New-found fundamentals of bacterial persistence

被引:112
作者
Kint, Cyrielle I. [1 ]
Verstraeten, Natalie [1 ]
Fauvart, Maarten [1 ]
Michiels, Jan [1 ]
机构
[1] KU Leuven Univ Leuven, Ctr Microbial & Plant Genet, B-3001 Heverlee, Belgium
关键词
antibiotic tolerance; toxin-antitoxin modules; noise; heterogeneity; chronic infections; cancer; TOXIN-ANTITOXIN SYSTEMS; ESCHERICHIA-COLI; MULTIDRUG TOLERANCE; GENE-EXPRESSION; ANTIBIOTIC PERSISTENCE; CELLS; DEATH; MECHANISM; GROWTH; HIPA;
D O I
10.1016/j.tim.2012.08.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Persister cells display tolerance to high doses of bactericidal antibiotics and typically comprise a small fraction of a bacterial population. Recently, evidence was provided for a causal link between therapy failure and the presence of persister cells in chronic infections, underscoring the need for research on bacterial persistence. A series of recent breakthroughs have shed light on the multiplicity of persister genes, the contribution of gene expression noise to persister formation, the importance of active responses to antibiotic tolerance and heterogeneity among persister cells. Moreover, the development of in vivo model systems has highlighted the clinical relevance of persistence. This review discusses these recent advances and how this knowledge fundamentally changes the way in which we will perceive the problem of antibiotic tolerance in years to come.
引用
收藏
页码:577 / 585
页数:9
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