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两种肉桂酰羟肟酸作为潜在的群体感应抑制剂对抗 。

Two cinnamoyl hydroxamates as potential quorum sensing inhibitors against .

机构信息

Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, China.

Key Laboratory of Tropical Biological Resources of Ministry of Education, School of Pharmaceutical Sciences, Hainan University, Haikou, China.

出版信息

Front Cell Infect Microbiol. 2024 Aug 6;14:1424038. doi: 10.3389/fcimb.2024.1424038. eCollection 2024.

Abstract

INTRODUCTION

is a ubiquitous pathogen that causes various infectious diseases through the regulation of quorum sensing (QS). The strategy of interfering with the QS systems of , coupled with a reduction in the dosage of conventional antibiotics, presents a potential solution to treating infection and mitigating antibiotic resistance. In this study, seven cinnamoyl hydroxamates were synthesized to evaluate their inhibitory effects on QS of . Among these cinnamic acid derivatives, we found cinnamoyl hydroxamic acid (CHA) and 3-methoxy-cinnamoyl hydroxamic acid (MCHA) were the two most effective candidates. Furtherly, the effect of CHA and MCHA on the production of virulence factors and biofilm of were evaluated. Ultimately, our study may offer promising potential for treating infections and reducing its virulence.

METHODS

The disc diffusion test were conducted to evaluate inhibitory effects on QS of seven cinnamoyl hydroxamates. The influence of CHA and MCHA on the production of virulence and flagellar motility of was furtherly explored. Scanning electron microscopy (SEM) experiment were conducted to evaluate the suppression of CHA and MCHA on the formed biofilm of . RT-qPCR was used to detect rhlI, lasA, lasB, rhlA, rhlB, and oprL genes in . docking study was performed to explore the molecular mechanism of CHA and MCHA. The synergistic effects of CHA with gentamicin were detected on biofilm cell dispersal.

RESULT

After treatment of CHA or MCHA, the production of multiple virulence factors, including pyocyanin, proteases, rhamnolipid, and siderophore, and swimming and swarming motilities in were inhibited significantly. And our results showed CHA and MCHA could eliminate the formed biofilm of . RT-qPCR revealed that CHA and MCHA inhibited the expression of QS related genes in . Molecular docking indicated that CHA and MCHA primarily inhibited the RhlI/R system in by competing with the cognate signaling molecule C4-HSL.Additionally, CHA exhibited potent synergistic effects with gentamicin on biofilm cell dispersal.

DISCUSSION

is one of the most clinically and epidemiologically important bacteria and a primary cause of catheter-related urinary tract infections and ventilator-associated pneumonia. This study aims to explore whether cinnamoyl hydroxamates have inhibitory effects on QS. And our results indicate that CHA and MCHA, as two novel QSIs, offer promising potential for treating P. aeruginosa infections and reducing its virulence.

摘要

简介

铜绿假单胞菌是一种普遍存在的病原体,通过群体感应(QS)调节导致各种传染病。干扰铜绿假单胞菌 QS 系统的策略,加上减少常规抗生素的剂量,为治疗感染和减轻抗生素耐药性提供了一种潜在的解决方案。在这项研究中,合成了七种肉桂酰羟肟酸来评估它们对铜绿假单胞菌 QS 的抑制作用。在这些肉桂酸衍生物中,我们发现肉桂酰羟肟酸(CHA)和 3-甲氧基肉桂酰羟肟酸(MCHA)是两种最有效的候选物。此外,还评估了 CHA 和 MCHA 对铜绿假单胞菌毒力因子和生物膜形成的影响。最终,我们的研究可能为治疗铜绿假单胞菌感染和降低其毒力提供了有前景的潜力。

方法

采用圆盘扩散试验评价七种肉桂酰羟肟酸对 QS 的抑制作用。进一步探讨了 CHA 和 MCHA 对铜绿假单胞菌毒力和鞭毛运动的影响。扫描电子显微镜(SEM)实验评价了 CHA 和 MCHA 对生物膜形成的抑制作用。采用 RT-qPCR 检测铜绿假单胞菌中 rhlI、lasA、lasB、rhlA、rhlB 和 oprL 基因。分子对接研究探讨了 CHA 和 MCHA 的分子机制。检测 CHA 与庆大霉素联合对生物膜细胞分散的协同作用。

结果

用 CHA 或 MCHA 处理后,铜绿假单胞菌多种毒力因子(如绿脓菌素、蛋白酶、鼠李糖脂和铁载体)的产生以及泳动和群集运动均受到显著抑制。结果表明,CHA 和 MCHA 可消除铜绿假单胞菌形成的生物膜。RT-qPCR 显示 CHA 和 MCHA 抑制了铜绿假单胞菌中 QS 相关基因的表达。分子对接表明,CHA 和 MCHA 主要通过与同源信号分子 C4-HSL 竞争抑制 RhlI/R 系统来抑制铜绿假单胞菌。此外,CHA 与庆大霉素联合对生物膜细胞分散具有显著的协同作用。

讨论

铜绿假单胞菌是临床和流行病学上最重要的细菌之一,是导管相关尿路感染和呼吸机相关性肺炎的主要病原体。本研究旨在探讨肉桂酰羟肟酸是否对 QS 有抑制作用。结果表明,CHA 和 MCHA 作为两种新型 QSIs,为治疗铜绿假单胞菌感染和降低其毒力提供了有前景的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b52/11333444/96b9236f09f1/fcimb-14-1424038-g001.jpg

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