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Activity of Imipenem-Relebactam and Meropenem-Vaborbactam against Carbapenem-Resistant, SME-Producing Serratia marcescens

Mark Biagi, Aisha Shajee, A. Vialichka, M. Jurkovic, X. Tan, Eric Wenzler

2020Antimicrobial Agents and Chemotherapy19 citationsDOIOpen Access PDF

Abstract

enzyme (SME) is a chromosomally encoded carbapenemase with no known optimal treatment. Various β-lactam/β-lactamase inhibitors and comparators were evaluated against 8 SME producers via broth microdilution. Four isolates were subsequently tested via time-kill analyses. All isolates were resistant to imipenem, imipenem-relebactam, and meropenem but susceptible to ceftazidime, ceftazidime-avibactam, and meropenem-vaborbactam. Ceftazidime, imipenem-relebactam, and meropenem-vaborbactam were bactericidal against 3, 0, and 4 isolates, respectively. Meropenem-vaborbactam may be a potential option for severe SME-producing infections.

Topics & Concepts

Serratia marcescensMeropenemCeftazidime/avibactamMicrobiologyImipenemCarbapenemBroth microdilutionCeftazidimeEnterobacteriaceaeSerratiaAntibacterial agentBiologyMedicineAntibioticsBacteriaAntibiotic resistanceMinimum inhibitory concentrationEscherichia coliPseudomonas aeruginosaPseudomonasGeneGeneticsBiochemistryAntibiotic Resistance in BacteriaVibrio bacteria research studiesPharmaceutical and Antibiotic Environmental Impacts
Activity of Imipenem-Relebactam and Meropenem-Vaborbactam against Carbapenem-Resistant, SME-Producing Serratia marcescens | Litcius