IntroductionAcinetobacter baumannii is a gram-negative, nonfermentative coccobacillus. It is increasingly recognized as a major pathogen causing nosocomial infections, including ventilator-associated pneumonia, bacteremia, meningitis, urinary tract, and wound infections, particularly in patients admitted to burn therapy and intensive care units (1). One of the most alarming characteristics of this bacterium is its ability to develop resistance to the majority of available antibiotics, including carbapenems, which are drugs of choice in severe infections (2). Several mechanisms responsible for resistance to carbapenems have been described in A. baumannii isolates: decreased outermembrane permeability, efflux-pumps, target-site modifications, and synthesis of carbapenemases (3). Among these, production of carbapenem-hydrolyzing oxacillinases (CHOs) or class D carbapenemases stands out as the most common resistance mechanism (4,5). The Amber class D carbapenemases of A. baumannii can be divided into six subgroups: OXA-51-like (intrinsic-chromosomal), OXA-23-like, OXA-40/24-like, OXA-58-like, OXA-143-like, and OXA-235-like (6). Types and frequency of CHOs may vary among different countries and centers. The aim of this study was to investigate the prevalence of primary CHO types in clinical A. baumannii strains isolated from a 2000bed regional university hospital.
Materials and methods
Bacterial strains and determination of imipenem minimum inhibitory concentration valuesSeventy-six carbapenem nonsusceptible clinical A. baumannii isolates, one per patient, were selected from 122 clinical isolates collected between January and March 2012 by Ege University Hospital, Turkey. Isolates were obtained from blood (n = 18), tracheal aspirates (n = 28), bronchial Background/aim: Acinetobacter baumannii is an important causative agent of nosocomial infections, and carbapenems have been frequently used in the treatment of these infections. This study was designed to investigate the prevalence of primary carbapenem hydrolyzing oxacillinase (CHO) types in clinical A. bumannii strains.Materials and methods: Minimum inhibitory concentration (MIC) values of 76 imipenem nonsusceptible A. baumannii strains, isolated from a tertiary care hospital, were determined by microdilution method. The clonal relationship of the isolates was analyzed with enterobacterial repetitive intergenic consensus (ERIC)-PCR, and the presence of CHO major groups (OXA-23; OXA-24, OXA-51, and OXA-58 groups) was investigated with multiplex PCR.Results: According to the ERIC-PCR patterns, the isolates were distributed in 13 different clones, the largest of which had 40 members. bla OXA-51-group was detected in representatives of all clones, whereas bla OXA-23-group was detected in representatives of all but two small clones. Additionally, the presence of bla OXA-58-group was discovered in the members of two small clones, whereas bla OXA-24-group was not encountered in any of the examined strains.
Conclusion:Molecular fingerprinting revealed that most imipenem-resi...