Transcriptional responses of Mycobacterium tuberculosis exposed to adverse conditions in vitro

被引:11
作者
Bacon, Joanna [1 ]
Marsh, Philip D. [1 ]
机构
[1] Hlth Protect Agcy, CEPR, TB Res, Salisbury SP4 0JG, Wilts, England
基金
英国惠康基金;
关键词
latency; chemostat; iron-limitation; regulation; hypoxia; nitric oxide; carbon starvation; re-activation;
D O I
10.2174/156652407780598566
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mycobacterium tuberculosis encounters a range of stimuli in the host. Understanding the environmental cues that initiate the transcriptional response of M. tuberculosis, which enable the bacterium to replicate and/or survive in the host, will provide markers that are specific to different stages of disease, further refining the search for improved treatments and vaccines. Studying M. tuberculosis gene expression in vivo is technically challenging and more amenable in vitro. experiments are being used to aid interpretation and to dissect the signals that are responsible for controlling subsets of genes. Key parameters that affect the growth of a pathogen in the host include nutrient status, environmental pH, oxygen availability, and host defences. Studying gene expression, pathogenicity, and physiology of M. tuberculosis that has been exposed to these relevant host conditions in vitro will further increase our understanding of the virulence factors that M. tuberculosis requires to establish disease. Complementary information obtained by metabolic flux analysis, proteomics, and regulatory networks analysis will enable a clearer picture of how transcriptional responses translate to changes in the metabolome and physiology of the organism.
引用
收藏
页码:277 / 286
页数:10
相关论文
共 92 条
[1]   The influence of reduced oxygen availability on pathogenicity and gene expression in Mycobacterium tuberculosis [J].
Bacon, J ;
James, BW ;
Wernisch, L ;
Williams, A ;
Morley, KA ;
Hatch, GJ ;
Mangan, JA ;
Hinds, J ;
Stoker, NG ;
Butcher, PD ;
Marsh, PD .
TUBERCULOSIS, 2004, 84 (3-4) :205-217
[2]   MECHANISM OF PASTEUR EFFECT [J].
BARKER, J ;
KHAN, MAA ;
SOLOMOS, T .
NATURE, 1966, 211 (5048) :547-+
[3]   Novel Mycobacterium tuberculosis anti-σ factor antagonists control σF activity by distinct mechanisms [J].
Beaucher, J ;
Rodrigue, S ;
Jacques, PÉ ;
Smith, I ;
Brzezinski, R ;
Gaudreau, L .
MOLECULAR MICROBIOLOGY, 2002, 45 (06) :1527-1540
[4]   Compiling a molecular inventory for Mycobacterium bovis BCG at two growth rates:: Evidence for growth rate-mediated regulation of ribosome biosynthesis and lipid metabolism [J].
Beste, DJV ;
Peters, J ;
Hooper, T ;
Avignone-Rossa, C ;
Bushell, ME ;
McFadden, J .
JOURNAL OF BACTERIOLOGY, 2005, 187 (05) :1677-1684
[5]   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
[6]   Reconstruction of amino acid biosynthesis pathways from the complete genome sequence [J].
Bono, H ;
Ogata, H ;
Goto, S ;
Kanehisa, M .
GENOME RESEARCH, 1998, 8 (03) :203-210
[7]   DnaE2 polymerase contributes to in vivo survival and the emergence of drug resistance in Mycobacterium tuberculosis [J].
Boshoff, HIM ;
Reed, MB ;
Barry, CE ;
Mizrahi, V .
CELL, 2003, 113 (02) :183-193
[8]   CHARACTERIZATION OF THE MYCOBACTERIUM-TUBERCULOSIS PHAGOSOME AND EVIDENCE THAT PHAGOSOMAL MATURATION IS INHIBITED [J].
CLEMENS, DL ;
HORWITZ, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (01) :257-270
[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]   Complex lipid determine tissue specific replication of Mycobacterium tuberculosis in mice [J].
Cox, JS ;
Chen, B ;
McNeil, M ;
Jacobs, WR .
NATURE, 1999, 402 (6757) :79-83