Impact of Minor Carbapenemases on Susceptibility to Novel β-Lactam/β-Lactamase Inhibitor Combinations and Cefiderocol in Enterobacterales

被引:8
作者
Sadek, Mustafa [1 ,2 ]
Duran, Juan Bosch [1 ]
Poirel, Laurent [1 ,3 ]
Nordmann, Patrice [1 ,3 ,4 ]
机构
[1] Univ Fribourg, Fac Sci & Med, Med & Mol Microbiol, Fribourg, Switzerland
[2] South Valley Univ, Fac Vet Med, Dept Food Hyg & Control, Qena, Egypt
[3] Univ Fribourg, Swiss Natl Reference Ctr Emerging Antibiot Resista, Fribourg, Switzerland
[4] Univ Lausanne, Univ Hosp Ctr, Inst Microbiol, Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
minor carbapenemases; SME; Enterobacterales; imipenem-relebactam; FRI; NMC-A; carbapenemase;
D O I
10.1128/aac.00078-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The in vitro activity of imipenem-relebactam, meropenem-vaborbactam, ceftazidime-avibactam, and cefiderocol was evaluated against both clinical and isogenic enterobacterial isolates producing carbapenemases of the SME, NmcA, FRI, and IMI types. Ceftazidime-avibactam and meropenem-vaborbactam showed the highest activity against all tested isolates; imipenem-relebactam showed only moderate activity. All isolates remained susceptible to cefiderocol. Furthermore, avibactam and vaborbactam have greater inhibitory activity than relebactam against the tested carbapenemases. Overall, ceftazidime-avibactam, meropenem-vaborbactam, and cefiderocol were the most effective therapeutic options for treating infections caused by the tested minor carbapenemase producers.
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页数:5
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