# Evaluation of Different DNA Vaccines against Porcine Reproductive and Respiratory Syndrome (PRRS) in Pigs

**Authors:** Stefano Petrini, Giorgio Ramadori, Riccardo Villa, Paolo Borghetti, Elena de Angelis, Anna Maria Cantoni, Attilio Corradi, Augusto Amici, Maura Ferrari

PMC · DOI: 10.3390/vaccines1040463 · Vaccines · 2013-10-18

## TL;DR

This study tested five DNA vaccines against PRRS in pigs and found that while none fully protected against the virus, some reduced symptoms and triggered immune responses.

## Contribution

The study evaluates the immune responses and efficacy of five different DNA vaccines against PRRS in pigs.

## Key findings

- Vaccines A and B reduced clinical signs of PRRS infection.
- ELISA IgM was detected 30 days after vaccination with A or B, and IgG was detected 90 days after vaccination with B or C.
- Vaccine C induced IFN-γ 90 days post-vaccination and increased after challenge.

## 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-γ were detected 90 days after first vaccination, and after challenge exposure they increased. In the other groups, the IFN-γ 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.

## Linked entities

- **Diseases:** porcine reproductive and respiratory syndrome (MONDO:0025494), PRRS (MONDO:0025494)

## Full-text entities

- **Genes:** CD8B (CD8 subunit beta) [NCBI Gene 396636], CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, Myc (Myc proto-oncogene, bHLH transcription factor) [NCBI Gene 17869] {aka Myc2, Niard, Nird, bHLHe39}, IFNG (interferon gamma) [NCBI Gene 396991], CD36 (CD36 molecule (CD36 blood group)) [NCBI Gene 948] {aka BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV}, CD4 (CD4 molecule) [NCBI Gene 404704], GP5 (glycoprotein V platelet) [NCBI Gene 100523640], IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, Cttnbp2 (cortactin binding protein 2) [NCBI Gene 30785] {aka 3010022N24Rik, 4732477G22Rik, 6430526E05, 9130022E09Rik, Cortbp2, ORF4}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, Rwdd2b (RWD domain containing 2B) [NCBI Gene 53858] {aka ORF5}, IFN-ALPHA-14 (interferon-alpha-14) [NCBI Gene 100310804] {aka IFN-alpha}, IL15 (interleukin 15) [NCBI Gene 397683] {aka IL-15}, IFNG (Interferon-gamma level) [NCBI Gene 103158290], GP2 (glycoprotein 2) [NCBI Gene 2813] {aka ZAP75}, GP5 (glycoprotein V platelet) [NCBI Gene 2814] {aka CD42d, GPV}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** Viremia (MESH:D014766), PCD (MESH:C538057), hyperplasia (MESH:D006965), Challenge infection (MESH:D007239), PRRS (MESH:D019318), lethargy (MESH:D053609), reproductive failure (MESH:D051437), Fever (MESH:D005334), Inappetence Cough Dyspnoea (MESH:D003371)
- **Chemicals:** B (MESH:D001895), oligonucleotide (MESH:D009841), H&amp;E (MESH:D006371), water (MESH:D014867), wax (MESH:D014885), ODN 2135 (-), formalin (MESH:D005557), E (MESH:D004540), C (MESH:D002244), A (MESH:D001151), Paraffin (MESH:D010232), NH4Cl (MESH:D000643), FITC (MESH:D016650), lipofectamine (MESH:C086724), ODN (MESH:D009838), phosphate (MESH:D010710)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Escherichia coli DH5[alpha] (strain) [taxon 668369], Porcine reproductive and respiratory syndrome virus (no rank) [taxon 28344], KV [taxon 2844101], Escherichia coli (E. coli, species) [taxon 562], Lelystad virus (no rank) [taxon 11049], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** MARC 145 — Chlorocebus pygerythrus (Vervet monkey), Spontaneously immortalized cell line (CVCL_4540), NIH-3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594), 48CpG-NeuL — Mus musculus (Mouse), Hybridoma (CVCL_J728), mouse — Mus musculus (Mouse), Undefined cell line type (CVCL_ZE35)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4494207/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC4494207/full.md

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Source: https://tomesphere.com/paper/PMC4494207