Activity of Aztreonam-Avibactam against Enterobacteriaceae and Pseudomonas aeruginosa Isolated by Clinical Laboratories in 40 Countries from 2012 to 2015.

Antimicrob Agents Chemother 2017 09 24;61(9). Epub 2017 Aug 24.

AstraZeneca Pharmaceuticals, Waltham, Massachusetts, USA.

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 , a difficult-to-treat subtype of carbapenem-resistant for which therapeutic options are currently very limited. The present study tested clinically significant isolates of ( = 51,352) and ( = 11,842) collected from hospitalized patients in 208 medical center laboratories from 40 countries from 2012 to 2015 for 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 MICs of aztreonam-avibactam and aztreonam were 0.12 and 64 μg/ml, respectively, for all isolates; >99.9% of all isolates and 99.8% of meropenem-nonsusceptible isolates ( = 1,498) were inhibited by aztreonam-avibactam at a concentration of ≤8 μg/ml. PCR and DNA sequencing identified 267 isolates positive for MBL genes (NDM, VIM, IMP); all carrying MBLs demonstrated aztreonam-avibactam MICs of ≤8 μg/ml and a MIC of 1 μg/ml. Against all isolates tested, the MIC of both aztreonam-avibactam and aztreonam was 32 μg/ml; against MBL-positive isolates ( = 452), MIC values for aztreonam-avibactam and aztreonam were 32 and 64 μg/ml, respectively. The current study demonstrated that aztreonam-avibactam possesses potent activity against a recent, sizeable global collection of clinical isolates, including isolates that were meropenem nonsusceptible, and against MBL-positive isolates of , for which there are few treatment options.

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http://dx.doi.org/10.1128/AAC.00472-17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571336PMC
September 2017
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