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Can Ceftazidime-Avibactam and Aztreonam Overcome β-Lactam Resistance Conferred by Metallo-β-Lactamases in Enterobacteriaceae?
- Source :
-
Antimicrobial agents and chemotherapy [Antimicrob Agents Chemother] 2017 Mar 24; Vol. 61 (4). Date of Electronic Publication: 2017 Mar 24 (Print Publication: 2017). - Publication Year :
- 2017
-
Abstract
- 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 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 bla <subscript>IMP</subscript> , bla <subscript>NDM</subscript> , bla <subscript>OXA-48</subscript> , bla <subscript>CTX-M</subscript> , bla <subscript>AmpC</subscript> , 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-log <subscript>10</subscript> -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-log <subscript>10</subscript> -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 .<br /> (Copyright © 2017 American Society for Microbiology.)
- Subjects :
- Animals
Colony Count, Microbial
Cyclophosphamide
Drug Administration Schedule
Drug Combinations
Drug Therapy, Combination
Enterobacteriaceae enzymology
Enterobacteriaceae genetics
Enterobacteriaceae growth & development
Enterobacteriaceae Infections microbiology
Female
Gene Expression
Humans
Klebsiella Infections complications
Klebsiella Infections drug therapy
Klebsiella Infections microbiology
Klebsiella pneumoniae drug effects
Klebsiella pneumoniae enzymology
Klebsiella pneumoniae genetics
Klebsiella pneumoniae growth & development
Mice
Microbial Sensitivity Tests
Neutropenia chemically induced
Neutropenia complications
Neutropenia drug therapy
Neutropenia microbiology
Plasmids chemistry
Plasmids metabolism
Soft Tissue Infections complications
Soft Tissue Infections drug therapy
Soft Tissue Infections microbiology
Thigh
beta-Lactam Resistance drug effects
beta-Lactam Resistance genetics
beta-Lactamases genetics
beta-Lactamases metabolism
Anti-Bacterial Agents pharmacology
Azabicyclo Compounds pharmacology
Aztreonam pharmacology
Ceftazidime pharmacology
Enterobacteriaceae drug effects
Enterobacteriaceae Infections drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1098-6596
- Volume :
- 61
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Antimicrobial agents and chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 28167541
- Full Text :
- https://doi.org/10.1128/AAC.02243-16