Mycobacterium tuberculosis gene expression during adaptation to stationary phase and low-oxygen dormancy

被引:345
作者
Voskuil, MI
Visconti, KC
Schoolnik, GK
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Microbiol, Denver, CO 80262 USA
[2] Stanford Univ, Sch Med, Div Infect Dis & Geog Med, Dept Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
关键词
Mycobacterium tuberculosis; stationary phase; dormancy; microarray;
D O I
10.1016/j.tube.2004.02.003
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 innate mechanisms used by Mycobacterium tuberculosis to persist during periods of non-proliferation are central to understanding the physiology of the bacilli during latent disease. We have used whole genome expression profiling to expose adaptive mechanisms initiated by M. tuberculosis in two common models of M. tuberculosis non-proliferation. The first of these models was a standard growth curve in which gene expression changes were followed from exponential growth through the transition to stationary phase. In the second model, we followed the adaptive process of M. tuberculosis during transition from aerobic growth to a state of anaerobic non-replicating persistence. The most striking finding from these experiments was the strong induction of the entire DosR "dormancy" regulon over approximately 20 days during the long transition to an anaerobic state. This is contrasted by the muted overall response to aerated stationary phase with only a partial dormancy regulon response. From the results presented here we conclude that the respiration-limited environment of the oxygen-depleted NRP model recreates at least one fundamental factor for which the genome of M. tuberculosis encodes a decisive adaptive program. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:218 / 227
页数:10
相关论文
共 28 条
[1]   Bacterial senescence:: protein oxidation in non-proliferating cells is dictated by the accuracy of the ribosomes [J].
Ballesteros, M ;
Fredriksson, Å ;
Henriksson, J ;
Nyström, T .
EMBO JOURNAL, 2001, 20 (18) :5280-5289
[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]   Peroxynitrite reductase activity of bacterial peroxiredoxins [J].
Bryk, R ;
Griffin, P ;
Nathan, C .
NATURE, 2000, 407 (6801) :211-215
[4]   Metabolic enzymes of mycobacteria linked to antioxidant defense by a thioredoxin-like protein [J].
Bryk, R ;
Lima, CD ;
Erdjument-Bromage, H ;
Tempst, P ;
Nathan, C .
SCIENCE, 2002, 295 (5557) :1073-1077
[5]  
Canetti G, 1955, TUBERCLE BACILLUS PU
[6]  
CORPER H. J., 1933, AMER REV TUBERC, V28, P856
[7]   A stationary-phase stress-response sigma factor from Mycobacterium tuberculosis [J].
DeMaio, J ;
Zhang, Y ;
Ko, C ;
Young, DB ;
Bishai, WR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :2790-2794
[8]   Dormant tubercle bacilli: the key to more effective TB chemotherapy? [J].
Dick, T .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 47 (01) :117-118
[9]   Sorting out bacterial viability with optical tweezers [J].
Ericsson, M ;
Hanstorp, D ;
Hagberg, P ;
Enger, J ;
Nyström, T .
JOURNAL OF BACTERIOLOGY, 2000, 182 (19) :5551-5555
[10]   The transcriptional profile of early to middle sporulation in Bacillus subtilis [J].
Fawcett, P ;
Eichenberger, P ;
Losick, R ;
Youngman, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (14) :8063-8068