In Vitro Activity of Gepotidacin, a Novel Triazaacenaphthylene Bacterial Topoisomerase Inhibitor, against a Broad Spectrum of Bacterial Pathogens

被引:103
|
作者
Biedenbach, D. J. [1 ]
Bouchillon, S. K. [1 ]
Hackel, M. [1 ]
Miller, L. A. [2 ]
Scangarella-Oman, N. E. [2 ]
Jakielaszek, C. [2 ]
Sahm, D. F. [1 ]
机构
[1] Int Hlth Management Associates Inc, Schaumburg, IL USA
[2] GlaxoSmithKline, Collegeville, PA USA
关键词
D O I
10.1128/AAC.02820-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Gepotidacin inhibits bacterial DNA replication through a mode different from that of fluoroquinolones. Gepotidacin and comparators were tested by broth and agar dilution against clinical isolates. The in vitro activities of gepotidacin were comparable against methicillin-susceptible and -resistant Staphylococcus aureus (MSSA and MRSA, respectively) isolates (MIC90, 0.5 mu g/ml). The gepotidacin MIC(90)s were as follows (in micrograms per milliliter) for the indicated bacteria: Streptococcus pyogenes, 0.25; Escherichia coli, 2; Moraxella catarrhalis, <= 0.06; Streptococcus pneumoniae (0.25), Haemophilus influenzae, 1; Clostridium perfringens, 0.5; and Shigella spp., 1, including levofloxacin-resistant subsets. Gepotidacin warrants further investigation for clinical development.
引用
收藏
页码:1918 / 1923
页数:6
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