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Unique Cell Adhesion and Invasion Properties of Yersinia enterocolitica O:3 the Most Frequent Cause of Human Yersiniosis

机译:小肠结肠炎耶尔森菌O:3的独特细胞粘附和侵袭特性这是人类耶尔森菌病最常见的原因

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摘要

Many enteric pathogens are equipped with multiple cell adhesion factors which are important for host tissue colonization and virulence. Y. enterocolitica, a common food-borne pathogen with invasive properties, uses the surface proteins invasin and YadA for host cell binding and entry. In this study, we demonstrate unique cell adhesion and invasion properties of Y. enterocolitica serotype O:3 strains, the most frequent cause of human yersiniosis, and show that these differences are mainly attributable to variations affecting the function and expression of invasin in response to temperature. In contrast to other enteric Yersinia strains, invasin production in O:3 strains is constitutive and largely enhanced compared to other Y. enterocolitica serotypes, in which invA expression is temperature-regulated and significantly reduced at 37°C. Increase of invasin levels is caused by (i) an IS1667 insertion into the invA promoter region, which includes an additional promoter and RovA and H-NS binding sites, and (ii) a P98S substitution in the invA activator protein RovA rendering the regulator less susceptible to proteolysis. Both variations were shown to influence bacterial colonization in a murine infection model. Furthermore, we found that co-expression of YadA and down-regulation of the O-antigen at 37°C is required to allow efficient internalization by the InvA protein. We conclude that even small variations in the expression of virulence factors can provoke a major difference in the virulence properties of closely related pathogens which may confer better survival or a higher pathogenic potential in a certain host or host environment.
机译:许多肠道病原体都具有多种细胞粘附因子,这对于宿主组织的定殖和毒力很重要。小肠结肠炎耶尔森氏菌(Y. enterocolitica)是一种常见的具有侵袭性的食源性病原体,它利用表面蛋白侵入蛋白和YadA进行宿主细胞的结合和进入。在这项研究中,我们证明了耶尔森菌肠炎耶尔森菌O:3菌株的独特细胞粘附和侵袭特性,这是人类耶尔森氏菌病的最常见原因,并且表明这些差异主要归因于影响血管紧张素转换酶功能和表达的变异。温度。与其他肠溶耶尔森菌菌株相比,O:3菌株的入侵素生产是组成型的,并且与invA表达受温度调节且在37°C时显着降低的其他肠结肠炎耶尔森氏菌血清型相比大大增强。血管紧张素水平升高是由于(i)IS1667插入invA启动子区域,其中包括一个额外的启动子以及RovA和H-NS结合位点,以及(ii)invA激活蛋白RovA中的P98S取代,使得调节剂较少易于蛋白水解。在鼠感染模型中,两种变体均显示影响细菌定植。此外,我们发现YadA的共表达和O-抗原在37°C下调是允许InvA蛋白有效内在化的必要条件。我们得出的结论是,即使毒力因子表达的微小变化也可能引起密切相关的病原体在毒力特性方面的重大差异,这可能会在某些宿主或宿主环境中提供更好的存活率或更高的致病潜力。

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