Abstract
Treatment options for multidrug-resistant Gram-negative infections are scarce and therefore alternatives with a narrow spectrum or new agents are sought. Antimicrobial susceptibility to temocillin, mecillinam, ceftazidime, and ceftazidime/avibactam was determined using Etest and disk diffusion according to European Committee on Antimicrobial Susceptibility Testing (EUCAST) methodology. A total of 77 carbapenem-nonsusceptible Enterobacteriaceae were studied, including Klebsiella pneumoniae (26 %), Escherichia coli (26 %), Enterobacter cloacae (26 %), and Enterobacter aerogenes (22 %). Several phenotypic tests, PCRs followed by sequencing and a microbiological bioassay excluded carbapenemase production in all isolates. Antimicrobial susceptibility rates were low for temocillin (15.6 %, minimum inhibitory concentration [MIC] range 2 to >1,024 μg/ml), moderate for mecillinam (59.7 %, MIC range 0.25 to >256 μg/ml), and excellent for ceftazidime/avibactam (100 %, zone diameter range 19 to 32 mm, median 25 mm). 5.2 % of the isolates were susceptible to ceftazidime alone (zone diameter range 6 to 32 mm). In this study, mecillinam exhibited moderate and ceftazidime/avibactam excellent in vitro antimicrobial activity against carbapenem-nonsusceptible Enterobacteriaceae without carbapenemase production. Ceftazidime/avibactam was able to restore previously reduced susceptibility to ceftazidime in all isolates, thus potentiating its activity. Temocillin only exhibited low in vitro antimicrobial activity against the isolates. Further evaluation of mecillinam and ceftazidime/avibactam with regard to the potential clinical utility against infections caused by these pathogens has to be performed.
Original language | English |
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Journal | European Journal of Clinical Microbiology and Infectious Diseases |
Volume | 34 |
Issue number | 12 |
Pages (from-to) | 2429-2437 |
Number of pages | 9 |
ISSN | 0934-9723 |
DOIs | |
Publication status | Published - 01.12.2015 |
Research Areas and Centers
- Academic Focus: Center for Infection and Inflammation Research (ZIEL)