In vitro activity of aztreonam-avibactam against metallo-β-lactamase-producing Enterobacteriaceae - A multicenter study in China Journal Article


Authors: Zhang, B.; Zhu, Z.; Jia, W.; Qu, F.; Huang, B.; Shan, B.; Yu, H.; Tang, Y.; Chen, L.; Du, H.
Article Title: In vitro activity of aztreonam-avibactam against metallo-β-lactamase-producing Enterobacteriaceae - A multicenter study in China
Abstract: Objectives: To study the molecular epidemiology of clinical metallo-β-lactamase (MBL)-producing Enterobacteriaceae isolates in China and to evaluate the antimicrobial susceptibility of MBL-Enterobacteriaceae isolates to aztreonam–avibactam. Methods: Bacterial speciation was determined using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. PCR was used to screen for common carbapenemase genes. Antimicrobial susceptibility testing of common clinical antibiotics and aztreonam–avibactam was performed using the standard broth microdilution method. Results: A total of 161 MBL-Enterobacteriaceae isolates were included, with Klebsiella pneumoniae (n = 73, 45.4%) and Escherichia coli (n = 53, 32.9%) being the most common species. Among the 161 isolates, blaNDM (n = 151), blaIMP (n = 13), and blaVIM (n = 2) were detected, including five strains (3.1%) co-harboring two MBLs. MBL-Enterobacteriaceae isolates frequently contained two (n = 55, 34.2%) or more (n = 89, 55.3%) additional serine β-lactamase genes (blaKPC, blaCTX-M, blaTEM, or blaSHV). Antimicrobial susceptibility testing showed that 81.4% of isolates (n = 131) were resistant to aztreonam. The rates of resistance to cefazolin, ceftazidime, ceftriaxone, cefotaxime, ampicillin–sulbactam, amoxicillin–clavulanic acid, and piperacillin–tazobactam were all over 90%. The addition of avibactam (4 μg/ml) significantly reduced the minimum inhibitory concentrations (MICs) of the aztreonam-resistant isolates by more than 8-fold (range ≤0.125 to 4 μg/ml), with a MIC50/MIC90 of ≤0.125/1 μg/ml among the 131 isolates. Overall, 96.9% (n = 156) of the total isolates were inhibited at an aztreonam–avibactam concentration of ≤1 μg/ml. Univariate and multivariate logistic regression analysis found that in patients with MBL-Enterobacteriaceae infections, the presence of pre-existing lung disease (adjusted odds ratio 8.267, 95% confidence interval 1.925–28.297; p = 0.004) was associated with a hazard effect on worse disease outcomes. Conclusions: The combined use of aztreonam–avibactam is highly potent against MBL-Enterobacteriaceae and may serve as a new candidate for the treatment of infections caused by MBL-Enterobacteriaceae in China. © 2020 The Author(s)
Keywords: adult; treatment outcome; aged; major clinical study; drug potentiation; nonhuman; polymerase chain reaction; lung disease; antifungal agent; in vitro study; bacterial strain; escherichia coli; multivariate logistic regression analysis; bacterium isolate; molecular epidemiology; cre; linezolid; matrix assisted laser desorption ionization time of flight mass spectrometry; univariate analysis; penicillin derivative; antibiotic sensitivity; resistance; china; ceftriaxone; piperacillin plus tazobactam; bacterial gene; antibacterial activity; cefazolin; aminoglycoside; cephalosporin derivative; sultamicillin; ceftazidime; minimum inhibitory concentration; amoxicillin plus clavulanic acid; klebsiella pneumoniae; enterobacteriaceae; carbapenem derivative; quinolone derivative; human; male; female; article; evaluation study; tigecycline; aztreonam; enterobacteriaceae infection; broth dilution; cefotaxime; penicillinase; aztreonam–avibactam; carbapenems; metallo-β-lactamase (mbl); avibactam; carbapenemase producing enterobacteriaceae; extended spectrum beta lactamase producing enterobacteriaceae
Journal Title: International Journal of Infectious Diseases
Volume: 97
ISSN: 1201-9712
Publisher: Elsevier Science, Inc.  
Date Published: 2020-08-01
Start Page: 11
End Page: 18
Language: English
DOI: 10.1016/j.ijid.2020.05.075
PUBMED: 32473388
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 1 July 2020 -- Source: Scopus
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  1. Yi-Wei Tang
    188 Tang