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Antimicrobial Agents and Chemotherapy, January 2001, p. 345-348, Vol. 45, No. 1
Microbial Research
Laboratory1 and Department of
Pathology,2 Los Angeles County- University
of Southern California Medical Center, Los Angeles, California
Received 7 March 2000/Returned for modification 29 July
2000/Accepted 17 October 2000
The activity of ABT-773, a novel ketolide antibiotic, against
clinical isolates of anaerobic bacteria was determined and
compared to the activities of other antimicrobial agents. MICs at which 90% of isolates were inhibited (MIC90s) were
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.1.345-348.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Comparative In Vitro Activities of ABT-773
against 362 Clinical Isolates of Anaerobic Bacteria
0.06
µg/ml for Actinomyces spp., Clostridium
perfringens, Peptostreptococcus spp.,
Propionibacterium spp., and Porphyromonas
spp. The MIC50s and MIC90s were
0.06 and >32
µg/ml, respectively, for Eubacterium spp.,
Lactobacillus spp., Clostridium
difficile, and Clostridium ramosum. The
MIC90 for Bilophila wadsworthia,
Bacteroides ureolyticus, and Campylobacter gracilis was 1 µg/ml, and that for Prevotella
bivia and other Prevotella spp.
was 0.5 µg/ml. The MIC90 for Fusobacterium
nucleatum was 8 µg/ml, and that for Fusobacterium
mortiferum and Fusobacterium varium was >32
µg/ml. The MIC90s for the
Bacteroides fragilis group were as follows: for
B. fragilis, 8 µg/ml; for Bacteroides thetaiotaomicron, Bacteroides ovatus,
Bacteroides distasonis, and Bacteroides
uniformis, >32 µg/ml; and for Bacteroides
vulgatus, 4 µg/ml. Telithromycin MICs for the B.
fragilis group were usually 1 to 2 dilutions higher than
ABT-773 MICs. For all strains, ABT-773 was more active than
erythromycin by 4 or more dilutions, and for some strains this drug was
more active than clindamycin.
*
Corresponding author. Mailing address: LAC+USC Medical
Center, General Labs Bldg., Room 2G-24, 1801 East Marengo St., Los Angeles, CA 90033. Phone: (323) 226-3749. Fax: (323) 226-7021. E-mail: dcitron{at}hsc.usc.edu.
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