Abstract

Porcine Circovirus 2 (PCV2) vaccines are based on either inactivated whole virion, or recombinant ORF2 capsid protein assembled into Virus-like Particles (VLPs). No data are available about the immunizing properties of free, non-assembled capsid protein. To investigate this issue, ORF2 of a reference PCV2b strain was expressed in a Baculovirus-based expression system without assembly into VLPs. The free purified protein was formulated into an oil vaccine at three distinct Ag payloads: 10.8/3.6/1.2 micrograms/dose. Each dose was injected intramuscularly into five, 37-day old piglets, carefully matched for maternally-derived antibody. Five control piglets were injected with sterile PBS in oil adjuvant. Twenty-eight days later, all the pigs were challenged intranasally with 105.3 TCID50 of PCV2b strain DV6503. After challenge infection, all the pigs remained in good clinical conditions. The recombinant vaccine did not induce significant antibody and PCV2-specific IFN-γ responses. ELISPOT and lymphocyte proliferation data confirmed poor induction of cell-mediated immunity. In terms of PCV2 viremia, there was no significant difference between vaccinated and control animals. The histological data indicated the absence of a detectable viral load and of PCVAD lesions in both vaccinated and control animals, as well as of histiocytes and multi-nucleated giant cells. We conclude that free, non-assembled ORF2 capsid protein does not induce protective immunity.

Highlights

  • The Porcine Circovirus Associated Disease (PCVAD) complex includes a series of devasting syndromes [1]

  • Viremia after challenge was observed in all the control and vaccinated pigs, starting at days post infection (DPI) 14 (Table 1)

  • Our results unambiguously show that non-assembled ORF2 protein does not induce protective immunity in pigs even at much higher doses, compared with conventional, whole virus, inactivated vaccines [8,9]

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Summary

Introduction

The Porcine Circovirus Associated Disease (PCVAD) complex includes a series of devasting syndromes [1]. PCVAD is sustained by Porcine Circovirus 2 (PCV2), a small, nonenveloped virus of the family Circoviridae [2]. PCVAD is triggered by PCV2 in association with other pathogens, as well as environmental, non-infectious stressors [3]. Plenty of nucleotide substitutions underlay the rapid emergence of new PCV2 strains worldwide. This way, in addition to the two original main groups designed as genotype “a” (PCV2a) and “b” (PCV2b), further genotypes later emerged in the field (PCV2c, PCV2d, PCV2e) [4,5]. Several vaccines were developed to reduce PCV2 infection and PCVAD occurrence

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