Shafikhani Sasha H, Morales Christina, Engel Joanne
Department of Medicine, University of California, San Francisco, CA 94143, USA.
Cell Microbiol. 2008 Apr;10(4):994-1007. doi: 10.1111/j.1462-5822.2007.01102.x. Epub 2007 Dec 4.
Type III secreted (T3SS) effectors are important virulence factors in acute infections caused by Pseudomonas aeruginosa. PA103, a well-studied human lung isolate, encodes and secretes two effectors, ExoU and ExoT. ExoU is a potent cytotoxin that causes necrotic cell death. In addition, PA103 can induce cell death in macrophages in an ExoU-independent but T3SS-dependent manner. We now demonstrate that ExoT is both necessary and sufficient to cause apoptosis in HeLa cells and that it activates the mitochondrial/cytochrome c-dependent apoptotic pathway. We further show that ExoT induction of cell death is primarily dependent on its ADP ribosyltransferase domain activity. Our data also indicate that the T3SS apparatus can cause necrotic cell death, which is effectively blocked by ExoT, suggesting that P. aeruginosa may have evolved strategies to prevent T3SS-induced necrosis.
III型分泌(T3SS)效应蛋白是铜绿假单胞菌引起的急性感染中的重要毒力因子。PA103是一株经过充分研究的人肺分离株,编码并分泌两种效应蛋白ExoU和ExoT。ExoU是一种强效细胞毒素,可导致坏死性细胞死亡。此外,PA103可以以不依赖ExoU但依赖T3SS的方式诱导巨噬细胞死亡。我们现在证明,ExoT对于导致HeLa细胞凋亡既是必要的也是充分的,并且它激活线粒体/细胞色素c依赖性凋亡途径。我们进一步表明,ExoT诱导细胞死亡主要依赖于其ADP核糖基转移酶结构域的活性。我们的数据还表明,T3SS装置可导致坏死性细胞死亡,而ExoT可有效阻断这种死亡,这表明铜绿假单胞菌可能已经进化出防止T3SS诱导坏死的策略。