Bacterial cell division as a target for new antibiotics

被引:70
|
作者
Sass, Peter [1 ]
Broetz-Oesterhelt, Heike [1 ]
机构
[1] Univ Dusseldorf, Inst Pharmaceut Biol & Biotechnol, D-40225 Dusseldorf, Germany
关键词
SMALL-MOLECULE INHIBITORS; PROTEIN FTSZ; STAPHYLOCOCCUS-AUREUS; ANTIBACTERIAL; CLPP; CURCUMIN; ACYLDEPSIPEPTIDES; IDENTIFICATION; MECHANISM; PC190723;
D O I
10.1016/j.mib.2013.07.006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacterial resistance to currently applied antibiotics complicates the treatment of infections and demands the evaluation of new strategies to counteract multidrug-resistant bacteria. In recent years, the inhibition of the bacterial divisome, mainly by targeting the central cell division mediator FtsZ, has been recognized as a promising strategy for antibiotic attack. New antibiotics were shown to either interfere with the natural dynamics and functions of FtsZ during the cell cycle or to activate a bacterial protease to degrade FtsZ and thus bring about bacterial death in a suicidal manner. Their efficacy in animal models of infection together with resistance-breaking properties prove the potential of such drugs and validate the inhibition of bacterial cell division as an attractive approach for antibiotic intervention.
引用
收藏
页码:522 / 530
页数:9
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