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Volume 38, Issue 4, Pages 308-314 (May 2010)


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

Karina Eugênia Schimith Bier, MSca, Simone Oliveira Luiz, MScb, Mara Cristina Scheffer, MScac, Ana Cristina Gales, PhDd, Maria Cristina Paganini, MScae, Agnaldo José do Nascimento, PhDf, Evelyn Carignano, BSe, Libera Maria Dalla Costa, PhDagCorresponding Author Informationemail address

published online 02 February 2010.

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 β-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 blaOXA-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 blaOXA-23–like gene was the main mechanism associated with carbapenem resistance among the isolates studied.

a Clinical Hospital, Federal University of Paraná, Curitiba, Brazil

b Microbiology, Parasitology and Pathology Post-Graduate Program, Federal University of Paraná, Curitiba, Brazil

c Clinical Hospital of Federal University of Santa Catarina, Florianópolis, Brazil

d Infectious Disease Department, Federal University of São Paulo (UNIFESP), São Paulo, Brazil

e Tuiuti University of Paraná, Curitiba, Brazil

f Pharmaceutical Sciences Post-Graduate Program, Federal University of Paraná, Curitiba, Brazil

g Pequeno Príncipe College—Pelé Pequeno Príncipe Research Institute (FPP/IPPPP), Curitiba, Brazil

Corresponding Author InformationAddress correspondence to Libera Dalla Costa, Universidade Federal do Paraná (UFPR), Hospital de Clínicas, Laboratório de Bacteriologia, UAD, Rua Padre Camargo, 280–1° andar, Curitiba, PR, 80060-240 Brazil.

 Conflict of interest: A.C.G. is a research fellow for the Brazilian National Council for Scientific and Technological Development, Ministry of Science and Technology (under Grant 307714/2006-3), and has received research funding, speaking grants, conference support, and consulting fees from Janssen Cylag, Novartis, Sanofi-Aventis, and Wyeth.

PII: S0196-6553(09)00944-4

doi:10.1016/j.ajic.2009.09.012


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