In vitro efficacies of oseltamivir carboxylate and zanamivir against equine influenza A viruses

J Vet Med Sci. 2006 Apr;68(4):405-8. doi: 10.1292/jvms.68.405.

Abstract

To investigate the possibilities of two NA inhibitors [oseltamivir carboxylate (OC) and zanamivir (ZA)] as the clinical agents for equine influenza A virus (EIV) infection, we examined the efficacies of these inhibitors against twelve EIVs in vitro. OC and ZA inhibited NA activities of all EIVs with 50% inhibitory concentrations with ranging from 0.017 to 0.130 and from 0.010 to 0.074 microM, respectively. OC and ZA inhibited plaque-forming of all EIVs in MDCK cells with 50% effective concentrations with ranging from 0.015 to 0.097 and from 0.016 to 0.089 microM, respectively, except for one strain (13.328 microM and 6.729 microM). These results suggest that these inhibitors are effective against most EIVs and might be useful for treatment of EI in horses.

MeSH terms

  • Acetamides / pharmacology*
  • Animals
  • Antiviral Agents / pharmacology*
  • Guanidines / pharmacology*
  • Horses / virology*
  • Influenza A virus / drug effects*
  • Inhibitory Concentration 50
  • Oseltamivir
  • Pyrans / pharmacology*
  • Sialic Acids / pharmacology*
  • Zanamivir

Substances

  • Acetamides
  • Antiviral Agents
  • Guanidines
  • Pyrans
  • Sialic Acids
  • Oseltamivir
  • Zanamivir