Evaluation of Different DNA Vaccines against Porcine Reproductive and Respiratory Syndrome (PRRS) in Pigs
- PMID: 26344342
- PMCID: PMC4494207
- DOI: 10.3390/vaccines1040463
Evaluation of Different DNA Vaccines against Porcine Reproductive and Respiratory Syndrome (PRRS) in Pigs
Abstract
In veterinary medicine, there have been different experiences with the plasmid DNA vaccination. In this area and with the hypothesis to demonstrate the effectiveness of different plasmids encoding porcine respiratory and reproductive syndrome (PRRS), five DNA vaccines against PRRS were evaluated for their innocuity and efficacy in pigs. Eighteen animals were divided into five groups which were injected with five (A, B, C, D, E) different DNA vaccines. Albeit, none of the proposed vaccines were able to protect the animals against PRRS virus. Only vaccines A and B were able to reduce the clinical signs of the infection. ELISA IgM were detected 30 days after the first vaccination in the pigs injected by Vaccine A or B. ELISA IgG were detected 90 days after the first vaccination in the pigs injected by Vaccine B or C. Neutralizing antibody were detected Post Challenge Days 61 (PCD) in all groups. In the pigs inoculated with Vaccine C, IFN-g were detected 90 days after first vaccination, and after challenge exposure they increased. In the other groups, the IFN-g were detected after challenge infection. Pigs injected with each of the vaccines A, B, C, D and E showed a significantly higher level of CD4(-)CD8⁺ lymphocytes (p < 0.001) after infection in comparison with their controls.
Keywords: CpG; DNA vaccines; NeuL; ORF4; ORF5; PRRS; UbilacI; pigs.
Figures








Similar articles
-
Lymphocyte activation as cytokine gene expression and secretion is related to the porcine reproductive and respiratory syndrome virus (PRRSV) isolate after in vitro homologous and heterologous recall of peripheral blood mononuclear cells (PBMC) from pigs vaccinated and exposed to natural infection.Vet Immunol Immunopathol. 2013 Feb 15;151(3-4):193-206. doi: 10.1016/j.vetimm.2012.11.006. Epub 2012 Nov 19. Vet Immunol Immunopathol. 2013. PMID: 23228653
-
Protection and immune response in pigs intradermally vaccinated against porcine reproductive and respiratory syndrome (PRRS) and subsequently exposed to a heterologous European (Italian cluster) field strain.Vaccine. 2007 Apr 30;25(17):3400-8. doi: 10.1016/j.vaccine.2006.12.050. Epub 2007 Jan 5. Vaccine. 2007. PMID: 17276558
-
Efficacy of a modified live porcine reproductive and respiratory syndrome virus (PRRSV) vaccine in pigs naturally exposed to a heterologous European (Italian cluster) field strain: Clinical protection and cell-mediated immunity.Vaccine. 2009 Jun 8;27(28):3788-99. doi: 10.1016/j.vaccine.2009.03.028. Epub 2009 Apr 3. Vaccine. 2009. PMID: 19442420
-
Enhanced immune responses in pigs by DNA vaccine coexpressing GP3 and GP5 of European type porcine reproductive and respiratory syndrome virus.J Virol Methods. 2014 Sep;206:27-37. doi: 10.1016/j.jviromet.2014.05.021. Epub 2014 May 29. J Virol Methods. 2014. PMID: 24882496
-
Field evaluation of the efficacy, compatibility and serologic profiling of a combined vaccine against porcine reproductive and respiratory syndrome and Haemophilus parasuis in nursery pigs.Prev Vet Med. 2015 May 1;119(3-4):134-40. doi: 10.1016/j.prevetmed.2015.03.005. Epub 2015 Mar 17. Prev Vet Med. 2015. PMID: 25819628 Clinical Trial.
Cited by
-
Glycoprotein 5-Derived Peptides Induce a Protective T-Cell Response in Swine against the Porcine Reproductive and Respiratory Syndrome Virus.Viruses. 2023 Dec 21;16(1):14. doi: 10.3390/v16010014. Viruses. 2023. PMID: 38275949 Free PMC article.
References
-
- Cavanagh D. Nidovirales: A new order comprising Coronaviridae and Arteriviridae. Arch. Virol. 1997;142:629–633. - PubMed
-
- Costers S., Lefebvre D.J., van Doorsselaere J., Vanhee M., Delputte P.L., Nauwynck H.J. GP4 of porcine reproductive and respiratory syndrome virus contains a neutralizing epitope that is susceptible to immunoselection in vitro. Arch. Virol. 2010;155:371–378. doi: 10.1007/s00705-009-0582-7. - DOI - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials