Bacterial resistance to antibiotics: Modified target sites

被引:213
作者
Lambert, PA [1 ]
机构
[1] Aston Univ, Birmingham B4 7ET, W Midlands, England
关键词
bacterial resistance; antibiotics; modified targets; resistance genes; genetic exchange;
D O I
10.1016/j.addr.2005.04.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alteration in the target sites of antibiotics is a common mechanism of resistance. Examples of clinical strains showing resistance can be found for every class of antibiotic, regardless of the mechanism of action. Target site changes often result from spontaneous mutation of a bacterial gene on the chromosome and selection in the presence of the antibiotic. Examples include mutations in RNA polymerase and DNA gyrase, resulting in resistance to the rifamycins and quinolones, respectively. In other cases, acquisition of resistance may involve transfer of resistance genes from other organisms by some form of genetic exchange (conjugation, transduction, or transformation). Examples of these mechanisms include acquisition of the mecA genes encoding methicillin resistance in Staphylococcus aureus and the various van genes in enterococci encoding resistance to glycopeptides. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1471 / 1485
页数:15
相关论文
共 149 条
[1]   New gene cassettes for trimethoprim resistance, dfr13, and streptomycin-spectinomycin resistance, aadA4, inserted on a class 1 integron [J].
Adrian, PV ;
Thomson, CJ ;
Klugman, KP ;
Amyes, SGB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (02) :355-361
[2]   Mutations affecting the Rossman fold of isoleucyl-tRNA synthetase are correlated with low-level mupirocin resistance in Staphylococcus aureus [J].
Antonio, M ;
McFerran, N ;
Pallen, MJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (02) :438-442
[3]   Linezolid-resistant enterococci: report of the first isolates in the United Kingdom [J].
Auckland, C ;
Teare, L ;
Cooke, F ;
Kaufmann, ME ;
Warner, M ;
Jones, G ;
Bamford, K ;
Ayles, H ;
Johnson, AP .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (05) :743-746
[4]   PROPERTIES OF PENICILLIN-BINDING PROTEINS IN NEISSERIA-GONORRHOEAE [J].
BARBOUR, AG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 19 (02) :316-322
[5]   Mechanism of isoniazid uptake in Mycobacterium tuberculosis [J].
Bardou, F ;
Raynaud, C ;
Ramos, C ;
Lanéelle, MA ;
Lanéelle, G .
MICROBIOLOGY-UK, 1998, 144 :2539-2544
[6]   Mechanisms of isoniazid resistance in Mycobacterium tuberculosis:: Enzymatic characterization of enoyl reductase mutants identified in isoniazid-resistant clinical isolates [J].
Basso, LA ;
Zheng, RJ ;
Musser, JM ;
Jacobs, WR ;
Blanchard, JS .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (03) :769-775
[7]   NOVEL RESISTANCE TO IMIPENEM ASSOCIATED WITH AN ALTERED PBP-4 IN A PSEUDOMONAS-AERUGINOSA CLINICAL ISOLATE [J].
BELLIDO, F ;
VEUTHEY, C ;
BLASER, J ;
BAUERNFEIND, A ;
PECHERE, JC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1990, 25 (01) :57-68
[8]   Molecular analysis of fusidic acid resistance in Staphylococcus aureus [J].
Besier, S ;
Ludwig, A ;
Brade, V ;
Wichelhaus, TA .
MOLECULAR MICROBIOLOGY, 2003, 47 (02) :463-469
[9]   INTERSPECIES RECOMBINATION BETWEEN THE PENA GENES OF NEISSERIA-MENINGITIDIS AND COMMENSAL NEISSERIA SPECIES DURING THE EMERGENCE OF PENICILLIN RESISTANCE IN N-MENINGITIDIS - NATURAL EVENTS AND LABORATORY SIMULATION [J].
BOWLER, LD ;
ZHANG, QY ;
RIOU, JY ;
SPRATT, BG .
JOURNAL OF BACTERIOLOGY, 1994, 176 (02) :333-337
[10]   Oxazolidinones: activity, mode of action, and mechanism of resistance [J].
Bozdogan, B ;
Appelbaum, PC .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2004, 23 (02) :113-119