Temporal evolution of carbapenem-resistant Acinetobacter baumannii in Curitiba, southern Brazil

被引:31
作者
Schimith, Karina Eugenia
Luiz, Simone Oliveira [2 ]
Scheffer, Mara Cristina [3 ]
Gales, Ana Cristina [4 ]
Paganini, Maria Cristina [5 ]
do Nascimento, Agnaldo Jose [6 ]
Carignano, Evelyn [5 ]
Dalla Costa, Libera Maria [1 ,7 ]
机构
[1] UFPR, Hosp Clin, Bacteriol Lab, UAD, BR-80060240 Curitiba, Parana, Brazil
[2] UFPR, Microbiol Parasitol & Pathol Postgrad Program, BR-80060240 Curitiba, Parana, Brazil
[3] Univ Fed Santa Catarina, Clin Hosp, Florianopolis, SC, Brazil
[4] Univ Fed Sao Paulo, Dept Infect Dis, Sao Paulo, Brazil
[5] Univ Tuiuti Parana, Curitiba, Parana, Brazil
[6] UFPR, Pharmaceut Sci Postgrad Program, BR-80060240 Curitiba, Parana, Brazil
[7] Pequeno Principe Coll Pele Pequeno Res Inst FPP I, Curitiba, Parana, Brazil
关键词
Acinetobacter baumannii; carbapenem resistance; OXA-23; METALLO-BETA-LACTAMASE; PSEUDOMONAS-AERUGINOSA; OXA-23; CARBAPENEMASE; OUTBREAK; DISSEMINATION; GENES; SPP; TIGECYCLINE; INFECTIONS; EMERGENCE;
D O I
10.1016/j.ajic.2009.09.012
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: In the last few years, carbapenem-resistant Acinetobacter baumannii isolates (CR-AB) have been identified worldwide. The first description of OXA-23-producing A baumannii in Brazil was from the city of Curitiba in 2003. The aim of the present study was to evaluate the persistence and dissemination of the first OXA-23-producing A baumannii clone isolated from patients in Hospital de Clinicas, Curitiba, Brazil. Methods: An antimicrobial susceptibility profile of the isolates was determined by the standard agar dilution method. Molecular detection of beta-lactamase genes was done by polymerase chain reaction. The clonal relationship of the isolates was analyzed by pulsed-field gel electrophoresis (PFGE). Epidemiologic and clinical features were evaluated as well. Results: Genotypic analysis of 172 CR-AB isolates by PFGE identified 3 distinct major PFGE clusters (A, B, and C, accounting for 36, 69, and 65 isolates, respectively). All isolates carried the bla(OXA-23)-like gene and were multidrug-resistant, but were susceptible to tigecycline and polymixin B. The mortality rate related to CR-AB infection was 45.4%, and ventilator-associated pneumonia and bloodstream infections were the most frequent clinical manifestations. Conclusions: The presence of 3 clones among the CR-AB isolates suggests that cross-transmission was the main mechanism responsible for dissemination of OXA-23 producers. PFGE pattern A was genotypically similar to that of the first OXA-23-producing A baumannii clone identified in Curitiba in 1999. This clone persisted in the same hospital until April 2004. The presence of the bla(OXA-23)-like gene was the main mechanism associated with carbapenem resistance among the isolates studied.
引用
收藏
页码:308 / 314
页数:7
相关论文
共 44 条
  • [1] OXA β-lactamases in Acinetobacter:: the story so far
    Brown, S
    Amyes, S
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 57 (01) : 1 - 3
  • [2] Dissemination of multidrug-resistant Acinetobacter baumannii genotypes carrying blaOXA-23 collected from hospitals in Rio de Janeiro, Brazil
    Carvalho, Karyne Rangel
    D'Alincourt Carvalho-Assef, Ana Paula
    Peirano, Gisele
    Galvao dos Santos, Lia Cristina
    Felix Pereira, Maria Jose
    Asensi, Marise Dutra
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2009, 34 (01) : 25 - 28
  • [3] Clinical and Laboratory Standards Institute, 2006, METH DIL ANT SUSC TE, V7
  • [4] Clinical and Laboratory Standards Institute, 2006, M100S16 CLIN LAB STA
  • [5] Outbreak of carbapenem-resistant Acinetobacter baumannii producing the OXA-23 enzyme in Curitiba, Brazil
    Dalla-Costa, LM
    Coelho, JM
    Souza, HAPHM
    Castro, MES
    Stier, CJN
    Bragagnolo, KL
    Rea-Neto, A
    Penteado, SR
    Livermore, DM
    Woodford, N
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (07) : 3403 - 3406
  • [6] Effect of divalent metal cations on the dimerization of OXA-10 and-14 class D β-lactamases from Pseudomonas aeruginosa
    Danel, F
    Paetzel, M
    Strynadka, NCJ
    Page, MGP
    [J]. BIOCHEMISTRY, 2001, 40 (31) : 9412 - 9420
  • [7] An increasing threat in hospitals:: multidrug-resistant Acinetobacter baumannii
    Dijkshoorn, Lenie
    Nemec, Alexandr
    Seifert, Harald
    [J]. NATURE REVIEWS MICROBIOLOGY, 2007, 5 (12) : 939 - 951
  • [8] Risk factors for the isolation of multi-drug-resistant Acinetobacter baumannii and Pseudomonas aeruginosa:: a systematic review of the literature
    Falagas, M. E.
    Kopterides, P.
    [J]. JOURNAL OF HOSPITAL INFECTION, 2006, 64 (01) : 7 - 15
  • [9] High Concentrations of Manganese in Mueller-Hinton Agar Increase MICs of Tigecycline Determined by Etest
    Fernandez-Mazarrasa, Carlos
    Mazarrasa, Olav
    Calvo, Jorge
    del Arco, Asuncion
    Martinez-Martinez, Luis
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2009, 47 (03) : 827 - 829
  • [10] Emergence of an IMP-like metallo-enzyme in an Acinetobacter baumannii clinical strain from a Brazilian teaching hospital
    Gales, AC
    Tognim, MCB
    Reis, AO
    Jones, RN
    Sader, HS
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2003, 45 (01) : 77 - 79