Literature DB >> 11680784

Bacterial protein toxins inhibiting low-molecular-mass GTP-binding proteins.

I Just1, F Hofmann, H Genth, R Gerhard.   

Abstract

The Rho GTPases, which belong to the Ras superfamily of low-molecular-mass GTP-binding proteins, are the preferred intracellular targets of bacterial protein toxins. The Rho GTPases RhoA/B/C, Rac1/2 and Cdc42 are the master regulators of the actin cytoskeleton. Clostridium difficile toxins A and B, the causative agents of the antibiotic-associated pseudomembranous colitis, are intracellularly acting cytotoxins which mono-glucosylate the Rho GTPases. Clostridium botulinum C3 toxin, which is not related to the clostridial neurotoxins, catalyses ADP-ribosylation of RhoA/B/C but not of other Rho GTPases. Glucosylation as well as ADP-ribosylation result in functional inactivation of Rho causing disassembly of the actin cytoskeleton.

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Year:  2001        PMID: 11680784     DOI: 10.1078/1438-4221-00127

Source DB:  PubMed          Journal:  Int J Med Microbiol        ISSN: 1438-4221            Impact factor:   3.473


  10 in total

1.  Localization of the C3-Like ADP-ribosyltransferase from Staphylococcus aureus during bacterial invasion of mammalian cells.

Authors:  Gabriella Molinari; Manfred Rohde; Christian Wilde; Ingo Just; Klaus Aktories; Gursharan S Chhatwal
Journal:  Infect Immun       Date:  2006-06       Impact factor: 3.441

Review 2.  Clostridium difficile infection: molecular pathogenesis and novel therapeutics.

Authors:  Ardeshir Rineh; Michael J Kelso; Fatma Vatansever; George P Tegos; Michael R Hamblin
Journal:  Expert Rev Anti Infect Ther       Date:  2014-01       Impact factor: 5.091

3.  Difference in the cytotoxic effects of toxin B from Clostridium difficile strain VPI 10463 and toxin B from variant Clostridium difficile strain 1470.

Authors:  Johannes Huelsenbeck; Stefanie Dreger; Ralf Gerhard; Holger Barth; Ingo Just; Harald Genth
Journal:  Infect Immun       Date:  2006-12-04       Impact factor: 3.441

4.  RhoA GTPase is dispensable for actomyosin regulation but is essential for mitosis in primary mouse embryonic fibroblasts.

Authors:  Jaime Melendez; Kristy Stengel; Xuan Zhou; Bharesh K Chauhan; Marcella Debidda; Paul Andreassen; Richard A Lang; Yi Zheng
Journal:  J Biol Chem       Date:  2011-03-14       Impact factor: 5.157

Review 5.  From signal transduction to protein toxins-a narrative review about milestones on the research route of C. difficile toxins.

Authors:  Klaus Aktories
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2022-10-07       Impact factor: 3.195

6.  Ileal smooth muscle motility depression on rabbit induced by toxin A from Clostridium difficile.

Authors:  Crystianne Calado Lima; João Luis Carvalho-de-Souza; Aldo Angelo Moreira Lima; José Henrique Leal-Cardoso
Journal:  Dig Dis Sci       Date:  2008-06       Impact factor: 3.199

7.  Vibrio parahaemolyticus inhibition of Rho family GTPase activation requires a functional chromosome I type III secretion system.

Authors:  Timothy Casselli; Tarah Lynch; Carolyn M Southward; Bryan W Jones; Rebekah DeVinney
Journal:  Infect Immun       Date:  2008-03-17       Impact factor: 3.441

8.  Inhibition of RHO-ROCK signaling enhances ICM and suppresses TE characteristics through activation of Hippo signaling in the mouse blastocyst.

Authors:  Kanako Kono; Dana Ann A Tamashiro; Vernadeth B Alarcon
Journal:  Dev Biol       Date:  2014-07-02       Impact factor: 3.582

9.  Muscarinic modulation of erg potassium current.

Authors:  Wiebke Hirdes; Lisa F Horowitz; Bertil Hille
Journal:  J Physiol       Date:  2004-07-02       Impact factor: 5.182

10.  Emergence of new PCR ribotypes from the hypervirulent Clostridium difficile 027 lineage.

Authors:  Esmeralda Valiente; Lisa F Dawson; Michelle D Cairns; Richard A Stabler; Brendan W Wren
Journal:  J Med Microbiol       Date:  2011-09-08       Impact factor: 2.472

  10 in total

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