Collins D M, Kawakami R P, de Lisle G W, Pascopella L, Bloom B R, Jacobs W R
AgResearch, Wallaceville Animal Research Centre, Upper Hutt, New Zealand.
Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):8036-40. doi: 10.1073/pnas.92.17.8036.
Tuberculosis continues to be responsible for the deaths of millions of people, yet the virulence factors of the causative pathogens remain unknown. Genetic complementation experiments with strains of the Mycobacterium tuberculosis complex have identified a gene from a virulent strain that restores virulence to an attenuated strain. The gene, designated rpoV, has a high degree of homology with principal transcription or sigma factors from other bacteria, particularly Mycobacterium smegmatis and Streptomyces griseus. The homologous rpoV gene of the attenuated strain has a point mutation causing an arginine-->histidine change in a domain known to interact with promoters. To our knowledge, association of loss of bacterial virulence with a mutation in the principal sigma factor has not been previously reported. The results indicate either that tuberculosis organisms have an alternative principal sigma factor that promotes virulence genes or, more probably, that this particular mutant principal sigma factor is unable to promote expression of one or more genes required for virulence. Study of genes and proteins differentially regulated by the mutant transcription factor should facilitate identification of further virulence factors.
结核病仍然导致数百万人死亡,但其致病病原体的毒力因子仍不为人知。对结核分枝杆菌复合群菌株进行的基因互补实验,已从一株强毒株中鉴定出一个基因,该基因可使减毒株恢复毒力。这个名为rpoV的基因与其他细菌(特别是耻垢分枝杆菌和灰色链霉菌)的主要转录或σ因子具有高度同源性。减毒株的同源rpoV基因发生了一个点突变,导致在一个已知与启动子相互作用的结构域中发生精氨酸→组氨酸的变化。据我们所知,此前尚未报道过细菌毒力丧失与主要σ因子突变之间的关联。结果表明,要么结核杆菌有一个促进毒力基因表达的替代主要σ因子,要么更有可能的是,这个特定的突变主要σ因子无法促进一个或多个毒力所需基因的表达。对受突变转录因子差异调节的基因和蛋白质进行研究,应有助于识别更多的毒力因子。