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6-聚氨基甾体衍生物对耐抗生素细菌的抗生物膜和抗毒力特性

Antibiofilm and Antivirulence Properties of 6-Polyaminosteroid Derivatives against Antibiotic-Resistant Bacteria.

作者信息

Vergoz Delphine, Le Hung, Bernay Benoit, Schaumann Annick, Barreau Magalie, Nilly Flore, Desriac Florie, Tahrioui Ali, Giard Jean-Christophe, Lesouhaitier Olivier, Chevalier Sylvie, Brunel Jean Michel, Muller Cécile, Dé Emmanuelle

机构信息

Univ Rouen Normandie, INSA Rouen Normandie, CNRS, Normandie Univ, PBS UMR 6270, F-76000 Rouen, France.

Univ Caen Normandie, Proteogen Platform, US EMERODE, F-14000 Caen, France.

出版信息

Antibiotics (Basel). 2023 Dec 20;13(1):8. doi: 10.3390/antibiotics13010008.

Abstract

The emergence of multi-drug resistant pathogens is a major public health problem, leading us to rethink and innovate our bacterial control strategies. Here, we explore the antibiofilm and antivirulence activities of nineteen 6-polyaminosterol derivatives (squalamine-based), presenting a modulation of their polyamine side chain on four major pathogens, i.e., carbapenem-resistant (CRAB) and (CRPA), methicillin-resistant (MRSA), and vancomycin-resistant (VRE) strains. We screened the effect of these derivatives on biofilm formation and eradication. Derivatives (for CRAB, VRE, and MRSA) and (for all the strains) were the most potent ones and displayed activities as good as those of conventional antibiotics. We also identified 11 compounds able to decrease by more than 40% the production of pyocyanin, a major virulence factor of . We demonstrated that treatment acts against bacterial infections in and significantly prolonged larvae survival (from 50% to 80%) after 24 h of CRAB, VRE, and MRSA infections. As shown by proteomic studies, triggered distinct cellular responses depending on the bacterial species but essentially linked to cell envelope. Its interesting antibiofilm and antivirulence properties make it a promising a candidate for use in therapeutics.

摘要

多重耐药病原体的出现是一个重大的公共卫生问题,促使我们重新思考并创新细菌控制策略。在此,我们探究了19种6-聚氨基甾醇衍生物(基于鲨胺)的抗生物膜和抗毒力活性,展示了其多胺侧链对四种主要病原体的调控作用,即耐碳青霉烯类(CRAB)和耐碳青霉烯类肺炎克雷伯菌(CRPA)、耐甲氧西林金黄色葡萄球菌(MRSA)以及耐万古霉素肠球菌(VRE)菌株。我们筛选了这些衍生物对生物膜形成和消除的影响。衍生物(针对CRAB、VRE和MRSA)以及(针对所有菌株)是最有效的,并且表现出与传统抗生素相当的活性。我们还鉴定出11种能够使绿脓菌素(一种主要毒力因子)的产生减少40%以上的化合物。我们证明了处理对感染有效,并显著延长了CRAB、VRE和MRSA感染24小时后幼虫的存活时间(从50%延长至80%)。蛋白质组学研究表明,根据细菌种类引发不同的细胞反应,但基本上与细胞包膜相关。其有趣的抗生物膜和抗毒力特性使其成为一种有前景的治疗候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d60/10812528/08956ba3e564/antibiotics-13-00008-g001.jpg

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