Dissemination in distinct Brazilian regions of an epidemic carbapenem-resistant Pseudomonas aeruginosa producing SPM metallo-β-lactamase

被引:190
作者
Gales, AC
Menezes, LC
Silbert, S
Sader, HS
机构
[1] Univ Fed Sao Paulo, Lab Alerta, BR-04025010 Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Div Infect Dis, Lab Especial Microbiol Clin, BR-04025010 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Gram-negative bacilli; carbapenem resistance; Brazil;
D O I
10.1093/jac/dkg416
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: In Brazil, carbapenem use has been limited by high carbapenem-resistance rates among Pseudomonas aeruginosa isolates. Objective: The main objective of this study was to evaluate the presence of an epidemic P. aeruginosa strain in unrelated Brazilian hospitals. We also aimed to search for the gene bla(SPM), which encodes production of SPM, a novel metallo-beta-lactamase (MBL). Methods: A reference broth microdilution method was used for antimicrobial susceptibility testing. The isolates were typed by ribotyping and pulsed-field gel electrophoresis (PFGE). A disc-approximation test using MBL inhibitors was employed to screen isolates for MBL production. PCR was used to search for the gene bla(SPM). Results: A total of 43 clinical isolates of carbapenem-resistant P. aeruginosa were collected from 12 hospitals. Colistin retained greatest activity in vitro. A single ribogroup included 17 P. aeruginosa isolates (39.5%) collected from seven unrelated hospitals located in five Brazilian states. Sixteen of these isolates showed an identical PFGE pattern, and 15 produced an SPM-1-like MBL. The remaining 26 isolates were grouped into 25 diverse ribogroups; none were MBL producers. Conclusions: The emergence and dissemination of an epidemic clone has contributed to the high carbapenem resistance rates among P. aeruginosa isolates in Brazil. In addition, the production of SPM MBL has an important role in carbapenem resistance in this region. This is the first report of dissemination of an SPM-1-like-MBL-producing strain of P. aeruginosa among unrelated Brazilian hospitals.
引用
收藏
页码:699 / 702
页数:4
相关论文
共 10 条
  • [1] [Anonymous], 2002, M100S12 NCCLS
  • [2] Arakawa Y, 2000, J CLIN MICROBIOL, V38, P40
  • [3] Endemicity, molecular diversity and colonisation routes of Pseudomonas aeruginosa in intensive care units
    Bertrand, X
    Thouverez, M
    Talon, D
    Boillot, A
    Capellier, G
    Floriot, C
    Hélias, JP
    [J]. INTENSIVE CARE MEDICINE, 2001, 27 (08) : 1263 - 1268
  • [4] Characterization of Pseudomonas aeruginosa isolates:: Occurrence rates, antimicrobial susceptibility patterns, and molecular typing in the global SENTRY Antimicrobial Surveillance Program, 1997-1999
    Gales, AC
    Jones, RN
    Turnidge, J
    Rennie, R
    Ramphal, R
    [J]. CLINICAL INFECTIOUS DISEASES, 2001, 32 : S146 - S155
  • [5] Multiple mechanisms of antimicrobial resistance in Pseudomonas aeruginosa:: Our worst nightmare?
    Livermore, DM
    [J]. CLINICAL INFECTIOUS DISEASES, 2002, 34 (05) : 634 - 640
  • [6] Emerging carbapenemases in Gram-negative aerobes
    Nordmann, P
    Poirel, L
    [J]. CLINICAL MICROBIOLOGY AND INFECTION, 2002, 8 (06) : 321 - 331
  • [7] Occurrence of a multidrug-resistant Pseudomonas aeruginosa clone in different hospitals in Rio de Janeiro, Brazil
    Pellegrino, FLPC
    Teixeira, LM
    Carvalho, MD
    Nouér, SA
    de Oliveira, MP
    Sampaio, JLM
    Freitas, AD
    Ferreira, ALP
    Amorim, ED
    Riley, LW
    Moreira, BM
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (07) : 2420 - 2424
  • [8] Nosocomial infections in medical intensive care units in the United States
    Richards, MJ
    Edwards, JR
    Culver, DH
    Gaynes, RP
    [J]. CRITICAL CARE MEDICINE, 1999, 27 (05) : 887 - 892
  • [9] Sader H S, 2001, Braz J Infect Dis, V5, P200
  • [10] Molecular characterization of SPM-1, a novel metallo-β-lactamase isolated in Latin America:: report from the SENTRY antimicrobial surveillance programme
    Toleman, MA
    Simm, AM
    Murphy, TA
    Gales, AC
    Biedenbach, DJ
    Jones, RN
    Walsh, TR
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (05) : 673 - 679