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首页> 外文期刊>International journal of medical microbiology: IJMM >Differential compartmentalization of Streptococcus pyogenes virulence factors and host protein binding properties as a mechanism for host adaptation
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Differential compartmentalization of Streptococcus pyogenes virulence factors and host protein binding properties as a mechanism for host adaptation

机译:化脓性链球菌毒力因子和宿主蛋白结合特性的差异区室化作为宿主适应的机制

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Streptococcus pyogenes is an important human pathogen responsible for substantial morbidity and mortality worldwide. Although S. pyogenes is a strictly human pathogen with no other known animal reservoir, several murine infection models exist to explore different aspects of the bacterial pathogenesis. Inoculating mice with wild-type S. pyogenes strains can result in the generation of new bacterial phenotypes that are hypervirulent compared to the original inoculum. In this study, we used a serial mass spectrometry based proteomics strategy to investigate if these hypervirulent strains have an altered distribution of virulence proteins across the intracellular, surface associated and secreted bacterial compartments and if any change in compartmentalization can alter the protein-protein interaction network between bacteria and host proteins. Quantitative analysis of the S. pyogenes surface and secreted proteomes revealed that animal passaged strains are associated with significantly higher amount of virulence factors on the bacterial surface and in the media. This altered virulence factor compartmentalization results in increased binding of several mouse plasma proteins to the bacterial surface, a trend that was consistent for mouse plasma from several different mouse strains. In general, both the wild-type strain and animal passaged strain were capable of binding high amounts of human plasma proteins. However, compared to the non-passaged strains, the animal passaged strains displayed an increased ability to bind mouse plasma proteins, in particular for M protein binders, indicating that the increased affinity for mouse blood plasma proteins is a consequence of host adaptation of this pathogen to a new host. In conclusion, plotting the total amount of virulence factors against the total amount of plasma proteins associated to the bacterial surface could clearly separate out animal passaged strains from wild type strains indicating a virulence model that could predict the virulence of a S. pyogenes strain in mice and which could be used to identify key aspects of this bacteria's pathogenesis. (C) 2016 Elsevier GmbH. All rights reserved.
机译:化脓性链球菌是重要的人类病原体,其在全世界范围内引起大量发病和死亡。尽管化脓性链球菌是严格的人类病原体,没有其他已知的动物宿主,但仍存在几种鼠类感染模型来探索细菌发病机理的不同方面。用野生型化脓性链球菌菌株接种小鼠可导致产生与原始接种物相比具有高毒力的新细菌表型。在这项研究中,我们使用了基于串联质谱的蛋白质组学策略,研究这些高毒力菌株在细胞内,表面相关和分泌的细菌区室中毒力蛋白的分布是否发生改变,以及区室化的任何变化是否可以改变蛋白质-蛋白质相互作用网络在细菌和宿主蛋白之间。化脓性链球菌表面和分泌的蛋白质组的定量分析表明,动物传代的菌株与细菌表面和培养基中大量的毒力因子有关。这种改变的毒力因子区室化导致几种小鼠血浆蛋白与细菌表面的结合增加,这种趋势对于来自几种不同小鼠品系的小鼠血浆是一致的。通常,野生型菌株和动物传代菌株都能够结合大量的人血浆蛋白。但是,与非传代菌株相比,动物传代菌株显示出更高的结合小鼠血浆蛋白的能力,特别是与M蛋白结合剂的结合力,表明与小鼠血浆蛋白的亲和力提高是宿主对这种病原体适应的结果到新主机。总之,将毒力因子的总量与与细菌表面相关的血浆蛋白总量作图可以清楚地从野生型菌株中分离出动物传代菌株,表明可以预测小鼠化脓性链球菌菌株的毒力的毒力模型。可以用来确定这种细菌发病机理的关键方面。 (C)2016 Elsevier GmbH。版权所有。

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