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红景天提取物抑制致龋口腔病原体变形链球菌生物膜的形成和毒力基因的表达。

Rhodiola rosea extract inhibits the biofilm formation and the expression of virulence genes of cariogenic oral pathogen Streptococcus mutans.

机构信息

State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, PR China.

West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu 610041, PR China.

出版信息

Arch Oral Biol. 2020 Aug;116:104762. doi: 10.1016/j.archoralbio.2020.104762. Epub 2020 May 19.

Abstract

OBJECTIVE

The present study aimed to evaluate the effect of Rhodiola rosea extract (RE) on Streptococcus mutans biofilm formation and the relevant mechanism of its action.

METHODS

The effect of RE on the biofilm formation and extracellular polysaccharides (EPS) synthesis of S. mutans was assessed by confocal laser scanning microscopy (CLSM), crystal violet staining and CFU counting method. Scanning electron microscopy (SEM) was applied to observe the surface morphology of S. mutans biofilms formed on glass coverslips and dental enamel. To study the relevant mechanism, quantitative real time PCR (qRT-PCR) and zymogram assay were applied to measure the expression of virulence genes and the enzymatic activity of glucosyltransferases (Gtfs) under the treatment of RE. The CCK-8 assay was also performed on macrophages (RAWs) and human oral keratinocytes (HOKs) in order to evaluate its biocompatibility.

RESULTS

As a result, RE inhibited the biofilm formation and EPS synthesis of S. mutans. RE also suppressed the expression of gtf genes and quorum sensing (QS) system as well as the enzymatic activity of Gtf proteins. Moreover, RE exhibited a good biocompatibility to human cells.

CONCLUSIONS

This study provides the evidence for RE as a novel anti-biofilm agent for clinical use.

摘要

目的

本研究旨在评估红景天提取物(RE)对变形链球菌生物膜形成的影响及其作用机制。

方法

通过共聚焦激光扫描显微镜(CLSM)、结晶紫染色和 CFU 计数法评估 RE 对变形链球菌生物膜形成和胞外多糖(EPS)合成的影响。扫描电子显微镜(SEM)用于观察玻璃载玻片和牙釉质上形成的变形链球菌生物膜的表面形态。为了研究相关机制,采用定量实时 PCR(qRT-PCR)和酶谱分析测定 RE 处理下毒力基因和葡糖基转移酶(Gtfs)的酶活性表达。还通过细胞活力试剂盒(CCK-8)检测 RE 在巨噬细胞(RAWs)和人口腔角质细胞(HOKs)中的生物相容性。

结果

RE 抑制了变形链球菌的生物膜形成和 EPS 合成。RE 还抑制了 gtf 基因和群体感应(QS)系统的表达以及 Gtf 蛋白的酶活性。此外,RE 对人细胞表现出良好的生物相容性。

结论

本研究为 RE 作为一种新型临床应用的抗生物膜剂提供了证据。

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