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抗生素发现的科学。

The Science of Antibiotic Discovery.

机构信息

Antimicrobial Discovery Center, Department of Biology, Northeastern University, Boston, MA 02115, USA.

出版信息

Cell. 2020 Apr 2;181(1):29-45. doi: 10.1016/j.cell.2020.02.056. Epub 2020 Mar 19.

Abstract

We are experiencing an antimicrobial resistance (AMR) crisis, brought on by the drying up of the antibiotic discovery pipeline and the resulting unchecked spread of resistant pathogens. Traditional methods of screening environmental isolates or compound libraries have not produced a new drug in over 30 years. Antibiotic discovery is uniquely difficult due to a highly restrictive penetration barrier and other mechanisms that allow bacteria to survive in the presence of toxic compounds. In this Perspective, we analyze the challenges facing discovery and discuss an emerging new platform for antibiotic discovery. The penetration barrier makes screening conventional synthetic compound libraries largely impractical, and actinomycetes, the main source of natural product compounds, have been overmined. The emerging platform is based on understanding the rules that guide the permeation of molecules into bacteria and on advances in microbiology, which enable us to identify and access attractive groups of secondary metabolite producers. Establishing this platform will enable reliable production of lead compounds to combat AMR.

摘要

我们正面临着抗生素耐药性(AMR)危机,这是由于抗生素发现管道的枯竭以及由此导致的耐药病原体的不受控制的传播所带来的。传统的筛选环境分离物或化合物库的方法已经超过 30 年没有产生新的药物了。由于存在高度限制穿透的障碍和其他使细菌能够在有毒化合物存在下生存的机制,抗生素的发现非常困难。在这篇观点文章中,我们分析了发现所面临的挑战,并讨论了一个新兴的抗生素发现新平台。穿透障碍使得筛选传统的合成化合物库在很大程度上变得不切实际,而放线菌,天然产物化合物的主要来源,已经被过度开采。新兴的平台基于对指导分子进入细菌的渗透规则的理解,以及微生物学的进步,这使我们能够识别和接触有吸引力的次级代谢产物产生者群体。建立这个平台将能够可靠地生产出对抗 AMR 的先导化合物。

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