Neeld Dennis, Jin Yongxin, Bichsel Candace, Jia Jinghua, Guo Jianhui, Bai Fang, Wu Weihui, Ha Un-Hwan, Terada Naohiro, Jin Shouguang
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL, USA.
Department of Microbiology, College of Life Sciences, Nankai University, Tianjin, PR China.
Microbiology (Reading). 2014 Jul;160(Pt 7):1417-1426. doi: 10.1099/mic.0.078139-0. Epub 2014 Apr 3.
Pseudomonas aeruginosa is a Gram-negative opportunistic human pathogen possessing a type III secretion system (T3SS) which injects toxic effector proteins into mammalian host cells. In previous studies, P. aeruginosa strains lacking all of the known type III effectors were shown to cause cytotoxicity upon prolonged infection time. In this study, we report the identification of a new cytotoxin, nucleoside diphosphate kinase (NDK), which is injected into eukaryotic cells in a T3SS-dependent manner. Injection of NDK is inhibited by the presence of previously known effectors of the T3SS, with an effectorless strain injecting the highest amount, suggesting active competition with the known T3SS effectors. NDK is shown to cause a cytotoxic response when expressed in eukaryotic cells, and P. aeruginosa strains harbouring NDK also show a greater toxicity than strains lacking it. Interestingly, the cytotoxic effect of intracellular NDK is independent of its kinase activity. In previous studies, NDK was shown to be secreted into culture supernatants via a type I secretion system and cause cytotoxicity in a kinase-dependent manner. Therefore, the current study highlights an alternative route of NDK secretion as well as two different cytotoxic mechanisms of NDK, depending on the extra- or intra-cellular location of the protein.
铜绿假单胞菌是一种革兰氏阴性机会性人类病原体,拥有III型分泌系统(T3SS),该系统可将有毒效应蛋白注入哺乳动物宿主细胞。在先前的研究中,已证明缺乏所有已知III型效应子的铜绿假单胞菌菌株在延长感染时间后会引起细胞毒性。在本研究中,我们报告了一种新细胞毒素——核苷二磷酸激酶(NDK)的鉴定,它以T3SS依赖的方式注入真核细胞。T3SS的已知效应子的存在会抑制NDK的注入,效应子缺失菌株注入的量最高,这表明它与已知的T3SS效应子存在活性竞争。当在真核细胞中表达时,NDK会引起细胞毒性反应,携带NDK的铜绿假单胞菌菌株也比缺乏它的菌株表现出更大的毒性。有趣的是,细胞内NDK的细胞毒性作用与其激酶活性无关。在先前的研究中,NDK被证明通过I型分泌系统分泌到培养上清液中,并以激酶依赖的方式引起细胞毒性。因此,当前研究突出了NDK分泌的另一种途径以及NDK的两种不同细胞毒性机制,这取决于该蛋白在细胞外或细胞内的位置。