Molecular mechanisms of antibacterial multidrug resistance

被引:1159
作者
Alekshun, Michael N.
Levy, Stuart B.
机构
[1] Schering Plough Res Inst, Kenilworth, NJ 07033 USA
[2] Tufts Univ, Sch Med, Ctr Adaptat Genet & Drug Resistance, Dept Mol Biol & Microbiol, Boston, MA 02111 USA
[3] Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA
基金
美国国家卫生研究院;
关键词
STAPHYLOCOCCUS-AUREUS; ESCHERICHIA-COLI; FLUOROQUINOLONE RESISTANCE; TETRACYCLINE-RESISTANCE; PSEUDOMONAS-AERUGINOSA; VANCOMYCIN RESISTANCE; BACTERIAL-RESISTANCE; MACROLIDE RESISTANCE; BACILLUS-SUBTILIS; DRUG-RESISTANCE;
D O I
10.1016/j.cell.2007.03.004
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
Treatment of infections is compromised worldwide by the emergence of bacteria that are resistant to multiple antibiotics. Although classically attributed to chromosomal mutations, resistance is most commonly associated with extrachromosomal elements acquired from other bacteria in the environment. These include different types of mobile DNA segments, such as plasmids, transposons, and integrons. However, intrinsic mechanisms not commonly specified by mobile elements-such as efflux pumps that expel multiple kinds of antibiotics-are now recognized as major contributors to multidrug resistance in bacteria. Once established, multidrug-resistant organisms persist and spread worldwide, causing clinical failures in the treatment of infections and public health crises.
引用
收藏
页码:1037 / 1050
页数:14
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