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Conservation of Ebp-Type Pilus Genes among Enterococci and Demonstration of Their Role in Adherence of Enterococcus faecalis to Human Platelets

机译:肠球菌中Ebp型毛囊基因的保守性及其在粪肠球菌对人血小板粘附中的作用的证明

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摘要

Ebp are endocarditis- and biofilm-associated pili of Enterococcus faecalis that are also important in experimental urinary tract infections (UTIs). Our analyses, using available genomes, found that the ebp locus is unique to enterococci. In E. faecalis, the ebp locus is very highly conserved and only 1/473 E. faecalis isolates tested lacked ebpABC, while only 1.2% had the bee pilus locus. No other pilus-encoding operon was identified in 55 available genomes, indicating that the vast majority of E. faecalis strains (unlike Enterococcus faecium and streptococci) have a single pilus locus. Surface expression studies showed that Ebp pili were produced in vitro by 91/91 brain heart infusion (BHI) plus serum-grown E. faecalis isolates and that strain OG1RF expressed pili at even higher levels in rat endocarditis vegetations. However, Ebp expression was restricted to 30 to 72% of E. faecalis cells, consistent with a bistability mode of expression. We also evaluated E. faecalis interactions with human platelets and found that growth of E. faecalis in BHI plus serum significantly enhanced adherence to human platelets and that sortase deletion mutants (the ΔsrtA, Δbps, and ΔbpsΔsrtA mutants) were markedly defective. Further studies identified that Ebp pili, but not the microbial surface components recognizing adhesive matrix molecules (MSCRAMMs) Ace and Fss2, mediate adherence of E. faecalis to platelets. Taken together, our data show that the immunogenic (in human endocarditis patients) and commonly expressed Ebp pili, which are known to be important for experimental endocarditis, are highly conserved and mediate adherence to platelets, suggesting that Ebp pili may be a reasonable immunotherapeutic target for prevention or possibly treatment of endocarditis caused by this species.
机译:Ebp是粪肠球菌的心内膜炎和生物膜相关菌毛,在实验性尿路感染(UTI)中也很重要。我们使用现有基因组进行的分析发现,ebp基因座对于肠球菌而言是独特的。在粪肠球菌中,ebp基因座非常保守,只有1/473个粪肠球菌分离株缺乏ebpABC,而只有1.2%的蜜蜂有菌毛基因座。在55个可用基因组中没有发现其他菌毛编码操纵子,这表明绝大多数粪肠球菌菌株(与粪肠球菌和链球菌不同)只有一个菌毛基因座。表面表达研究表明,Ebp菌毛是由91/91脑心脏输液(BHI)加上血清生长的粪肠球菌分离株体外产生的,并且OG1RF菌株在大鼠心内膜炎植被中的菌毛表达水平更高。但是,Ebp的表达限于粪肠球菌细胞的30​​%至72%,这与双稳态表达模式一致。我们还评估了粪肠球菌与人血小板的相互作用,发现粪便肠球菌在BHI和血清中的生长显着增强了对人血小板的粘附力以及分选酶缺失突变体(ΔsrtA,Δbps和Δ bps Δ srtA 突变)明显有缺陷。进一步的研究表明,Ebp菌毛而非介导粘附基质分子(MSCRAMMs)Ace和Fss2的微生物表面成分介导了 E的粘附。粪便至血小板。综上所述,我们的数据表明,免疫原性(在人心内膜炎患者中)和通常表达的Ebp菌毛是高度保守的,可介导血小板粘附,这被认为对实验性心内膜炎很重要,这提示Ebp菌毛可能是合理的免疫治疗靶点用于预防或可能治疗由该物种引起的心内膜炎。

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