Raman S, Song T, Puyang X, Bardarov S, Jacobs W R, Husson R N
Division of Infectious Diseases, Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Bacteriol. 2001 Oct;183(20):6119-25. doi: 10.1128/JB.183.20.6119-6125.2001.
Mycobacterium tuberculosis is a specialized intracellular pathogen that must regulate gene expression to overcome stresses produced by host defenses during infection. SigH is an alternative sigma factor that we have previously shown plays a role in the response to stress of the saprophyte Mycobacterium smegmatis. In this work we investigated the role of sigH in the M. tuberculosis response to heat and oxidative stress. We determined that a M. tuberculosis sigH mutant is more susceptible to oxidative stresses and that the inducible expression of the thioredoxin reductase/thioredoxin genes trxB2/trxC and a gene of unknown function, Rv2466c, is regulated by sigH via expression from promoters directly recognized by SigH. We also determined that the sigH mutant is more susceptible to heat stress and that inducible expression of the heat shock genes dnaK and clpB is positively regulated by sigH. The induction of these heat shock gene promoters but not of other SigH-dependent promoters was markedly greater in response to heat versus oxidative stress, consistent with their additional regulation by a heat-labile repressor. To further understand the role of sigH in the M. tuberculosis stress response, we investigated the regulation of the stress-responsive sigma factor genes sigE and sigB. We determined that inducible expression of sigE is regulated by sigH and that basal and inducible expression of sigB is dependent on sigE and sigH. These data indicate that sigH plays a central role in a network that regulates heat and oxidative-stress responses that are likely to be important in M. tuberculosis pathogenesis.
结核分枝杆菌是一种特殊的胞内病原体,在感染过程中必须调节基因表达以克服宿主防御产生的应激。SigH是一种替代sigma因子,我们之前已表明它在腐生耻垢分枝杆菌的应激反应中发挥作用。在这项研究中,我们调查了sigH在结核分枝杆菌对热应激和氧化应激反应中的作用。我们确定结核分枝杆菌sigH突变体对氧化应激更敏感,并且硫氧还蛋白还原酶/硫氧还蛋白基因trxB2/trxC以及一个功能未知的基因Rv2466c的可诱导表达受sigH调控,通过SigH直接识别的启动子进行表达。我们还确定sigH突变体对热应激更敏感,并且热休克基因dnaK和clpB的可诱导表达受sigH正调控。与它们通过热不稳定阻遏物的额外调控一致,这些热休克基因启动子的诱导在热应激下比氧化应激下明显更强,而其他SigH依赖的启动子则不然。为了进一步了解sigH在结核分枝杆菌应激反应中的作用,我们研究了应激反应性sigma因子基因sigE和sigB的调控。我们确定sigE的可诱导表达受sigH调控,并且sigB的基础表达和可诱导表达依赖于sigE和sigH。这些数据表明sigH在一个调节热应激和氧化应激反应的网络中起核心作用,这在结核分枝杆菌发病机制中可能很重要。