Targeting iron assimilation to develop new antibacterials

被引:71
作者
Foley, Timothy L. [1 ]
Simeonov, Anton [1 ]
机构
[1] NIH, Natl Ctr Adv Translat Sci, Div Preclin Innovat, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
antibacterial; antibiotic; chelation therapy; high-throughput screening; iron assimilation; siderophore; UROPATHOGENIC ESCHERICHIA-COLI; IN-VITRO CHARACTERIZATION; MYCOBACTERIUM-TUBERCULOSIS; STRUCTURAL-CHARACTERIZATION; SIDEROPHORE BIOSYNTHESIS; BAD BUGS; PSEUDOMONAS-AERUGINOSA; TRANSFERRIN-BINDING; GENE-CLUSTER; NO DRUGS;
D O I
10.1517/17460441.2012.708335
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Since the first application of antibiotics to treat bacterial infections, the development and spread of resistance has been a persistent threat. An ever evolving pipeline of next-generation therapeutics is required for modern medicine to remain one step ahead of pathogens. Areas covered: This review describes recent efforts to develop drugs that interrupt the assimilation of iron by bacteria: a process that is vital to cellular homeostasis and is not currently targeted by antibiotics used in the clinic. This review also covers the mechanisms by which bacteria acquire iron for their environment, and details efforts to intervene in these processes, using small molecule inhibitors that target key steps in these pathways, with a special emphasis on recent advances published during the 2010 - 2012 period. Expert opinion: For decades, the routes used by bacteria to assimilate iron from host and environmental settings have been the subject of intense study. While numerous investigations have identified inhibitors of these pathways, many have stopped short of translating the in vitro results to in vivo proof of concept experiments. The extension of preliminary findings in this manner will significantly increase the impact of the field.
引用
收藏
页码:831 / 847
页数:17
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