Inhibition of transcription of herpes simplex virus immediate early genes in interferon-treated human cells

J Gen Virol. 1988 Jun:69 ( Pt 6):1167-77. doi: 10.1099/0022-1317-69-6-1167.

Abstract

The effect of interferon (IFN) treatment on the early stages of herpes simplex virus type 1 (HSV-1) replication in three types of human cells was investigated. Interferon pretreatment was shown to reduce the steady state levels of both total and polysomebound HSV-1 immediate early alpha mRNAs. Using the nuclear run-off transcription assay, we showed that IFN selectively inhibited transcription of the HSV-1 genes, with no effect on transcription of total cellular RNA or that of the beta-tubulin RNA. Thus, IFN appears to inhibit the initiation of HSV-1 alpha gene transcription rather than affect the stability of the respective mRNAs. IFN did not prevent the HSV-1-induced early shut-off of host cellular protein synthesis caused by a structural protein of infecting virus. This observation indicated that the IFN-mediated inhibition of HSV-1 replication is at a stage beyond viral penetration into the cytoplasm. These results suggested that IFN blocked HSV-1 replication primarily at a very early stage, during the onset of alpha mRNA transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Encephalomyocarditis virus / physiology
  • Fibroblasts
  • Gene Expression Regulation
  • Genes, Viral
  • HeLa Cells
  • Humans
  • Immediate-Early Proteins*
  • Interferons / pharmacology*
  • Kinetics
  • Nucleic Acid Hybridization
  • Nucleic Acid Synthesis Inhibitors
  • RNA, Messenger / genetics
  • RNA, Viral / genetics
  • Recombinant Proteins / pharmacology
  • Simplexvirus / genetics*
  • Simplexvirus / physiology
  • Transcription, Genetic*
  • Viral Proteins / biosynthesis
  • Viral Proteins / genetics*
  • Virus Replication

Substances

  • IE1 protein, Human herpesvirus 1
  • Immediate-Early Proteins
  • Nucleic Acid Synthesis Inhibitors
  • RNA, Messenger
  • RNA, Viral
  • Recombinant Proteins
  • Viral Proteins
  • Interferons