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Renaissance of vancomycin: approaches for breaking antibiotic resistance in multidrug-resistant bacteria

机译:万古霉素的文艺复兴:在多药物抗性细菌中破坏抗生素抗性的方法

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摘要

The emergence of multidrug-resistant bacteria demands innovations in the development of new antibiotics. For decades, the glycopeptide antibiotic vancomycin has been considered as the “last resort” treatment of severe infections caused by Gram-positive bacteria. Since the discovery of the first vancomycin-resistant enterococci strains in the late 1980s, the number of resistances has been steadily rising, with often life-threatening consequences. As an alternative to the generation of completely new substances, novel approaches focus on structural modifications of established antibiotics such as vancomycin to overcome these resistances. Here, we provide an overview of several promising modifications of vancomycin to restore its efficacy against vancomycin-resistant enterococci.
机译:多药物抗性细菌的出现需要在新抗生素的发展方面的创新。 几十年来,糖肽抗生素万古霉素被认为是革兰氏阳性细菌引起的严重感染的“最后手段”治疗。 自20世纪80年代后期发现第一个万古霉素抗菌肠杆菌菌株以来,电阻的次数一直在稳步上升,经常威胁危及生命的后果。 作为一代完全新物质的替代方案,新颖的方法侧重于建立抗生素如万古霉素的结构修饰,以克服这些抗性。 在这里,我们概述了若干有希望的万古霉素修饰,以恢复其对抗万古霉素的肠球菌的功效。

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