The in vitro activity of BMS-284756, a new des-fluorinated quinolone

被引:31
作者
Weller, TMA [1 ]
Andrews, JM [1 ]
Jevons, G [1 ]
Wise, R [1 ]
机构
[1] City Hosp NHS Trust, Dept Med Microbiol, Birmingham B18 7QH, W Midlands, England
关键词
D O I
10.1093/jac/49.1.177
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The in vitro activity of BMS-284756 (previously T-3811ME), a des-fluoro(6) quinolone, was investigated and compared with those of six other antimicrobial agents. Susceptibility tests were performed on 919 Gram-positive, Gram-negative (including nine quinolone-resistant Escherichia coli) and anaerobic bacteria, three Chlamydia isolates and four Mycobacteria spp. BMS-284756 was marginally less active against the Enterobacteriaceae, but was the most active quinolone against staphylococci, enterococci and peptostreptococci. Against Streptococcus pneumoniae, BMS-284756 and gemifloxacin were more active than other quinolones. The MIC90 of BMS-284756 was greater than or equal to 2 mg/L for the following bacteria: E. coli (MIC90 16 mg/L), Acinetobacter spp. (8 mg/L), Pseudomonas aeruginosa (64 mg/L) and Enterococcus faecium (4 mg/L). The MIC of BMS-284756 for Mycobacterium spp. was within one dilution of the MIC of ciprofloxacin. BMS-284756 was markedly more active than ciprofloxacin against the Chlamydia isolates tested.
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页码:177 / 184
页数:8
相关论文
共 11 条
  • [1] [Anonymous], 1991, J Antimicrob Chemother, V27 Suppl D, P1
  • [2] A review of the comparative in-vitro activities of 12 antimicrobial agents, with a focus on five new 'respiratory quinolones'
    Blondeau, JM
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 43 : 1 - 11
  • [3] CISNEROS RL, 2000, 40 INT C ANT AG CHEM, P55
  • [4] COTTAGNOUD P, 2000, 40 INT C ANT AG CHEM, P51
  • [5] STRUCTURE-ACTIVITY AND STRUCTURE-SIDE-EFFECT RELATIONSHIPS FOR THE QUINOLONE ANTIBACTERIALS
    DOMAGALA, JM
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1994, 33 (04) : 685 - 706
  • [6] Antibacterial spectrum of a novel des-fluoro(6) quinolone, BMS-284756
    Fung-Tomc, JC
    Minassian, B
    Kolek, B
    Huczko, E
    Aleksunes, L
    Stickle, T
    Washo, T
    Gradelski, E
    Valera, L
    Bonner, DP
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (12) : 3351 - 3356
  • [7] RANDOMIZED, DOUBLE-BLIND COMPARATIVE-STUDY OF INTRAVENOUS CIPROFLOXACIN VERSUS CEFTAZIDIME IN THE TREATMENT OF SERIOUS INFECTIONS
    LEVINE, DP
    MCNEIL, P
    LERNER, SA
    [J]. AMERICAN JOURNAL OF MEDICINE, 1989, 87 (5A) : S160 - S163
  • [8] ACTIVITIES OF CLARITHROMYCIN, SULFISOXAZOLE, AND RIFABUTIN AGAINST MYCOBACTERIUM-AVIUM COMPLEX MULTIPLICATION WITHIN HUMAN MACROPHAGES
    PERRONNE, C
    GIKAS, A
    TRUFFOTPERNOT, C
    GROSSET, J
    POCIDALO, JJ
    VILDE, JL
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1990, 34 (08) : 1508 - 1511
  • [9] In vitro and in vivo antimicrobial activities of T-3811ME, a novel des-F(6)-quinolone
    Takahata, M
    Mitsuyama, J
    Yamashiro, Y
    Yonezawa, M
    Araki, H
    Todo, Y
    Minami, S
    Watanabe, Y
    Narita, H
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (05) : 1077 - 1084
  • [10] COMMERCIALLY AVAILABLE FLUORESCEIN-CONJUGATED MONOCLONAL-ANTIBODY FOR DETERMINING THE INVITRO ACTIVITY OF ANTIMICROBIAL AGENTS AGAINST CHLAMYDIA-TRACHOMATIS
    WEBBERLEY, JM
    MATTHEWS, RS
    ANDREWS, JM
    WISE, R
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1987, 6 (05) : 587 - 589