The antibiotic resistome: the nexus of chemical and genetic diversity

被引:920
作者
Wright, Gerard D. [1 ]
机构
[1] McMaster Univ, Antimicrobial Res Ctr, Dept Biochem & Biomed Sci, DeGroote Sch Med, Hamilton, ON L8N 3Z5, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
D O I
10.1038/nrmicro1614
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Over the millennia, microorganisms have evolved evasion strategies to overcome a myriad of chemical and environmental challenges, including antimicrobial drugs. Even before the first clinical use of antibiotics more than 60 years ago, resistant organisms had been isolated. Moreover, the potential problem of the widespread distribution of antibiotic resistant bacteria was recognized by scientists and healthcare specialists from the initial use of these drugs. Why is resistance inevitable and where does it come from? Understanding the molecular diversity that underlies resistance will inform our use of these drugs and guide efforts to develop new efficacious antibiotics.
引用
收藏
页码:175 / 186
页数:12
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共 99 条
[81]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680
[82]   Spectinomycin kinase from Legionella pneumophila -: Characterization of substrate specificity and identification of catalytically important residues [J].
Thompson, PR ;
Hughes, DW ;
Cianciotto, NP ;
Wright, GD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) :14788-14795
[83]   ISCR elements:: Novel gene-capturing systems of the 21st century? [J].
Toleman, MA ;
Bennett, PM ;
Walsh, TR .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2006, 70 (02) :296-+
[84]   Dual effects of MLS antibiotics: Transcriptional modulation and interactions on the ribosome [J].
Tsui, WHW ;
Yim, G ;
Wang, HHM ;
McClure, JE ;
Surette, MG ;
Davies, J .
CHEMISTRY & BIOLOGY, 2004, 11 (09) :1307-1316
[85]   Structure and functions of the GNAT superfamily of acetyltransferases [J].
Vetting, MW ;
de Carvalho, LPS ;
Yu, M ;
Hegde, SS ;
Magnet, S ;
Roderick, SL ;
Blanchard, JS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2005, 433 (01) :212-226
[86]   A bacterial acetyltransferase capable of regioselective N-acetylation of antibiotics and histones [J].
Vetting, MW ;
Magnet, S ;
Nieves, E ;
Roderick, SL ;
Blanchard, JS .
CHEMISTRY & BIOLOGY, 2004, 11 (04) :565-573
[87]   Aminoglycoside 2′-N-acetyltransferase from Mycobacterium tuberculosis in complex with coenzyme A and aminoglycoside substrates [J].
Vetting, MW ;
Hegde, SS ;
Javid-Majd, F ;
Blanchard, JS ;
Roderick, SL .
NATURE STRUCTURAL BIOLOGY, 2002, 9 (09) :653-658
[88]   Polyketide and nonribosomal peptide antibiotics: Modularity and versatility [J].
Walsh, CT .
SCIENCE, 2004, 303 (5665) :1805-1810
[89]   Bacterial resistance to vancomycin: Five genes and one missing hydrogen bond tell the story [J].
Walsh, CT ;
Fisher, SL ;
Park, IS ;
Prahalad, M ;
Wu, Z .
CHEMISTRY & BIOLOGY, 1996, 3 (01) :21-28
[90]   Vancomycin-resistant Staphylococcus aureus in the absence of vancomycin exposure [J].
Whitener, CJ ;
Park, SY ;
Browne, FA ;
Parent, LJ ;
Julian, K ;
Bozdogan, B ;
Appelbaum, PC ;
Chaitram, J ;
Weigel, LM ;
Jernigan, J ;
McDougal, LK ;
Tenover, FC ;
Fridkin, SK .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (08) :1049-1055