Literature DB >> 15981456

Bacterial virulence strategies that utilize Rho GTPases.

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Abstract

The ability to modify central host cellular functions is a major advantage to many bacterial pathogens that use such strategies as part of their virulence mechanisms. Small GTPases, including Rho GTPases, make particularly attractive targets for pathogens because of their central roles in modulating cellular functions such as cytoskeletal control. Such modifications of these GTPases can include direct chemical modification of the GTPase or interfacing with some of the regulatory elements associated with GTPase control. Pathogens use these alterations in GTPase functions for a variety of functions, including killing the host cell, mediating bacterial uptake into the host cell (invasion), reprogramming actin to form a lesion in host cells underlying adherent bacteria, to mediate intracellular survival by affecting intracellular trafficking, or to provide polymerized actin mechanisms to propel microbes around inside host cells and into adjacent cells. Collectively, these examples represent many key microbial virulence mechanisms that have led to a much deeper understanding of both microbial pathogens and GTPase functions.

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Year:  2005        PMID: 15981456     DOI: 10.1007/3-540-27511-8_1

Source DB:  PubMed          Journal:  Curr Top Microbiol Immunol        ISSN: 0070-217X            Impact factor:   4.291


  18 in total

1.  Sequestering of Rac by the Yersinia effector YopO blocks Fcgamma receptor-mediated phagocytosis.

Authors:  Eleanor Groves; Katrin Rittinger; Marlise Amstutz; Sara Berry; David W Holden; Guy R Cornelis; Emmanuelle Caron
Journal:  J Biol Chem       Date:  2009-11-19       Impact factor: 5.157

2.  Helicobacter pylori CagA induces AGS cell elongation through a cell retraction defect that is independent of Cdc42, Rac1, and Arp2/3.

Authors:  Kevin M Bourzac; Crystal M Botham; Karen Guillemin
Journal:  Infect Immun       Date:  2006-12-28       Impact factor: 3.441

3.  Klebsiella pneumoniae translocates across the intestinal epithelium via Rho GTPase- and phosphatidylinositol 3-kinase/Akt-dependent cell invasion.

Authors:  Chun-Ru Hsu; Yi-Jiun Pan; Ju-Yun Liu; Chun-Tang Chen; Tzu-Lung Lin; Jin-Town Wang
Journal:  Infect Immun       Date:  2014-12-01       Impact factor: 3.441

4.  Modulation of RhoGTPases improves the behavioral phenotype and reverses astrocytic deficits in a mouse model of Rett syndrome.

Authors:  Bianca De Filippis; Alessia Fabbri; Daiana Simone; Rossella Canese; Laura Ricceri; Fiorella Malchiodi-Albedi; Giovanni Laviola; Carla Fiorentini
Journal:  Neuropsychopharmacology       Date:  2011-12-07       Impact factor: 7.853

5.  Cryptococcus neoformans activates RhoGTPase proteins followed by protein kinase C, focal adhesion kinase, and ezrin to promote traversal across the blood-brain barrier.

Authors:  Jong-Chul Kim; Benjamin Crary; Yun C Chang; Kyung J Kwon-Chung; Kee J Kim
Journal:  J Biol Chem       Date:  2012-08-16       Impact factor: 5.157

6.  Staphylococcus aureus protein A mediates invasion across airway epithelial cells through activation of RhoA GTPase signaling and proteolytic activity.

Authors:  Grace Soong; Francis J Martin; Jarin Chun; Taylor S Cohen; Danielle S Ahn; Alice Prince
Journal:  J Biol Chem       Date:  2011-08-30       Impact factor: 5.157

Review 7.  Bacterial guanine nucleotide exchange factors SopE-like and WxxxE effectors.

Authors:  Richard Bulgin; Benoit Raymond; James A Garnett; Gad Frankel; Valerie F Crepin; Cedric N Berger; Ana Arbeloa
Journal:  Infect Immun       Date:  2010-02-01       Impact factor: 3.441

8.  Modulation of host microtubule dynamics by pathogenic bacteria.

Authors:  Girish K Radhakrishnan; Gary A Splitter
Journal:  Biomol Concepts       Date:  2012-12-01

9.  Cdc42 and the phosphatidylinositol 3-kinase-Akt pathway are essential for PspC-mediated internalization of pneumococci by respiratory epithelial cells.

Authors:  Vaibhav Agarwal; Sven Hammerschmidt
Journal:  J Biol Chem       Date:  2009-05-27       Impact factor: 5.157

10.  EspM2 is a RhoA guanine nucleotide exchange factor.

Authors:  Ana Arbeloa; James Garnett; James Lillington; Richard R Bulgin; Cedric N Berger; Susan M Lea; Steve Matthews; Gad Frankel
Journal:  Cell Microbiol       Date:  2009-12-21       Impact factor: 3.715

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