Literature DB >> 18835713

PhoP, a key player in Mycobacterium tuberculosis virulence.

Michelle Ryndak1, Shuishu Wang, Issar Smith.   

Abstract

The Mycobacterium tuberculosis PhoPR two-component system is essential for virulence in animal models of tuberculosis. Recent articles have shown that among the reasons for the attenuation of the M. tuberculosis H37Ra strain is a mutation in the phoP gene that prevents the secretion of proteins that are important for virulence. There is a need for new anti-tubercular therapies because of the emergence of multi-drug-resistant M. tuberculosis strains and also the variable efficacy of the currently used bacille Calmette-Guérin vaccine. Because of its major role in M. tuberculosis pathogenicity, PhoP is a potential target candidate. This review summarizes our understanding of PhoPR's role in virulence and discusses areas in which our knowledge is limited.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18835713     DOI: 10.1016/j.tim.2008.08.006

Source DB:  PubMed          Journal:  Trends Microbiol        ISSN: 0966-842X            Impact factor:   17.079


  46 in total

1.  Structure of the response regulator PhoP from Mycobacterium tuberculosis reveals a dimer through the receiver domain.

Authors:  Smita Menon; Shuishu Wang
Journal:  Biochemistry       Date:  2011-06-13       Impact factor: 3.162

2.  Phosphorylation of PhoP protein plays direct regulatory role in lipid biosynthesis of Mycobacterium tuberculosis.

Authors:  Rajni Goyal; Arijit Kumar Das; Ranjeet Singh; Pradip K Singh; Suresh Korpole; Dibyendu Sarkar
Journal:  J Biol Chem       Date:  2011-11-09       Impact factor: 5.157

3.  Domain structure of virulence-associated response regulator PhoP of Mycobacterium tuberculosis: role of the linker region in regulator-promoter interaction(s).

Authors:  Anuj Pathak; Rajni Goyal; Akesh Sinha; Dibyendu Sarkar
Journal:  J Biol Chem       Date:  2010-09-02       Impact factor: 5.157

4.  Analysis of a Borrelia burgdorferi phosphodiesterase demonstrates a role for cyclic-di-guanosine monophosphate in motility and virulence.

Authors:  Syed Z Sultan; Joshua E Pitzer; Michael R Miller; Md A Motaleb
Journal:  Mol Microbiol       Date:  2010-04-27       Impact factor: 3.501

5.  Functional analysis of the EspR binding sites upstream of espR in Mycobacterium tuberculosis.

Authors:  Guangxiang Cao; Susan T Howard; Peipei Zhang; Guihua Hou; Xiuhua Pang
Journal:  Curr Microbiol       Date:  2013-06-07       Impact factor: 2.188

6.  Mycobacterium tuberculosis PhoP recognizes two adjacent direct-repeat sequences to form head-to-head dimers.

Authors:  Sankalp Gupta; Anuj Pathak; Akesh Sinha; Dibyendu Sarkar
Journal:  J Bacteriol       Date:  2009-10-09       Impact factor: 3.490

7.  Withdrawn

Authors: 
Journal:  Infect Disord Drug Targets       Date:  2012-11-16

8.  Comparative genomics of the Mycobacterium signaling architecture and implications for a novel live attenuated Tuberculosis vaccine.

Authors:  Peifu Zhou; Jianping Xie
Journal:  Hum Vaccin Immunother       Date:  2013-09-06       Impact factor: 3.452

9.  The type I NADH dehydrogenase of Mycobacterium tuberculosis counters phagosomal NOX2 activity to inhibit TNF-alpha-mediated host cell apoptosis.

Authors:  Jessica L Miller; Kamalakannan Velmurugan; Mark J Cowan; Volker Briken
Journal:  PLoS Pathog       Date:  2010-04-22       Impact factor: 6.823

10.  EspR-dependent ESAT-6 Protein Secretion of Mycobacterium tuberculosis Requires the Presence of Virulence Regulator PhoP.

Authors:  Vijjamarri Anil Kumar; Rajni Goyal; Roohi Bansal; Nisha Singh; Ritesh Rajesh Sevalkar; Ashwani Kumar; Dibyendu Sarkar
Journal:  J Biol Chem       Date:  2016-07-21       Impact factor: 5.157

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.