Annals of Clinical Microbiology, The official Journal of the Korean Society of Clinical Microbiology

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pISSN 2288-0585 eISSN 2288-6850

Prevalence of OXA-23 Extended-Spectrum β-Lactamase-Producing Clinical Isolates of Acinetobacter baumannii in a University Hospital, Busan, Korea

Original article

Annals of Clinical Microbiology (Ann Clin Microbiol) 2004 December Volume 7, Issue 2, pages 139-147.


https://doi.org/10.5145/ACM.2004.07.2.139

Prevalence of OXA-23 Extended-Spectrum β-Lactamase-Producing Clinical Isolates of Acinetobacter baumannii in a University Hospital, Busan, Korea

Byung-Chan Jeon2, Ki-Young Kwon2, Seok Hoon Jeong1, Il Kwon Bae1, Su Bong Kwon1, Byung Kyu Cho1, Dongeun Yong3, Kyungwon Lee3
Departments of Laboratory Medicine1, Neurosurgery2, Kosin University College of Medicine; Department of Laboratory Medicine3, Yonsei University College of Medicine

Abstract

Background : Acinetobacter baumannii is a glucose-nonfermenting gram-negative rod and is a well-recognized nosocomial pathogen. In recent years, A. baumannii strains showing resistance to carbapenems by producing metallo-β-lactamases or OXA-type β-lactamases have increased, and it is considered to be a serious clinical problem. But genotypes of carbapenemases produced by A. baumannii isolates in Korea have been rarely reported. The purpose of this study was to investigate the prevalence of imipenem-resistant A. baumannii and to determine the mechanism of resistance.

Methods : During the period of January through September, 2003, susceptibilities to imipenem of A. baumannii isolates from patients admitted in Kosin University Gospel Hospital in Busan, Korea were investigated. The modified Hodge and EDTA-disk synergy tests were performed for screening of carbapenemase and metallo-β-lactamase-production. Minimal inhibitory concentrations (MICs) were determined by the agar dilution method. For detection of IMP, VIM and OXA-type β-lactamases genes, polymerase chain reactions (PCR) were performed, and the DNA sequences of OXA-type β-lactamases genes were determined by using the dideoxy-chain termination method. The isoelectric points of β-lactamases were determined by isoelectric focusing. Pulsed-field gel electrophresis (PFGE) of the SmaI-digested genomic DNA was performed.

Results : A total of 193 strains of A. baumannii were collected from patients during the surveillance period. Twenty-seven percents (52/193) of A. baumannii isolates were resistant to imipenem. Among the 52 imipenem-resistant isolates, 41 isolates (78.8%) showed positive results in the modified Hodge test, but none of the isolates showed positive results in the EDTA-disk synergy test. Thirty-eight modified Hodge test-positive isolates harbored blaOXA-23 gene, but none of the isolates harbored IMP- or VIM-type metallo-β-lactamases genes. Analytical isoelectric focusing revealed that all the 38 isolates had a nitrocefin-positive band at pI of 6.65. Thirty-five OXA-23-producing isolates showed a similar PFGE pattern when digested by SmaI endonuclease.

Conclusion : Thirty-eight clinical isolates of A. baumannii acquired resistance to imipenem by producing OXA-23 β-lactamase. Among them were 35 isolates thought to be originated from the same source, because they contained a similar chromosomal type. To the best of our knowledge, this is the first time that OXA-23 β-lactamase has been detected in Korea. (Korean J Clin Microbiol 2004;7(2):139-147)

Keywords

Acinetobacter baumannii, Imipenem, OXA-23 β-lactamase