The PCV3 Cap Virus-like Particle Vaccine with the Chimeric PCV2-Neutralizing Epitope Gene Is Effective in Mice

• Published in: Veterinary sciences 2024-06, Vol.11 (6), p.264
• Main Authors: Wu, Xingchen, Wang, Qikai, Lu, Wang, Wang, Ying, Han, Zehao, Liang, Libin, Gao, Shimin, Ma, Haili, Luo, Xiaomao
• Format: Article
• Language: English
• Subjects: Animal experimentation; Antigenic determinants; Antigens; Biotechnology; capsid; Cell-mediated immunity; Cells; Cross-protection; Design; E coli; Enzymes; Epitopes; Genes; Genomes; Health aspects; Hogs; Immune response (cell-mediated); Immune response (humoral); Immunization; Immunogenicity; Infections; Localization; Mammalian cells; Mice; Mutation; neutralizing epitope; Peptides; Plasmids; porcine circovirus type 3; Proteins; Vaccine development; Vaccines; virus-like particle vaccine; Virus-like particles; Viruses
• ISSN: 2306-7381; 2306-7381
• DOI: 10.3390/vetsci11060264

Porcine circovirus type 3 (PCV3) infection can cause symptoms similar to those of porcine circovirus type 2 (PCV2) infection, and coinfections with both PCV2 and PCV3 are observed in the swine industry. Consequently, developing chimeric vaccines is essential to prevent and control porcine circovirus infections. In this study, we used both and mammalian expression systems to express PCV3 Cap (Cap3) and a chimeric gene containing the PCV2-neutralizing epitope within the PCV3 Cap (Cap3-Cap2E), which were assembled into virus-like particle (VLP) vaccines. We found that Cap3 lacking nuclear localization signal (NLS) could not form VLPs, while Cap3 with a His-tag successfully assembled into VLPs. Additionally, the chimeric of PCV2-neutralizing epitopes did not interfere with the assembly process of VLPs. Various immunization approaches revealed that pCap3-Cap2E VLP vaccines were capable of activating high PCV3 Cap-specific antibody levels and effectively neutralizing both PCV3 and PCV2. Furthermore, pCap3-Cap2E VLPs demonstrated a potent ability to activate cellular immunity, protecting against PCV3 infection and preventing lung damage in mice. In conclusion, this study successfully developed a PCV3 Cap VLP vaccine incorporating chimeric PCV2-neutralizing epitope genes, providing new perspectives for PCV3 vaccine development.