JAC Advance Access originally published online on January 23, 2006
Journal of Antimicrobial Chemotherapy 2006 57(3):557-561; doi:10.1093/jac/dkl004
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Outbreak of multiple clones of imipenem-resistant Acinetobacter baumannii isolates expressing OXA-58 carbapenemase in an intensive care unit
1 Department of Microbiology, Medical School, University of Thessaly, Mezourlo, Larissa, Greece; 2 Department of Microbiology, Medical School, University of Athens, 11527 Athens, Greece; 3 Department of Clinical Microbiology, Red Cross Hospital, Athens, Greece
Received 17 November 2005; returned 6 December 2005; revised 16 December 2005; accepted 23 December 2005
* Corresponding author. Tel: +30-210-746-2140; Fax: +30-210-746-1489; E-mail: atsakris{at}med.uoa.gr
Objectives: To investigate the resistance mechanisms and the genetic relationship of imipenem-resistant Acinetobacter baumannii isolates recovered in the intensive care unit (ICU) of a tertiary care hospital.
Methods: Imipenem-resistant A. baumannii clinical and environmental isolates were collected in the ICU of the Red Cross General Hospital, Athens, Greece between March and October 2002. The isolates were tested by Etest MBL, PCR, RT–PCR and sequencing for carbapenemase-encoding genes, PFGE and synergy experiments using meropenem and the efflux pump inhibitor carbonyl cyanide chlorophenylhydrazone.
Results: During the study period, 15 clinical and two environmental imipenem-resistant (MIC 8 to >128 mg/L) A. baumannii isolates were recovered. PFGE showed six different clones that included both clinical and environmental isolates. All 17 isolates were negative by Etest MBL and PCR for genes blaIMP, blaVIM, blaSPM, blaOXA-23-like and blaOXA-24-like. Genes blaOXA-51-like and blaOXA-58-like were amplified from 15 and 14 isolates, respectively. Sequencing of blaOXA-51-like amplicons identified blaOXA-66 (nine cases) and blaOXA-69 (six cases), whereas blaOXA-58-like sequences were classical blaOXA-58. Reverse transcriptase-PCR showed that blaOXA-51-like genes were expressed in 12 and blaOXA-58 in 10 isolates; in these isolates, inhibition of OXA enzymes by 200 mM of NaCl reduced carbapenem MICs by up to 4-fold. Overexpression of proton-gradient dependent efflux pumps did not contribute to carbapenem resistance in any isolate. Similarly, although AmpC expression was demonstrated in eight isolates, inhibition of AmpC with cloxacillin did not reduce the MICs of carbapenems significantly.
Conclusions: These findings indicate wide dissemination of OXA-58 carbapenemase, which contributes, at least partially, to the imipenem resistance of unrelated A. baumannii isolates in our ICU.
Keywords: oxacillinase , carbapenems , blaOXA-51 , blaOXA-58 , RT–PCR
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