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Antimicrobial Agents and Chemotherapy, December 1999, p. 3001-3004, Vol. 43, No. 12
Department of Microbiology and
Immunology1 and Department of
Dermatology,2 Shimane Medical University,
Izumo, Shimane 693-8501, National Sanatorium Minami-Okayama
Hospital, Okayama 710-0304,3 and
National Sanatorium Kinki-Chuo Hospital, Osaka
591-8555,4 Japan
Received 9 April 1999/Returned for modification 13 August
1999/Accepted 28 September 1999
We compared the in vitro antimycobacterial activity of a new
fluoroquinolone, HSR-903, with strong activity against gram-positive cocci with those of levofloxacin (LVFX), sitafloxacin (STFX), and
gatifloxacin (GFLX). The MICs of the quinolones for Mycobacterium tuberculosis and Mycobacterium avium complex were in
the order STFX
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Comparative In Vitro Antimicrobial Activities of the Newly
Synthesized Quinolone HSR-903, Sitafloxacin (DU-6859a),
Gatifloxacin (AM-1155), and Levofloxacin against
Mycobacterium tuberculosis and Mycobacterium
avium Complex
GFLX < LVFX
HSR-903 and STFX
GFLX
HSR-903
LVFX, respectively. HSR-903 effectively
eliminated intramacrophagial M. tuberculosis, as did LVFX,
and exhibited bacteriostatic effects against M. tuberculosis replicating in type II alveolar cells.
*
Corresponding author. Mailing address: Department of
Microbiology and Immunology, Shimane Medical University, Izumo, Shimane 693-8501, Japan. Phone: 81 (853) 20-2146. Fax: 81 (853) 20-2145. E-mail: tomioka{at}shimane-med.ac.jp.
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