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Antimicrobial Agents and Chemotherapy, December 2001, p. 3640-3643, Vol. 45, No. 12
Center for the Study of Emerging and
Re-emerging Pathogens,1 Division of
Infectious Diseases, Department of Internal
Medicine,2 and Department of
Microbiology and Molecular Genetics,3 The
University of Texas Medical School, Houston, Texas 77030
Received 1 February 2001/Returned for modification 14 August
2001/Accepted 18 September 2001
The in vitro activities of ABT-773 were evaluated against 324 strains of gram-positive bacteria, including multidrug-resistant Staphylococcus spp. and Enterococcus spp.
ABT-773 had lower MIC ranges, MICs at which 50% of isolates are
inhibited (MIC50s), and MIC90s than
erythromycin or clindamycin for almost all isolates tested. The
MICs of ABT-773 were also lower than those of quinupristin-dalfopristin (Q-D) for methicillin-susceptible Staphylococcus aureus,
Rhodococcus spp., and Streptococcus spp., while
the MICs of Q-D were lower than those of ABT-773 for
methicillin-resistant S. aureus and Enterococcus
faecium, including vancomycin-resistant isolates.
0066-4804/01/$04.00+0 DOI: 10.1128/AAC.45.12.3640-3643.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
In Vitro Activities of a New Ketolide, ABT-773,
against Multidrug-Resistant Gram-Positive Cocci
and
*
Corresponding author. Mailing address: Center for the
Study of Emerging and Re-emerging Pathogens, University of Texas
Medical School-Houston, 6431 Fannin, 1.728 JFB, Houston, TX 77030. Phone: (713) 500-6758. Fax: (713) 500-5495. E-mail:
Kavindra.Singh{at}uth.tmc.edu.
Present address: Division of Infectious Diseases, Department of
Internal Medicine, Ramathibodi Hospital, Rajjatheve, Bangkok, Thailand.
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