Targeting bacterial growth in biofilm conditions: rational design of novel inhibitors to mitigate clinical and food contamination using QSAR

IF 5.6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Maria Galvez-Llompart, Jesús Hierrezuelo, Mariluz Blasco, Riccardo Zanni, Jorge Galvez, A. de Vicente, A. Pérez-García, D. Romero
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引用次数: 0

Abstract

Abstract Antimicrobial resistance (AMR) is a pressing global issue exacerbated by the abuse of antibiotics and the formation of bacterial biofilms, which cause up to 80% of human bacterial infections. This study presents a computational strategy to address AMR by developing three novel quantitative structure–activity relationship (QSAR) models based on molecular topology to identify potential anti-biofilm and antibacterial agents. The models aim to determine the chemo-topological pattern of Gram (+) antibacterial, Gram (−) antibacterial, and biofilm formation inhibition activity. The models were applied to the virtual screening of a commercial chemical database, resulting in the selection of 58 compounds. Subsequent in vitro assays showed that three of these compounds exhibited the most promising antibacterial activity, with potential applications in enhancing food and medical device safety.
针对生物膜条件下的细菌生长:利用 QSAR 合理设计新型抑制剂,减轻临床和食品污染
摘要 抗菌药耐药性(AMR)是一个紧迫的全球性问题,抗生素的滥用和细菌生物膜的形成加剧了这一问题,导致高达 80% 的人类细菌感染。本研究提出了一种解决 AMR 问题的计算策略,即基于分子拓扑学开发三种新型定量结构-活性关系 (QSAR) 模型,以确定潜在的抗生物膜和抗菌剂。这些模型旨在确定革兰氏(+)抗菌、革兰氏(-)抗菌和抑制生物膜形成活性的化学拓扑模式。这些模型被应用于商业化学数据库的虚拟筛选,最终选出了 58 种化合物。随后的体外试验表明,其中三种化合物具有最有前途的抗菌活性,可用于提高食品和医疗器械的安全性。
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来源期刊
CiteScore
10.30
自引率
10.70%
发文量
195
审稿时长
4-8 weeks
期刊介绍: Journal of Enzyme Inhibition and Medicinal Chemistry publishes open access research on enzyme inhibitors, inhibitory processes, and agonist/antagonist receptor interactions in the development of medicinal and anti-cancer agents. Journal of Enzyme Inhibition and Medicinal Chemistry aims to provide an international and interdisciplinary platform for the latest findings in enzyme inhibition research. The journal’s focus includes current developments in: Enzymology; Cell biology; Chemical biology; Microbiology; Physiology; Pharmacology leading to drug design; Molecular recognition processes; Distribution and metabolism of biologically active compounds.
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