Inhibition of plasmid conjugation by some recently synthetized 4-quinolone compounds.
F. Scazzocchio, Laura Selan, B Oliva, Serena Schippa, Luigina Cellini, G Renzini
Abstract
F. Scazzocchio, Laura Selan, B Oliva, Serena Schippa, Luigina Cellini, G Renzini
Abstract
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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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.
Key concepts: Pefloxacin, Nalidixic acid, Ofloxacin, Plasmid, Norfloxacin, Ciprofloxacin, Microbiology, Chemistry