Abstract
The susceptibility of 53 clinical isolates of Bacteroides fragilis to cephamycins was examined. Judging from the MICs for 50% of the strains tested, moxalactam was the most active, however, judging from the MICs for 90% of the strains tested, cefbuperazone was more effective than moxalactam. A correlation was observed between in vitro activity of benzylpenicillin and cephaloridine and beta-lactamase production. Inactivation due to enzymatic hydrolysis of cephamycins over a short time was not observed; however, inactivation was detected by a double disk diffusion test, and moxalactam was most easily inactivated. We conclude that inactivation due to enzymatic hydrolysis of cephamycins over a long time may play an important role in resistance to some cephamycins in strains of B. fragilis.
MeSH Terms
Bacteroides fragilis/drug effects,enzymology
Cephalosporins/metabolism,pharmacology
Cephamycins/metabolism,pharmacology
Clavulanic Acid
Clavulanic Acids/pharmacology
Hydrolysis
Microbial Sensitivity Tests
Moxalactam/pharmacology
Penicillin G/pharmacology
beta-Lactamase Inhibitors
beta-Lactamases/metabolism
Chemicals
Cephalosporins
Cephamycins
Clavulanic Acids
beta-Lactamase Inhibitors
Clavulanic Acid
beta-Lactamases
Penicillin G
Moxalactam
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Yotsuji A
Minami S
Kakizawa H
Yasuda T
Takai A
Saikawa I
Inoue M
Mitsuhashi S
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