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

被引:88
作者
Pang, Xiuhua
Vu, Phong
Byrd, Thomas F.
Ghanny, Saleena
Soteropoulos, Patricia
Mukamolova, Galina V.
Wu, Shiping
Samten, Buka
Howard, Susan T.
机构
[1] Univ Texas Hlth Ctr, Dept Microbiol & Immunol, Ctr Pulm & Infect Dis, Tyler, TX 75708 USA
[2] Albuquerque Vet Affairs Med Ctr, Dept Med, Albuquerque, NM 87108 USA
[3] Ctr Appl Genom, Publ Hlth Res Inst, Newark, NJ 07103 USA
来源
MICROBIOLOGY-SGM | 2007年 / 153卷
关键词
D O I
10.1099/mic.0.29281-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 SIDS 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 monoctyes, was upregulated in the deletion mutant under SIDS 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 SIDS. Surprisingly, the deletion mutant had increased resistance to SIDS 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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页码:1229 / 1242
页数:14
相关论文
共 69 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]   Mycobacterium bovis BCG response regulator essential for hypoxic dormancy [J].
Boon, C ;
Dick, T .
JOURNAL OF BACTERIOLOGY, 2002, 184 (24) :6760-6767
[4]   Transcription activation by catabolite activator protein (CAP) [J].
Busby, S ;
Ebright, RH .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 293 (02) :199-213
[5]   Tumor necrosis factor alpha (TNF alpha) promotes growth of virulent Mycobacterium tuberculosis in human monocytes - Iron-mediated growth suppression is correlated with decreased release of TNF alpha from iron-treated infected monocytes [J].
Byrd, TF .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (10) :2518-2529
[7]   The Mycobacterium tuberculosis SigD sigma factor controls the expression of ribosome-associated gene products in stationary phase and is required for full virulence [J].
Calamita, H ;
Ko, C ;
Tyagi, S ;
Yoshimatsu, T ;
Morrison, NE ;
Bishai, WR .
CELLULAR MICROBIOLOGY, 2005, 7 (02) :233-244
[8]   The structure of a resuscitation-promoting factor domain from Mycobacterium tuberculosis shows homology to lysozymes [J].
Cohen-Gonsaud, M ;
Barthe, P ;
Bagnéris, C ;
Henderson, B ;
Ward, J ;
Roumestand, C ;
Keep, NH .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (03) :270-273
[9]   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-+
[10]  
Corbett L, 2005, TUBERCULOSIS AND THE TUBERCLE BACILLUS, P3