Examining the activity of cefepime-taniborbactam against Burkholderia cepacia complex and Burkholderia gladioli isolated from cystic fibrosis patients in the United States

被引:1
作者
Mojica, Maria F. [1 ,2 ,3 ]
Zeiser, Elise T. [2 ]
Becka, Scott A. [2 ]
Lipuma, John J. [4 ]
Six, David A. [5 ]
Moeck, Greg [5 ]
Papp-Wallace, Krisztina M. [2 ,6 ,7 ]
机构
[1] Case Western Reserve Univ, Dept Mol Biol & Microbiol, Cleveland, OH USA
[2] Vet Affairs Northeast Ohio Healthcare Syst, Res Serv, Cincinnati, OH 44106 USA
[3] CASE VA Ctr Antimicrobial Resistance & Epidemiol, Cleveland, OH 44106 USA
[4] Univ Michigan, Ann Arbor, MI USA
[5] Venatorx Pharmaceut Inc, Malyern, PA USA
[6] Case Western Reserve Univ, Dept Med, Cleveland, OH 44106 USA
[7] Case Western Reserve Univ, Dept Biochem, Cleveland, OH 44106 USA
关键词
beta-lactamases; Burkholderia; beta-lactam; PenA; carbapenemase; beta-lactamase inhibitor; cefepime-taniborbactam; BETA-LACTAMASES; RESISTANCE; CEFEPIME/TANIBORBACTAM; SUSCEPTIBILITY; COMBINATION; CEFTAZIDIME; PSEUDOMONAS; VNRX-5133;
D O I
10.1128/aac.00498-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The novel clinical-stage beta-lactam-beta-lactamase inhibitor combination, cefepime-taniborbactam, demonstrates promising activity toward many Gram-negative bacteria producing class A, B, C, and/or D beta-lactamases. We tested this combination against a panel of 150 Burkholderia cepacia complex (Bcc) and Burkholderia gladioli strains. The addition of taniborbactam to cefepime shifted cefepime minimum inhibitory concentrations toward the provisionally susceptible range in 59% of the isolates tested. Therefore, cefepime-taniborbactam possessed similar activity as first-line agents, ceftazidime and trimethoprim-sulfamethoxazole, supporting further development.
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页数:7
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