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Antimicrobial Agents and Chemotherapy, March 2009, p. 1221-1224, Vol. 53, No. 3
0066-4804/09/$08.00+0 doi:10.1128/AAC.01260-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

JMI Laboratories, North Liberty, Iowa 52317,1 Tufts University School of Medicine, Boston, Massachusetts 021112
Received 19 September 2008/ Returned for modification 13 November 2008/ Accepted 22 December 2008
Prulifloxacin, the prodrug of ulifloxacin (active component), is a newer fluoroquinolone with broad activity against enteric and nonenteric gram-negative bacilli. Ulifloxacin and other oral comparator agents were tested for activity against 582 gastroenteritis strains from global surveillance studies. Ulifloxacin was highly active against Escherichia coli, Salmonella spp., Shigella spp., Yersinia spp., Vibrio spp., Aeromonas spp., and Plesiomonas spp. (MIC50s and MIC90s,
0.03 µg/ml and
0.06 µg/ml, respectively). Only rare Aeromonas spp., Campylobacter spp., and E. coli displayed elevated MIC results (
4 µg/ml). Ciprofloxacin exhibited similar activity but was two- to fourfold less potent. Presently approved for clinical use in certain European countries and Japan, ulifloxacin was the most active of the antimicrobial agents tested against these gastroenteritis-causing pathogens.
Published ahead of print on 29 December 2008.
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