Comparative in vitro activity of SM7338, a new carbapenem antimicrobial agent
Open Access
- 1 August 1989
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 33 (8) , 1232-1236
- https://doi.org/10.1128/aac.33.8.1232
Abstract
The comparative in vitro activity of SM7338 was tested against 670 routine clinical isolates and 130 cefoperazone-resistant isolates of bacteria by agar dilution methods. SM7338 was at least as active as imipenem against gram-negative organisms but was slightly less active against gram-positive organisms. SM7338 was particularly active against members of the family Enterobacteriaceae, with MICs for 90% of strains of less than or equal to 0.125 micrograms/ml for all species tested. Differences in activity between SM7338 and imipenem were particularly striking against Proteus vulgaris, Proteus mirabilis, and Morganella morganii, against which MICs of SM7338 and imipenem for 90% of strains were 0.125 and 4 micrograms/ml, respectively. The presence of unique plasmid-mediated beta-lactamases in Pseudomonas aeruginosa PU21 transconjugants did not affect activity substantially, except in the case of OXA-2 (eightfold-increased MIC) and OXA-3 (fourfold-increased MIC). SM7338 was also active against a laboratory-derived strain of P. aeruginosa which hyperproduced chromosomal beta-lactamase, inhibiting both the wild type and the mutant at a concentration of 1.0 micrograms/ml.This publication has 8 references indexed in Scilit:
- Type I -Lactamases of Gram-Negative Bacteria: Interactions with -Lactam AntibioticsThe Journal of Infectious Diseases, 1986
- New plasmid-mediated oxacillin-hydrolyzing β-lactamase in Pseudomonas aeruginosaJournal of Antimicrobial Chemotherapy, 1986
- Properties of a novel carbenicillin-hydrolyzing beta-lactamase (CARB-4) specified by an IncP-2 plasmid from Pseudomonas aeruginosaAntimicrobial Agents and Chemotherapy, 1986
- Five novel plasmid-determined beta-lactamasesAntimicrobial Agents and Chemotherapy, 1985
- Effects of azlocillin in combination with clavulanic acid, sulbactam, and N-formimidoyl thienamycin against beta-lactamase-producing, carbenicillin-resistant Pseudomonas aeruginosaAntimicrobial Agents and Chemotherapy, 1982
- In-vitro activity of Sch 29482 in comparison with other oral antibioticsJournal of Antimicrobial Chemotherapy, 1982
- Susceptibility of enterococci and Listeria monocytogenes to N-Formimidoyl thienamycin alone and in combination with an aminoglycosideAntimicrobial Agents and Chemotherapy, 1981