Author:
Reinhardt J F,Fowlston S,Jones J,George W L
Abstract
MICs of 14 antimicrobial agents for 29 strains of Edwardsiella tarda were determined by an agar dilution method. Of the agents tested, ciprofloxacin, enoxacin, and norfloxacin were the most active on a weight basis. All strains were also susceptible to clinically achievable concentrations of ampicillin, chloramphenicol, tetracycline, trimethoprim, sulfamethoxazole, trimethoprim plus sulfamethoxazole, cefotaxime, and gentamicin. Ninety percent of the strains demonstrated high-level resistance to polymyxin B and colistin.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference13 articles.
1. Comparative in vitro activities of ten antimicrobial agents against bacterial enteropathogens;Carlson J. R.;Antimicrob. Agents Chemother.,1983
2. Edwardsiella tardaidentification and clinical significance;Chatty H. B.;Cleveland Clin. Q.,1968
3. Extraintestinal human infection caused by Edwardsiella tarda;Clarridge J. E.;J. Clin. Microbiol.,1980
4. Farmer J. J III and A. C. McWhorter. 1984. Genus X. Edwardsiella Ewing and McWhorter 1965 37AL p. 486491. In N. R. Kreig and J. G. Holt (ed.) Bergey's manual of systematic bacteriology vol. 1. The Williams & Wilkins Co. Baltimore.
5. Comparative in vitro activity of ciprofloxacin against Campylobacter spp. and other bacterial enteric pathogens. Antimicrob;Goodman L. J.;Agents Chemother.,1984
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