Inhibition of replication of rinderpest virus by 5-fluorouracil

Antiviral Res. 1996 Jun;31(1-2):35-44. doi: 10.1016/0166-3542(96)00943-6.

Abstract

5-Fluorouracil (5FU), an analogue of uracil, was found to inhibit the production of infectious particles of rinderpest virus (RPV) in Vero cells (African green monkey kidney cells) by 99%, at a concentration of 1 microgram/ml. The levels of individual mRNA specific for five of the virus genes were also reduced drastically, while the level of mRNA for a cellular housekeeping gene-glyceraldehyde-3-phosphate dehydrogenase (GAPDH)-was unaltered by fluorouracil treatment of infected cells. Both virus RNA and protein synthesis showed inhibition in a dose-dependent manner. The virions which budded out of 5-fluorouracil-treated cells also contained reduced amounts of virus proteins compared with virus particles from untreated cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology*
  • Chlorocebus aethiops
  • Fluorouracil / pharmacology*
  • RNA, Messenger
  • Rinderpest virus / drug effects*
  • Rinderpest virus / genetics
  • Rinderpest virus / growth & development
  • Rinderpest virus / physiology
  • Vero Cells
  • Viral Proteins / biosynthesis
  • Virus Replication

Substances

  • Antiviral Agents
  • RNA, Messenger
  • Viral Proteins
  • Fluorouracil