Dissemination of multidrug-resistant Acinetobacter baumannii genotypes carrying blaOXA-23 collected from hospitals in Rio de Janeiro, Brazil

被引:71
作者
Carvalho, Karyne Rangel [1 ]
D'Alincourt Carvalho-Assef, Ana Paula [1 ]
Peirano, Gisele [1 ]
Galvao dos Santos, Lia Cristina [2 ]
Felix Pereira, Maria Jose [1 ]
Asensi, Marise Dutra [1 ]
机构
[1] Fiocruz MS, Inst Oswaldo Cruz, BR-21040360 Rio De Janeiro, Brazil
[2] Bonsucesso Gen Hosp, BR-21041030 Rio De Janeiro, Brazil
关键词
Multidrug resistance; Acinetobacter baumannii; OXA-23; Molecular typing; OXA BETA-LACTAMASES; PSEUDOMONAS-AERUGINOSA; OUTBREAK; SUSCEPTIBILITY; TIGECYCLINE; IDENTIFICATION; CARBAPENEMASE; HODGE; SPP;
D O I
10.1016/j.ijantimicag.2008.12.009
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The present study reports the dissemination of multidrug-resistant (MDR) OXA-23-producing Acinetobacter baumannii clones throughout hospitals in Rio de Janeiro, Brazil. A total of 110 imipenem-resistant A. baumannii isolates were obtained from January 2006 to September 2007 in eight hospitals. The modified Hodge test was performed to screen for carbapenemase production. Polymerase chain reaction (PCR) and DNA sequencing were performed for the detection of bla(IMP), bla(VIM), bla(OXA-23-like), bla(OXA-24-like), bla(OXA-58) and the class 1 integron. Isolates were typed by pulsed-field gel electrophoresis (PFGE) following digestion with ApaI. All the isolates were MDR and 96 (87.3%) produced the carbapenemase OXA-23. No isolates produced OXA-24, OXA-58 or the metallo-beta-lactamases IMP and VIM. The class 1 integron was absent in all isolates. The A. baumannii isolates were separated into five genotypes, with the highest prevalence of genotype A (71.8%) followed by genotype B (22.7%). Genotype A was present in seven hospitals, whilst genotype B had spread in five hospitals. The OXA-23-producing isolates belonged to all genotypes. The presence of MDR OXA-23-producing A. baumannii in different hospitals in Rio de Janeiro emphasises the need to control the use of carbapenems and to prevent the spread of these organisms in Rio de Janeiro. (C) 2009 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:25 / 28
页数:4
相关论文
共 31 条
[1]   OXA β-lactamases in Acinetobacter:: the story so far [J].
Brown, S ;
Amyes, S .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 57 (01) :1-3
[2]  
CAETANOANOLLES G, 1997, CHARACTERIZATION CLA, P151
[3]  
*CLIN LAB STAND I, 2008, M100S18 NCCLS CLIN S
[4]   Genetics and expression of the carbapenem-hydrolyzing oxacillinase gene blaOXA-23 in Acinetobacter baumannii [J].
Corvec, Stephane ;
Poirel, Laurent ;
Naas, Thierry ;
Drugeon, Henri ;
Nordmann, Patrice .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (04) :1530-1533
[5]   Outbreak of carbapenem-resistant Acinetobacter baumannii producing the OXA-23 enzyme in Curitiba, Brazil [J].
Dalla-Costa, LM ;
Coelho, JM ;
Souza, HAPHM ;
Castro, MES ;
Stier, CJN ;
Bragagnolo, KL ;
Rea-Neto, A ;
Penteado, SR ;
Livermore, DM ;
Woodford, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (07) :3403-3406
[6]   Evaluation of amplified ribosomal DNA restriction analysis for identification of Acinetobacter genomic species [J].
Dijkshoorn, L ;
van Harsselaar, B ;
Tjernberg, I ;
Bouvet, PJM ;
Vaneechoutte, M .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 1998, 21 (01) :33-39
[7]   An increasing threat in hospitals:: multidrug-resistant Acinetobacter baumannii [J].
Dijkshoorn, Lenie ;
Nemec, Alexandr ;
Seifert, Harald .
NATURE REVIEWS MICROBIOLOGY, 2007, 5 (12) :939-951
[8]   Investigation of a nosocomial outbreak of imipenem-resistant Acinetobacter baumannii producing the OXA-23 β-lactamase in Korea [J].
Jeon, BC ;
Jeong, SH ;
Bae, IK ;
Kwon, SB ;
Lee, K ;
Young, D ;
Lee, JH ;
Song, JS ;
Lee, SH .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (05) :2241-2245
[9]  
Jeong SH, 2006, J MICROBIOL, V44, P423
[10]   Multicenter studies of tigecycline disk diffusion susceptibility results for Acinetobacter spp. [J].
Jones, Ronald N. ;
Ferraro, Mary Jane ;
Reller, L. Barth ;
Schreckenberger, Paul C. ;
Swenson, Jana M. ;
Sader, Helio S. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2007, 45 (01) :227-230