The in vitro activity of DU-6859a, a new fluoroquinolone, was compared with those of other fluoroquinolones against clinical isolates of anaerobic bacteria and Gardnerella vaginalis. DU-6859a was the most active agent; it inhibited 90% of isolates of almost all species tested, including Bacteroides fragilis at ≤0.39 μg/mL. Although the other quinolones tested were active against most gram-positive anaerobes, inhibiting their growth at ≤1.56 μg/mL, these agents were less active against the B. fragilis group and Prevotella bivia (90% of which were inhibited at ≤6.25 μg/mL). Mobiluncus species and G. vaginalis, which are well associated with bacterial vaginosis, were inhibited by DU-6859a at 0.1 μg/mL. These results suggest that DU- 6859a is a promising oral agent for the treatment of bacterial infections due to anaerobic bacteria; however, further studies, including determination of vaginal levels of this compound, should be performed to study the role of DU- 6859a in the treatment of bacterial vaginosis.
CITATION STYLE
Kato, N., Kato, H., Tanaka-Bando, K., Watanabe, K., & Ueno, K. (1996). Comparison of in vitro activities of DU-6859a and other fluoroquinolones against Japanese isolates of anaerobic bacteria. Clinical Infectious Diseases, 23(SUPPL. 1). https://doi.org/10.1093/clinids/23.supplement_1.s31
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