Antimicrobial Agents and Chemotherapy · 2020 · 19 citations · 21 references
Life SciencesInfectious DiseasesMicrobiologyAntimicrobial ResistanceBacteriologyMedical MicrobiologyAntibacterial ResistanceAntibacterial TherapyAntibiotic ResistanceBeta-lactam ResistanceCarbapenem ResistanceResistance In Gram-positive BacteriaBeta-lactamase InhibitorsCarbapenem AntibioticsCarbapenem-hydrolyzing EnzymesCarbapenemase EnzymesOptimal Treatment RegimesTime-kill AssaysTime-kill Kineticsβ-Lactam Antibiotics
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.
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Identification of acquired antimicrobial resistance genes
Ea Zankari, Henrik Hasman, Salvatore Cosentino et al. · Journal of Antimicrobial Chemotherapy · 2012 · 5.2K citations · Full text
Hesna Yigit, Anne Marie Queenan, Gregory J. Anderson et al. · Antimicrobial Agents and Chemotherapy · 2001 · 1.6K citations · Full text