Affiliation:
1. Department of Medical Microbiology, College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada
2. International Health Management Associates, Inc., Schaumburg, Illinois, USA
3. AstraZeneca Pharmaceuticals, Waltham, Massachusetts, USA
Abstract
ABSTRACT
The combination of the monobactam aztreonam and the non-β-lactam β-lactamase inhibitor avibactam is currently in clinical development for the treatment of serious infections caused by metallo-β-lactamase (MBL)-producing
Enterobacteriaceae
, a difficult-to-treat subtype of carbapenem-resistant
Enterobacteriaceae
for which therapeutic options are currently very limited. The present study tested clinically significant isolates of
Enterobacteriaceae
(
n
= 51,352) and
Pseudomonas aeruginosa
(
n
= 11,842) collected from hospitalized patients in 208 medical center laboratories from 40 countries from 2012 to 2015 for
in vitro
susceptibility to aztreonam-avibactam, aztreonam, and comparator antimicrobial agents using a standard broth microdilution methodology. Avibactam was tested at a fixed concentration of 4 μg/ml in combination with 2-fold dilutions of aztreonam. The MIC
90
s of aztreonam-avibactam and aztreonam were 0.12 and 64 μg/ml, respectively, for all
Enterobacteriaceae
isolates; >99.9% of all isolates and 99.8% of meropenem-nonsusceptible isolates (
n
= 1,498) were inhibited by aztreonam-avibactam at a concentration of ≤8 μg/ml. PCR and DNA sequencing identified 267
Enterobacteriaceae
isolates positive for MBL genes (NDM, VIM, IMP); all
Enterobacteriaceae
carrying MBLs demonstrated aztreonam-avibactam MICs of ≤8 μg/ml and a MIC
90
of 1 μg/ml. Against all
P. aeruginosa
isolates tested, the MIC
90
of both aztreonam-avibactam and aztreonam was 32 μg/ml; against MBL-positive
P. aeruginosa
isolates (
n
= 452), MIC
90
values for aztreonam-avibactam and aztreonam were 32 and 64 μg/ml, respectively. The current study demonstrated that aztreonam-avibactam possesses potent
in vitro
activity against a recent, sizeable global collection of
Enterobacteriaceae
clinical isolates, including isolates that were meropenem nonsusceptible, and against MBL-positive isolates of
Enterobacteriaceae
, for which there are few treatment options.
Funder
AstraZeneca Pharmaceuticals
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
145 articles.
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