MERTK is a host factor that promotes classical swine fever virus entry and antagonizes innate immune response in PK-15 cells

Emerg Microbes Infect. 2020 Mar 14;9(1):571-581. doi: 10.1080/22221751.2020.1738278. eCollection 2020.

Abstract

Classical swine fever virus (CSFV) is a member of the genus Pestivirus in the Flaviviridae family. To date, the host factors required for CSFV entry remain poorly characterized. To identify the functional membrane protein(s) involved in CSFV infection, we analyzed the transcriptomic data from previous studies describing gene expression profiles for CSFV, and found twelve novel candidate proteins. One of these proteins, MERTK, significantly reduced CSFV protein expression by RNA interference screening using a recombinant CSFV that contains a luciferase reporter to measure CSFV protein expression. Furthermore, our results demonstrated that either anti-MERTK antibodies or soluble MERTK ectodomain could reduce CSFV infection in PK-15 cells in a dose-dependent manner. Mechanistically, MERTK interacted with the E2 protein of CSFV and facilitated virus entry. After virus entry, MERTK downregulates of mRNA expression of IFN-β and promotes CSFV infection. Interestingly, the soluble MERTK ectodomain could also reduce the infection of bovine viral diarrhea virus (BVDV), another pestivirus. Taken together, our results suggested that MERTK is a CSFV entry factor that synergistically dampens innate immune responses in PK-15 cells and is also involved in BVDV infection.

Keywords: MERTK; TAM receptors; classical swine fever virus; entry; innate immune response.

MeSH terms

  • Animals
  • Cattle
  • Cell Line
  • Classical Swine Fever / immunology*
  • Classical Swine Fever Virus / physiology*
  • Humans
  • Immunity, Innate*
  • Recombination, Genetic
  • Swine
  • Viral Envelope Proteins / genetics
  • Viral Envelope Proteins / metabolism
  • Virus Internalization*
  • c-Mer Tyrosine Kinase / genetics
  • c-Mer Tyrosine Kinase / metabolism*

Substances

  • Viral Envelope Proteins
  • c-Mer Tyrosine Kinase

Grants and funding

This study was supported by the National Natural Science Foundation of China (grants 31630080, 31672537, 31572540, 31702220, and 31902264).