In vivo imaging assay for the convenient evaluation of antiviral compounds against cytomegalovirus in mice

Antiviral Res. 2010 Oct;88(1):45-52. doi: 10.1016/j.antiviral.2010.07.002. Epub 2010 Jul 13.

Abstract

Evaluation of newly identified antiviral compounds against cytomegalovirus (CMV) in vivo still requires laborious and time-consuming experiments using a large number of animals. In this study, we examined an in vivo imaging assay for the evaluation of antiviral compounds using a recombinant murine CMV expressing EGFP (MCMV-GFP). We found the followings: (1) Fluorescent signals were detectable from 1 day after subcutaneous inoculation of the viruses into the backs of mice, and reached to the peak within 2-4 days. (2) Incubation period required for the signal appearance and peak signal intensities depended on the inoculated dose. (3) Not only BALB/c but also a hairless mouse strain, HR1, can be used for the assay, and no need to shave the HR1 mice added to the convenience of the assay. (4) However, BALB/c mice showed better sensitivity and dose-response to the inoculated virus, and inoculation with 200 PFUs of MCMV-GFP still yielded the signals. (5) Demonstration of the antiviral effect of ganciclovir provided a proof-of-concept. Thus, the in vivo imaging assay can allow the fast and convenient initial evaluation of anti-CMV candidate compounds in animals prior to comprehensive analyses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology*
  • Antiviral Agents / therapeutic use
  • Cytomegalovirus / drug effects*
  • Cytomegalovirus Infections / drug therapy
  • Fluorescence
  • Fluorescent Antibody Technique, Indirect
  • Ganciclovir / pharmacology*
  • Ganciclovir / therapeutic use
  • Green Fluorescent Proteins / analysis
  • Herpesviridae Infections / drug therapy
  • Herpesviridae Infections / virology*
  • Mice
  • Mice, Hairless
  • Mice, Inbred BALB C
  • Microbial Sensitivity Tests / methods*
  • Muromegalovirus / drug effects*
  • Muromegalovirus / genetics
  • Muromegalovirus / growth & development
  • Muromegalovirus / isolation & purification
  • Polymerase Chain Reaction

Substances

  • Antiviral Agents
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • Ganciclovir