Phenotypic ESBL Detection in Acinetobacter baumannii: A Real Challenge
Geetanjali M. Litake, Vikram S. Ghole, Krishna B. Niphadkar and Suresh G. Joshi
DOI : 10.3844/ajidsp.2015.48.53
American Journal of Infectious Diseases
Volume 11, Issue 3
Clinical Laboratory Standards Institute (CLSI) recommends two-step approach for extended-spectrum-Î²-lactamase (ESBL) detection which includes the screening of recommended agents and the phenotypic confirmation of ESBL using a combination of screening agent and Î²-lactamase inhibitor. To investigate this approach, we screened 145 Î²-lactamase-producing Acinetobacter baumannii isolates for ESBL from tracheal secretions using double disk synergy test (DDST) and phenotypic confirmatory disc diffusion test (PCDDT), the determination of minimum inhibitory concentration (MIC) for ceftazidime and cefotaxime (with/without clavulanic acid), and the unique disc placement scheme. Eighteen of 145 (12.4%) isolates showed ESBL production. All 18 isolates showed positive PCDDT. MIC of these isolates were extremely high (>512 Âµg/ml), and eight fold decrease in MIC was shown by only one isolate. The unique disc placement scheme detected 13 (72.2%) and 3 (16.7%) of ESBL producers and ampC producers, respectively. High level resistance to cefoxitin and cefotaxime among these isolates is suggestive of the derepressed mutants. The PCDDT was most effective ESBL detection method while the unique disc placement scheme showed advantage of detection of ampC Î²-lactamase, derepressed mutants and multiple Î²-lactam resistance mechanism in these isolates. This is a rare report comparing different tests for phenotypic ESBL detection in clinical isolates of A. baumannii.
© 2015 Geetanjali M. Litake, Vikram S. Ghole, Krishna B. Niphadkar and Suresh G. Joshi. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.