Type I Interferon Response Limits Astrovirus Replication and Protects against Increased Barrier Permeability In Vitro and In Vivo

J Virol. 2015 Dec 9;90(4):1988-96. doi: 10.1128/JVI.02367-15. Print 2016 Feb 15.

Abstract

Little is known about intrinsic epithelial cell responses against astrovirus infection. Here we show that human astrovirus type 1 (HAstV-1) infection induces type I interferon (beta interferon [IFN-β]) production in differentiated Caco2 cells, which not only inhibits viral replication by blocking positive-strand viral RNA and capsid protein synthesis but also protects against HAstV-1-increased barrier permeability. Excitingly, we found similar results in vivo using a murine astrovirus (MuAstV) model, providing new evidence that virus-induced type I IFNs may protect against astrovirus replication and pathogenesis in vivo.

Importance: Human astroviruses are a major cause of pediatric diarrhea, yet little is known about the immune response. Here we show that type I interferon limits astrovirus infection and preserves barrier permeability both in vitro and in vivo. Importantly, we characterized a new mouse model for studying astrovirus replication and pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astroviridae Infections / pathology
  • Astroviridae Infections / virology
  • Caco-2 Cells
  • Disease Models, Animal
  • Epithelial Cells / immunology*
  • Epithelial Cells / virology*
  • Female
  • Humans
  • Interferon Type I / immunology*
  • Male
  • Mamastrovirus / immunology*
  • Mamastrovirus / physiology*
  • Mice, Inbred C57BL
  • Permeability*
  • Virus Replication*

Substances

  • Interferon Type I

Grants and funding

ALSAC and The Hartwell Foundation provided funding to Stacey Schultz-Cherry.