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Glucosyltransferases of Viridans Streptococci Are Modulins of Interleukin-6 Induction in Infective Endocarditis

机译:绿藻链球菌的葡萄糖基转移酶是感染性心内膜炎中白介素6诱导的调节蛋白。

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摘要

The glucosyltransferases (GTFs) of viridans streptococci, common pathogens of infective endocarditis, are extracellular proteins that convert sucrose into exopolysaccharides and glucans. GTFs B, C, and D of Streptococcus mutans are modulins that induce, in vitro and in vivo, the production of cytokines, in particular interleukin-6 (IL-6), from monocytes. The roles of S. mutans GTFs in infectivity and inflammation in situ were tested in a rat experimental model of endocarditis. No significant differences in infectivity, in terms of 95% infective dose and densities of bacteria inside vegetations, were observed between laboratory strain GS-5 and two clinical isolates or isogenic mutant NHS1DD, defective in the expression of GTFs. In aortic valves and surrounding tissues, IL-6 was detected by Western blots and immunostaining 24 h after GS-5 infection, was maintained over 72 h, and was followed by production of tumor necrosis factor alpha but not IL-1β. Animals infected with NHS1DD showed markedly lower levels of IL-6 (less than 5% of that of parental GS-5-infected rats), while tumor necrosis factor alpha was unaffected. In contrast, animals infected with NHR1DD, another isogenic mutant expressing only GtfB, showed a much smaller reduction (down to 56%). These results suggest that GTFs are specific modulins that act during acute inflammation, inducing IL-6 from endothelial cells surrounding the infected valves without affecting bacterial colonization in vegetations, and that IL-6 might persist in chronic inflammation in endocarditis.
机译:绿脓杆菌链球菌是感染性心内膜炎的常见病原体,其糖基转移酶(GTF)是将蔗糖转化为胞外多糖和葡聚糖的细胞外蛋白。变形链球菌的GTF B,C和D是调节蛋白,可在体外和体内诱导单核细胞产生细胞因子,特别是白介素6(IL-6)。在心内膜炎的大鼠实验模型中测试了变形链球菌GTF在感染性和原位炎症中的作用。在实验室菌株GS-5和两种临床分离株或同基因突变体NHS1DD之间,在GTF表达方面存在缺陷,在95%的感染剂量和植被内细菌的密度方面,没有观察到明显的感染性差异。在主动脉瓣和周围组织中,通过Western印迹检测到IL-6,并在GS-5感染后24 h进行免疫染色,维持72 h以上,随后产生肿瘤坏死因子α,但没有IL-1β。被NHS1DD感染的动物表现出明显较低的IL-6水平(不到GS-5感染的父母的5%),而肿瘤坏死因子α则不受影响。相反,感染了NHR1DD(仅表达GtfB的另一种等基因突变体)的动物,其减少的幅度要小得多(降至56%)。这些结果表明,GTF是在急性炎症过程中起作用的特定调节蛋白,可从感染瓣膜周围的内皮细胞中诱导IL-6,而不会影响植物中细菌的定殖,并且IL-6可能在心内膜炎的慢性炎症中持续存在。

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