Abstract
Three beta-lactamase inhibitors were combined with ampicillin in a fixed 2:1 ratio. The activity of ampicillin was enhanced by tazobactam and by clavulanic acid, and to a lesser extent by sulbactam when tested against fresh clinical isolates ofEnterobacteriaceae. At a concentration of 8 µg/ml, ampicillin alone inhibited 49.6 % of 2,434 consecutive isolates of enteric bacilli compared to 81 % inhibited by ampicillin combined with tazobactam or clavulanic acid and 69.3 % inhibited by the sulbactam/ampicillin combination. A four-fold or greater reduction in ampicillin MICs was observed in comparable numbers of isolates with all three combinations, but the most marked effects were seen with strains that were highly resistant to ampicillin.
Similar content being viewed by others
References
Aronoff SC, Jacobs MR, Johenning S, Yamabe S: Comparative activities of the beta-lactamase inhibitors YTR 830, sodium clavulanate, and sulbactam combined with amoxicillin or ampicillin. Antimicrobial Agents and Chemotherapy 1984, 26: 580–582.
Fuchs PC, Barry AL, Thornsberry C, Jones RN: In vitro activity of ticarcillin plus clavulanic acid against 632 clinical isolates. Antimicrobial Agents and Chemotherapy 1984, 25: 392–394.
Klastersky J, Van der Auwera P: In vitro activity of sulbactam in combination with various beta-lactam antibiotics. Diagnostic Microbiology and Infectious Disease 1989, 12, Supplement 4: 165–169.
Sawai T, Yamaguchi A: Mechanism of beta-lactamase inhibition: differences between sulbactam and other inhibitors. Diagnostic Microbiology and Infectious Disease 1989, 12, Supplement 4: 121–129.
Gutmann L, Kitzis MD, Yamabe S, Acar JF: Comparative evaluation of a new beta-lactamase inhibitor, YTR 830, combined with different beta-lactam antibiotics against bacteria harboring known beta-lactamases. Antimicrobial Agents and Chemotherapy 1986, 29: 955–957.
Jacobs MR, Aronoff SC, Johenning S, Shlaes DM, Yamabe S: Comparative activities of the beta-lactamase inhibitors YTR 830, clavulanate and sulbactam combined with ampicillin and broad spectrum penicillins against defined beta-lactamase-producing aerobic gram-negative bacilli. Antimicrobial Agents and Chemotherapy 1986, 29: 980–985.
Moosdeen F, Williams JC, Yamabe S: Antibacterial characteristics of YTR 830, a sulfone β-lactamase inhibitor, compared with those of clavulanic acid and sulbactam. Antimicrobial Agents and Chemotherapy 1988, 32: 925–927.
Jones RN, Pfaller MA, Fuchs PC, Aldrige K, Allen SD, Gerlach EH: Piperacillin/tazobactam (YTR 830) combination: comparative antimicrobial activity against 5889 recent aerobic clinical isolates and 60Bacteroides fragilis group strains. Diagnostic Microbiology and Infectious Disease 1989, 12: 489–494.
Weber DA, Saunders CC: Diverse potential of β-lactamase inhibitors to induce class I enzymes. Antimicrobial Agents and Chemotherapy 1990, 34: 156–158.
Eliopoulos GM, Klimm K, Ferraro MJ, Jacoby GA, Moellering RC: Comparative in vitro activity of piperacillin combined with the beta-lactamase inhibitor tazobactam (YTR 830). Diagnostic Microbiology and Infectious Disease 1989, 12: 481–488.
Fass RJ, Prior RB: Comparative in vitro activities of piperacillin-tazobactam and ticarcillin-clavulanate. Antimicrobial Agents and Chemotherapy 1989, 33: 1268–1274.
Jones RN, Barry AL: Studies to optimize the in vitro testing of piperacillin combined with taxobactam (YTR 830). Diagnostic Microbiology and Infectious Disease 1989, 12: 495–510.
Kuck NA, Jacobus NV, Petersen PJ, Weiss WJ, Testa RT: Comparative in vitro and in vivo activities of piperacillin combined with the β-lactamase inhibitors tazobactam, clavulanic acid, and sulbactam. Antimicrobial Agents and Chemotherapy 1989, 33: 1964–1969.
Mehter S, Drabu YJ, Blakemore PH: The in vitro activity of piperacillin/tazobactam, ciprofloxacin, ceftazidime and imipenem against multiple resistant gram-negative bacteria. Journal of Antimicrobial Chemotherapy 1990, 25: 915–919.
National Committee for Clinical Laboratory Standards: Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. Approved Standard M7-A2. NCCLS, Villanova, PA, 1990.
Sanders CC, Iaconis JP, Bodey GP, Samonis G: Resistance to ticarcillin-potassium clavulanate among clinical isolates of the familyEnterobacteriaceae: role of PSE-1 beta-lactamase and high level TEM-1 and SHV-1 and problems with false susceptibility in disk diffusion tests. Antimicrobial Agents and Chemotherapy 1988, 32: 1365–1369.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Pfaller, M., Barry, A., Fuchs, P. et al. Relative efficacy of tazobactam, sulbactam and clavulanic acid in enhancing the potency of ampicillin against clinical isolates ofEnterobacteriaceae . Eur. J. Clin. Microbiol. Infect. Dis. 12, 200–205 (1993). https://doi.org/10.1007/BF01967112
Issue Date:
DOI: https://doi.org/10.1007/BF01967112