In vitro comparative activity of the new beta-lactamase inhibitor taniborbactam with cefepime or meropenem against Klebsiella pneumoniae and cefepime against Pseudomonas aeruginosa metallo-beta-lactamase-producing clinical isolates

被引:28
作者
Meletiadis, Joseph [1 ]
Paranos, Paschalis [1 ]
Georgiou, Panagiota-Christina [1 ]
Vourli, Sofia [1 ]
Antonopoulou, Stavroula [2 ]
Michelaki, Aikaterini [2 ]
Vagiakou, Eleni [2 ]
Pournaras, Spyros [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Attikon Univ Hosp, Med Sch, Clin Microbiol Lab, Athens, Greece
[2] Gen Hosp G Gennimatas, Dept Microbiol, Athens, Greece
关键词
beta-lactamase inhibitor; metallo-beta-lactamase-producing isolates; K; pneumoniae; P; aeruginosa; COMBINATION;
D O I
10.1016/j.ijantimicag.2021.106440
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Metallo-beta-lactamase (MBL)-producing Gram-negative bacteria are increasing worldwide and very few agents are active against these pathogens. Taniborbactam (formerly VNRX-5133) is a newly developed bicyclic boronate beta-lactamase inhibitor that directly inhibits all four Ambler classes of beta-lactamases. In the present study the in vitro activity of cefepime or meropenem combined with taniborbactam against 100 Klebsiella pneumoniae and cefepime combined with taniborbactam against 100 Pseudomonas aeruginosa molecularly characterized MBL-producing strains were investigated using ISO standard broth microdilution assays and compared with a panel of antimicrobial agents that are used in clinical practice (amikacin, aztreonam, ciprofloxacin, levofloxacin, gentamicin, piperacillin/tazobactam, imipenem, tigecycline, ceftolozane-tazobactam, cefepime-tazobactam, meropenem-vaborbactam, ceftazidime-avibactam). For K. pneumoniae isolates, the MIC90 values were >= 64 mg/L for all drugs except cefepime-taniborbactam (16 mg/L; 87% inhibited at <= 8/4 mg/L), meropenem-taniborbactam (4 mg/L; 94% inhibited at <= 8/4 mg/L) and tigecycline (8 mg/L), with high levels of resistance (>= 65%) found for all approved comparator antimicrobials tested. For P. aeruginosa, the MIC90 values were >= 64 mg/L for all drugs except aztreonam (32 mg/L), cefepime-taniborbactam (32 mg/L; 88% inhibited at <= 16/4 mg/L) and ciprofloxacin (32 mg/L), with high levels of resistance (>= 73%) for all approved drugs except aztreonam (27%). Taniborbactam reduced cefepime and meropenem MICs by a median 5 and 7 two-fold dilutions to <= 8 mg/L in 87% and 94% of MBL-producing K. pneumoniae isolates, and cefepime MICs by a median 5 two-fold dilutions to <= 16 mg/L in 86% of MBL-producing P. aeruginosa, respectively . The combinations cefepime-taniborbactam and meropenem-taniborbactam are promising alternative treatment options for infections by MBL-producing isolates. (C) 2021 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.
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