蜜糠苯并吡喃破坏铜绿假单胞菌生物膜及抑制相关毒力因子的研究。

IF 3.3 3区 医学 Q3 IMMUNOLOGY
Microbial pathogenesis Pub Date : 2025-08-01 Epub Date: 2025-05-17 DOI:10.1016/j.micpath.2025.107711
Rajendra Moorthy Rajendran, Parthiban Brindha Devi
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引用次数: 0

摘要

含呋喃苯吡喃衍生物(海草碱)的中草药海草(Ammi visnaga)具有治疗作用,但其在铜绿假单胞菌中破坏生物膜形成和抑制通过Las群体感应系统介导的毒力因子的潜力尚未被探索。本研究通过分子对接和动力学模拟,研究了大虾藻素在≤9 μg/mL的亚最小抑制浓度(sub-MIC)水平下抑制生物膜形成、抑制生物膜相关毒力因子的作用,并对其与激光辐射的相互作用进行了评价。使用“aBiofilm”网络工具进行的计算机分析预测了大肠杆菌具有很强的抗生物膜潜力,此前没有此类活性的报道。共聚焦激光扫描显微镜证实了这一预测,在9 μg/mL的浓度下,生物膜具有明显的抑制作用,并伴有明显的微生物畸变。进一步的评估表明,亚mic水平的贝壳素以剂量依赖的方式有效地降低了生物膜相关的毒力因子,包括游泳和蜂群运动、鼠李糖脂含量、细胞表面疏水性、海藻酸盐和胞外多糖的产生,尽管这些因子的抑制程度各不相同。分子对接分析结果为-7.285 kcal/mol,表明与靶蛋白的相互作用良好;“分子力学广义出生表面积”结合自由能为-28.32 kcal/mol,表明与靶蛋白的相互作用稳定且能量有利。利用“液体模拟优化电位-全原子”力场模型进行100 ns分子动力学模拟,验证了khellin-protein复合物的稳定性。均方根偏差、均方根波动、旋转半径、分子内氢键、分子表面积、溶剂可及表面积和极性表面积的结果证实了khellin在整个模拟过程中保持稳定的相互作用。这些发现表明,大虾壳菌素是治疗假单胞菌相关生物膜感染的潜在候选药物,并提供了强有力的证据,证明大虾壳菌素可能是铜绿假单胞菌LasR蛋白的群体感应抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of furobenzopyran from Ammi visnaga in disrupting Pseudomonas aeruginosa biofilms and suppressing associated virulence factors.

Ammi visnaga, an herbal plant containing the furobenzopyran derivative (khellin) with therapeutic effects, remains unexplored for its potential to disrupt the biofilm formation and suppress the virulence factors mediated through the Las quorum-sensing system in Pseudomonas aeruginosa. The current study investigates the efficacy of khellin in inhibiting biofilm formation, suppressing biofilm-associated virulence factors at sub-minimum inhibitory concentration (sub-MIC) levels of ≤9 μg/mL, and its interactions with LasR are evaluated through molecular docking and dynamics simulation. In-silico analysis using the 'aBiofilm' web tool predicted a strong antibiofilm potential for khellin, with no prior reports of such activity. This prediction was supported by confocal laser scanning microscopy, which demonstrated significant biofilm inhibition at 9 μg/mL, along with noticeable microbial distortion. Further assessments showed that sub-MIC levels of khellin effectively reduced biofilm-associated virulence factors, including swimming and swarming motility, rhamnolipid content, cell surface hydrophobicity, alginate, and exopolysaccharide production, in a dose-dependent manner, though the extent of inhibition varied among these factors. Molecular docking analysis yielded a score of -7.285 kcal/mol, indicating a favorable binding, and 'Molecular Mechanics Generalized Born Surface Area' binding free energy of -28.32 kcal/mol confirms a stable and energetically favorable interaction with the target protein. The stability of the khellin-protein complex was validated through a 100 ns molecular dynamics simulation using the 'Optimized Potentials for Liquid Simulations-All Atom' force field model. Results of root mean square deviation, root mean square fluctuation, radius of gyration, intramolecular hydrogen bonds, molecular surface area, solvent accessible surface area, and polar surface area confirmed that khellin maintained stable interactions throughout the simulation. These findings suggest khellin as a potential candidate for treating Pseudomonas-associated biofilm infections and provide strong evidence that khellin may function as a quorum-sensing inhibitor of the P.aeruginosa's LasR protein.

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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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