Generation and immunogenicity of virus-like particles based on mink enteritis virus capsid protein VP2 expressed in

Hongchao Wu1, Hongli Jin2, Lingxiao Wang1

  • 1National Research Center for Veterinary Medicine, No. 3 Cuiwei Road, High-Tech District, Luoyang, 471003, Henan, China.

Insights

Mink enteritis virus (MEV) capsid protein VP2 was used to create virus-like particles (VLPs). These MEV VLPs provided complete protection against virulent MEV infection in mink for over six months.

Area of Science:

  • Veterinary Virology
  • Immunology
  • Molecular Biology

Background:

  • Mink enteritis virus (MEV) causes severe gastrointestinal illness in mink.
  • The VP2 capsid protein of MEV is a key target for immune responses and vaccine development.

Purpose of the Study:

  • To express and characterize the MEV VP2 protein.
  • To evaluate the immunogenicity and protective efficacy of self-assembled MEV virus-like particles (VLPs) in mink.

Main Methods:

  • Recombinant baculovirus expression system used to produce MEV VP2 in Spodoptera frugiperda 9 cells.
  • Characterization of self-assembled VLPs, including hemagglutination (HA) titer determination.
  • Vaccination of mink with a single dose of MEV VLPs followed by challenge with virulent MEV.

Main Results:

  • MEV VP2 self-assembled into VLPs with a high hemagglutination titer (1:2^16).
  • A single VLP injection (HA titer, 1:256) conferred complete protection against virulent MEV challenge.
  • Protection was sustained for at least 180 days post-vaccination.

Conclusions:

  • MEV VLPs are highly immunogenic and capable of inducing long-lasting protective immunity.
  • MEV VLPs represent a promising candidate for a novel vaccine against mink enteritis.

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