Dependence of echovirus 9 on the enterovirus RNA replication inhibitor 2-(alpha-Hydroxybenzyl)-benzimidazole maps to nonstructural protein 2C

J Virol. 1999 Dec;73(12):10536-9. doi: 10.1128/JVI.73.12.10536-10539.1999.

Abstract

HBB [2-(alpha-hydroxybenzyl)-benzimidazole] selectively inhibits RNA synthesis of most enteroviruses. However, isolation of HBB-dependent variants is possible. Sequence analysis and characterization of recombinant viruses revealed that HBB dependence maps to the nonstructural protein 2C. A single point mutation at position C(4782)U is sufficient to establish the HBB-dependent phenotype in our echovirus 9 model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / pharmacology*
  • Benzimidazoles / pharmacology*
  • Cloning, Molecular
  • Enterovirus B, Human / drug effects*
  • Enterovirus B, Human / enzymology
  • Enterovirus B, Human / genetics
  • Enterovirus B, Human / physiology
  • Humans
  • Point Mutation
  • RNA Helicases / genetics*
  • RNA, Viral / biosynthesis
  • Viral Proteins

Substances

  • Antiviral Agents
  • Benzimidazoles
  • RNA, Viral
  • Viral Proteins
  • HBBPC
  • 2C helicase
  • RNA Helicases