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红树植物无梗倍半萜醇通过破坏初始附着和细胞间黏附抑制表皮葡萄球菌生物膜形成和毒力产生。

Quebrachitol from Rhizophora mucronata inhibits biofilm formation and virulence production in Staphylococcus epidermidis by impairment of initial attachment and intercellular adhesion.

机构信息

Centre of Advanced Study in Marine Biology, Annamalai University, Parangipettai, Tamil Nadu, 608 502, India.

出版信息

Arch Microbiol. 2020 Aug;202(6):1327-1340. doi: 10.1007/s00203-020-01844-9. Epub 2020 Mar 7.

Abstract

Staphylococcus epidermidis is well recognized nosocomial pathogen in clinical settings for their implants associated infections. Biofilm and virulence production executes a S. epidermidis pathogenesis against host. Hence, interfering of biofilm formation has become an auspicious to control the pathogenesis of S. epidermidis. The present study evaluates antibiofilm potential of Rhizophora mucronata against S. epidermidis biofilms. Rhizophora mucronata leaves extract significantly inhibited the biofilm formation and quebrachitol was identified as an active compound responsible for the biofilm inhibition. Quebrachitol significantly inhibited biofilm formation at concentration dependent manner without exhibit non-bactericidal property. And, quebrachitol reduced the biofilm building components such as exopolysaccharides, lipase and proteins production. Confocal laser scanning microscopic studies obtained quebrachitol surface independent biofilm efficacy against S. epidermidis. Notably, quebrachitol significantly reduced S. epidermidis adherence on biotic (coated with type I collagen and fibrinogen) and abiotic (hydrophobic and hydrophilic) surfaces. Addition of quebrachitol inhibits autolysis mediated initial attachment and accumulation associated aggregation process. Moreover, quebrachitol significantly reduced the hydrolases virulence production which supports S. epidermidis invasion into the host. Furthermore, gene expression analysis revealed the ability of quebrachitol to downregulate the virulence genes expression which are mainly involved in biofilm formation and virulence production. The results obtained from the present study suggest that quebrachitol as an ideal candidate for the therapeutic action against S. epidermidis pathogenesis.

摘要

表皮葡萄球菌是临床植入物相关感染的重要医院获得性病原体。生物膜和毒力产生使表皮葡萄球菌对宿主产生致病性。因此,干扰生物膜的形成已成为控制表皮葡萄球菌发病机制的一种有希望的方法。本研究评估了红厚壳对表皮葡萄球菌生物膜的抗生物膜潜力。红厚壳叶提取物显著抑制生物膜的形成,鉴定出 quebrachitol 是一种负责生物膜抑制的活性化合物。Quebrachitol 以浓度依赖的方式显著抑制生物膜形成,而没有表现出非杀菌特性。而且,quebrachitol 减少了生物膜形成成分,如胞外多糖、脂肪酶和蛋白质的产生。共聚焦激光扫描显微镜研究获得了 quebrachitol 对表皮葡萄球菌的表面非依赖性生物膜功效。值得注意的是,quebrachitol 显著减少了表皮葡萄球菌在生物(涂有 I 型胶原蛋白和纤维蛋白原)和非生物(疏水性和亲水性)表面的粘附。添加 quebrachitol 可抑制自溶介导的初始附着和聚集相关的聚集过程。此外,quebrachitol 显著降低了水解酶的毒力产生,这支持表皮葡萄球菌侵入宿主。此外,基因表达分析显示,quebrachitol 能够下调与生物膜形成和毒力产生有关的毒力基因表达。本研究的结果表明,quebrachitol 是一种针对表皮葡萄球菌发病机制的治疗作用的理想候选物。

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