What's new in antibiotic resistance? Focus on beta-lactamases

被引:160
作者
Babic, Maja
Hujer, Andrea M.
Bonomo, Robert A.
机构
[1] Case Western Reserve Univ, Vet Affairs Med Ctr, Infect Dis Sect, Dept Mol Biol & Microbiol, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Pharmacol, Cleveland, OH 44106 USA
[3] Univ Hosp Cleveland, Dept Med, Div Infect Dis, Cleveland, OH 44106 USA
关键词
beta-lactamases; cephalosporinases; carbapenemases; extended-spectrum beta-lactamases; ESBLs;
D O I
10.1016/j.drup.2006.05.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In gram-negative bacteria, beta-lactamases are the most important mechanism of resistance to beta-lactam antibiotics. Currently, the beta-lactamases receiving the most attention are the extended-spectrum beta-lactamases (ESBLs), inhibitor-resistant beta-lactamases and carbapenemases. When found in Escherichia coli and Klebsiella spp., ESBLs confer resistance to extended-spectrum cephalosporins, such as ceftazidime, cefotaxime and cefepime. Hence, ESBLs limit the choice of beta-lactam therapy to carbapenems. A worrisome trend is the increasing number of pathogens found in isolates from patients in the community that possess ESBLs. It is equally distressing that carbapenemases (serine and metallo-beta-lactamases) are being found in many of the same bacteria that harbor ESBLs, for example Klebsiella pneumoniae. Despite many years studying beta-lactamases, important clinical and scientific questions still remain. Published by Elsevier Ltd.
引用
收藏
页码:142 / 156
页数:15
相关论文
共 140 条
  • [71] Panresistance in VIM-1-producing Klebsiella pneumoniae
    Miriagou, V
    Tzelepi, E
    Daikos, GL
    Tassios, PT
    Tzouvelekis, LS
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 55 (05) : 810 - 811
  • [72] Escherichia coli with a self-transferable, multiresistant plasmid coding for metallo-β-lactamase VIM-1
    Miriagou, V
    Tzelepi, E
    Gianneli, D
    Tzouvelekis, LS
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (01) : 395 - 397
  • [73] Plasmid-mediated, carbapenem-hydrolysing β-lactamase, KPC-2, in Klebsiella pneumoniae isolates
    Moland, ES
    Hanson, ND
    Herrera, VL
    Black, JA
    Lockhart, TJ
    Hossain, A
    Johnson, JA
    Goering, RV
    Thomson, KS
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (03) : 711 - 714
  • [74] Nanomolar inhibitors of AmpC β-lactamase
    Morandi, F
    Caselli, E
    Morandi, S
    Focia, PJ
    Blázquez, J
    Shoichet, BK
    Prati, F
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (03) : 685 - 695
  • [75] CHARACTERIZATION OF AN LYSR FAMILY PROTEIN, SMER FROM SERRATIA-MARCESCENS S6, ITS EFFECT ON EXPRESSION OF THE CARBAPENEM-HYDROLYZING BETA-LACTAMASE SME-1, AND COMPARISON OF THIS REGULATOR WITH OTHER BETA-LACTAMASE REGULATORS
    NAAS, T
    LIVERMORE, DM
    NORDMANN, P
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (03) : 629 - 637
  • [76] CLONING AND SEQUENCE-ANALYSIS OF THE GENE FOR A CARBAPENEM-HYDROLYZING CLASS-A BETA-LACTAMASE, SME-1, FROM SERRATIA-MARCESCENS S6
    NAAS, T
    VANDEL, L
    SOUGAKOFF, W
    LIVERMORE, DM
    NORDMANN, P
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (06) : 1262 - 1270
  • [77] Molecular characterization of OXA-20, a novel class D β-lactamase, and its integron from Pseudomonas aeruginosa
    Naas, T
    Sougakoff, W
    Casetta, A
    Nordmann, P
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (08) : 2074 - 2083
  • [78] TEM-89 β-lactamase produced by a Proteus mirabilis clinical isolate:: New complex mutant (CMT 3) with mutations in both TEM-59 (IRT-17) and TEM-3
    Neuwirth, C
    Madec, S
    Siebor, E
    Pechinot, A
    Duez, JM
    Pruneaux, M
    Fouchereau-Peron, M
    Kazmierczak, A
    Labia, R
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (12) : 3591 - 3594
  • [79] BIOCHEMICAL-PROPERTIES OF A CARBAPENEM-HYDROLYZING BETA-LACTAMASE FROM ENTEROBACTER-CLOACAE AND CLONING OF THE GENE INTO ESCHERICHIA-COLI
    NORDMANN, P
    MARIOTTE, S
    NAAS, T
    LABIA, R
    NICOLAS, MH
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (05) : 939 - 946
  • [80] Trends in β-lactam resistance among enterobacteriaceae
    Nordmann, P
    [J]. CLINICAL INFECTIOUS DISEASES, 1998, 27 : S100 - S106