Assessing the antibacterial potential of 6-gingerol: Combined experimental and computational approaches

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Mahmoud A. Elfaky , Hassan M. Okairy , Hossam M. Abdallah , Abdulrahman E. Koshak , Gamal A. Mohamed , Sabrin R.M. Ibrahim , Abdulrahim A. Alzain , Wael A.H. Hegazy , El-Sayed Khafagy , Noura M. Seleem
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引用次数: 0

Abstract

The rise of antibiotic resistance in bacteria is becoming a global concern, particularly due to the dwindling supply of new antibiotics. This situation mandates the discovery of new antimicrobial candidates. Plant-derived natural compounds have historically played a crucial role in the development of antibiotics, serving as a rich source of substances possessing antimicrobial properties. Numerous studies have supported the reputation of 6-gingerol, a prominent compound found in the ginger family, for its antibacterial properties. In this study, the antibacterial activities of 6-gingerol were evaluated against Gram-negative bacteria, Acinetobacter baumannii and Klebsiella pneumoniae, with a particular focus on the clinically significant Gram-negative Pseudomonas aeruginosa and Gram-positive bacteria Staphylococcus aureus. Furthermore, the anti-virulence activities were assessed in vitro, in vivo, and in silico. The current findings showed that 6-gingerol’s antibacterial activity is due to its significant effect on the disruption of the bacterial cell membrane and efflux pumps, as it significantly decreased the efflux and disrupted the cell membrane of S. aureus and P. aeruginosa. Furthermore, 6-gingerol significantly decreased the biofilm formation and production of virulence factors in S. aureus and P. aeruginosa in concentrations below MICs. The anti-virulence properties of 6-gingerol could be attributed to its capacity to disrupt bacterial virulence-regulating systems; quorum sensing (QS). 6-Gingerol was found to interact with QS receptors and downregulate the genes responsible for QS. In addition, molecular docking, and molecular dynamics (MD) simulation results indicated that 6-gingerol showed a comparable binding affinity to the co-crystalized ligands of different P. aeruginosa QS targets as well as stable interactions during 100 ns MD simulations. These findings suggest that 6-gingerol holds promise as an anti-virulence agent that can be combined with antibiotics for the treatment of severe infections.

评估 6-姜酚的抗菌潜力:实验与计算相结合的方法
细菌中抗生素耐药性的增加正成为全球关注的问题,特别是由于新抗生素的供应日益减少。这种情况要求发现新的抗菌候选药物。植物提取的天然化合物在抗生素的开发过程中一直发挥着至关重要的作用,是具有抗菌特性物质的丰富来源。姜科植物中的一种重要化合物 6-姜酚具有抗菌特性,大量研究证实了这一点。本研究评估了 6-gingerol 对革兰氏阴性菌、鲍曼不动杆菌和肺炎克雷伯菌的抗菌活性,特别是对临床上重要的革兰氏阴性绿脓杆菌和革兰氏阳性菌金黄色葡萄球菌的抗菌活性。此外,还对其体外、体内和硅学中的抗病毒活性进行了评估。目前的研究结果表明,6-姜酚的抗菌活性是由于它对破坏细菌细胞膜和外流泵有显著效果,因为它能显著减少金黄色葡萄球菌和铜绿假单胞菌的外流并破坏其细胞膜。此外,在低于 MIC 的浓度下,6-姜酚还能明显减少金黄色葡萄球菌和铜绿假单胞菌生物膜的形成和毒力因子的产生。6- 姜酚的抗病毒特性可归因于其破坏细菌毒力调节系统的能力,即法定量感应(QS)。研究发现,6-姜酚能与 QS 受体相互作用,并下调负责 QS 的基因。此外,分子对接和分子动力学(MD)模拟结果表明,6-姜酚与不同铜绿假单胞菌 QS 靶标的共晶体配体具有相当的结合亲和力,并且在 100 ns MD 模拟期间具有稳定的相互作用。这些研究结果表明,6-姜酚有望成为一种抗病毒剂,可与抗生素联合用于治疗严重感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Saudi Pharmaceutical Journal
Saudi Pharmaceutical Journal PHARMACOLOGY & PHARMACY-
CiteScore
6.10
自引率
2.40%
发文量
194
审稿时长
67 days
期刊介绍: The Saudi Pharmaceutical Journal (SPJ) is the official journal of the Saudi Pharmaceutical Society (SPS) publishing high quality clinically oriented submissions which encompass the various disciplines of pharmaceutical sciences and related subjects. SPJ publishes 8 issues per year by the Saudi Pharmaceutical Society, with the cooperation of the College of Pharmacy, King Saud University.
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