JAC Advance Access originally published online on May 18, 2004
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Journal of Antimicrobial Chemotherapy 2004 54(1):134-138; doi:10.1093/jac/dkh274
JAC vol.54 no.1 © The British Society for Antimicrobial Chemotherapy 2004; all rights reserved.
Evaluation of a new cefepimeclavulanate ESBL Etest to detect extended-spectrum ß-lactamases in an Enterobacteriaceae strain collection
Institut für Infektionsmedizin, Zentrum für Klinisch-Theoretische Medizin I, Universitätsklinikum Hamburg-Eppendorf, Martinistrasse 52, D-20246 Hamburg, Germany
* Corresponding author. Tel: +49-40-42803-3147; Fax: +49-40-42803-4881; Email: e.stuerenburg{at}uke.uni-hamburg.de
Objectives: In this study, we evaluated the performance of a new ESBL Etest configuration based on clavulanate synergy with cefepime compared with cefotaximeclavulanate and ceftazidimeclavulanate ESBL Etest strips for the detection of extended-spectrum ß-lactamases (ESBL) in an Enterobacteriaceae strain collection, with special focus on Enterobacter spp.
Methods: Overall, a total of 54 clinical isolates of ESBL-producing Enterobacteriaceae species were evaluated: Enterobacter aerogenes (n=3), Enterobacter cloacae (n=10), Escherichia coli (n=10), Klebsiella oxytoca (n=3), Klebsiella pneumoniae (n=25) and Proteus mirabilis (n=3). To check Etest behaviour with resistance phenotypes similar to ESBL, our panel was expanded by six clinical isolates of K. oxytoca that were identified as putative producers of their chromosomal K1 ß-lactamase.
Results: With this panel, ESBL Etest was 98% sensitive with cefepimeclavulanate, 83% with cefotaximeclavulanate, and 74% with ceftazidimeclavulanate strips. Concentrating on Enterobacter spp., reliable ESBL detection could only be achieved by the new cefepimeclavulanate strip since it confirmed ESBL production in all strains (100% sensitivity) whereas only 4/13 (31%) of Enterobacter strains were positive using cefotaximeclavulanate or ceftazidimeclavulanate strips. A limitation of using the new cefepime strip was less than optimal specificity with K1 phenotypes of K. oxytoca: among six strains, four isolates were scored false-positive by Etest strips containing cefepimeclavulanate.
Conclusion: The new Etest ESBL strip containing cefepimeclavulanate is a valuable supplement to current methods for detection of ESBLs. In our study collection, the cefepimeclavulanate strip was the best configuration for detection of ESBLs, particularly in Enterobacter spp.
Keywords: ESBL detection , Etest methodology
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