Comparison of antimicrobial activity between ceftolozane–tazobactam and ceftazidime–avibactam against multidrug-resistant isolates of Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa

Abstract

ObjectiveThis study compared the activity of ceftolozane–tazobactam and ceftazidime–avibactam against 120 bacterial strains, including extended-spectrum beta-lactamase (ESBL) producers, carbapenem-resistant Enterobacteriaceae (CRE), and Pseudomonas aeruginosa, isolated from patients admitted to Cleveland Clinic Abu Dhabi, United Arab Emirates. MethodsIn vitro susceptibility was tested using the Etest strip minimum inhibitory concentration (MIC) method, and PCR was used to characterize the carbapenemase enzymes produced by CRE strains. ResultsAll 29 ESBL isolates were susceptible to ceftazidime–avibactam (MIC50 0.125μg/ml), whereas all but one were susceptible to ceftolozane–tazobactam (MIC50 0.38μg/ml). Twenty-seven (45%) CRE isolates were susceptible to ceftazidime–avibactam (MIC50 ≥256μg/ml), whereas only six (10%) isolates were susceptible to ceftolozane–tazobactam (MIC50 ≥256μg/ml). Very few NDM-1 isolates were susceptible to ceftazidime–avibactam, whereas the majority of OXA-48 isolates were susceptible. Twenty-nine (94%) P. aeruginosa isolates were susceptible to ceftazidime–avibactam (MIC50 1.5μg/ml), whereas 30 (97%) isolates were susceptible to ceftolozane–tazobactam (MIC50 0.75μg/ml). ConclusionsCeftolozane–tazobactam and ceftazidime–avibactam showed comparable activity against ESBL and P. aeruginosa, with ceftazidime–avibactam having lower MICs against ESBL isolates and ceftolozane–tazobactam having lower MICs against P. aeruginosa. Ceftazidime–avibactam showed better activity against all CRE isolates except for those carrying the NDM-1 enzyme.