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Changes in the Frequencies of β-Lactamase Genes among Enterobacteriaceae Isolates in U.S. Hospitals, 2012 to 2014: Activity of Ceftazidime-Avibactam Tested against β-Lactamase-Producing Isolates
Author(s) -
Mariana Castanheira,
Rodrigo E. Mendes,
Ronald N. Jones,
Hélio S. Sader
Publication year - 2016
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.00540-16
Subject(s) - klebsiella pneumoniae , enterobacteriaceae , microbiology and biotechnology , ceftazidime/avibactam , ceftazidime , biology , carbapenem , escherichia coli , beta lactamase , carbapenem resistant enterobacteriaceae , gene , antibiotics , bacteria , pseudomonas aeruginosa , genetics
Among 15,588Enterobacteriaceae isolates collected in 63 U.S. hospitals from 2012 to 2014, 2,129 (13.7%) displayed an extended-spectrum β-lactamase (ESBL) phenotype. These rates were similar over time (13.2 to 13.9%); however, differences amongEscherichia coli (12.7 and 15.1% in 2012 and 2014;P = 0.007) andKlebsiella pneumoniae (18.9 and 15.5% in 2012 and 2014;P = 0.006) were noted when comparing 2014 and 2012. Carbapenem-resistantEnterobacteriaceae (CRE) (2.3 and 1.8%) and carbapenem-resistantK. pneumoniae (6.8 and 5.1%;P = 0.003) rates were lower in 2014 than in 2012. Isolates carryingbla CTX-M-15 -like genes were stable (42.1 to 42.4%), but a decrease amongE. coli isolates (59.1 and 49.7%;P = 0.008) and an increase amongK. pneumoniae isolates (32.7 and 41.2%;P = 0.022) in 2014 were observed. Isolates carryingbla KPC (304) decreased over the years (16.5 and 10.9%;P = 0.008), mainly due to the decrease inK. pneumoniae isolates harboringbla KPC (n = 285; 35.6 and 28.4%;P = 0.041) in hospitals in the Mid-Atlantic and South Atlantic regions, where these isolates were highly prevalent during 2012 and 2013. Isolates carryingbla CMY-2- like andbla CTX-M-14- like genes increased (8.2 and 11.9% and 9.1 and 12.9%, respectively;P = 0.04 for both), and those producingbla SHV ESBL decreased (24.9 and 12.7%;P < 0.001) over the studied years, due to a decreased occurrence of the enzymes amongK. pneumoniae isolates. Other enzymes were detected in smaller numbers of isolates, including fourK. pneumoniae isolates carryingbla NDM-1 metallo-β-lactamase (two in 2012 and two in 2014). Ceftazidime-avibactam, a recently approved β-lactamase inhibitor combination, was very active against the ESBL phenotype isolates (MIC50/90 , 0.12 and 1 μg/ml; 99.7% susceptible) and CRE strains (MIC50/90 , 0.5 and 2 μg/ml; 98.5% susceptible) that displayed elevated MIC values for many comparator agents. In conclusion, significant changes were noted in the frequencies of isolates harboring various β-lactamases among U.S. hospitals between 2012 and 2014 that will require continued monitoring.

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