Literature DB >> 17379732

Evidence for complex interactions of stress-associated regulons in an mprAB deletion mutant of Mycobacterium tuberculosis.

Xiuhua Pang1, Phong Vu1, Thomas F Byrd2, Saleena Ghanny3, Patricia Soteropoulos3, Galina V Mukamolova1, Shiping Wu1, Buka Samten1, Susan T Howard1.   

Abstract

Two-component systems are important constituents of bacterial regulatory networks. Results of this investigation into the role of the MprAB two-component system of Mycobacterium tuberculosis indicate that it is associated with the regulation of several stress-responsive regulons. Using a deletion mutant lacking portions of the response regulator, MprA, and the histidine kinase, MprB, it was demonstrated by real-time PCR, primer extension analyses and DNA microarrays that MprAB activates sigma factor genes sigE and sigB, under SDS stress and during exponential growth. SDS-inducible, MprA-dependent transcriptional start points were identified for mprA, sigE and sigB, and variations in distance between these points and MprA-binding sites suggest that MprA is involved in different mechanisms of promoter activation. Although most of the SigE regulon was downregulated in the deletion mutant, the cluster of genes Rv1129c, Rv1130 and Rv1131, which is associated with growth in monocytes, was upregulated in the deletion mutant under SDS stress, and this upregulation was dependent upon atmospheric growth conditions. Multiple stress-associated genes of the DosR, SigD and IdeR regulons were also upregulated in the deletion mutant, during exponential growth and/or in the presence of SDS. Surprisingly, the deletion mutant had increased resistance to SDS compared to the parental strain, and enhanced growth in human peripheral blood monocytes, characteristics which may result from a loss of repression of stress-associated genes.

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Year:  2007        PMID: 17379732     DOI: 10.1099/mic.0.29281-0

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  56 in total

1.  Critical role of a single position in the -35 element for promoter recognition by Mycobacterium tuberculosis SigE and SigH.

Authors:  Taeksun Song; Seung-Eun Song; Sahadevan Raman; Mauricio Anaya; Robert N Husson
Journal:  J Bacteriol       Date:  2008-01-11       Impact factor: 3.490

2.  Evidence of complex transcriptional, translational, and posttranslational regulation of the extracytoplasmic function sigma factor sigmaE in Mycobacterium tuberculosis.

Authors:  Valentina Donà; Sébastien Rodrigue; Elisa Dainese; Giorgio Palù; Luc Gaudreau; Riccardo Manganelli; Roberta Provvedi
Journal:  J Bacteriol       Date:  2008-07-07       Impact factor: 3.490

3.  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

Review 4.  Phosphate responsive regulation provides insights for ESX-5 function in Mycobacterium tuberculosis.

Authors:  Sarah R Elliott; Anna D Tischler
Journal:  Curr Genet       Date:  2016-04-22       Impact factor: 3.886

Review 5.  Virulence factors of the Mycobacterium tuberculosis complex.

Authors:  Marina A Forrellad; Laura I Klepp; Andrea Gioffré; Julia Sabio y García; Hector R Morbidoni; María de la Paz Santangelo; Angel A Cataldi; Fabiana Bigi
Journal:  Virulence       Date:  2012-10-17       Impact factor: 5.882

6.  MprAB regulates the espA operon in Mycobacterium tuberculosis and modulates ESX-1 function and host cytokine response.

Authors:  Xiuhua Pang; Buka Samten; Guangxiang Cao; Xisheng Wang; Amy R Tvinnereim; Xiu-Lan Chen; Susan T Howard
Journal:  J Bacteriol       Date:  2012-10-26       Impact factor: 3.490

7.  EspA acts as a critical mediator of ESX1-dependent virulence in Mycobacterium tuberculosis by affecting bacterial cell wall integrity.

Authors:  Alejandra Garces; Krishnamohan Atmakuri; Michael R Chase; Joshua S Woodworth; Bryan Krastins; Alissa C Rothchild; Talia L Ramsdell; Mary F Lopez; Samuel M Behar; David A Sarracino; Sarah M Fortune
Journal:  PLoS Pathog       Date:  2010-06-24       Impact factor: 6.823

8.  A Mycobacterium tuberculosis sigma factor network responds to cell-envelope damage by the promising anti-mycobacterial thioridazine.

Authors:  Noton K Dutta; Smriti Mehra; Deepak Kaushal
Journal:  PLoS One       Date:  2010-04-08       Impact factor: 3.240

9.  Cooperative binding of phosphorylated DevR to upstream sites is necessary and sufficient for activation of the Rv3134c-devRS operon in Mycobacterium tuberculosis: implication in the induction of DevR target genes.

Authors:  Santosh Chauhan; Jaya Sivaswami Tyagi
Journal:  J Bacteriol       Date:  2008-03-21       Impact factor: 3.490

10.  The genetic requirements for fast and slow growth in mycobacteria.

Authors:  Dany J V Beste; Mateus Espasa; Bhushan Bonde; Andrzej M Kierzek; Graham R Stewart; Johnjoe McFadden
Journal:  PLoS One       Date:  2009-04-28       Impact factor: 3.240

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