In Vitro Activity of Ceftibuten/VNRX-5236 against Urinary Tract Infection Isolates of Antimicrobial-Resistant Enterobacterales

被引:8
作者
Karlowsky, James A. [1 ,2 ]
Hackel, Meredith A. [1 ]
Sahm, Daniel F. [1 ]
机构
[1] IHMA, Schaumburg, IL 60173 USA
[2] Univ Manitoba, Max Rady Coll Med, Dept Med Microbiol & Infect Dis, Winnipeg, MB, Canada
基金
美国国家卫生研究院;
关键词
VNRX-5236; VNRX-7145; ceftibuten; urinary tract infection; oral therapy; Enterobacterales;
D O I
10.1128/AAC.01304-21
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Ceftibuten/VNRX-7145 is a cephalosporin/boronate beta-lactamase inhibitor combination under development as an oral treatment for complicated urinary tract infections caused by Enterobacterales producing serine beta-lactamases (Ambler class A, C, and D). In vivo, VNRX-7145 (VNRX-5236 etzadroxil) is cleaved to the active inhibitor, VNRX-5236. We assessed the in vitro activity of ceftibuten/VNRX-5236 against 1,066 urinary isolates of Enterobacterales from a 2014-2016 global culture collection. Each isolate tested was preselected to possess a multidrug-resistant (MDR) phenotype that included nonsusceptibility to amoxicillin-clavulanate and resistance to levofloxacin. MICs were determined by CLSI broth microdilution. VNRX-5236 was tested at a fixed concentration of 4 mu g/ml. Ceftibuten/VNRX-5236 inhibited 90% of all isolates tested (MIC90) at 2 mu g/ml; MIC(90)s for ESBL-(n = 566), serine carbapenemase-(n = 116), and acquired AmpC-positive (n = 58) isolate subsets were <= 0.25, >32, and 8 mu g/ml, respectively. At concentrations of <= 1, <= 2, and <= 4 mu g/ml, ceftibuten/VNRX-5236 inhibited 89.1, 91.7, and 93.1% of all isolates tested; 96.5, 97.7, and 98.4% of ESBL-positive isolates; 75.9, 81.9, and 81.9% of serine carbapenemase-positive isolates; and 70.7, 81.0, and 87.9% of acquired AmpC-positive isolates. Ceftibuten/VNRX-5236 at concentrations of <= 1, <= 2, and <= 4 mu g/ml inhibited 85-89, 89-91, and 91-92% of isolates that were not susceptible (defined by CLSI and EUCAST breakpoint criteria) to nitrofurantoin, trimethoprim-sulfamethoxazole, and/or fosfomycin, (as part of their MDR phenotype), oral agents commonly prescribed to treat uncomplicated urinary tract infections. The potency of ceftibuten/VNRX-5236 (MIC90, 2 mu g/ml) was similar (within one doubling-dilution) to intravenous-only agents ceftazidime-avibactam (MIC90 2 mu g/ml) and meropenem-vaborbactam (MIC90 1 mu g/ml). Continued investigation of ceftibuten/VNRX-5236 is warranted.
引用
收藏
页数:13
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