In vitro susceptibility of Mycobacterium fortuitum to N-formimidoyl thienamycin and several cephamycins
- 1 December 1982
- journal article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 22 (6), 1079-1081
- https://doi.org/10.1128/aac.22.6.1079
Abstract
The comparative in vitro activity of N-formimidoyl thienamycin, cefmetazole, cefoxitin, cefotetan (YM-09330), and moxalactam against 13 isolates of Mycobacterium fortuitum was evaluated by agar dilution susceptibility testing. N-Formimidoyl thienamycin inhibited 10 to 12 strains at 6.25 micrograms/ml, cefmetazole inhibited 12 of 13 strains at 12.5 micrograms/ml, cefoxitin inhibited 11 of 13 strains at 25 micrograms/ml, and cefotetan inhibited 11 of 13 strains at 50 micrograms/ml. Moxalactam was less active than the other compounds tested, inhibiting only 9 of 13 strains at 50 micrograms/ml.Keywords
This publication has 3 references indexed in Scilit:
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- Description and classification of the newer cephalosporins and their relationships with the established compoundsJournal of Antimicrobial Chemotherapy, 1979
- Susceptibility of Organisms in the Mycobacterium fortuitum Complex to Antituberculous and Other Antimicrobial AgentsAntimicrobial Agents and Chemotherapy, 1977