Hygromycin B inhibits synthesis of murine coronavirus RNA

G. Macintyre, D. E. Woods, R. Anderson

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

The aminoglycoside hygromycin B inhibits the infection of mouse hepatitis virus (MHV) A59 both in vitro and in vivo. In probing the mechanism by which hygromycin B exerts its antiviral effect, we describe here studies which point to inhibition of viral RNA synthesis as the key step in virus replication which is affected by the drug. Cells which are infected with MHV do not take up higher levels of hygromycin B than do uninfected ones. Comparative assays of MHV replication and MHV protein synthesis in the presence of hygromycin B and another aminoglycoside, neomycin, indicate that hygromycin B is the more-effective antiviral agent and that its antiviral activity likely does not involve phosphoinositide-mediated processes such as those inhibited by neomycin.

Original languageEnglish
Pages (from-to)2630-2633
Number of pages4
JournalAntimicrobial Agents and Chemotherapy
Volume35
Issue number12
DOIs
Publication statusPublished - 1991
Externally publishedYes

ASJC Scopus Subject Areas

  • Pharmacology
  • Pharmacology (medical)
  • Infectious Diseases

PubMed: MeSH publication types

  • Comparative Study
  • Journal Article
  • Research Support, Non-U.S. Gov't

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