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黄芩苷与左氧氟沙星联合对生物膜相关感染的作用

Combination effects of baicalin with levofloxacin against biofilm-related infections.

作者信息

Du Zhongye, Huang Yingying, Chen Yan, Chen Yiqiang

机构信息

Department of Pulmonary and Critical Care Medicine, First Affiliated Hospital of Guangxi Medical University, Guangxi Medical University Nanning, China.

Department of Respiratory Disease, Second Affiliated Hospital of Guangxi Medical University, Guangxi Medical University Nanning, China.

出版信息

Am J Transl Res. 2019 Mar 15;11(3):1270-1281. eCollection 2019.

Abstract

It is important to improve the existing techniques and develop new strategies to prevent bacterial biofilm formation. In this in vitro study, biofilms were established by a clinically isolated strain of 17546 (t037). Different concentrations of baicalin were added to 3- and 7-day biofilms. Based on colony counts and quantitative analysis of the biomass, sub-minimum inhibitory concentrations (sub-MICs) (1024, 512 or 256 μg/mL) of baicalin clearly decreased the number of bacterial colonies and biomass in vitro. Fluorescence microscopy revealed that sub-MICs (1024, 512, or 256 μg/mL) of baicalin inhibited bacterial adherence to the carrier surface and decreased polysaccharide production. Moreover, baicalin disrupted biofilms and exhibited synergistic effects with levofloxacin. Virulence factors were assessed by western blotting and real-time quantitative polymerase chain reaction, confirming that staphylococcal enterotoxin A, α-haemolysin and coagulase production decreased after baicalin treatment. Additionally, baicalin increased production of thermonuclease in , and baicalin at 1024 and 512 μg/mL downregulated agrA expression. Based on these findings, the combination of baicalin with levofloxacin might be a new, feasible strategy for treating biofilm-related infections. Baicalin may serve as a new inhibitor that modulates virulence factors.

摘要

改进现有技术并开发新策略以防止细菌生物膜形成很重要。在这项体外研究中,生物膜由临床分离菌株17546(t037)形成。将不同浓度的黄芩苷添加到3天和7天的生物膜中。基于菌落计数和生物量的定量分析,黄芩苷的亚最小抑菌浓度(sub-MICs)(1024、512或256μg/mL)明显减少了体外细菌菌落数量和生物量。荧光显微镜显示,黄芩苷的亚最小抑菌浓度(1024、512或256μg/mL)抑制细菌黏附于载体表面并减少多糖产生。此外,黄芩苷破坏生物膜并与左氧氟沙星表现出协同作用。通过蛋白质印迹法和实时定量聚合酶链反应评估毒力因子,证实黄芩苷处理后葡萄球菌肠毒素A、α-溶血素和凝固酶的产生减少。此外,黄芩苷增加了热核酸酶的产生,并且1024和512μg/mL的黄芩苷下调了agrA表达。基于这些发现,黄芩苷与左氧氟沙星联合使用可能是治疗生物膜相关感染的一种新的可行策略。黄芩苷可能作为一种调节毒力因子的新型抑制剂。

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