Affiliation:
1. Department of Medicine, University of Washington and Harborview Medical Center, Seattle, Washington 98104
Abstract
Cefoxitin and cefamandole were evaluated in vitro against 263 organisms. Studies were performed in Mueller-Hinton and nutrient broth and agar employing inoculum sizes of 10
6
and 10
8
organisms per ml. At obtainable serum levels both antibiotics were bactericidal for nearly all strains of
Escherichia coli, Klebsiella, Proteus mirabilis
, and
Staphylococcus aureus
but were inactive against
Pseudomonas aeruginosa
and enterococcus. In agar, cefamandole appeared to be active against most strains of
Enterobacter
and indole-positive
Proteus
, whereas cefoxitin was active against indole-positive
Proteus
but not
Enterobacter
. Moreover, in broth medium most strains of
Enterobacter
were not readily inhibited by either antibiotic and only 40 and 73% of indole-positive
Proteus
were inhibited by 10 μg of cefamandole per ml in Mueller-Hinton and nutrient broth, respectively. However, in both broth media, 10 μg of cefoxitin per ml continued to be inhibitory and bactericidal for most isolates of indole-positive
Proteus
. Cefoxitin also was bactericidal against four cephalothin-resistant strains of
E. coli
. These data suggest that cefoxitin broadens the spectrum of existing cephalosporins by enhancing the activity against indole-positive
Proteus
species as well as some other
Enterobacteriaceae
. On the other hand, with the exception of strains of
Enterobacter aerogenes
, the apparent increased in vitro activity of cefamandole was demonstrated in agar and not in broth.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
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