一些新合成的4-喹诺酮类化合物对质粒偶联的抑制作用。

F Scazzocchio, L Selan, B Oliva, S Schippa, L Cellini, G Renzini
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引用次数: 0

摘要

比较了四种氟喹诺酮类药物(诺氟沙星、环丙沙星、氧氟沙星和培氟沙星)与萘啶酸对偶联质粒转移的抑制作用。在大肠杆菌k12遗传背景下,用不同亚抑制浓度的药物组合和3种不同的质粒进行配对实验,观察了这种抑制作用。氟喹诺酮类药物比萘啶酸更能抑制质粒转移。氧氟沙星和培氟沙星一直是最有效的药物,在所有研究的交配系统中,质粒转移的抑制率为90%至100%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of plasmid conjugation by some recently synthetized 4-quinolone compounds.

Four fluoroquinolones (norfloxacin, ciprofloxacin, ofloxacin, and pefloxacin) were compared with nalidixic acid for their inhibitory effect on conjugal plasmid transfer. The inhibition was observed in mating experiments using various combinations of drugs at subinhibitory concentrations and 3 different plasmids in the E. coli k12 genetic background. Fluoroquinolones inhibited plasmid transfer to a greater extent than nalidixic acid. Ofloxacin and pefloxacin were consistently the most active agents, causing 90 to 100% inhibition of plasmid transfer in all mating systems studied.

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