A Single Point Mutation Creating a Furin Cleavage Site in the Spike Protein Renders Porcine Epidemic Diarrhea Coronavirus Trypsin Independent for Cell Entry and Fusion

J Virol. 2015 Aug;89(15):8077-81. doi: 10.1128/JVI.00356-15. Epub 2015 May 13.

Abstract

The emerging porcine epidemic diarrhea virus (PEDV) requires trypsin supplementation to activate its S protein for membrane fusion and virus propagation in cell culture. By substitution of a single amino acid in the S protein, we created a recombinant PEDV with an artificial furin protease cleavage site N terminal of the putative fusion peptide (PEDV-SFCS). PEDV-SFCS exhibited trypsin-independent cell-cell fusion and was able to replicate in culture cells independently of trypsin, though to low titer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Substitution
  • Animals
  • Coronavirus Infections / enzymology
  • Coronavirus Infections / veterinary*
  • Coronavirus Infections / virology
  • Furin / metabolism*
  • Point Mutation*
  • Porcine epidemic diarrhea virus / chemistry
  • Porcine epidemic diarrhea virus / genetics*
  • Porcine epidemic diarrhea virus / physiology
  • Protein Processing, Post-Translational
  • Spike Glycoprotein, Coronavirus / chemistry
  • Spike Glycoprotein, Coronavirus / genetics*
  • Spike Glycoprotein, Coronavirus / metabolism*
  • Swine
  • Swine Diseases / enzymology*
  • Swine Diseases / virology
  • Trypsin / metabolism*
  • Virus Internalization*

Substances

  • Spike Glycoprotein, Coronavirus
  • Trypsin
  • Furin