Ha U, Jin S
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida 32610, USA.
Infect Immun. 2001 Jul;69(7):4398-406. doi: 10.1128/IAI.69.7.4398-4406.2001.
Clinical isolates of Pseudomonas aeruginosa are classified into invasive and noninvasive (cytolytic) strains. In a noninvasive PA103 background, ExoS and ExoT have recently been shown to function as anti-internalization factors. However, these two factors seemed not to have such a function in an invasive strain PAK background. In this study, using HeLa tissue culture cells, we observed that the internalization of invasive strain PAK is dependent on its growth phases, with the stationary-phase cells internalized about 100-fold more efficiently than the exponential-phase cells. This growth phase-dependent internalization was not observed in the noninvasive PA103 strain. Further analysis of various mutant derivatives of the invasive PAK and the noninvasive PA103 strains demonstrated that ExoS or ExoT that is injected into host cells by a type III secretion machinery functions as an anti-internalization factor in both types of strains. In correlation with the growth phase-dependent internalization, the invasive strain PAK translocates much higher amount of ExoS and ExoT into HeLa cells when it is in an exponential-growth phase than when it is in a stationary-growth phase, whereas the translocation of ExoT by the noninvasive strain PA103 is consistently high regardless of the growth phases, suggesting a difference in the regulatory mechanism of type III secretion between the two types of strains. Consistent with the invasive phenotype of the parent strain, an internalized PAK derivative survived well within the HeLa cells, whereas the viability of internalized PA103 derivative was dramatically decreased and completely cleared within 48 h. These results indicate that the invasive strains of P. aeruginosa have evolved the mechanism of intracellular survival, whereas the noninvasive P. aeruginosa strains have lost or not acquired the ability to survive within the epithelial cells.
铜绿假单胞菌的临床分离株可分为侵袭性和非侵袭性(细胞溶解性)菌株。在非侵袭性PA103背景下,最近研究表明外毒素S(ExoS)和外毒素T(ExoT)可作为抗内化因子发挥作用。然而,在侵袭性菌株PAK背景下,这两种因子似乎没有这种功能。在本研究中,我们使用HeLa组织培养细胞观察到,侵袭性菌株PAK的内化作用取决于其生长阶段,稳定期细胞的内化效率比指数期细胞高约100倍。在非侵袭性PA103菌株中未观察到这种生长阶段依赖性内化现象。对侵袭性PAK和非侵袭性PA103菌株的各种突变衍生物进行进一步分析表明,通过III型分泌机制注入宿主细胞的ExoS或ExoT在这两种菌株中均作为抗内化因子发挥作用。与生长阶段依赖性内化相关的是,侵袭性菌株PAK在指数生长期比稳定生长期向HeLa细胞转运的ExoS和ExoT量要高得多,而非侵袭性菌株PA103的ExoT转运量无论生长阶段如何都始终很高,这表明两种菌株在III型分泌调节机制上存在差异。与亲本菌株的侵袭表型一致,内化的PAK衍生物在HeLa细胞内存活良好,而内化的PA103衍生物的活力则显著下降,并在48小时内完全清除。这些结果表明,铜绿假单胞菌的侵袭性菌株已经进化出细胞内存活机制,而非侵袭性铜绿假单胞菌菌株已经丧失或未获得在上皮细胞内存活的能力。