Robinson Nirmal, Wolke Martina, Ernestus Karen, Plum Georg
Institute for Medical Microbiology, University of Cologne, 50935 Cologne, Germany.
Infect Immun. 2007 Feb;75(2):581-91. doi: 10.1128/IAI.00997-06. Epub 2006 Nov 6.
Virulent mycobacteria cause arrest of phagosome maturation as a part of their survival strategy in hosts. This process is mediated through multiple virulence factors, whose molecular nature remains elusive. Using Mycobacterium marinum as a model, we performed a genome-wide screen to identify mutants whose ability to inhibit phagosome maturation was impaired, and we succeeded in isolating a comprehensive set of mutants that were not able to occupy an early endosome-like phagosomal compartment in mammalian macrophages. Categorizing and ordering the multiple mutations according to their gene families demonstrated that the genes modulating the cell envelope are the principal factors in arresting phagosome maturation. In particular, we identified a novel gene, pmiA, which is capable of influencing the constitution of the cell envelope lipids, thereby leading to the phagosome maturation block. The pmiA mutant was not able to resist phagosome maturation and was severely attenuated in mice. Complementing the mutant with the wild-type gene restored the attenuated virulence to wild-type levels in mice.
致病性分枝杆菌会导致吞噬体成熟停滞,这是它们在宿主体内生存策略的一部分。这个过程是由多种毒力因子介导的,但其分子本质仍然难以捉摸。我们以海分枝杆菌为模型,进行了全基因组筛选,以鉴定那些抑制吞噬体成熟能力受损的突变体,并且成功分离出了一组完整的突变体,这些突变体无法在哺乳动物巨噬细胞中占据早期内体样的吞噬体区室。根据基因家族对多个突变进行分类和排序表明,调节细胞壁的基因是阻止吞噬体成熟的主要因素。特别是,我们鉴定出了一个新基因pmiA,它能够影响细胞壁脂质的组成,从而导致吞噬体成熟受阻。pmiA突变体无法抵抗吞噬体成熟,并且在小鼠中严重减毒。用野生型基因对该突变体进行互补,可使小鼠体内减弱的毒力恢复到野生型水平。