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双靶向策略降解生物膜基质并增强杀菌效果。

Dual-Targeting Approach Degrades Biofilm Matrix and Enhances Bacterial Killing.

机构信息

1 State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Cariology and Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, P.R. China.

2 Biofilm Research Laboratories, Levy Center for Oral Health, Department of Orthodontics and Divisions of Pediatric Dentistry & Community Oral Health, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

J Dent Res. 2019 Mar;98(3):322-330. doi: 10.1177/0022034518818480. Epub 2019 Jan 24.

Abstract

Biofilm formation is a key virulence factor responsible for a wide range of infectious diseases, including dental caries. Cariogenic biofilms are structured microbial communities embedded in an extracellular matrix that affords bacterial adhesion-cohesion and drug tolerance, making them difficult to treat using conventional antimicrobial monotherapy. Here, we investigated a multitargeted approach combining exopolysaccharide (EPS) matrix-degrading glucanohydrolases with a clinically used essential oils-based antimicrobial to potentiate antibiofilm efficacy. Our data showed that dextranase and mutanase can synergistically break down the EPS glucan matrix in preformed cariogenic biofilms, markedly enhancing bacterial killing by the antimicrobial agent (3-log increase versus antimicrobial alone). Further analyses revealed that an EPS-degrading/antimicrobial (EDA) approach disassembles the matrix scaffold, exposing the bacterial cells for efficient killing while concurrently causing cellular dispersion and "physical collapse" of the bacterial clusters. Unexpectedly, we found that the EDA approach can also selectively target the EPS-producing cariogenic bacteria Streptococcus mutans with higher killing specificity (versus other species) within mixed biofilms, disrupting their accumulation and promoting dominance of commensal bacteria. Together, these results demonstrate a dual-targeting approach that can enhance antibiofilm efficacy and precision by dismantling the EPS matrix and its protective microenvironment, amplifying the killing of pathogenic bacteria within.

摘要

生物膜的形成是导致多种感染性疾病(包括龋齿)的关键毒力因子。致龋生物膜是嵌入细胞外基质中的结构化微生物群落,为细菌的黏附和耐药提供了支持,这使得它们难以通过传统的抗菌单药治疗。在这里,我们研究了一种多靶点方法,将胞外多糖(EPS)基质降解葡聚糖水解酶与临床使用的基于精油的抗菌剂结合,以增强抗生物膜功效。我们的数据表明,葡聚糖酶和黏菌素可以协同作用,破坏已形成的致龋生物膜中的 EPS 聚糖基质,显著增强抗菌剂的杀菌效果(与单独使用抗菌剂相比,增加了 3 个对数)。进一步的分析表明,EPS 降解/抗菌(EDA)方法会破坏基质支架,使细菌细胞易于被杀死,同时还会导致细胞分散和细菌簇的“物理崩溃”。出乎意料的是,我们发现 EDA 方法还可以选择性地针对 EPS 产生的致龋细菌变形链球菌,在混合生物膜中具有更高的杀菌特异性(与其他物种相比),破坏它们的聚集并促进共生菌的优势。总之,这些结果表明,这种双重靶向方法可以通过破坏 EPS 基质及其保护微环境来增强抗生物膜功效和精准性,放大对致病性细菌的杀伤作用。

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