The use of microarray analysis to determine the gene expression profiles of Mycobacterium tuberculosis in response to anti-bacterial compounds

被引:91
作者
Waddell, SJ
Stabler, RA
Laing, K
Kremer, L
Reynolds, RC
Besra, GS
机构
[1] St George Hosp, Sch Med, Dept Cellular & Mol Med, London SW17 0RE, England
[2] Inst Pasteur, INSERM, U447, IBL, F-59019 Lille, France
[3] So Res Inst, Dept Organ Chem, Birmingham, AL 35255 USA
[4] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
基金
英国惠康基金;
关键词
Mycobacterium tuberculosis; innate drug resistance; microarray; isoniazid; isoxyl; tetrahydrolipstatin;
D O I
10.1016/j.tube.2003.12.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The response of Mycobacterium tuberculosis to six anti-microbial agents was determined by microarray analysis in an attempt to define mechanisms of innate resistance in M. tuberculosis. The gene expression profiles of M. tuberculosis after treatment at the minimal inhibitory concentration (MIC) for 4h with isoniazid, isoxyl, tetrahydrolipstatin, SRI#221, SR1#967 and SR1#9190 were compared to untreated M. tuberculosis. A common response to drug exposure was defined, and this expression profile overlapped with a number of other mycobacterial stress responses recently identified by microarray analysis. Compound-specific responses were also distinguished including a number of putative transcriptional regulators and translocation-related genes. These genes may contribute to the intrinsic resistance of M. tuberculosis to anti-microbial compounds. Further investigation into these mechanisms may elucidate novel pathways contributing to mycobacterial drug resistance and influence anti-mycobacterial drug development strategies. (C) 2004 Elsevier Ltd. ALL rights reserved.
引用
收藏
页码:263 / 274
页数:12
相关论文
共 42 条
[1]   Aminoglycoside 2'-N-acetyltransferase genes are universally present in mycobacteria: Characterization of the aac(2')-lc gene from Mycobacterium tuberculosis and the aac(2')-ld gene from Mycobacterium smegmatis [J].
Ainsa, JA ;
Perez, E ;
Pelicic, V ;
Berthet, FX ;
Gicquel, B ;
Martin, C .
MOLECULAR MICROBIOLOGY, 1997, 24 (02) :431-441
[2]   The eukaryotic-like Ser/Thr protein kinases of Mycobacterium tuberculosis [J].
Av-Gay, Y ;
Everett, M .
TRENDS IN MICROBIOLOGY, 2000, 8 (05) :238-244
[3]   The mabA gene from the inhA operon of Mycobacterium tuberculosis encodes a 3-ketoacyl reductase that fails to confer isoniazid resistance [J].
Banerjee, A ;
Sugantino, M ;
Sacchettini, JC ;
Jacobs, WR .
MICROBIOLOGY-SGM, 1998, 144 :2697-2704
[4]   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
[5]   Signature gene expression profiles discriminate between isoniazid-, thiolactomycin-, and triclosan-treated Mycobacterium tuberculosis [J].
Betts, JC ;
McLaren, A ;
Lennon, MG ;
Kelly, FM ;
Lukey, PT ;
Blakemore, SJ ;
Duncan, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (09) :2903-2913
[6]   Stereotyped and specific gene expression programs in human innate immune responses to bacteria [J].
Boldrick, JC ;
Alizadeh, AA ;
Diehn, M ;
Dudoit, S ;
Liu, CL ;
Belcher, CE ;
Botstein, D ;
Staudt, LM ;
Brown, PO ;
Relman, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :972-977
[7]   The ATP binding cassette (ABC) transport systems of Mycobacterium tuberculosis [J].
Braibant, M ;
Gilot, P ;
Content, J .
FEMS MICROBIOLOGY REVIEWS, 2000, 24 (04) :449-467
[8]   THE ENVELOPE OF MYCOBACTERIA [J].
BRENNAN, PJ ;
NIKAIDO, H .
ANNUAL REVIEW OF BIOCHEMISTRY, 1995, 64 :29-63
[9]   Identification of some DNA damage-inducible genes of Mycobacterium tuberculosis:: Apparent lack of correlation with LexA binding [J].
Brooks, PC ;
Movahedzadeh, F ;
Davis, EO .
JOURNAL OF BACTERIOLOGY, 2001, 183 (15) :4459-4467
[10]   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-+