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探索植物大麻素对抗多重耐药细菌的潜力。

Exploring the Potential of Phytocannabinoids Against Multidrug-Resistant Bacteria.

作者信息

Sirignano Carmina, De Vita Simona, Gargiulo Ernesto, Lucidi Massimiliano, Visaggio Daniela, Chini Maria Giovanna, Lauro Gianluigi, Chianese Giuseppina, Visca Paolo, Bifulco Giuseppe, Taglialatela-Scafati Orazio

机构信息

Department of Pharmacy, University of Naples Federico II, Via Domenico Montesano 49, 80131 Napoli, Italy.

Department of Pharmacy, University of Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Italy.

出版信息

Plants (Basel). 2025 Jun 20;14(13):1901. doi: 10.3390/plants14131901.

Abstract

The rapid emergence of multidrug-resistant (MDR) bacterial pathogens poses a critical threat to global health, creating an urgent need for novel antimicrobial agents. In this study, we evaluated a small library of natural and semisynthetic phytocannabinoids against a broad panel of MDR Gram-positive bacterial strains, evidencing very good activity in the low µM range. We provide evidence of the antibacterial activity of the two separated enantiomers of cannabidiol, offering novel insights into the stereochemical aspects of their bioactivity. To investigate the possible molecular targets and clarify the mechanism of action, we employed Inverse Virtual Screening (IVS), a computational approach optimized for predicting potential protein-ligand interactions, on three selected MDR bacterial species. Interestingly, key targets belonging to important bacterial metabolic pathways and defense mechanisms were retrieved, and the results were used to rationalize the observed biological activities. To the best of our knowledge, this study marks the first application of IVS to microorganisms, offering a novel strategy for identifying bacterial protein targets. The results pave the way for future experimental validation, structure-based drug design, and the development of novel antibacterial agents.

摘要

多重耐药(MDR)细菌病原体的迅速出现对全球健康构成了严重威胁,迫切需要新型抗菌药物。在本研究中,我们评估了一个由天然和半合成植物大麻素组成的小型文库对多种MDR革兰氏阳性细菌菌株的作用,结果表明其在低 microM 范围内具有很好的活性。我们提供了大麻二酚两种分离对映体的抗菌活性证据,为其生物活性的立体化学方面提供了新的见解。为了研究可能的分子靶点并阐明作用机制,我们对三种选定的MDR细菌物种采用了反向虚拟筛选(IVS),这是一种为预测潜在蛋白质-配体相互作用而优化的计算方法。有趣的是,检索到了属于重要细菌代谢途径和防御机制的关键靶点,并利用这些结果来解释观察到的生物活性。据我们所知,本研究标志着IVS首次应用于微生物,为鉴定细菌蛋白质靶点提供了一种新策略。这些结果为未来的实验验证、基于结构的药物设计以及新型抗菌药物的开发铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b849/12251955/689ed41e67b5/plants-14-01901-g001.jpg

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