullah Khan; Allan M Goldstein; David S Newburg; Andrea Quaroni; Dennis Brown; W Allan Walker
Journal:  Gastroenterology       Date:  2008-03-22       Impact factor: 22.682

7.  Generating an unfoldase from thioredoxin-like domains.

Authors:  Michele L Forster; James J Mahn; Billy Tsai
Journal:  J Biol Chem       Date:  2009-03-16       Impact factor: 5.157

8.  ADP-ribosylation factors regulate the development of CT signaling in immature human enterocytes.

Authors:  Lei Lu; Abdullah Khan; W Allan Walker
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2009-04-09       Impact factor: 4.052

9.  The Aggregatibacter actinomycetemcomitans Cytolethal Distending Toxin Active Subunit CdtB Contains a Cholesterol Recognition Sequence Required for Toxin Binding and Subunit Internalization.

Authors:  Kathleen Boesze-Battaglia; Lisa P Walker; Ali Zekavat; Mensur Dlakić; Monika Damek Scuron; Patrik Nygren; Bruce J Shenker
Journal:  Infect Immun       Date:  2015-07-27       Impact factor: 3.441

Review 10.  Principles and clinical implications of the brain-gut-enteric microbiota axis.

Authors:  Sang H Rhee; Charalabos Pothoulakis; Emeran A Mayer
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2009-05       Impact factor: 46.802

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