The Stringent Response Is Required for Full Virulence of Mycobacterium tuberculosis in Guinea Pigs

被引:76
作者
Klinkenberg, Lee G. [1 ]
Lee, Jong-Hee [1 ]
Bishai, William R. [1 ,2 ]
Karakousis, Petros C. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Ctr TB Res, Sch Med, Dept Med, Baltimore, MD 21231 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
CYTOKINE PRODUCTION; INFECTED MICE; EXPRESSION; GRANULOMAS; MODEL; MACROPHAGES; (P)PPGPP; POLYPHOSPHATE; TRANSCRIPTION; SMEGMATIS;
D O I
10.1086/656524
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During human latent tuberculosis infection, Mycobacterium tuberculosis likely resides within the nutrient-starved environment of caseous lung granulomas. The stringent response alarmone (p)ppGpp is synthesized by Rel in response to nutrient starvation, thus enabling tubercle bacilli to restrict growth and shut down metabolism in a coordinated fashion. In this study, we investigated the virulence of a rel-deficient M. tuberculosis mutant in the guinea pig model. Quantitative reverse-transcription polymerase chain reaction was used to study the effect of (p)ppGpp deficiency on expression of key cytokine and chemokine genes in guinea pig lungs. The rel-deficient mutant showed impaired initial growth and survival relative to the wild-type strain. Loss of Rel was associated with the striking absence of tubercle lesions grossly and of caseous granulomas histologically. The attenuated phenotype of the rel-deficient mutant was not associated with increased expression of genes encoding the proinflammatory cytokines interferon-gamma and tumor necrosis factor alpha in the lungs 28 days after infection.
引用
收藏
页码:1397 / 1404
页数:8
相关论文
共 43 条
[1]   Coordinate cytokine gene expression in vivo following induction of tuberculous pleurisy in guinea pigs [J].
Allen, SS ;
McMurray, DN .
INFECTION AND IMMUNITY, 2003, 71 (08) :4271-4277
[2]   Oxygen status of lung granulomas in Mycobacterium tuberculosis-infected mice [J].
Aly, S. ;
Wagner, K. ;
Keller, C. ;
Malm, S. ;
Malzan, A. ;
Brandau, S. ;
Bange, F-C ;
Ehlers, S. .
JOURNAL OF PATHOLOGY, 2006, 210 (03) :298-305
[3]   Structural basis for transcription regulation by alarmone ppGpp [J].
Artsimovitch, I ;
Patlan, V ;
Sekine, SI ;
Vassylyeva, MN ;
Hosaka, T ;
Ochi, K ;
Yokoyama, S ;
Vassylyev, DG .
CELL, 2004, 117 (03) :299-310
[4]  
Ausubel F. M., 1991, CURRENT PROTOCOLS MO
[5]   Functional regulation of the opposing (p)ppGpp synthetase/hydrolase activities of RelMtb from Mycobacterium tuberculosis [J].
Avarbock, A ;
Avarbock, D ;
Teh, JS ;
Buckstein, M ;
Wang, ZM ;
Rubin, H .
BIOCHEMISTRY, 2005, 44 (29) :9913-9923
[6]   Cloning and characterization of a bifunctional RelA SpoT homologue from Mycobacterium tuberculosis [J].
Avarbock, D ;
Salem, J ;
Li, LS ;
Wang, ZM ;
Rubin, H .
GENE, 1999, 233 (1-2) :261-269
[7]   New horizons for (p)ppGpp in bacterial and plant physiology [J].
Braeken, K ;
Moris, M ;
Daniels, R ;
Vanderleyden, J ;
Michiels, J .
TRENDS IN MICROBIOLOGY, 2006, 14 (01) :45-54
[8]   Evidence that mycobacterial PE_PGRS proteins are cell surface constituents that influence interactions with other cells [J].
Brennan, MJ ;
Delogu, G ;
Chen, YP ;
Bardarov, S ;
Kriakov, J ;
Alavi, M ;
Jacobs, WR .
INFECTION AND IMMUNITY, 2001, 69 (12) :7326-7333
[9]   Recombinant guinea pig tumor necrosis factor alpha stimulates the expression of interleukin-12 and the inhibition of Mycobacterium tuberculosis growth in macrophages [J].
Cho, H ;
Lasco, TM ;
Allen, SS ;
Yoshimura, T ;
McMurray, DN .
INFECTION AND IMMUNITY, 2005, 73 (03) :1367-1376
[10]   Role of the dosR- dosS Two-Component Regulatory System in Mycobacterium tuberculosis Virulence in Three Animal Models [J].
Converse, Paul J. ;
Karakousis, Petros C. ;
Klinkenberg, Lee G. ;
Kesavan, Anup K. ;
Ly, Lan H. ;
Allen, Shannon Sedberry ;
Grosset, Jacques H. ;
Jain, Sanjay K. ;
Lamichhane, Gyanu ;
Manabe, Yukari C. ;
McMurray, David N. ;
Nuermberger, Eric L. ;
Bishai, William R. .
INFECTION AND IMMUNITY, 2009, 77 (03) :1230-1237