Coxsackievirus Mutants That Can Bypass Host Factor PI4KIIIβ and the Need for High Levels of PI4P Lipids for Replication

Cell Res. 2012 Nov;22(11):1576-92. doi: 10.1038/cr.2012.129. Epub 2012 Sep 4.

Abstract

RNA viruses can rapidly mutate and acquire resistance to drugs that directly target viral enzymes, which poses serious problems in a clinical context. Therefore, there is a growing interest in the development of antiviral drugs that target host factors critical for viral replication, since they are unlikely to mutate in response to therapy. We recently demonstrated that phosphatidylinositol-4-kinase IIIβ (PI4KIIIβ) and its product phosphatidylinositol-4-phosphate (PI4P) are essential for replication of enteroviruses, a group of medically important RNA viruses including poliovirus (PV), coxsackievirus, rhinovirus, and enterovirus 71. Here, we show that enviroxime and GW5074 decreased PI4P levels at the Golgi complex by directly inhibiting PI4KIIIβ. Coxsackievirus mutants resistant to these inhibitors harbor single point mutations in the non-structural protein 3A. These 3A mutations did not confer compound-resistance by restoring the activity of PI4KIIIβ in the presence of the compounds. Instead, replication of the mutant viruses no longer depended on PI4KIIIβ, since their replication was insensitive to siRNA-mediated depletion of PI4KIIIβ. The mutant viruses also did not rely on other isoforms of PI4K. Consistently, no high level of PI4P could be detected at the replication sites induced by the mutant viruses in the presence of the compounds. Collectively, these findings indicate that through specific single point mutations in 3A, CVB3 can bypass an essential host factor and lipid for its propagation, which is a new example of RNA viruses acquiring resistance against antiviral compounds, even when they directly target host factors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Phosphatidylinositol 4-Kinase / antagonists & inhibitors*
  • 1-Phosphatidylinositol 4-Kinase / metabolism
  • Animals
  • Antiviral Agents / pharmacology*
  • Benzimidazoles / pharmacology
  • Cell Line, Tumor
  • Chlorocebus aethiops
  • Drug Resistance, Viral / genetics
  • Enterovirus B, Human / drug effects*
  • Enterovirus B, Human / genetics
  • Enterovirus B, Human / physiology*
  • HeLa Cells
  • Humans
  • Indoles / pharmacology
  • Phenols / pharmacology
  • Phosphatidylinositol Phosphates / metabolism*
  • Phosphotransferases (Alcohol Group Acceptor) / antagonists & inhibitors*
  • Phosphotransferases (Alcohol Group Acceptor) / genetics
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Point Mutation
  • RNA Interference
  • RNA, Small Interfering
  • Viral Nonstructural Proteins / genetics*
  • Virus Replication / drug effects

Substances

  • 5-iodo-3-((3,5-dibromo-4-hydroxyphenyl)methylene)-2-indolinone
  • Antiviral Agents
  • Benzimidazoles
  • Indoles
  • Phenols
  • Phosphatidylinositol Phosphates
  • RNA, Small Interfering
  • Viral Nonstructural Proteins
  • phosphatidylinositol 4-phosphate
  • enviroxime
  • Phosphotransferases (Alcohol Group Acceptor)
  • 1-Phosphatidylinositol 4-Kinase
  • phosphatidylinositol 4-kinase IIIbeta, human