Zahrt T C, Deretic V
Department of Microbiology and Immunology, University of Michigan Medical School, 5641 Medical Science Building II, Ann Arbor, MI 48109-0620, USA.
Proc Natl Acad Sci U S A. 2001 Oct 23;98(22):12706-11. doi: 10.1073/pnas.221272198.
It is estimated that nearly 2 billion people currently suffer from latent Mycobacterium tuberculosis infection. Although the key front-line antituberculosis drugs are effective in treating individuals with acute tuberculosis, these drugs are ineffective in eliminating M. tuberculosis during the persistent stages of latent infection. Consequently, therapeutics that directly target persistent bacilli are urgently needed. We have conducted a global analysis on a group of regulatory determinants that may play a role in M. tuberculosis virulence, and identified a two-component response regulator whose expression is required for entrance into and maintenance of persistent infection. Inactivation of this response regulator, Rv0981 (termed here mprA for mycobacterial persistence regulator), affected M. tuberculosis H37Rv growth in vivo in an organ- and infection stage-specific fashion. These results indicate that two-component systems are important for adaptation of the tubercle bacillus during stages of persistent infection.
据估计,目前有近20亿人患有潜伏性结核分枝杆菌感染。尽管一线关键抗结核药物在治疗急性结核病患者方面有效,但这些药物在潜伏感染的持续阶段无法消除结核分枝杆菌。因此,迫切需要直接针对持续存在的杆菌的治疗方法。我们对一组可能在结核分枝杆菌毒力中起作用的调控决定因素进行了全球分析,并鉴定出一种双组分反应调节因子,其表达是进入和维持持续感染所必需的。这种反应调节因子Rv0981(在此称为mprA,即分枝杆菌持续调节因子)的失活,以器官和感染阶段特异性的方式影响结核分枝杆菌H37Rv在体内的生长。这些结果表明,双组分系统在结核杆菌持续感染阶段的适应过程中很重要。