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Antimicrobial Agents and Chemotherapy, January 2008, p. 77-84, Vol. 52, No. 1
0066-4804/08/$08.00+0 doi:10.1128/AAC.01229-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Department of Pathology (Clinical Microbiology), Hershey Medical Center, Hershey, Pennsylvania 17033
Received 18 September 2007/ Returned for modification 30 September 2007/ Accepted 8 October 2007
DC-159a yielded MICs of
1 µg/ml against 316 strains of both quinolone-susceptible and -resistant pneumococci (resistance was defined as a levofloxacin MIC
4 µg/ml). Although the MICs for DC-159a against quinolone-susceptible pneumococci were a few dilutions higher than those of gemifloxacin, the MICs of these two compounds against 28 quinolone-resistant pneumococci were identical. The DC-159a MICs against quinolone-resistant strains did not appear to depend on the number or the type of mutations in the quinolone resistance-determining region. DC-159a, as well as the other quinolones tested, was bactericidal after 24 h at 2x MIC against 11 of 12 strains tested. Two of the strains were additionally tested at 1 and 2 h, and DC-159a at 4x MIC showed significant killing as early as 2 h. Multistep resistance selection studies showed that even after 50 consecutive subcultures of 10 strains in the presence of sub-MICs, DC-159a produced only two mutants with maximum MICs of 1 µg/ml.
Published ahead of print on 15 October 2007.
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