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      Dual inhibitory activity of sitafloxacin (DU-6859a) against DNA gyrase and topoisomerase IV of Streptococcus pneumoniae.

      1 , , ,
      The Journal of antimicrobial chemotherapy

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          Abstract

          The in-vitro inhibitory activities of sitafloxacin (DU-6859a) and other quinolones against Streptococcus pneumoniae DNA gyrase and topoisomerase IV were measured. IC50s of levofloxacin, ciprofloxacin, sparfloxacin and tosufloxacin against DNA gyrase were almost three to 12 times higher than those against topoisomerase IV. On the other hand, sitafloxacin showed dual inhibitory activity against both enzymes and its IC50s were the lowest among those of the quinolones tested. These results suggest that sitafloxacin is an effective agent against pneumococcal infections and that the incidence of drug-resistant mutants is low.

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          Author and article information

          Journal
          J. Antimicrob. Chemother.
          The Journal of antimicrobial chemotherapy
          0305-7453
          0305-7453
          Oct 1999
          : 44
          : 4
          Affiliations
          [1 ] New Product Research Laboratories I, Daiichi Pharmaceutical Co., Ltd, Tokyo, Japan. onode90j@daiichipharm.co.jp
          Article
          10588315
          5afe6932-6aa8-447a-8bcd-80d792d34862
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