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具有亲脂亲水性的胆汁酸功能化抗菌剂:对抗致病细菌、真菌及其生物膜。

Facially Amphiphilic Bile Acid-Functionalized Antimicrobials: Combating Pathogenic Bacteria, Fungi, and Their Biofilms.

机构信息

Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208, United States.

Department of Environmental Health Sciences, University of South Carolina, Columbia, South Carolina 29208, United States.

出版信息

ACS Infect Dis. 2023 Sep 8;9(9):1769-1782. doi: 10.1021/acsinfecdis.3c00266. Epub 2023 Aug 3.

Abstract

We report facially amphiphilic bile acid-based antimicrobials with a broad spectrum of activity against both bacterial and fungal pathogens and negligible detrimental effects on mammalian cells. Two lead compounds eliminated dormant subpopulations of various bacterial species, unlike conventional antibiotics. The lead compounds were also effective in eradicating biofilms of methicillin-resistant (MRSA), , and . Additionally, these compounds substantially inhibited the formation of fungal biofilms (). Mechanistic investigations revealed the membrane-active nature and endogenous reactive oxygen species (ROS) induction ability of these compounds. Finally, no detectable resistance was developed by the bacterial strains against this class of membrane-targeting antimicrobials.

摘要

我们报告了具有广谱抗细菌和真菌病原体活性的两亲性胆汁酸类抗菌药物,对哺乳动物细胞几乎没有不良影响。与传统抗生素不同,两种先导化合物消除了各种细菌休眠亚群。这两种先导化合物对耐甲氧西林金黄色葡萄球菌(MRSA)、 和 的生物膜也有清除作用。此外,这些化合物还能显著抑制真菌生物膜的形成()。机制研究揭示了这些化合物的膜活性性质和内源性活性氧(ROS)诱导能力。最后,细菌菌株对这类靶向细胞膜的抗菌药物没有产生可检测的耐药性。

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