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首页> 外文期刊>Infection and immunity >Edwardsiella tarda EscE (Orf13 Protein) Is a Type III Secretion System-Secreted Protein That Is Required for the Injection of Effectors, Secretion of Translocators, and Pathogenesis in Fish
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Edwardsiella tarda EscE (Orf13 Protein) Is a Type III Secretion System-Secreted Protein That Is Required for the Injection of Effectors, Secretion of Translocators, and Pathogenesis in Fish

机译:爱德华氏菌EscE(Orf13蛋白)是一种III型分泌系统分泌的蛋白,是注入效应子,转运蛋白的分泌和鱼的发病机理所必需的

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The type III secretion system (T3SS) of Edwardsiella tarda is crucial for its intracellular survival and pathogenesis in fish. The orf13 gene (escE) of E. tarda is located 84 nucleotides (nt) upstream of esrC in the T3SS gene cluster. We found that EscE is secreted and translocated in a T3SS-dependent manner and that amino acids 2 to 15 in the N terminus were required for a completely functional T3SS in E. tarda. Deletion of escE abolished the secretion of T3SS translocators, as well as the secretion and translocation of T3SS effectors, but did not influence their intracellular protein levels in E. tarda. Complementation of the escE mutant with a secretion-incompetent EscE derivative restored the secretion of translocators and effectors. Interestingly, the effectors that were secreted and translocated were positively correlated with the EscE protein level in E. tarda. The escE mutant was attenuated in the blue gourami fish infection model, as its 50% lethal dose (LD50) increased to 4 times that of the wild type. The survival rate of the escE mutant-strain-infected fish was 69%, which was much higher than that of the fish infected with the wild-type bacteria (6%). Overall, EscE represents a secreted T3SS regulator that controls effector injection and translocator secretion, thus contributing to E. tarda pathogenesis in fish. The homology of EscE within the T3SSs of other bacterial species suggests that the mechanism of secretion and translocation control used by E. tarda may be commonly used by other bacterial pathogens.
机译:爱德华氏菌的III型分泌系统(T3SS)对其在鱼类中的细胞内存活和发病机理至关重要。 tar。E. tarf的orf13基因(escE)位于T3SS基因簇中esrC上游84个核苷酸(nt)。我们发现EscE是以T3SS依赖性方式分泌和转运的,N末端2至15位氨基酸是tar.E.中完全功能性T3SS所必需的。 escE的删除消除了T3SS易位子的分泌,以及T3SS效应子的分泌和易位,但不影响其在大肠杆菌中的细胞内蛋白水平。 escE突变体与无分泌功能的EscE衍生物互补,恢复了易位子和效应子的分泌。有趣的是,分泌和易位的效应子与塔氏大肠杆菌中的EscE蛋白水平呈正相关。 escE突变体在蓝色古拉米鱼感染模型中减弱,因为其50%致死剂量(LD50)增加到野生型的4倍。受escE突变株感染的鱼的成活率为69%,远高于被野生型细菌感染的鱼的成活率(6%)。总体而言,EscE代表一种分泌的T3SS调节剂,可控制效应子的注射和易位子的分泌,从而促进鱼类的塔氏肠杆菌发病机理。 EscE在其他细菌物种的T3SS内的同源性表明,tar。E. tarta使用的分泌和易位控制机制可能被其他细菌病原体普遍使用。

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