Emergence of serine carbapenemases (KPC and SME) among clinical strains of Enterobacteriaceae isolated in the United States Medical Centers: Report from the MYSTIC Program (1999-2005)

被引:113
作者
Deshpande, Lalitagauri M.
Rhomberg, Paul R.
Sader, Helio S.
Jones, Ronald N.
机构
[1] JMI Labs, Iowa City, IA 52317 USA
[2] Univ Fed Sao Paulo, Sao Paulo, Brazil
[3] Tufts Univ, Sch Med, Medford, MA 02155 USA
关键词
KPC; SME; New York; MYSTIC program; Enterobacteriaceae;
D O I
10.1016/j.diagmicrobio.2006.07.004
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Among 8885 Enterobacteriaceae tested in the 1999 to 2005 period as part of the USA Meropenem Yearly Susceptibility Test Information Collection (MYSTIC) Program, 51 strains with increased imipenem and meropenem MIC values (>= 2 mu g/mL) were detected. bla(KPC) was identified from 28 Klebsiella pneumoniae from 3 medical centers in the New York City area (8 ribotypes), 2 Klebsiella oxytoca from Arkansas (same ribotype), 7 Citrobacter freundii (6 from New York [5 ribotypes] and I from Delaware), 4 Enterobacter spp. from New York (2 species, different ribotypes), 3 Escherichia coli (2 from New York and I from Ohio, same ribotype), and I Serratia marcescens (New York), Sequencing confirmed KPC-2 or -3 in all of the strains. S. marcescens strains harboring SME-1 (2 isolates, same ribotype) and SME-2 (I isolate) were identified from medical centers in Illinois and Washington state, respectively. Our results indicate that bla(KPC-2/3) has emerged widely (New York City area, Arkansas, Delaware, and Ohio) among Enterobacteriaceae isolated in the MYSTIC Program participant sites (2000-2005) and continues to be isolated from multiple species, as a result of clonal expansion and horizontal gene transfer. The escalating occurrence (0.35%) of serine carbapenemases could compromise the role of carbapenems and other beta-lactams in USA clinical practice although observed in only a few locations to date. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:367 / 372
页数:6
相关论文
共 31 条
  • [1] Kinetics study of KPC-3, a plasmid-encoded class a carbapenem-hydrolyzing β-lactamase
    Alba, J
    Ishii, Y
    Thomson, K
    Moland, ES
    Yamaguchi, K
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (11) : 4760 - 4762
  • [2] Arakawa Y, 2000, J CLIN MICROBIOL, V38, P40
  • [3] BRADFIELD HL, 1997, IEEE IND APPL MAG, V3, P41
  • [4] Emergence of carbapenem-resistant Klebsiella species possessing the class A carbapenem-hydrolyzing KPC-2 and inhibitor-resistant TEM-30 β-lactamases in New York City
    Bradford, PA
    Bratu, S
    Urban, C
    Visalli, M
    Mariano, N
    Landman, D
    Rahal, JJ
    Brooks, S
    Cebular, S
    Quale, J
    [J]. CLINICAL INFECTIOUS DISEASES, 2004, 39 (01) : 55 - 60
  • [5] Carbapenemase-producing Klebsiella pneumoniae in Brooklyn, NY:: molecular epidemiology and in vitro activity of polymyxin B and other agents
    Bratu, S
    Tolaney, P
    Karumudi, U
    Quale, J
    Mooty, M
    Nichani, S
    Landman, D
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 56 (01) : 128 - 132
  • [6] Detection of KPC carbapenem-hydrolyzing enzymes in Enterobacter spp. from Brooklyn, New York
    Bratu, S
    Landman, D
    Alam, M
    Tolentino, E
    Quale, J
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (02) : 776 - 778
  • [7] Rapid spread of carbapenem-resistant Klebsiella pneumoniae in New York City -: A new threat to our antibiotic armamentarium
    Bratu, S
    Landman, D
    Haag, R
    Recco, R
    Eramo, A
    Alam, M
    Quale, J
    [J]. ARCHIVES OF INTERNAL MEDICINE, 2005, 165 (12) : 1430 - 1435
  • [8] Emergence of imipenem resistance in Klebsiella pneumoniae owing to combination of plasmid-mediated CMY-4 and permeability alteration
    Cao, VTB
    Arlet, G
    Ericsson, BM
    Tammelin, A
    Courvalin, P
    Lambert, T
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 46 (06) : 895 - 900
  • [9] *CLIN LAB STAND I, 2006, M100S16 CLSI
  • [10] Clinical and Laboratory Standards Institute, 2006, M7A7 CLSI