Indian Journal of Comparative Microbiology, Immunology and Infectious Diseases
  • Year: 2024
  • Volume: 45
  • Issue: 1

Development and evaluation of inactivated Porcine circovirus 2 vaccine using predominantly circulating genotypes in India

  • Author:
  • S. Parthiban1, A. Ramesh2,*, A.K. Karuppannan2, G.D. Raj1, M. Parthiban1, S. Hemalatha3, K. Senthilkumar4, D. Balasubramaniyam5
  • Total Page Count: 12
  • Published Online: Sep 25, 2024
  • Page Number: 42 to 53

1Department of Animal Biotechnology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, Chennai, Tamil Nadu, India

2Department of Veterinary Microbiology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, Chennai, Tamil Nadu, India

3Department of Veterinary Pathology, Madras Veterinary College, Tamil Nadu Veterinary and Animal Sciences University, Chennai, Tamil Nadu, India

4Department of Veterinary and Animal Husbandry Extension Education, Veterinary College and Research Institute, Tamil Nadu Veterinary and Animal Sciences University, Salem, Tamil Nadu, India

5Post Graduate Research Institute in Animal Sciences, Tamil Nadu Veterinary and Animal Sciences University, Chennai, Tamil Nadu, India

*Corresponding author E-mail id: drvetaramesh2021@gmail.com

Online Published on 4 October, 2024.

Abstract

The present study aimed to develop and evaluate an inactivated porcine circovirus 2 (PCV2) vaccine using predominantly circulating genotypes under field conditions in India. The two most commonly circulating genotypes, PCV2d (INDTN07- BC3) and PCV2b (INDTNCHN56-4T), isolated and genotyped in southern India, were further propagated in PK-15 cells and titrated at the eleventh passage, with the titer of 106.3TCID50/ml and 105.4TCID50/ml for PCV2b and PCV2d, respectively. They were then inactivated using binary ethylenimine (BEI) and developed into individual genotype-specific inactivated PCV2 vaccines. The safety and immunogenicity of the developed inactivated PCV2b and PCV2d vaccines were evaluated individually through experimental trials in piglets. The post-vaccinal serum antibody response against PCV2 was measured using a commercial ELISA, and its neutralizing titer was measured through a fluorescent antibody virus neutralization assay (FAVN) at 21 days post-vaccination (dpv). The animals used in the immunogenicity study were further sub-grouped and kept as non-booster and booster groups within each vaccine group. In the booster group, the second dose of their respective inactivated PCV2 vaccine was given on the 28th day post-primary vaccination, and the duration of serum antibody response and neutralizing antibody response were evaluated for the period of 120 dpv. Both the genotype-specific inactivated PCV2b and PCV2d vaccines developed in this study were found to be safe and showed a significant rise in serum antibody response with the required neutralizing PCV2 antibody titer at 21 dpv. This response was maintained up to 120 dpv in both the booster and non-booster groups of both PCV2 vaccines when compared with the unvaccinated control group. Heterologous cross-protection of PCV2b vaccinated serum to the wild PCV2d genotype and vice versa was evidenced at 21 dpv for both vaccines.

Keywords

Safety, Immunogenicity, Cross-protection