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Antimicrobial Agents and Chemotherapy, 05 1997, 1037-1041, Vol 41, No. 5
LM Ednie, SK Spangler, MR Jacobs and PC Appelbaum
Agar dilution methodology (with added Oxyrase in the case of the macrolide
group to allow incubation without added CO2) was used to compare the
activity of RU 64004, a new ketolide, with the activities of erythromycin,
azithromycin, clarithromycin, roxithromycin, clindamycin, amoxicillin with
and without clavulanate, piperacillin with and without tazobactam,
metronidazole, and imipenem against 379 anaerobes. Overall, RU 64004
yielded an MIC at which 50% of the isolates are inhibited (MIC50) of 1.0
microg/ml and an MIC90 of 16.0 microg/ml. In comparison, MIC50s and MIC90s
of erythromycin, azithromycin, clarithromycin, and roxithromycin were 2.0
to 8.0 and >64.0 microg/ml, respectively. MICs of macrolides, including
RU 64004, were higher for Bacteroides ovatus, Fusobacterium varium,
Fusobacterium mortiferum, and Clostridium difficile than for the other
species. RU 64004 was more active against gram-positive rods and cocci,
Prevotella and Porphyromonas spp., and fusobacteria other than F.
mortiferum and F. varium than against the Bacteroides fragilis group.
Overall MIC50s and MIC90s (in micrograms per milliliter), respectively, of
other compounds were as follows: clindamycin, 1.0 and 16.0; amoxicillin,
4.0 and 64.0; amoxicillin-clavulanate, 0.5 and 4.0; piperacillin, 8.0 and
>64.0; piperacillin-tazobactam, 1.0 and 16.0; metronidazole, 1.0 and
4.0; and imipenem, 0.25 and 1.0.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Antianaerobic activity of the ketolide RU 64004 compared to activities of four macrolides, five beta-lactams, clindamycin, and metronidazole
Department of Pathology (Clinical Microbiology), Hershey Medical Center, Pennsylvania 17033, USA.
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