An evaluation of the bacteriolytic and biochemical properties of ceftiolene (42980RP)
- 1 December 1984
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Antimicrobial Chemotherapy
- Vol. 14 (6) , 581-593
- https://doi.org/10.1093/jac/14.6.581
Abstract
Ceftiolene (42980RP) is a new cephalosporin with a broad antibacterial spectrum similar to cefotaxime or ceftriaxone. The characteristics of ceftiolene have been tested in a variety of assays involving various biochemical aspects of the mode of action of β-lactam antibiotics. The affinities of ceftiolene for penicillin-binding proteins were very comparable with those of ceftriaxone and cefotaxime for Escherichia coli, and generally greater than those of latamoxef (moxalactam) for the higher molecular weight PBPs of E. coli. Enterobacter cloacae. Proteus mirabilis and Pseudomonas aeruginosa. The affinity of ceftiolene for PBP1 of Staphylococcus aureus was greater than those of cefotaxime or latamoxef, but comparable with these antibiotics for PBP3. The bacteriolytic activity of ceftiolene at defined concentrations against Gram-negative organisms was similar to that of ceftriaxone, and significantly better than that of the other third-generation cephalosporins tested. Introduction of plasmid-encoded β-lactamases into E. coli reduced the wide variation in bacteriolytic effect of the different cephalosporins, and a significant inoculum effect was observed for the bacteriolysis. Chloramphenicol was less antagonistic against ceftiolene- or ceftriaxone-induced lysis than was observed for cefotaxime or latamoxef. Growth of Staph. aureus at low concentrations of ceftiolene caused the bacteria to become more sensitive to lysis by lysostaphin than organisms grown with cefotaxime or latamoxef under the same conditions. These observations confirm the necessity to use techniques other than routine MIC determinations to distinguish between antibiotics which would otherwise appear very similar.Keywords
This publication has 13 references indexed in Scilit:
- Mode of action of azthreonamAntimicrobial Agents and Chemotherapy, 1982
- Induction of cell lysis in Escherichia coli: cooperative effect of nocardicin A and mecillinamAntimicrobial Agents and Chemotherapy, 1982
- The Role of Penicillin‐Binding Proteins in the Action of Cephalosporins against Escherichia coli and Salmonella typhimuriumEuropean Journal of Biochemistry, 1981
- Activity of a new cephalosporin antibiotic, Ro 13-9904 against dense populations of selected enterobacteriaAntimicrobial Agents and Chemotherapy, 1981
- Alteration of Escherichia coli murein during amino acid starvationJournal of Bacteriology, 1980
- Lethal Effect of a Heterologous Murein Hydrolase on Penicillin-Treated Streptococcus sanguisAntimicrobial Agents and Chemotherapy, 1980
- Affinities of penicillins and cephalosporins for the penicillin-binding proteins of Escherichia coli K-12 and their antibacterial activityAntimicrobial Agents and Chemotherapy, 1979
- Modification of Peptidoglycan Structure by Penicillin Action in Cell Walls of Proteus mirabilisEuropean Journal of Biochemistry, 1979
- Solubilization and Isolation of the Membrane-Bound dd-Carboxypeptidase of Streptococcus faecalis ATCC 9790. Properties of the Purified EnzymeEuropean Journal of Biochemistry, 1978
- Properties of the Penicillin‐Binding Proteins of Escherichia coli K12European Journal of Biochemistry, 1977