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The major outer membrane protein OmpU of Vibrio splendidus contributes to host antimicrobial peptide resistance and is required for virulence in the oyster Crassostrea gigas

机译:锦绣弧菌的主要外膜蛋白OmpU有助于宿主抗菌肽的耐药性,是牡蛎Crassostrea gigas的致病力所必需的

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Vibrio splendidus, strain LGP32, is an oyster pathogen associated with the summer mortalities affecting the production of Crassostrea gigas oysters worldwide. Vibrio splendidus LGP32 was shown to resist to up to 10 mu M Cg-Def defensin and Cg-BPI bactericidal permeability increasing protein, two antimicrobial peptides/proteins (AMPs) involved in C. gigas immunity. The resistance to both oyster Cg-Def and Cg-BPI and standard AMPs (polymyxin B, protegrin, human BPI) was dependent on the ompU gene. Indeed, upon ompU inactivation, minimal bactericidal concentrations decreased by up to fourfold. AMP resistance was restored upon ectopic expression of ompU. The susceptibility of bacterial membranes to AMP-induced damages was independent of the ompU-mediated AMP resistance. Besides its role in AMP resistance, ompU proved to be essential for the adherence of V. splendidus LGP32 to fibronectin. Interestingly, in vivo, ompU was identified as a major determinant of V. spiendidus pathogenicity in oyster experimental infections. Indeed, the V. splendidus-induced oyster mortalities dropped from 56% to 11% upon ompU mutation (Kaplan Meier survival curves, P < 0.01). Moreover, in co-infection assays, the ompU mutant was out competed by the wild-type strain with competitive indexes in the range of 0.1-0.2. From this study, ompU is required for virulence of V. splendidus. Contributing to AMP resistance, conferring adhesive properties to V. splendidus, and being essential for in vivo fitness, the OmpU porin appears as an essential effector of the C. gigas/V. splendidus interaction.
机译:锦绣弧菌是LGP32菌株,是与夏季死亡率相关的牡蛎病原体,影响了全球Crassostrea gigas牡蛎的生产。脾脏弧菌LGP32被证明能抵抗高达10μM的Cg-Def防御素和Cg-BPI杀菌通透性增加蛋白,两种抗微生物肽/蛋白(AMPs)参与到C. gigas免疫中。对牡蛎Cg-Def和Cg-BPI以及标准AMP(多粘菌素B,protegrin,人BPI)的抗性均取决于ompU基因。实际上,在ompU灭活后,最小的杀菌浓度最多降低了四倍。 ompU异位表达后,AMP抗性得以恢复。细菌膜对AMP诱导的损伤的敏感性与ompU介导的AMP抗性无关。除了在AMP耐药性中的作用外,ompU还被证明对于锦绣葡萄菌LGP32与纤连蛋白的粘附至关重要。有趣的是,在体内,ompU被确定为牡蛎实验性感染中孢子菌弧菌致病性的主要决定因素。的确,在ompU突变后,锦绣葡萄球菌引起的牡蛎死亡率从56%降至11%(Kaplan Meier生存曲线,P <0.01)。而且,在共感染测定中,ompU突变体被野生型菌株竞争,竞争指数在0.1-0.2的范围内。从这项研究中,需要ompU才能感染脾炎弧菌。 OmpU孔蛋白有助于增强AMP抗性,赋予锦绣葡萄粘膜特性,并且对于体内适应性至关重要,它似乎是C. gigas / V的重要效应物。脾脏互动。

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