Efficacy of inactivated variant porcine epidemic diarrhea virus vaccines in growing pigs
- Author:
Seung Heon LEE
1
;
Dong Kun YANG
;
Ha Hyun KIM
;
In Soo CHO
Author Information
- Publication Type:Original Article
- Keywords: Porcine epidemic diarrhea virus; Vaccines; Adjuvant; Growing pigs
- MeSH: Antibody Formation; Disease Progression; Enzyme-Linked Immunosorbent Assay; Neutralization Tests; Porcine epidemic diarrhea virus; Swine; Vaccines; Vero Cells; Virus Shedding
- From:Clinical and Experimental Vaccine Research 2018;7(1):61-69
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: The first aim of this study was to develop a novel inactivated porcine epidemic diarrhea virus (PEDV) vaccine using the recently isolated Korean PEDV QIAP1401 strain and to evaluate its protective efficacy in growing pigs. The second was to determine the optimum adjuvant formulation of the inactivated PEDV vaccine that induces protection against viral challenge. MATERIALS AND METHODS: To generate high titers of infectious PEDV, the QIAP1401 isolate was passaged in Vero cells. The experimental vaccines were prepared from a binary ethyleneimine-inactivated QIAP1401 strain passaged sequentially 70 times (QIAP1401-p70), formulated with four commercial adjuvants, and administered twice intramuscularly to growing pigs. Challenge studies using a virulent homologous strain of PEDV QIAP1401-p11, which was passaged 11 times after isolation, were performed to assess protection against disease progression and viral shedding during the 15-day observation period. The vaccine-induced antibody responses were measured in serum samples collected at predetermined time points by indirect enzyme-linked immunosorbent assay and virus neutralization test. RESULTS: The QIAP1401-p70 strain had 42 amino acid (aa) mutations, including a 25 aa deletion, and was selected as the inactivated PEDV vaccine candidate. Although none of the pigs that received the experimental vaccines were completely protected against subsequent viral challenge, they exhibited a significantly higher immune response than did non-vaccinated control pigs. Among the vaccine groups, the highest antibody responses were observed in the pigs that received an oil-based multiphasic water/oil/water (W/O/W) emulsion adjuvanted vaccine, which delayed the onset of clinical symptoms and viral shedding. CONCLUSION: A novel inactivated PEDV vaccine formulated with a W/O/W emulsion adjuvant was both immunogenic and protective against viral challenge.
