Artículo

Can ceftazidime-avibactam and aztreonam overcome β-lactam resistance conferred by metallo-β-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 Jose Icon; Van Duin, David ; Kreiswirth, Barry N. ; Chambers, Henry F. ; Fowler Jr., Vance G. ; Jacobs, Michael R. ; Pulse, Mark E. ; Weiss, William J. ; Bonomo, Robert A.

Otros responsables

Fecha

04/2017

Editorial

American Society for Microbiology

Revista

Antimicrobial Agents and Chemotherapy

Título del libro

Nombre del evento

Fecha del evento

Institución organizadora

ISSN

0066-4804

eISSN

1098-6596

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

Based upon knowledge of the hydrolytic profile of major β-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-β-lactamases (MBLs). Disk diffusion and agarbased 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.

Colecciones

Aprobación

Revisión

Complementado por

Referenciado por

Licencia Creative Commons

Excepto donde se indique lo contrario, la licencia de este ítem se describe como by