Suppression of Zika Virus Infection in the Brain by the Antiretroviral Drug Rilpivirine

Mol Ther. 2019 Dec 4;27(12):2067-2079. doi: 10.1016/j.ymthe.2019.10.006. Epub 2019 Oct 11.

Abstract

Zika virus (ZIKV) infection is associated with microcephaly in neonates and Guillain-Barré syndrome in adults. ZIKV produces a class of nonstructural (NS) regulatory proteins that play a critical role in viral transcription and replication, including NS5, which possesses RNA-dependent RNA polymerase (RdRp) activity. Here we demonstrate that rilpivirine (RPV), a non-nucleoside reverse transcriptase inhibitor (NNRTI) used in the treatment of HIV-1 infection, inhibits the enzymatic activity of NS5 and suppresses ZIKV infection and replication in primary human astrocytes. Similarly, other members of the NNRTI family, including etravirine and efavirenz, showed inhibitory effects on viral infection of brain cells. Site-directed mutagenesis identified 14 amino acid residues within the NS5 RdRp domain (AA265-903), which are important for the RPV interaction and the inhibition of NS5 polymerase activity. Administration of RPV to ZIKV-infected interferon-alpha/beta receptor (IFN-A/R) knockout mice improved the clinical outcome and prevented ZIKV-induced mortality. Histopathological examination of the brains from infected animals revealed that RPV reduced ZIKV RNA levels in the hippocampus, frontal cortex, thalamus, and cerebellum. Repurposing of NNRTIs, such as RPV, for the inhibition of ZIKV replication offers a possible therapeutic strategy for the prevention and treatment of ZIKV-associated disease.

Keywords: NS5; Zika virus; animal model; astrocytes; rilpivirine.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Anti-HIV Agents / pharmacology*
  • Brain / drug effects*
  • Brain / virology
  • Humans
  • Mice
  • Mice, Knockout
  • Mutagenesis, Site-Directed
  • Mutation
  • Protein Binding
  • Protein Conformation
  • Receptor, Interferon alpha-beta / physiology*
  • Rilpivirine / pharmacology*
  • Viral Nonstructural Proteins / antagonists & inhibitors*
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / metabolism
  • Virus Replication
  • Zika Virus / drug effects*
  • Zika Virus Infection / drug therapy*
  • Zika Virus Infection / pathology
  • Zika Virus Infection / virology

Substances

  • Anti-HIV Agents
  • NS5 protein, flavivirus
  • Viral Nonstructural Proteins
  • Receptor, Interferon alpha-beta
  • Rilpivirine