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揭示石蒜叶提取物对[具体对象]的抗菌、抗生物膜和群体感应抑制潜力:一项体外-计算机模拟综合研究

Unveiling the Antimicrobial, Anti-Biofilm, and Anti-Quorum-Sensing Potential of Linn. Leaf Extract against : An Integrated In Vitro-In Silico Investigation.

作者信息

Santajit Sirijan, Tunyong Witawat, Horpet Dararat, Binmut Asma, Kong-Ngoen Thida, Wisessaowapak Churaibhon, Thavorasak Techit, Pumirat Pornpan, Indrawattana Nitaya

机构信息

Department of Medical Technology, School of Allied Health Sciences, Walailak University, Tha Sala 80160, Thailand.

Research Center in Tropical Pathobiology, Walailak University, Tha Sala 80160, Thailand.

出版信息

Antibiotics (Basel). 2024 Jul 1;13(7):613. doi: 10.3390/antibiotics13070613.

Abstract

Antimicrobial resistance poses a global health threat, with emerging as a notorious pathogen capable of forming stubborn biofilms and regulating virulence through quorum sensing (QS). In the quest for novel therapeutic strategies, this groundbreaking study unveils the therapeutic potential of Linn., an Asian medicinal plant containing various bioactive compounds, contributing to its antimicrobial activities, in the battle against . Through a comprehensive approach, we investigated the effect of ethanolic leaf extract on biofilms, QS, and antimicrobial activity. The extract exhibited promising inhibitory effects against including the biofilm-forming strain and MRSA. Real-time PCR analysis revealed significant downregulation of key virulence and biofilm genes, suggesting interference with QS. Biofilm assays quantified the extract's ability to disrupt and prevent biofilm formation. LC-MS/MS analysis identified quercetin and kaempferol glycosides as potential bioactive constituents, while molecular docking studies explored their binding to the QS transcriptional regulator SarA. Computational ADMET predictions highlighted favorable intestinal absorption but potential P-glycoprotein interactions limiting oral bioavailability. While promising anti-virulence effects were demonstrated, the high molecular weights and excessive hydrogen bond donors/acceptors of the flavonoid glycosides raise concerns regarding drug-likeness and permeability. This integrated study offers valuable insights for developing novel anti-virulence strategies to combat antimicrobial resistance.

摘要

抗菌耐药性对全球健康构成威胁,[某种病原体]作为一种臭名昭著的病原体出现,能够形成顽固的生物膜并通过群体感应(QS)调节毒力。在寻求新的治疗策略的过程中,这项开创性的研究揭示了[某种亚洲药用植物名称]的治疗潜力,这种植物含有多种生物活性化合物,在对抗[某种病原体]的斗争中有助于其抗菌活性。通过综合方法,我们研究了乙醇提取的[该植物名称]叶提取物对[某种病原体]生物膜、群体感应和抗菌活性的影响。该提取物对包括生物膜形成菌株和耐甲氧西林金黄色葡萄球菌(MRSA)在内的[某种病原体]表现出有前景的抑制作用。实时聚合酶链反应(PCR)分析显示关键毒力和生物膜基因显著下调,表明对群体感应有干扰。生物膜试验量化了提取物破坏和预防生物膜形成的能力。液相色谱 - 串联质谱(LC - MS/MS)分析确定槲皮素和山奈酚糖苷为潜在的生物活性成分,而分子对接研究探索了它们与群体感应转录调节因子SarA的结合。计算机化的药物代谢动力学(ADMET)预测突出了良好的肠道吸收,但潜在的P - 糖蛋白相互作用限制了口服生物利用度。虽然已证明有前景的抗毒力作用,但黄酮类糖苷的高分子量和过多的氢键供体/受体引发了对药物相似性和渗透性的担忧。这项综合研究为开发对抗抗菌耐药性的新型抗毒力策略提供了有价值的见解

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