Activity of Cefepime in Combination with the Novel β-Lactamase Inhibitor Taniborbactam (VNRX-5133) against Extended-Spectrum-β-Lactamase-Producing Isolates in In Vitro Checkerboard Assays

Extended-spectrum-beta-lactamase (ESBL)-producing strains are increasing worldwide, limiting therapeutic options. Taniborbactam (VNRX-5133) is a newly developed beta-lactamase inhibitor with a wide spectrum of activity covering both serine and metallo enzymes. We therefore evaluated cefepime-taniborbactam activity against ESBL-producing isolates and determined the concentrations to be used in MIC determinations in the clinical laboratory. The in vitro activity of cefepime (0.06 to 256 mg liter(-1)) combined with taniborbactam (0.03 to 32 mg liter(-1)) against 129 clinically and molecularly well-documented ESBL-producing isolates (42 Escherichia toll, 39 Klebsiella pneumoniae, 28 Pseudomonas aeruginosa, 16 Enterobacter cloacae, 2 Citrobacter freundil, and 2 Enterobacter aerogenes) was tested with a broth microdilution checkerboard method based on the ISO standard. The MICs of cefepime alone and in combination, together with percentage resistance at different concentrations of taniborbactam, were calculated for each species and resistance mechanism. The median (range)/MIC9, of cefepime was 32 (0.125 to 256)/256 mg liter' for all Enterobacterales isolates (n =101), with 72% being resistant, and 32 (8 to 256)/128 mg liter(-1) for the 28 P. aeruginosa isolates, with 86% being resistant. The median (range)/90th percentile concentration of taniborbactam required to restore Enterobacterales susceptibility to cefepime (MIC <= 1 mg liter(-1)) was 0.06 (<0.03 to 32)/4 mg liter(-1) and P. aeruginosa susceptibility to increased exposure to cefepime (MIC s8 mg liter(-1)) 1 (0.032 to 32)/32 mg liter(-1). At a fixed concentration of 4 mg liter(-1) of taniborbactam, cefepime median (range)/MIC90 were reduced to 0.125 (0.06 to 4)/1 mg liter(-1) for Enterobacterales with no resistant isolates found, and to 8 (2 to 64)/16 mg liter(-1) for P. aeruginosa isolates, where 36% remained resistant. The combination cefepime-taniborbactam demonstrated a potent activity against ESBL isolates, restoring susceptibility of all Enterobacterales and two-thirds of P. aeruginosa isolates.

Automated summary

The combination of taniborbactam and cefepime showed potent activity against ESBL-producing strains, restoring susceptibility in all Enterobacterales and two-thirds of P. aeruginosa isolates.