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首页> 外文期刊>International journal of antimicrobial agents >Use of the quorum sensing inhibitor furanone C-30 to interfere with biofilm formation by Streptococcus mutans and its luxS mutant strain
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Use of the quorum sensing inhibitor furanone C-30 to interfere with biofilm formation by Streptococcus mutans and its luxS mutant strain

机译:群体感应抑制剂呋喃酮C-30干扰变形链球菌及其luxS突变菌株形成生物膜的用途

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摘要

Streptococcus mutans is recognised as a major aetiological agent of dental caries. One of its important virulence factors is its ability to form biofilms on tooth surfaces. The aim of this study was to evaluate the effects of the quorum sensing inhibitor furanone C-30 on biofilm formation by S. mutans and its luxS mutant strain. The effects of furanone C-30 on biofilms of both strains formed on 96-well microtitre plates at 37°C were determined by a colorimetric technique (MTT assay). Different concentrations of furanone C-30 (0.0, 2.0 and 4.0 μg/mL) and different time points of biofilm formation (4, 14 and 24 h) were investigated. The structures and thickness of the biofilms were observed by confocal laser scanning microscopy (CLSM). Quorum sensing-related gene expression (ftf, smu630, brpA, gbpB, gtfB, vicR, comDE and relA) was investigated by real-time polymerase chain reaction (RT-PCR). The results showed that synthetic furanone C-30 can inhibit biofilm formation by S. mutans and its luxS mutant strain, although it does not affect the bacterial growth rate itself. The quantities of biofilm formed by both strains significantly decreased (P < 0.05) and the biofilms became thinner and looser as revealed by CLSM with increasing concentrations of furanone C-30. Expression of the genes tested was downregulated in the biofilms by the addition of furanone C-30. These results revealed that synthetic furanone C-30 can effectively inhibit biofilm formation by S. mutans and its luxS mutant strain.
机译:变形链球菌被认为是龋齿的主要病因。它的重要毒力因子之一是其在牙齿表面形成生物膜的能力。这项研究的目的是评估群体感应抑制剂呋喃酮C-30对变形链球菌及其luxS突变菌株形成生物膜的影响。通过比色技术(MTT分析)确定呋喃酮C-30对在37℃下在96孔微量滴定板上形成的两种菌株的生物膜的影响。研究了不同浓度的呋喃酮C-30(0.0、2.0和4.0μg/ mL)和生物膜形成的不同时间点(4、14和24 h)。通过共聚焦激光扫描显微镜(CLSM)观察生物膜的结构和厚度。通过实时聚合酶链反应(RT-PCR)研究了与群体感应相关的基因表达(ftf,smu630,brpA,gbpB,gtfB,vicR,comDE和relA)。结果表明,合成呋喃酮C-30可以抑制变形链球菌及其luxS突变株的生物膜形成,尽管它并不影响细菌自身的生长速度。 CLSM发现,随着呋喃酮C-30浓度的增加,两种菌株形成的生物膜数量均显着减少(P <0.05),生物膜变得更薄和更松散。通过添加呋喃酮C-30,可在生物膜中下调受测基因的表达。这些结果表明,合成的呋喃酮C-30可有效抑制变形链球菌及其luxS突变株的生物膜形成。

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