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Relative contributions of Enterococcus faecalis OG1RF sortase-encoding genes, srtA and bps (srtC), to biofilm formation and a murine model of urinary tract infection.

机译:粪肠球菌OG1RF分选酶编码基因srtA和bps(srtC)对生物膜形成和尿道感染的小鼠模型的相对贡献。

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摘要

Deletion mutants of the two sortase genes of Enterococcus faecalis OG1RF were constructed. srtC (renamed here bps for biofilm and pilus-associated sortase) was previously shown to be necessary for the production of Ebp pili and important for biofilm formation and endocarditis. Here, we report that a srtA deletion mutant showed a small (5%) yet significant (P = 0.037) reduction in biofilm relative to OG1RF, while a DeltasrtA Deltabps double mutant showed a much greater reduction (74% versus OG1RF and 44% versus the Deltabps mutant). In a murine urinary tract infection (UTI), the 50% infective doses of both the DeltasrtA Deltabps and Deltabps mutants were approximately 2 log10 greater than that of OG1RF or the DeltasrtA mutant. Similarly, approximately 2 log10 fewer bacteria were recovered from the kidneys after infection with the Deltabps mutant (P = 0.017) and the DeltasrtA Deltabps double mutant (P = 0.022) compared to wild-type strain OG1RF. In a competition UTI, the Deltabps mutant was slightly, but not significantly, less attenuated than the DeltasrtA Deltabps double mutant. Fluorescence-activated cell sorter analysis with Ebp-specific antibodies confirmed that a minority of OG1RF cells express Ebp pili on their surface in vitro and that Bps has a major role in Ebp pilus biogenesis but also indicated a function for SrtA in surface localization of the pilus subunit protein EbpA. In conclusion, deletion of bps had a major effect on virulence in murine UTIs, as well as biofilm; deletion of srtA from OG1RF had little effect on these phenotypes, but its deletion from a bps mutant had a pronounced effect on biofilm, suggesting that Bps and/or the proteins it anchors may compensate for the loss of some SrtA function(s).
机译:构建了粪肠球菌OG1RF的两个分选酶基因的缺失突变体。 srtC(在这里更名为生物膜和菌毛相关分选酶的bps)以前被证明对于产生Ebp菌毛是必需的,并且对生物膜的形成和心内膜炎很重要。在这里,我们报告说,相对于OG1RF,srtA缺失突变体显示出较小的(5%)显着(P = 0.037)生物膜减少,而DeltasrtA Deltabps双突变体显示出更大的减少(74%与OG1RF和44% Deltabps突变体)。在鼠尿道感染(UTI)中,DeltasrtA Deltabps和Deltabps突变体的50%感染剂量均比OG1RF或DeltasrtA突变体高约2 log10。同样,与野生型菌株OG1RF相比,用Deltabps突变体(P = 0.017)和DeltasrtA Deltabps双突变体(P = 0.022)感染后,从肾脏中回收的细菌减少了约2 log10。在竞争性UTI中,Deltabps突变体比DeltasrtA Deltabps双重突变体的衰减程度稍低,但不明显。用Ebp特异性抗体进行的荧光激活细胞分选分析证实,少数OG1RF细胞在体外表面表达Ebp菌毛,而Bps在Ebp菌毛的生物发生中起主要作用,但也表明SrtA在菌毛的表面定位中起作用亚基蛋白EbpA。总之,bps的缺失对鼠类UTI以及生物膜的毒力具有重要影响。从OG1RF缺失srtA对这些表型几乎没有影响,但从bps突变体中缺失对生物膜有显着影响,表明Bps和/或其锚定的蛋白质可能补偿某些SrtA功能的丧失。

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