DMO-CAP inhibits influenza virus replication by activating heme oxygenase-1-mediated IFN response

Virol J. 2019 Feb 20;16(1):21. doi: 10.1186/s12985-019-1125-9.

Abstract

Background: As a leading cause of respiratory disease, influenza A virus (IAV) infection remains a pandemic threat in annual seasonal outbreaks. Given the limitation of existing anti-influenza therapeutic drugs, development of new drugs is urgently required. Flavonoids extracted from Artemisia rupestris L. have an inhibitory effect on virus infections. Despite this fact, the antiviral properties of 6-demethoxy-4'-O-methylcapillarisin (DMO-CAP), one of such flavonoids, against the influenza virus have not been reported. Thus, the aim of this study is to investigate the anti-IAV virus efficacy and antiviral mechanism of DMO-CAP.

Methods: The inhibitory activity of DMO-CAP against IAV was detected in vitro using viral titers by Western blot analysis, qRT-PCR, and immunofluorescence assays. The mechanism of DMO-CAP against influenza virus was analyzed by Western blot analysis, qRT-PCR, and luciferase assay.

Results: DMO-CAP exhibits broad spectrum of antiviral activities against IAV in vitro. Mechanistically, DMO-CAP treatment induced the phosphorylation of p38 mitogen-activated protein kinase (MAPK), JNK MAPK, and ERK MAPK, which led to the activation of Nrf2/heme oxygenase-1 (HO-1) pathway. Then, the up-regulation of HO-1 expression activated the IFN response and induced the expression of IFN-stimulated genes, thereby leading to efficient anti-IAV effects.

Conclusions: DMO-CAP inhibited IAV replication by activating HO-1-mediated IFN response. DMO-CAP may be a potential agent or supplement against IAV infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Artemisia / chemistry
  • Dogs
  • Flavonoids / pharmacology*
  • HEK293 Cells
  • Heme Oxygenase-1 / metabolism*
  • Humans
  • Influenza A virus / drug effects*
  • Influenza A virus / physiology
  • Inhibitory Concentration 50
  • Interferons / immunology*
  • Madin Darby Canine Kidney Cells
  • Mice
  • RAW 264.7 Cells
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction / drug effects*
  • Virus Replication / drug effects*
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Flavonoids
  • Interferons
  • Heme Oxygenase-1
  • p38 Mitogen-Activated Protein Kinases