Cloning, expression, and antiviral activity of interferon β from the Chinese microbat, Myotis davidii

Virol Sin. 2015 Dec;30(6):425-32. doi: 10.1007/s12250-015-3668-2. Epub 2015 Dec 7.

Abstract

Bats are natural reservoir hosts for many viruses that produce no clinical symptoms in bats. Therefore, bats may have evolved effective mechanisms to control viral replication. However, little information is available on bat immune responses to viral infection. Type I interferon (IFN) plays a key role in controlling viral infections. In this study, we report the cloning, expression, and biological activity of interferon β (IFNβ) from the Chinese microbat species, Myotis davidii. We demonstrated the upregulation of IFNB and IFN-stimulated genes in a kidney cell line derived from M. davidii after treatment with polyI:C or infection with Sendai virus. Furthermore, the recombinant IFNβ inhibited vesicular stomatitis virus and bat adenovirus replication in cell lines from two bat species, M. davidii and Rhinolophus sinicus. We provide the first in vitro evidence of IFNβ antiviral activity in microbats, which has important implications for virus interactions with these hosts.

Keywords: IFN-stimulated genes; antiviral activity; bat; interferon.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antiviral Agents / pharmacology*
  • Cell Line
  • Chiroptera / genetics*
  • Chiroptera / immunology*
  • Chiroptera / virology
  • Cloning, Molecular*
  • Humans
  • Immunity, Innate
  • Interferon Type I / pharmacology
  • Interferon-beta / biosynthesis
  • Interferon-beta / genetics*
  • Interferon-beta / immunology*
  • Interferon-beta / pharmacology
  • Molecular Sequence Data
  • Phylogeny
  • Sequence Alignment
  • Sequence Analysis, Protein
  • Sequence Homology
  • Up-Regulation
  • Vesiculovirus / drug effects
  • Vesiculovirus / physiology

Substances

  • Antiviral Agents
  • Interferon Type I
  • Interferon-beta