MprAB is a stress-responsive two-component system that directly regulates expression of sigma factors SigB and SigE in Mycobacterium tuberculosis

被引:134
作者
He, HJ
Hovey, R
Kane, J
Singh, V
Zahrt, TC [1 ]
机构
[1] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
[2] Med Coll Wisconsin, Dept Pediat, Milwaukee, WI 53226 USA
关键词
D O I
10.1128/JB.188.6.2134-2143.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genetic mechanisms mediating the adaptation of Mycobacterium tuberculosis within the host are poorly understood. The best-characterized regulatory systems in this organism include sigma factors and two-component signal transduction systems. mprAB is a two-component system required by M. tuberculosis for growth in vivo during the persistent stage of infection. In this report, we demonstrate that MprAB is stress responsive and regulates the expression of numerous stress-responsive genes in M. tuberculosis. With DNA microarrays and quantitative real-time reverse transcription-PCR, genes regulated by MprA in M. tuberculosis that included two stress-responsive sigma factors were identified. Response regulator MprA bound to conserved motifs in the upstream regions of both sigB and sigE in vitro and regulated the in vivo expression of sigB and sigE in M. tuberculosis. In addition, mprA itself was induced following exposure to stress, establishing a direct role for this regulatory system in stress response pathways of M. tuberculosis. Induction of mprA and sigE by MprA in response to stress was mediated through the cognate sensor kinase MprB and required expression of the extracytoplasmic loop domain. These results provide the first evidence that recognition of and adaptation to specific stress in M. tuberculosis are mediated through activation of a two-component signal transduction system that directly regulates the expression of stress-responsive determinants.
引用
收藏
页码:2134 / 2143
页数:10
相关论文
共 36 条
[1]   Deletion of Mycobacterium tuberculosis sigma factor E results in delayed time to death with bacterial persistence in the lungs of aerosol-infected mice [J].
Ando, M ;
Yoshimatsu, T ;
Ko, C ;
Converse, PJ ;
Bishai, WR .
INFECTION AND IMMUNITY, 2003, 71 (12) :7170-7172
[2]   Evaluation of a nutrient starvation model of Mycobacterium tuberculosis persistence by gene and protein expression profiling [J].
Betts, JC ;
Lukey, PT ;
Robb, LC ;
McAdam, RA ;
Duncan, K .
MOLECULAR MICROBIOLOGY, 2002, 43 (03) :717-731
[3]   Molecular genetics of Mycobacterium tuberculosis pathogenesis [J].
Clark-Curtiss, JE ;
Haydel, SE .
ANNUAL REVIEW OF MICROBIOLOGY, 2003, 57 :517-549
[4]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[5]   The secret lives of the pathogenic mycobacteria [J].
Cosma, CL ;
Sherman, DR ;
Ramakrishnan, L .
ANNUAL REVIEW OF MICROBIOLOGY, 2003, 57 :641-676
[6]   Genome-wide profiling of promoter recognition by the two-component response regulator CpxR-P in Escherichia coli. [J].
De Wulf, P ;
McGuire, AM ;
Liu, XQ ;
Lin, ECC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (29) :26652-26661
[7]   Microarray analysis of the Mycobacterium tuberculosis transcriptional response to the acidic conditions found in phagosomes [J].
Fisher, MA ;
Plikaytis, BB ;
Shinnick, TM .
JOURNAL OF BACTERIOLOGY, 2002, 184 (14) :4025-4032
[8]   Identification of Mycobacterium tuberculosis RNAs synthesized in response to phagocytosis by human macrophages by selective capture of transcribed sequences (SCOTS) [J].
Graham, JE ;
Clark-Curtiss, JE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11554-11559
[9]   Identification and characterization of a regulatory sequence recognized by Mycobacterium tuberculosis persistence regulator MprA [J].
He, HJ ;
Zahrt, TC .
JOURNAL OF BACTERIOLOGY, 2005, 187 (01) :202-212
[10]   Utilization of a labeled tracking oligonucleotide for visualization and quality control of spotted 70-mer arrays [J].
Hessner, MJ ;
Singh, VK ;
Wang, XJ ;
Khan, S ;
Tschannen, MR ;
Zahrt, TC .
BMC GENOMICS, 2004, 5 (1)