Hauser A R, Engel J N
Departments of Medicine, University of California, San Francisco, San Francisco, California 94143, USA.
Infect Immun. 1999 Oct;67(10):5530-7. doi: 10.1128/IAI.67.10.5530-5537.1999.
Pseudomonas aeruginosa is a gram-negative opportunistic pathogen that is cytotoxic towards a variety of eukaryotic cells. To investigate the effect of this bacterium on macrophages, we infected J774A.1 cells and primary bone-marrow-derived murine macrophages with the P. aeruginosa strain PA103 in vitro. PA103 caused type-III-secretion-dependent killing of macrophages within 2 h of infection. Only a portion of the killing required the putative cytotoxin ExoU. By three criteria, terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling assays, cytoplasmic nucleosome assays, and Hoechst staining, the ExoU-independent but type-III-secretion-dependent killing exhibited features of apoptosis. Extracellular bacteria were capable of inducing apoptosis, and some laboratory and clinical isolates of P. aeruginosa induced significantly higher levels of this form of cell death than others. Interestingly, HeLa cells but not Madin-Darby canine kidney cells were susceptible to type-III-secretion-mediated apoptosis under the conditions of these assays. These findings are consistent with a model in which the P. aeruginosa type III secretion system transports at least two factors that kill macrophages: ExoU, which causes necrosis, and a second, as yet unidentified, effector protein, which induces apoptosis. Such killing may contribute to the ability of this organism to persist and disseminate within infected patients.
铜绿假单胞菌是一种革兰氏阴性机会致病菌,对多种真核细胞具有细胞毒性。为了研究这种细菌对巨噬细胞的影响,我们在体外将铜绿假单胞菌PA103菌株感染J774A.1细胞和原代骨髓来源的小鼠巨噬细胞。PA103在感染后2小时内导致巨噬细胞发生III型分泌依赖性杀伤。只有一部分杀伤需要假定的细胞毒素ExoU。通过三种标准,即末端脱氧核苷酸转移酶介导的dUTP-生物素缺口末端标记测定、细胞质核小体测定和Hoechst染色,ExoU非依赖性但III型分泌依赖性杀伤表现出凋亡特征。细胞外细菌能够诱导凋亡,并且一些铜绿假单胞菌的实验室和临床分离株比其他分离株诱导这种细胞死亡形式的水平显著更高。有趣的是,在这些测定条件下,HeLa细胞而非Madin-Darby犬肾细胞对III型分泌介导的凋亡敏感。这些发现与一种模型一致,即铜绿假单胞菌III型分泌系统转运至少两种杀伤巨噬细胞的因子:导致坏死的ExoU和第二种尚未鉴定的效应蛋白,其诱导凋亡。这种杀伤可能有助于该生物体在感染患者体内持续存在和传播的能力。