Impact of Acquired Broad Spectrum β-Lactamases on Susceptibility to Novel Combinations Made of β-Lactams (Aztreonam, Cefepime, Meropenem, and Imipenem) and Novel β-Lactamase Inhibitors in Escherichia coli and Pseudomonas aeruginosa

被引:30
作者
Le Terrier, Christophe [1 ,2 ]
Nordmann, Patrice [1 ,3 ,4 ,5 ]
Freret, Charlotte [1 ]
Seigneur, Marion [1 ]
Poirel, Laurent [1 ,3 ]
机构
[1] Univ Fribourg, Fac Sci & Med, Emerging Antibiot Resistance Unit, Med & Mol Microbiol, Fribourg, Switzerland
[2] Univ Hosp Geneva, Div Intens care unit, Geneva, Switzerland
[3] Swiss Natl Reference Ctr Emerging Antibiot Resista, Fribourg, Switzerland
[4] Univ Lausanne, Lausanne, Switzerland
[5] Univ Hosp Ctr, Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
zidebactam; taniborbactam; enmetazobactam; relebactam; vaborbactam; nacubactam; susceptibility testing; beta-lactamase; avibactam;
D O I
10.1128/aac.00339-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The impact of broad-spectrum beta-lactamases on the susceptibility to novel beta-lactamase/beta-lactamase inhibitor combinations was evaluated both in Pseudomonas aeruginosa and Escherichia coli using isogenic backgrounds. Cefepime-zidebactam displayed low MICs, mainly due to the significant intrinsic antibacterial activity of zidebactam. Cefepime-taniborbactam showed excellent activity against recombinant E. coli strains, including metallo-beta-lactamase producers, whereas aztreonam-avibactam remained the best therapeutic option against class B beta-lactamase-producing P. aeruginosa.
引用
收藏
页数:9
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