Journal of Antimicrobial Chemotherapy (2000) 45, 437-446
© 2000 The British Society for Antimicrobial Chemotherapy
In vitro antibacterial spectrum of a new broad-spectrum 8-methoxy fluoroquinolone, gatifloxacin
Department of Microbiology, Bristol-Myers Squibb Company, Wallingford, CT 06492, USA
The in vitro antibacterial spectrum of gatifloxacin was compared with those of ciprofloxacin and ofloxacin. Gatifloxacin was two- to four-fold more potent than comparator quinolones against staphylococci, streptococci, pneumococci and enterococci (gatifloxacin MIC90s,
1 mg/L, except 4 mg/L against methicillin-resistant Staphylococcus aureus and Enterococcus faecium). Gatifloxacin was two-fold less potent than ciprofloxacin, and the same as or two-fold more potent than ofloxacin against Enterobacteriaceae (MIC90s, 0.060.5 mg/L against most members of the Enterobacteriaceae and
1 mg/L against Proteus/Morganella spp.). Relative to the comparator quinolones, gatifloxacin was two- to four-fold more potent against Providencia spp., and had good potency against Acinetobacter spp. (MIC90s, 0.251 mg/L). Gatifloxacin and ofloxacin had similar anti-pseudomonal potency, with corresponding MIC90s of 4, 8 and 0.25 mg/L for Pseudomonas aeruginosa, Pseudomonas fluorescens and Pseudomonas stutzeri, while ciprofloxacin had two- to eight-fold more potency. The three quinolones were equipotent against Burkholderia cepacia (MIC90s, 8 mg/L), but gatifloxacin was two-fold more potent against Stenotrophomonas maltophilia (MIC90, 4 mg/L). Gatifloxacin was highly potent (MIC90s, 0.030.06 mg/L) against Haemophilus influenzae, Legionella spp., Helicobacter pylori and had at least eight-fold better anti-chlamydial and anti-mycoplasma potency (gatifloxacin MIC90s, 0.13 mg/L). The higher quinolone MICs for ureaplasma (MIC90s, 48 mg/L) may be due to the acidic pH of the ureaplasma test medium, which antagonizes quinolones. Like other quinolones, gatifloxacin had poor potency against Mycobacterium aviumintracellulare, though it was eight- to 16-fold more potent against Mycobacterium tuberculosis (MIC90, 0.25 mg/L). Of the three quinolones, only gatifloxacin had activity against Bacteroides fragilis and Clostridium difficile. In summary, gatifloxacin is a broad-spectrum 8-methoxy fluoroquinolone that is more potent than ciprofloxacin and ofloxacin against Gram-positive bacteria, chlamydia, mycoplasma, mycobacteria and anaerobes.
* Corresponding author. Tel: +1-203-677-6370; Fax: +1-203-677-6771; E-mail: fungtomj{at}bms.com
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
J. van den Boogaard, G. S. Kibiki, E. R. Kisanga, M. J. Boeree, and R. E. Aarnoutse New Drugs against Tuberculosis: Problems, Progress, and Evaluation of Agents in Clinical Development Antimicrob. Agents Chemother., March 1, 2009; 53(3): 849 - 862. [Full Text] [PDF] |
||||
![]() |
J. Lalucat, A. Bennasar, R. Bosch, E. Garcia-Valdes, and N. J. Palleroni Biology of Pseudomonas stutzeri Microbiol. Mol. Biol. Rev., June 1, 2006; 70(2): 510 - 547. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. V. Capparelli, M. D. Reed, J. S. Bradley, G. L. Kearns, R. F. Jacobs, B. D. Damle, J. L. Blumer, and D. M. Grasela Pharmacokinetics of Gatifloxacin in Infants and Children Antimicrob. Agents Chemother., March 1, 2005; 49(3): 1106 - 1112. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Rafii, M. Park, and J. S. Novak Alterations in DNA Gyrase and Topoisomerase IV in Resistant Mutants of Clostridium perfringens Found after In Vitro Treatment with Fluoroquinolones Antimicrob. Agents Chemother., February 1, 2005; 49(2): 488 - 492. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Pucci, J. J. Bronson, J. F. Barrett, K. L. DenBleyker, L. F. Discotto, J. C. Fung-Tomc, and Y. Ueda Antimicrobial Evaluation of Nocathiacins, a Thiazole Peptide Class of Antibiotics Antimicrob. Agents Chemother., October 1, 2004; 48(10): 3697 - 3701. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. M. Parrish, C. G. Ko, M. A. Hughes, C. A. Townsend, and J. D. Dick Effect of n-octanesulphonylacetamide (OSA) on ATP and protein expression in Mycobacterium bovis BCG J. Antimicrob. Chemother., October 1, 2004; 54(4): 722 - 729. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Pereyre, H. Renaudin, C. Bebear, and C. M. Bebear In Vitro Activities of the Newer Quinolones Garenoxacin, Gatifloxacin, and Gemifloxacin against Human Mycoplasmas Antimicrob. Agents Chemother., August 1, 2004; 48(8): 3165 - 3168. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. F. B. Cheng, W. W. Yew, E. W. C. Chan, M. L. Chin, M. M. M. Hui, and R. C. Y. Chan Multiplex PCR Amplimer Conformation Analysis for Rapid Detection of gyrA Mutations in Fluoroquinolone-Resistant Mycobacterium tuberculosis Clinical Isolates Antimicrob. Agents Chemother., February 1, 2004; 48(2): 596 - 601. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. W. Yew, C. K. Chan, C. C. Leung, C. H. Chau, C. M. Tam, P. C. Wong, and J. Lee Comparative Roles of Levofloxacin and Ofloxacin in the Treatment of Multidrug-Resistant Tuberculosis: Preliminary Results of a Retrospective Study From Hong Kong Chest, October 1, 2003; 124(4): 1476 - 1481. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Ameyama, Y. Shinmura, and M. Takahata Inhibitory Activities of Quinolones against DNA Gyrase of Chlamydia pneumoniae Antimicrob. Agents Chemother., July 1, 2003; 47(7): 2327 - 2329. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Dawis, H. D. Isenberg, K. A. France, and S. G. Jenkins In vitro activity of gatifloxacin alone and in combination with cefepime, meropenem, piperacillin and gentamicin against multidrug-resistant organisms J. Antimicrob. Chemother., May 1, 2003; 51(5): 1203 - 1211. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Bourgeois, J.-C. Ghnassia, and F. Doucet-Populaire In vitro activity of fluoroquinolones against erythromycin-susceptible and -resistant Bordetella pertussis J. Antimicrob. Chemother., March 1, 2003; 51(3): 742 - 743. [Full Text] [PDF] |
||||
![]() |
K. Tominaga, K. Higuchi, N. Hamasaki, M. Hamaguchi, T. Takashima, T. Tanigawa, T. Watanabe, Y. Fujiwara, Y. Tezuka, T. Nagaoka, et al. In vivo action of novel alkyl methyl quinolone alkaloids against Helicobacter pylori J. Antimicrob. Chemother., October 1, 2002; 50(4): 547 - 552. [Abstract] [Full Text] [PDF] |
||||
![]() |
H.-J. Yun, Y.-H. Min, J.-A Lim, J.-W. Kang, S.-Y. Kim, M.-J. Kim, J.-H. Jeong, Y.-J. Choi, H.-J. Kwon, Y.-H. Jung, et al. In Vitro and In Vivo Antibacterial Activities of DW286, a New Fluoronaphthyridone Antibiotic Antimicrob. Agents Chemother., September 1, 2002; 46(9): 3071 - 3074. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. A. Gordon, M. A. Pfaller, R. N. Jones, and the SENTRY Participants Group BMS284756 (formerly T-3811, a des-fluoroquinolone) potency and spectrum tested against over 10 000 bacterial bloodstream infection isolates from the SENTRY antimicrobial surveillance programme (2000) J. Antimicrob. Chemother., May 1, 2002; 49(5): 851 - 855. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Braback, K. Riesbeck, and A. Forsgren Susceptibilities of Mycobacteriummarinum to Gatifloxacin, Gemifloxacin, Levofloxacin, Linezolid, Moxifloxacin, Telithromycin, and Quinupristin-Dalfopristin (Synercid) Compared to Its Susceptibilities to Reference Macrolides and Quinolones Antimicrob. Agents Chemother., April 1, 2002; 46(4): 1114 - 1116. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Gradelski, L. Valera, D. Bonner, and J. Fung-Tomc Synergistic Activities of Gatifloxacin in Combination with Other Antimicrobial Agents against Pseudomonas aeruginosa and Related Species Antimicrob. Agents Chemother., November 1, 2001; 45(11): 3220 - 3222. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Ince and D. C. Hooper Mechanisms and Frequency of Resistance to Gatifloxacin in Comparison to AM-1121 and Ciprofloxacin in Staphylococcus aureus Antimicrob. Agents Chemother., October 1, 2001; 45(10): 2755 - 2764. [Abstract] [Full Text] |
||||
![]() |
R. J. O'BRIEN and P. P. NUNN The Need for New Drugs against Tuberculosis . Obstacles, Opportunities, and Next Steps Am. J. Respir. Crit. Care Med., April 1, 2001; 163(5): 1055 - 1058. [Full Text] |
||||
![]() |
J. C. Fung-Tomc, B. Minassian, B. Kolek, E. Huczko, L. Aleksunes, T. Stickle, T. Washo, E. Gradelski, L. Valera, and D. P. Bonner Antibacterial Spectrum of a Novel Des-Fluoro(6) Quinolone, BMS-284756 Antimicrob. Agents Chemother., December 1, 2000; 44(12): 3351 - 3356. [Abstract] [Full Text] |
||||




