Carbapenem-resistant Serratia marcescens isolates producing Bush group 2f β-lactamase (SME-1) in the United States:: Results from the MYSTIC Programme

被引:31
作者
Gales, AC
Biedenbach, DJ
Winokur, P
Hacek, DM
Pfaller, MA
Jones, RN
机构
[1] Univ Iowa, Coll Med, Dept Pathol, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[3] CAST Labs, Iowa City, IA USA
[4] Northwestern Univ, Dept Med, Chicago, IL 60611 USA
[5] Northwestern Univ, Dept Pathol, Chicago, IL 60611 USA
关键词
D O I
10.1016/S0732-8893(00)00222-4
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Two carbapanem (imipenem, meropenem)-resistant Serratia marcescens strains were isolated in the United States (Chicago, IL) through the 1999 MYSTIC (Meropenem Yearly Susceptibility Test Information Collection) Programme. The S. marcescens antimicrobial susceptible patterns were: susceptible to ceftriaxone, ceftazidime, and cefepime (MICs, less than or equal to0.25 mug/ml), and resistance to the carbapenems (imipenem and meropenem; MIC, > 32 mug/ml) and aztreonam (MIC, greater than or equal to 16 mug/ml). Each S. marcescens isolate shared an identical epidemiologic type (ribotype and PFGE) and the outer membrane protein profile was also identical to those of the wild type susceptible strains from the same medical center. The PCR utilizing bla(sme-1) primers amplified a gene product that was identified as consistent with SME-1 after DNA sequencing. Imipenem and meropenem resistance due to production of carbapenem-hydrolyzing enzymes among clinical isolates is still very rare, but microbiology laboratories should be aware of these chromosomally encoded enzymes among class C p-lactamases producing enteric bacilli such as S. marcescens and Enterobacter cloacae. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:125 / 127
页数:3
相关论文
共 15 条
  • [1] [Anonymous], [No title captured]
  • [2] A FUNCTIONAL CLASSIFICATION SCHEME FOR BETA-LACTAMASES AND ITS CORRELATION WITH MOLECULAR-STRUCTURE
    BUSH, K
    JACOBY, GA
    MEDEIROS, AA
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (06) : 1211 - 1233
  • [3] SOLUBILIZATION OF CYTOPLASMIC MEMBRANE OF ESCHERICHIA-COLI BY IONIC DETERGENT SODIUM-LAURYL SARCOSINATE
    FILIP, C
    FLETCHER, G
    WULFF, JL
    EARHART, CF
    [J]. JOURNAL OF BACTERIOLOGY, 1973, 115 (03) : 717 - 722
  • [4] Hejazi A, 1997, J MED MICROBIOL, V46, P903, DOI 10.1099/00222615-46-11-903
  • [5] Molecular characterization of the Serratia marcescens OmpF porin, and analysis of S-marcescens OmpF and OmpC osmoregulation
    Hutsul, JA
    Worobec, E
    [J]. MICROBIOLOGY-UK, 1997, 143 : 2797 - 2806
  • [6] PLASMID-MEDIATED DISSEMINATION OF THE METALLO-BETA-LACTAMASE GENE BLA(IMP) AMONG CLINICALLY ISOLATED STRAINS OF SERRATIA-MARCESCENS
    ITO, H
    ARAKAWA, Y
    OHSUKA, S
    WACHAROTAYANKUN, R
    KATO, N
    OHTA, M
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (04) : 824 - 829
  • [7] JONES RN, 1998, DIAGN MICROBIOL INFE, V31, P561
  • [8] Characterization of a new plasmid-mediated extended-spectrum beta-lactamase from Serratia marcescens
    Kunugita, C
    Higashitani, F
    Hyodo, A
    Unemi, N
    Inoue, M
    [J]. JOURNAL OF ANTIBIOTICS, 1995, 48 (12) : 1453 - 1459
  • [9] 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
  • [10] *NAT COMM CLIN LAB, 2000, M7A4 NAT COMM CLIN L