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Expression and evaluation of porcine circovirus type 2 capsid protein mediated by recombinant adeno-associated virus 8

  • Li, Shuang (National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University) ;
  • Wang, Bo (School of Chemistry and Life Science, Changchun University of Technology) ;
  • Jiang, Shun (National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University) ;
  • Lan, Xiaohui (The Second Hospital of Jilin University) ;
  • Qiao, Yongbo (National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University) ;
  • Nie, Jiaojiao (National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University) ;
  • Yin, Yuhe (School of Chemistry and Life Science, Changchun University of Technology) ;
  • Shi, Yuhua (National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University) ;
  • Kong, Wei (National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University) ;
  • Shan, Yaming (National Engineering Laboratory for AIDS Vaccine, School of Life Sciences, Jilin University)
  • Received : 2020.09.09
  • Accepted : 2020.11.29
  • Published : 2021.01.31

Abstract

Background: Porcine circovirus type 2 (PCV2) is an important infectious pathogen implicated in porcine circovirus-associated diseases (PCVAD), which has caused significant economic losses in the pig industry worldwide. Objectives: A suitable viral vector-mediated gene transfer platform for the expression of the capsid protein (Cap) is an attractive strategy. Methods: In the present study, a recombinant adeno-associated virus 8 (rAAV8) vector was constructed to encode Cap (Cap-rAAV) in vitro and in vivo after gene transfer. Results: The obtained results showed that Cap could be expressed in HEK293T cells and BABL/c mice. The results of lymphocytes proliferative, as well as immunoglobulin G (IgG) 2a and interferon-γ showed strong cellular immune responses induced by Cap-rAAV. The enzyme-linked immunosorbent assay titers obtained and the IgG1 and interleukin-4 levels showed that humoral immune responses were also induced by Cap-rAAV. Altogether, these results demonstrated that the rAAV8 vaccine Cap-rAAV can induce strong cellular and humoral immune responses, indicating a potential rAAV8 vaccine against PCV2. Conclusions: The injection of rAAV8 encoding PCV2 Cap genes into muscle tissue can ensure long-term, continuous, and systemic expression.

Keywords

Acknowledgement

This work was supported by National Natural Science Foundation of China (grant number: 31770996).

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