Frontiers in Veterinary Science (Dec 2023)

Immunoinformatics-aided rational design of a multi-epitope vaccine targeting feline infectious peritonitis virus

  • Mohit Chawla,
  • Andrés Felipe Cuspoca,
  • Andrés Felipe Cuspoca,
  • Nahid Akthar,
  • Jorge Samuel Leon Magdaleno,
  • Siriluk Rattanabunyong,
  • Chonticha Suwattanasophon,
  • Nathjanan Jongkon,
  • Kiattawee Choowongkomon,
  • Abdul Rajjak Shaikh,
  • Tabarak Malik,
  • Luigi Cavallo

DOI
https://doi.org/10.3389/fvets.2023.1280273
Journal volume & issue
Vol. 10

Abstract

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Feline infectious peritonitis (FIP) is a grave and frequently lethal ailment instigated by feline coronavirus (FCoV) in wild and domestic feline species. The spike (S) protein of FCoV assumes a critical function in viral ingress and infection, thereby presenting a promising avenue for the development of a vaccine. In this investigation, an immunoinformatics approach was employed to ascertain immunogenic epitopes within the S-protein of FIP and formulate an innovative vaccine candidate. By subjecting the amino acid sequence of the FIP S-protein to computational scrutiny, MHC-I binding T-cell epitopes were predicted, which were subsequently evaluated for their antigenicity, toxicity, and allergenicity through in silico tools. Our analyses yielded the identification of 11 potential epitopes capable of provoking a robust immune response against FIPV. Additionally, molecular docking analysis demonstrated the ability of these epitopes to bind with feline MHC class I molecules. Through the utilization of suitable linkers, these epitopes, along with adjuvants, were integrated to design a multi-epitope vaccine candidate. Furthermore, the stability of the interaction between the vaccine candidate and feline Toll-like receptor 4 (TLR4) was established via molecular docking and molecular dynamics simulation analyses. This suggests good prospects for future experimental validation to ascertain the efficacy of our vaccine candidate in inducing a protective immune response against FIP.

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