Platforms for antibiotic discovery

被引:1010
作者
Lewis, Kim [1 ,2 ]
机构
[1] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
[2] Northeastern Univ, Antimicrobial Discovery Ctr, Boston, MA 02115 USA
基金
比尔及梅琳达.盖茨基金会;
关键词
COMPLETE GENOME SEQUENCE; IN-SITU CULTIVATION; PSEUDOMONAS-AERUGINOSA; PERSISTER CELLS; MYCOBACTERIUM-TUBERCULOSIS; ESCHERICHIA-COLI; DRUG-RESISTANCE; STREPTOMYCES-COELICOLOR; HETEROLOGOUS EXPRESSION; ANTIBACTERIAL COMPOUNDS;
D O I
10.1038/nrd3975
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The spread of resistant bacteria, leading to untreatable infections, is a major public health threat but the pace of antibiotic discovery to combat these pathogens has slowed down. Most antibiotics were originally isolated by screening soil-derived actinomycetes during the golden era of antibiotic discovery in the 1940s to 1960s. However, diminishing returns from this discovery platform led to its collapse, and efforts to create a new platform based on target-focused screening of large libraries of synthetic compounds failed, in part owing to the lack of penetration of such compounds through the bacterial envelope. This article considers strategies to re-establish viable platforms for antibiotic discovery. These include investigating untapped natural product sources such as uncultured bacteria, establishing rules of compound penetration to enable the development of synthetic antibiotics, developing species-specific antibiotics and identifying prodrugs that have the potential to eradicate dormant persisters, which are often responsible for hard-to-treat infections.
引用
收藏
页码:371 / 387
页数:17
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