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Relative Inhibitory Activities of the Broad-spectrum β-lactamase Inhibitor Xeruborbactam in Comparison with Taniborbactam Against Metallo-β-lactamases Produced in and

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Abstract

Xeruborbactam is a newly developed β-lactamase inhibitor designed for metallo-β-lactamases (MBLs). This study assessed the relative inhibitory properties of this novel inhibitor in comparison with another MBL inhibitor, namely taniborbactam (TAN), against a wide range of acquired MBL produced either in or . As observed with taniborbactam, the combination of xeruborbactam (XER) with β-lactams, namely, ceftazidime, cefepime and meropenem, led to significantly decreased MIC values for a wide range of B1-type MBL-producing , including most recombinant strains producing NDM, VIM, IMP, GIM-1, and DIM-1 enzymes. Noteworthily, while TAN-based combinations significantly reduced MIC values of β-lactams for MBL-producing recombinant strains, those with XER were much less effective. We showed that this latter feature was related to the MexAB-OprM efflux pump significantly impacting MIC values when testing XER-based combinations in . The relative inhibitory concentrations (IC values) were similar for XER and TAN against NDM and VIM enzymes. Noteworthily, XER was effective against NDM-9, NDM-30, VIM-83, and most of IMP enzymes, although those latter enzymes were considered resistant to TAN. However, no significant inhibition was observed with XER against IMP-10, SPM-1, and SIM-1 as well as the representative subclass B2 and B3 enzymes, PFM-1 and AIM-1. The determination of the constant inhibition () of XER revealed a much higher value against IMP-10 than against NDM-1, VIM-2, and IMP-1. Hence, IMP-10 that differs from IMP-1 by a single amino-acid substitution (Val67Phe) can, therefore, be considered resistant to XER.

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References
1.
Lomovskaya O, Tsivkovski R, Nelson K, Rubio-Aparicio D, Sun D, Totrov M . Spectrum of Beta-Lactamase Inhibition by the Cyclic Boronate QPX7728, an Ultrabroad-Spectrum Beta-Lactamase Inhibitor of Serine and Metallo-Beta-Lactamases: Enhancement of Activity of Multiple Antibiotics against Isogenic Strains Expressing Single.... Antimicrob Agents Chemother. 2020; 64(6). PMC: 7269471. DOI: 10.1128/AAC.00212-20. View

2.
Nordmann P, Poirel L . Epidemiology and Diagnostics of Carbapenem Resistance in Gram-negative Bacteria. Clin Infect Dis. 2019; 69(Suppl 7):S521-S528. PMC: 6853758. DOI: 10.1093/cid/ciz824. View

3.
Alkasaby N, Zaki M . Molecular Study of Isolates for Metallo--Lactamases and Extended-Spectrum--Lactamases Genes in Intensive Care Unit, Mansoura University Hospital, Egypt. Int J Microbiol. 2017; 2017:3925868. PMC: 5439075. DOI: 10.1155/2017/3925868. View

4.
LaCuran A, Pegg K, Liu E, Bethel C, Ai N, Welsh W . Elucidating the Role of Residue 67 in IMP-Type Metallo-β-Lactamase Evolution. Antimicrob Agents Chemother. 2015; 59(12):7299-307. PMC: 4649200. DOI: 10.1128/AAC.01651-15. View

5.
Masuda N, Sakagawa E, Ohya S, Gotoh N, Tsujimoto H, Nishino T . Substrate specificities of MexAB-OprM, MexCD-OprJ, and MexXY-oprM efflux pumps in Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2000; 44(12):3322-7. PMC: 90200. DOI: 10.1128/AAC.44.12.3322-3327.2000. View