Novel antiviral activity and mechanism of bromocriptine as a Zika virus NS2B-NS3 protease inhibitor

Antiviral Res. 2017 May:141:29-37. doi: 10.1016/j.antiviral.2017.02.002. Epub 2017 Feb 7.

Abstract

Zika virus (ZIKV) infection is associated with congenital malformations in infected fetuses and severe neurological and other systemic complications in adults. There are currently limited anti-ZIKV treatment options that are readily available and safe for use in pregnancy. In this drug repurposing study, bromocriptine was found to have inhibitory effects on ZIKV replication in cytopathic effect inhibition, virus yield reduction, and plaque reduction assays. Time-of-drug-addition assay showed that bromocriptine exerted anti-ZIKV activity between 0 and 12 h post-ZIKV inoculation, corroborating with post-entry events in the virus replication cycle prior to budding. Our docking model showed that bromocriptine interacted with several active site residues of the proteolytic cavity involving H51 and S135 in the ZIKV-NS2B-NS3 protease protein, and might occupy the active site and inhibit the protease activity of the ZIKV-NS2B-NS3 protein. A fluorescence-based protease inhibition assay confirmed that bromocriptine inhibited ZIKV protease activity. Moreover, bromocriptine exhibited synergistic effect with interferon-α2b against ZIKV replication in cytopathic effect inhibition assay. The availability of per vagina administration of bromocriptine as suppositories or vaginoadhesive discs and the synergistic anti-ZIKV activity between bromocriptine and type I interferon may make bromocriptine a potentially useful and readily available treatment option for ZIKV infection. The anti-ZIKV effects of bromocriptine should be evaluated in a suitable animal model.

Keywords: Antiviral; Bromocriptine; Interferon; Protease; Treatment; Zika.

MeSH terms

  • Antiviral Agents / pharmacology*
  • Bromocriptine / pharmacology*
  • Bromocriptine / therapeutic use
  • Enzyme Assays
  • Fluorescence
  • Humans
  • Interferon alpha-2
  • Interferon-alpha / pharmacology
  • Peptide Hydrolases / drug effects
  • Recombinant Proteins / pharmacology
  • Serine Proteases / metabolism
  • Serine Proteinase Inhibitors / chemistry
  • Serine Proteinase Inhibitors / pharmacology*
  • Viral Nonstructural Proteins / antagonists & inhibitors*
  • Virus Replication / drug effects
  • Zika Virus / drug effects*
  • Zika Virus / enzymology
  • Zika Virus / physiology

Substances

  • Antiviral Agents
  • Interferon alpha-2
  • Interferon-alpha
  • Recombinant Proteins
  • Serine Proteinase Inhibitors
  • Viral Nonstructural Proteins
  • Bromocriptine
  • Peptide Hydrolases
  • Serine Proteases