Literature DB >> 22126994

Adaptation to environmental stimuli within the host: two-component signal transduction systems of Mycobacterium tuberculosis.

Daniel J Bretl1, Chrystalla Demetriadou, Thomas C Zahrt.   

Abstract

Pathogenic microorganisms encounter a variety of environmental stresses following infection of their respective hosts. Mycobacterium tuberculosis, the etiological agent of tuberculosis, is an unusual bacterial pathogen in that it is able to establish lifelong infections in individuals within granulomatous lesions that are formed following a productive immune response. Adaptation to this highly dynamic environment is thought to be mediated primarily through transcriptional reprogramming initiated in response to recognition of stimuli, including low-oxygen tension, nutrient depletion, reactive oxygen and nitrogen species, altered pH, toxic lipid moieties, cell wall/cell membrane-perturbing agents, and other environmental cues. To survive continued exposure to these potentially adverse factors, M. tuberculosis encodes a variety of regulatory factors, including 11 complete two-component signal transduction systems (TCSSs) and several orphaned response regulators (RRs) and sensor kinases (SKs). This report reviews our current knowledge of the TCSSs present in M. tuberculosis. In particular, we discuss the biochemical and functional characteristics of individual RRs and SKs, the environmental stimuli regulating their activation, the regulons controlled by the various TCSSs, and the known or postulated role(s) of individual TCSSs in the context of M. tuberculosis physiology and/or pathogenesis.

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Year:  2011        PMID: 22126994      PMCID: PMC3232741          DOI: 10.1128/MMBR.05004-11

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  183 in total

1.  K182G substitution in DevR or C₈G mutation in the Dev box impairs protein-DNA interaction and abrogates DevR-mediated gene induction in Mycobacterium tuberculosis.

Authors:  Rajesh Kumar Gupta; Santosh Chauhan; Jaya Sivaswami Tyagi
Journal:  FEBS J       Date:  2011-05-17       Impact factor: 5.542

2.  Mycobacterial bacilli are metabolically active during chronic tuberculosis in murine lungs: insights from genome-wide transcriptional profiling.

Authors:  Adel M Talaat; Sarah K Ward; Chia-Wei Wu; Elizabeth Rondon; Christine Tavano; John P Bannantine; Rick Lyons; Stephen A Johnston
Journal:  J Bacteriol       Date:  2007-03-23       Impact factor: 3.490

3.  Structure-based design of DevR inhibitor active against nonreplicating Mycobacterium tuberculosis.

Authors:  Rajesh Kumar Gupta; Tejender S Thakur; Gautam R Desiraju; Jaya Sivaswami Tyagi
Journal:  J Med Chem       Date:  2009-10-22       Impact factor: 7.446

4.  Nitric oxide dioxygenation reaction in DevS and the initial response to nitric oxide in Mycobacterium tuberculosis.

Authors:  Erik T Yukl; Alexandra Ioanoviciu; Santhosh Sivaramakrishnan; Michiko M Nakano; Paul R Ortiz de Montellano; Pierre Moënne-Loccoz
Journal:  Biochemistry       Date:  2011-01-20       Impact factor: 3.162

5.  Deletion of two-component regulatory systems increases the virulence of Mycobacterium tuberculosis.

Authors:  Tanya Parish; Debbie A Smith; Sharon Kendall; Nicola Casali; Gregory J Bancroft; Neil G Stoker
Journal:  Infect Immun       Date:  2003-03       Impact factor: 3.441

Review 6.  Bacterial response regulators: versatile regulatory strategies from common domains.

Authors:  Rong Gao; Timothy R Mack; Ann M Stock
Journal:  Trends Biochem Sci       Date:  2007-04-12       Impact factor: 13.807

7.  Domain orientation in the inactive response regulator Mycobacterium tuberculosis MtrA provides a barrier to activation.

Authors:  Natalia Friedland; Timothy R Mack; Minmin Yu; Li-Wei Hung; Thomas C Terwilliger; Geoffrey S Waldo; Ann M Stock
Journal:  Biochemistry       Date:  2007-05-19       Impact factor: 3.162

8.  The HtrA-like serine protease PepD interacts with and modulates the Mycobacterium tuberculosis 35-kDa antigen outer envelope protein.

Authors:  Mark J White; John P Savaryn; Daniel J Bretl; Hongjun He; Renee M Penoske; Scott S Terhune; Thomas C Zahrt
Journal:  PLoS One       Date:  2011-03-22       Impact factor: 3.240

9.  Determinants outside the DevR C-terminal domain are essential for cooperativity and robust activation of dormancy genes in Mycobacterium tuberculosis.

Authors:  Uma Shankar Gautam; Santosh Chauhan; Jaya Sivaswami Tyagi
Journal:  PLoS One       Date:  2011-01-27       Impact factor: 3.240

10.  The enduring hypoxic response of Mycobacterium tuberculosis.

Authors:  Tige R Rustad; Maria I Harrell; Reiling Liao; David R Sherman
Journal:  PLoS One       Date:  2008-01-30       Impact factor: 3.240

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  48 in total

Review 1.  Roles of two-component regulatory systems in antibiotic resistance.

Authors:  Aimee Rp Tierney; Philip N Rather
Journal:  Future Microbiol       Date:  2019-05-08       Impact factor: 3.165

Review 2.  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

3.  Discovery of a glycerol 3-phosphate phosphatase reveals glycerophospholipid polar head recycling in Mycobacterium tuberculosis.

Authors:  Gérald Larrouy-Maumus; Tapan Biswas; Debbie M Hunt; Geoff Kelly; Oleg V Tsodikov; Luiz Pedro Sório de Carvalho
Journal:  Proc Natl Acad Sci U S A       Date:  2013-06-25       Impact factor: 11.205

4.  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

5.  Analysis of DevR regulated genes in Mycobacterium tuberculosis.

Authors:  Arnab Bandyopadhyay; Soumi Biswas; Alok Kumar Maity; Suman K Banik
Journal:  Syst Synth Biol       Date:  2014-02-09

6.  The perilipin-like PPE15 protein in Mycobacterium tuberculosis is required for triacylglycerol accumulation under dormancy-inducing conditions.

Authors:  Jaiyanth Daniel; Nidhi Kapoor; Tatiana Sirakova; Rajesh Sinha; Pappachan Kolattukudy
Journal:  Mol Microbiol       Date:  2016-06-21       Impact factor: 3.501

7.  The Psp system of Mycobacterium tuberculosis integrates envelope stress-sensing and envelope-preserving functions.

Authors:  Pratik Datta; Janani Ravi; Valentina Guerrini; Rinki Chauhan; Matthew B Neiditch; Scarlet S Shell; Sarah M Fortune; Baris Hancioglu; Oleg A Igoshin; Maria Laura Gennaro
Journal:  Mol Microbiol       Date:  2015-05-26       Impact factor: 3.501

8.  Evidence of Robustness in a Two-Component System Using a Synthetic Circuit.

Authors:  Arkajyoti Dutta; Paulami Rudra; Suman Kumar Banik; Jayanta Mukhopadhyay
Journal:  J Bacteriol       Date:  2020-01-29       Impact factor: 3.490

9.  PhoPR Positively Regulates whiB3 Expression in Response to Low pH in Pathogenic Mycobacteria.

Authors:  Lipeng Feng; Shiyun Chen; Yangbo Hu
Journal:  J Bacteriol       Date:  2018-03-26       Impact factor: 3.490

10.  Unique N-terminal arm of Mycobacterium tuberculosis PhoP protein plays an unusual role in its regulatory function.

Authors:  Arijit Kumar Das; Vijjamarri Anil Kumar; Ritesh Rajesh Sevalkar; Roohi Bansal; Dibyendu Sarkar
Journal:  J Biol Chem       Date:  2013-08-20       Impact factor: 5.157

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