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革兰氏阳性选择性抗生素的小分子增效作用针对…… (原文不完整,翻译至此)

Small Molecule Potentiation of Gram-Positive Selective Antibiotics against .

作者信息

Martin Sara E, Melander Roberta J, Brackett Christopher M, Scott Alison J, Chandler Courtney E, Nguyen Catherine M, Minrovic Bradley M, Harrill Sarah E, Ernst Robert K, Manoil Colin, Melander Christian

机构信息

Department of Chemistry and Biochemistry , University of Notre Dame , 236 Cavanaugh Drive , Notre Dame , Indiana 46556 , United States.

Department of Chemistry , North Carolina State University , 2620 Yarbrough Drive , Raleigh , North Carolina 27695 , United States.

出版信息

ACS Infect Dis. 2019 Jul 12;5(7):1223-1230. doi: 10.1021/acsinfecdis.9b00067. Epub 2019 Apr 26.

Abstract

In 2016, the World Health Organization deemed antibiotic resistance one of the biggest threats to global health, food security, and development. The need for new methods to combat infections caused by antibiotic resistant pathogens will require a variety of approaches to identifying effective new therapeutic strategies. One approach is the identification of small molecule adjuvants that potentiate the activity of antibiotics of demonstrated utility, whose efficacy is abated by resistance, both acquired and intrinsic. To this end, we have identified compounds that enhance the efficacy of antibiotics normally ineffective against Gram-negative pathogens because of the outer membrane permeability barrier. We identified two adjuvant compounds that dramatically enhance sensitivity of to macrolide and glycopeptide antibiotics, with reductions in minimum inhibitory concentrations as high as 256-fold, and we observed activity across a variety of clinical isolates. Mode of action studies indicate that these adjuvants likely work by modulating lipopolysaccharide synthesis or assembly. The adjuvants were active in a infection model, indicating potential for use in mammalian infections.

摘要

2016年,世界卫生组织将抗生素耐药性视为对全球健康、粮食安全和发展的最大威胁之一。对抗由抗生素耐药病原体引起的感染的新方法的需求,将需要多种方法来确定有效的新治疗策略。一种方法是鉴定小分子佐剂,这些佐剂可增强已证明有用的抗生素的活性,其疗效因获得性和固有性耐药而减弱。为此,我们已经鉴定出一些化合物,这些化合物可以增强由于外膜通透性屏障而通常对革兰氏阴性病原体无效的抗生素的疗效。我们鉴定出两种佐剂化合物,它们能显著增强对大环内酯类和糖肽类抗生素的敏感性,最低抑菌浓度降低高达256倍,并且我们在多种临床分离株中观察到了活性。作用机制研究表明,这些佐剂可能通过调节脂多糖的合成或组装起作用。这些佐剂在感染模型中具有活性,表明其在哺乳动物感染中具有应用潜力。

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