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膜转导肽 gH625 及其类似物的多微生物抗生物膜活性。

Polymicrobial antibiofilm activity of the membranotropic peptide gH625 and its analogue.

机构信息

Department of Biology, University of Naples "Federico II", via Cinthia, 80100, Naples, Italy.

Department of Pharmacy, University of Naples "Federico II", Via Mezzocannone 16, 80134 Naples, Italy.

出版信息

Microb Pathog. 2018 Dec;125:189-195. doi: 10.1016/j.micpath.2018.09.027. Epub 2018 Sep 15.

Abstract

This work illustrates a new role for the membranotropic peptide gH625 and its derivative gH625-GCGKKK in impairing formation of polymicrobial biofilms. Mixed biofilms composed of Candida and bacterial species cause frequently infections and failure of medical silicone devices and also show a major drug resistance than single-species biofilms. Inhibition and eradication of biofilms were evaluated by complementary methods: XTT-reduction, and crystal violet staining (CV). Our results indicate that gH625-GCGKKKK, better than the native peptide, strongly inhibited formation of mixed biofilms of clinical isolates of C. tropicalis/S. marcescens and C. tropicalis/S. aureus and reduced the biofilm architecture, interfering with cell adhesion and polymeric matrix, as well as eradicated the long-term polymicrobial biofilms on silicone surface.

摘要

这项工作说明了膜转导肽 gH625 及其衍生物 gH625-GCGKKK 在破坏多微生物生物膜形成方面的新作用。由念珠菌和细菌物种组成的混合生物膜会导致经常发生感染和医用硅酮设备失效,并且比单物种生物膜表现出更大的耐药性。通过补充方法评估了生物膜的抑制和根除:XTT 还原和结晶紫染色(CV)。我们的结果表明,gH625-GCGKKKK 比天然肽更能强烈抑制临床分离株热带念珠菌/粘质沙雷氏菌和热带念珠菌/金黄色葡萄球菌的混合生物膜的形成,并降低生物膜结构,干扰细胞黏附和聚合物基质,以及根除硅酮表面上的长期多微生物生物膜。

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