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一种具有强效抗菌活性的新型合成类黄酮:体外活性及作用机制推测。

A novel synthetic flavonoid with potent antibacterial properties: In vitro activity and proposed mode of action.

机构信息

Faculty of Biology, Biology Department, The Alexandru Ioan Cuza University of Iasi, Iasi, Romania.

Integrated Center for Environmental Sciences Studies - North Eastern, CERNESIM, The Alexandru Ioan Cuza University of Iasi, Iasi, Romania.

出版信息

PLoS One. 2018 Apr 4;13(4):e0194898. doi: 10.1371/journal.pone.0194898. eCollection 2018.

Abstract

The emergence of pathogenic multidrug-resistant bacteria demands new approaches in finding effective antibacterial agents. Synthetic flavonoids could be a reliable solution due to their important antimicrobial activity. We report here the potent in vitro antibacterial activity of ClCl-flav-a novel synthetic tricyclic flavonoid. The antimicrobial effects were tested using the minimum inhibitory concentration (MIC), time kill and biofilm formation assays. Fluorescence microscopy and scanning electron microscopy were employed to study the mechanism of action. MTT test was used to assess the cytotoxicity of ClCl-flav. Our results showed that Gram positive bacteria were more sensitive (MIC = 0.24 μg/mL) to ClCl-flav compared to the Gram negative ones (MIC = 3.9 μg/mL). We found that our compound showed significantly enhanced antibacterial activities, 32 to 72-fold more active than other synthetic flavonoids. ClCl-flav showed bactericidal activity at concentrations ranging from 0.48 to 15.62 μg/mL. At twice the MIC, all Escherichia coli and Klebsiella pneumoniae cells were killed within 1 h. Also ClCl-flav presented good anti-biofilm activity. The mechanism of action is related to the impairment of the cell membrane integrity. No or very low cytotoxicity was evidenced at effective concentrations against Vero cells. Based on the strong antibacterial activity and cytotoxicity assessment, ClCl-flav has a good potential for the design of new antimicrobial agents.

摘要

致病的多药耐药菌的出现要求寻找有效抗菌剂的新方法。合成类黄酮由于其重要的抗菌活性,可能是一种可靠的解决方案。我们在这里报告一种新型合成三环类黄酮 ClCl-flav 的体外强力抗菌活性。使用最小抑菌浓度(MIC)、时间杀伤和生物膜形成测定来测试抗菌效果。荧光显微镜和扫描电子显微镜用于研究作用机制。MTT 试验用于评估 ClCl-flav 的细胞毒性。我们的结果表明,与革兰氏阴性菌(MIC = 3.9 μg/mL)相比,革兰氏阳性菌对 ClCl-flav 更敏感(MIC = 0.24 μg/mL)。我们发现我们的化合物表现出显著增强的抗菌活性,比其他合成类黄酮高 32 至 72 倍。ClCl-flav 在 0.48 至 15.62 μg/mL 的浓度范围内表现出杀菌活性。在 MIC 的两倍时,所有大肠杆菌和肺炎克雷伯菌细胞在 1 小时内被杀死。ClCl-flav 还表现出良好的抗生物膜活性。作用机制与细胞膜完整性的损害有关。在对 Vero 细胞的有效浓度下,没有或只有很低的细胞毒性。基于强大的抗菌活性和细胞毒性评估,ClCl-flav 具有设计新型抗菌剂的良好潜力。

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