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外排泵抑制剂增强粪肠球菌生物膜的抗菌光动力灭活作用。

Efflux pump inhibitor potentiates antimicrobial photodynamic inactivation of Enterococcus faecalis biofilm.

机构信息

Endodontics, Faculty of Dentistry, University of Toronto, Toronto, Canada.

出版信息

Photochem Photobiol. 2010 Nov-Dec;86(6):1343-9. doi: 10.1111/j.1751-1097.2010.00792.x. Epub 2010 Sep 22.

DOI:10.1111/j.1751-1097.2010.00792.x
PMID:20860692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2991588/
Abstract

Microbial biofilm architecture contains numerous protective features, including extracellular polymeric material that render biofilms impermeable to conventional antimicrobial agents. This study evaluated the efficacy of antimicrobial photodynamic inactivation (aPDI) of Enterococcus faecalis biofilms. The ability of a cationic, phenothiazinium photosensitizer, methylene blue (MB) and an anionic, xanthene photosensitizer, rose bengal (RB) to inactivate biofilms of E. faecalis (OG1RF and FA 2-2) and disrupt the biofilm structure was evaluated. Bacterial cells were tested as planktonic suspensions, intact biofilms and biofilm-derived suspensions obtained by the mechanical disruption of biofilms. The role of a specific microbial efflux pump inhibitor (EPI), verapamil hydrochloride in the MB-mediated aPDI of E. faecalis biofilms was also investigated. The results showed that E. faecalis biofilms exhibited significantly higher resistance to aPDI when compared with E. faecalis in suspension (P < 0.001). aPDI with cationic MB produced superior inactivation of E. faecalis strains in a biofilm along with significant destruction of biofilm structure when compared with anionic RB (P < 0.05). The ability to inactivate biofilm bacteria was further enhanced when the EPI was used with MB (P < 0.001). These experiments demonstrated the advantage of a cationic phenothiazinium photosensitizer combined with an EPI to inactivate biofilm bacteria and disrupt biofilm structure.

摘要

微生物生物膜结构包含许多保护特性,包括使生物膜对常规抗菌剂不可渗透的细胞外聚合物材料。本研究评估了抗菌光动力灭活(aPDI)对粪肠球菌生物膜的疗效。评估了阳离子吩噻嗪类光敏剂亚甲蓝(MB)和阴离子呫吨类光敏剂玫瑰红(RB)对粪肠球菌(OG1RF 和 FA 2-2)生物膜的灭活能力以及破坏生物膜结构的能力。测试了细菌细胞作为浮游悬液、完整生物膜和通过机械破坏生物膜获得的生物膜衍生悬浮液。还研究了特定微生物外排泵抑制剂(EPI)盐酸维拉帕米在 MB 介导的粪肠球菌生物膜 aPDI 中的作用。结果表明,与悬浮中的粪肠球菌相比,粪肠球菌生物膜对 aPDI 表现出明显更高的抗性(P<0.001)。与阴离子 RB 相比,阳离子 MB 进行的 aPDI 可更有效地灭活生物膜中的粪肠球菌菌株,同时显著破坏生物膜结构(P<0.05)。当使用 EPI 与 MB 结合时,灭活生物膜细菌的能力进一步增强(P<0.001)。这些实验证明了阳离子吩噻嗪类光敏剂与 EPI 结合用于灭活生物膜细菌和破坏生物膜结构的优势。

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