Antimicrobial Agents and Chemotherapy · 2022 · 47 citations · 13 references
Life SciencesMicrobiologyPharmacologyAntimicrobial PharmacologyAntimicrobial ResistanceMedical MicrobiologyAntibacterial PharmacologyAntibacterial PharmacotherapyAntibiotic ResistanceBeta-lactam ResistanceCarbapenem ResistanceCombination Antimicrobial TherapyBeta-lactamase InhibitorsCarbapenem AntibioticsCarbapenem-hydrolyzing EnzymesCarbapenem-resistant EnterobacteralesCarbapenemase Enzymes
Novel β-lactam–β-lactamase inhibitor combinations currently approved for clinical use are poorly active against metallo-β-lactamase (MBL)-producing strains. We evaluated the in vitro activity of cefepime-taniborbactam (FTB [formerly cefepime–VNRX-5133]) and comparator agents against carbapenemase-producing Enterobacterales ( n = 247) and carbapenem-resistant Pseudomonas species ( n = 170) clinical isolates prospectively collected from different clinical origins in patients admitted to 8 Spanish hospitals. FTB was the most active agent in both Enterobacterales (97.6% MIC FTB , ≤8/4 mg/L) and Pseudomonas (67.1% MIC FTB , ≤8/4 mg/L) populations.
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Bicyclic Boronate VNRX-5133 Inhibits Metallo- and Serine-β-Lactamases
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