Comparative Activities of Clavulanic Acid, Sulbactam, and Tazobactam Against Clinically Important Beta-lactamases
Overview
Authors
Affiliations
Clavulanic acid, sulbactam, and tazobactam are inhibitors of a variety of plasmid-mediated beta-lactamases. However, inhibition data for these three inhibitors with a wide range of different plasmid-mediated beta-lactamases have not yet been compared under the same experimental conditions. A number of groups have inferred that clavulanic acid inhibits extended-spectrum TEM and SHV beta-lactamases, but inhibition data have rarely been published. In this study, the 50% inhibitory concentrations of these three beta-lactamase inhibitors for 35 plasmid-mediated beta-lactamases have been determined. Of these 35 beta-lactamases, 20 were extended-spectrum TEM- or SHV-derived beta-lactamases. The other 15 enzymes were conventional-spectrum beta-lactamases such as TEM-1 and SHV-1. Clavulanic acid was a more potent inhibitor than sulbactam for 32 of the 35 plasmid-mediated beta-lactamases tested. In particular, clavulanic acid was 60 and 580 times more potent than sulbactam against TEM-1 and SHV-1, respectively, currently the two most clinically prevalent gram-negative plasmid-mediated beta-lactamases. Statistical analysis of the data of the 50% inhibitory concentrations showed that clavulanic acid was 20 times more active overall than sulbactam against the conventional-spectrum enzymes. In addition, clavulanic acid was 14 times more potent than sulbactam at inhibiting the extended-spectrum enzymes. Tazobactam also showed significantly greater activity than sulbactam against the two groups of beta-lactamases. There were no significant differences between the overall activities of tazobactam and clavulanic acid against the extended-spectrum TEM and SHV enzymes and conventional-spectrum enzymes, although differences in their inhibition profiles were observed.
Reeder J, OSullivan C, Xu M, Wu N, Ince D, Rogers W Antimicrob Agents Chemother. 2023; 67(4):e0124822.
PMID: 36920230 PMC: 10112153. DOI: 10.1128/aac.01248-22.
Zhang J, Wu M, Diao S, Zhu S, Song C, Yue J Pharmaceutics. 2023; 15(1).
PMID: 36678879 PMC: 9865866. DOI: 10.3390/pharmaceutics15010251.
Haines R, Putsathit P, Hammer K, Tai A Sci Rep. 2022; 12(1):16814.
PMID: 36207358 PMC: 9547053. DOI: 10.1038/s41598-022-21101-x.
Mithin U, Buragohain R, Das P, Mandal T, Hansda R, Joardar S ADMET DMPK. 2022; 10(3):180-196.
PMID: 36131891 PMC: 9484700. DOI: 10.5599/admet.1170.
A review on the mechanistic details of OXA enzymes of ESKAPE pathogens.
Avci F, Tastekil I, Jaisi A, Sarica P, Sariyar Akbulut B Pathog Glob Health. 2022; 117(3):219-234.
PMID: 35758005 PMC: 10081068. DOI: 10.1080/20477724.2022.2088496.