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Can Ceftazidime-Avibactam and Aztreonam Overcome ß-Lactam Resistance Conferred by Metallo-ß-Lactamases in Enterobacteriaceae?
Marshall, Steven; Hujer, Andrea M; Rojas, Laura J; Papp-Wallace, Krisztina M; Humphries, Romney M; Spellberg, Brad; Hujer, Kristine M; Marshall, Emma K; Rudin, Susan D; Perez, Federico; Wilson, Brigid M; Wasserman, Ronald B; Chikowski, Linda; Paterson, David L; Vila, Alejandro J; van Duin, David; Kreiswirth, Barry N; Chambers, Henry F; Fowler, Vance G; Jacobs, Michael R; Pulse, Mark E; Weiss, William J; Bonomo, Robert A.
Afiliação
  • Marshall S; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Hujer AM; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Rojas LJ; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Papp-Wallace KM; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Humphries RM; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Spellberg B; Department of Molecular Biology and Microbiology, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Hujer KM; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Marshall EK; Department of Pathology and Laboratory Medicine, University of California, Los Angeles, Los Angeles, California, USA.
  • Rudin SD; Division of Infectious Diseases, Keck School of Medicine at USC and the Los Angeles County-USC Medical Center, Los Angeles, California, USA.
  • Perez F; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Wilson BM; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Wasserman RB; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Chikowski L; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Paterson DL; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Vila AJ; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • van Duin D; Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.
  • Kreiswirth BN; Louis Stokes Cleveland Department of Veterans Affairs Medical Center, Cleveland, Ohio, USA.
  • Chambers HF; Infectious Disease Doctors Medical Group, Walnut Creek, California, USA.
  • Fowler VG; John Muir Health, Walnut Creek, California, USA.
  • Jacobs MR; The University of Queensland, UQ Centre for Clinical Research, Brisbane, Queensland, Australia.
  • Pulse ME; Instituto de Biología Molecular y Celular de Rosario Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina, Universidad Nacional de Rosario, Rosario, Argentina.
  • Weiss WJ; Division of Infectious Diseases, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Bonomo RA; Public Health Research Institute Center, New Jersey Medical School-Rutgers University, Newark, New Jersey, USA.
Article em En | MEDLINE | ID: mdl-28167541
ABSTRACT
Based upon knowledge of the hydrolytic profile of major ß-lactamases found in Gram-negative bacteria, we tested the efficacy of the combination of ceftazidime-avibactam (CAZ-AVI) with aztreonam (ATM) against carbapenem-resistant enteric bacteria possessing metallo-ß-lactamases (MBLs). Disk diffusion and agar-based antimicrobial susceptibility testing were initially performed to determine the in vitro efficacy of a unique combination of CAZ-AVI and ATM against 21 representative Enterobacteriaceae isolates with a complex molecular background that included blaIMP, blaNDM, blaOXA-48, blaCTX-M, blaAmpC, and combinations thereof. Time-kill assays were conducted, and the in vivo efficacy of this combination was assessed in a murine neutropenic thigh infection model. By disk diffusion assay, all 21 isolates were resistant to CAZ-AVI alone, and 19/21 were resistant to ATM. The in vitro activity of CAZ-AVI in combination with ATM against diverse Enterobacteriaceae possessing MBLs was demonstrated in 17/21 isolates, where the zone of inhibition was ≥21 mm. All isolates demonstrated a reduction in CAZ-AVI agar dilution MICs with the addition of ATM. At 2 h, time-kill assays demonstrated a ≥4-log10-CFU decrease for all groups that had CAZ-AVI with ATM (8 µg/ml) added, compared to the group treated with CAZ-AVI alone. In the murine neutropenic thigh infection model, an almost 4-log10-CFU reduction was noted at 24 h for CAZ-AVI (32 mg/kg every 8 h [q8h]) plus ATM (32 mg/kg q8h) versus CAZ-AVI (32 mg/kg q8h) alone. The data presented herein require us to carefully consider this new therapeutic combination to treat infections caused by MBL-producing Enterobacteriaceae.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aztreonam / Ceftazidima / Enterobacteriaceae / Infecções por Enterobacteriaceae / Compostos Azabicíclicos / Antibacterianos Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aztreonam / Ceftazidima / Enterobacteriaceae / Infecções por Enterobacteriaceae / Compostos Azabicíclicos / Antibacterianos Idioma: En Ano de publicação: 2017 Tipo de documento: Article