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Antimicrobial Agents and Chemotherapy, October 2008, p. 3776-3778, Vol. 52, No. 10
0066-4804/08/$08.00+0 doi:10.1128/AAC.00849-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama
Received 26 June 2008/ Accepted 14 July 2008
The in vitro susceptibilities of 151 unique clinical isolates of Mycoplasma pneumoniae, Mycoplasma hominis, Mycoplasma fermentans, Mycoplasma genitalium, and Ureaplasma species to DC-159a, an investigational fluoroquinolone, in comparison with those to other agents were determined. Macrolides were the most active agents against M. pneumoniae and M. genitalium, whereas clindamycin was most active against M. hominis. DC-159a MICs were
0.5 µg/ml for all Mycoplasma species and
4 µg/ml for ureaplasmas. DC-159a was the most active fluoroquinolone tested against M. pneumoniae and M. fermentans, and it was second to moxifloxacin against the other species. It was bactericidal against 10 M. pneumoniae isolates and demonstrated killing of
99.9% of the inoculum at 24 h for 2 isolates. The excellent in vitro activity of DC-159a demonstrates its potential for use in the treatment of infections due to mycoplasmas and ureaplasmas.
Published ahead of print on 28 July 2008.
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