Journal of Antimicrobial Chemotherapy, Vol 39, 247-249, Copyright © 1997 by The British Society for Antimicrobial Chemotherapy
T Deguchi, M Yasuda, M Nakano, E Kanematsu, S Ozeki, S Ishihara, I Saito and Y Kawada
The in-vitro antimicrobial activity of DU-6859a, a new fluoroquinolone, was
tested against 55 clinical isolates of Neisseria gonorrhoeae. The MIC of
DU-6859a inhibiting 90% (MIC90) of the isolates with genetic alterations of
both the GyrA subunit of DNA gyrase and the ParC subunit of topoisomerase
IV was 0.125 mg/L. The MIC90 for isolates with alterations of GyrA alone or
without alterations of GyrA or ParC was 0.03 mg/L and 0.004 mg/L,
respectively. The potency of DU-6859a against clinical isolates bearing
genetic alterations associated with quinolone resistance was significantly
greater than that of currently available fluoroquinolones.
JOURNAL ARTICLE
Antimicrobial activity of a new fluoroquinolone, DU-6859a, against quinolone-resistant clinical isolates of Neisseria gonorrhoeae with genetic alterations in the GyrA subunit of DNA gyrase and the ParC subunit of topoisomerase IV
Department of Urology, Gifu University School of Medicine, Gifu City, Japan.
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