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

Citation
H. Tomioka et al., 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, ANTIM AG CH, 43(12), 1999, pp. 3001-3004
Citations number
28
Categorie Soggetti
Microbiology
Journal title
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
ISSN journal
00664804 → ACNP
Volume
43
Issue
12
Year of publication
1999
Pages
3001 - 3004
Database
ISI
SICI code
0066-4804(199912)43:12<3001:CIVAAO>2.0.ZU;2-#
Abstract
We compared the in vitro antimycobacterial activity of a new fluoroquinolon e, 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 c omplex were in the order STFX approximate to GFLX < LVFX less than or equal to HSR-903 and STFX less than or equal to GFLX less than or equal to HSR-9 03 less than or equal to LVFX, respectively. HSR-903 effectively eliminated intramacrophagial M. tuberculosis, as did LVFX, and exhibited bacteriostat ic effects against M. tuberculosis replicating in type II alveolar cells.