A phage-displayed peptide recognizing porcine aminopeptidase N is a potent small molecule inhibitor of PEDV entry

Virology. 2014 May:456-457:20-7. doi: 10.1016/j.virol.2014.01.010. Epub 2014 Mar 25.

Abstract

Three phage-displayed peptides designated H, S and F that recognize porcine aminopeptidase N (pAPN), the cellular receptor of porcine transmissible gastroenteritis virus (TGEV) were able to inhibit cell infection by TGEV. These same peptides had no inhibitory effects on infection of Vero cells by porcine epidemic diarrhea virus (PEDV). However, when PEDV, TGEV and porcine pseudorabies virus were incubated with peptide H (HVTTTFAPPPPR), only infection of Vero cells by PEDV was inhibited. Immunofluoresence assays indicated that inhibition of PEDV infection by peptide H was independent of pAPN. Western blots demonstrated that peptide H interacted with PEDV spike protein and that pre-treatment of PEDV with peptide H led to a higher inhibition than synchronous incubation with cells. These results indicate direct interaction with the virus is necessary to inhibit infectivity. Temperature shift assays demonstrated that peptide H inhibited pre-attachment of the virus to the cells.

Keywords: Coronavirus; PEDV; Peptides; Virus attachment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / isolation & purification
  • Antiviral Agents / metabolism*
  • CD13 Antigens / metabolism*
  • Chlorocebus aethiops
  • Herpesvirus 1, Suid / drug effects
  • Herpesvirus 1, Suid / physiology
  • Peptide Library
  • Peptides / isolation & purification
  • Peptides / metabolism*
  • Porcine epidemic diarrhea virus / drug effects*
  • Porcine epidemic diarrhea virus / physiology*
  • Transmissible gastroenteritis virus / drug effects
  • Transmissible gastroenteritis virus / physiology
  • Vero Cells
  • Virus Internalization / drug effects*

Substances

  • Antiviral Agents
  • Peptide Library
  • Peptides
  • CD13 Antigens