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Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo
The porcine reproductive and respiratory syndrome virus (PRRSV) is a threat to the health of pigs worldwide, but commercially available vaccines offer limited protection against PRRSV infection. It is necessary to develop a more effective DNA vaccine. The immunological effects of DNA vaccines with t...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582230/ https://www.ncbi.nlm.nih.gov/pubmed/36275018 http://dx.doi.org/10.3389/fcimb.2022.1016897 |
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author | Zhao, Guanyu Zhang, Jiaqi Sun, Wenchao Xie, Changzhan Zhang, He Gao, Yan Wen, Shubo Ha, Zhuo Nan, Fulong Zhu, Xiangyu Feng, Sheng Cao, Xinyu Zhang, Ying Zhu, Yanzhu Jin, Ningyi Lu, Huijun |
author_facet | Zhao, Guanyu Zhang, Jiaqi Sun, Wenchao Xie, Changzhan Zhang, He Gao, Yan Wen, Shubo Ha, Zhuo Nan, Fulong Zhu, Xiangyu Feng, Sheng Cao, Xinyu Zhang, Ying Zhu, Yanzhu Jin, Ningyi Lu, Huijun |
author_sort | Zhao, Guanyu |
collection | PubMed |
description | The porcine reproductive and respiratory syndrome virus (PRRSV) is a threat to the health of pigs worldwide, but commercially available vaccines offer limited protection against PRRSV infection. It is necessary to develop a more effective DNA vaccine. The immunological effects of DNA vaccines with three adjuvants were examined in pigs (Susscrofa domestica) challenged with PRRSV. These DNA vaccines, which encoded PRRSV GP3 and GP5, were formulated with A1, A2, and A3. Serum specific and neutralizing antibodies, IL-4, IFN-γ, IL-2, IL-10, CD4(+) and CD8(+)T-lymphocytes, health status, histopathology, and viral loads were determined. The results showed that the use of adjuvant A3 led to higher levels of neutralizing antibodies and a lower viral load in pigs compared to the other adjuvants. The neutralizing antibody titers of the pVAX-GP35+A1 and pVAX-GP35+A3 groups reached a peak of 1:19 at 35 dpi. The maximum concentration of IL-4 was 136.77 pg/mL in the pVAX-GP35+A3 group. At 35 dpi, the IFN-γ concentration in the pVAX-GP35+A1 group was 227.4 pg/mL. pVAX-GP35+A3 group shows the highest IL-2 and IL-10 expression to the peak of 597.6 pg/mL and 189.1 pg/mL, respectively. We found a formulation demonstrated beneficial immune outcomes. This study provides an alternative vaccine to protect pigs from PRRSV. |
format | Online Article Text |
id | pubmed-9582230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95822302022-10-21 Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo Zhao, Guanyu Zhang, Jiaqi Sun, Wenchao Xie, Changzhan Zhang, He Gao, Yan Wen, Shubo Ha, Zhuo Nan, Fulong Zhu, Xiangyu Feng, Sheng Cao, Xinyu Zhang, Ying Zhu, Yanzhu Jin, Ningyi Lu, Huijun Front Cell Infect Microbiol Cellular and Infection Microbiology The porcine reproductive and respiratory syndrome virus (PRRSV) is a threat to the health of pigs worldwide, but commercially available vaccines offer limited protection against PRRSV infection. It is necessary to develop a more effective DNA vaccine. The immunological effects of DNA vaccines with three adjuvants were examined in pigs (Susscrofa domestica) challenged with PRRSV. These DNA vaccines, which encoded PRRSV GP3 and GP5, were formulated with A1, A2, and A3. Serum specific and neutralizing antibodies, IL-4, IFN-γ, IL-2, IL-10, CD4(+) and CD8(+)T-lymphocytes, health status, histopathology, and viral loads were determined. The results showed that the use of adjuvant A3 led to higher levels of neutralizing antibodies and a lower viral load in pigs compared to the other adjuvants. The neutralizing antibody titers of the pVAX-GP35+A1 and pVAX-GP35+A3 groups reached a peak of 1:19 at 35 dpi. The maximum concentration of IL-4 was 136.77 pg/mL in the pVAX-GP35+A3 group. At 35 dpi, the IFN-γ concentration in the pVAX-GP35+A1 group was 227.4 pg/mL. pVAX-GP35+A3 group shows the highest IL-2 and IL-10 expression to the peak of 597.6 pg/mL and 189.1 pg/mL, respectively. We found a formulation demonstrated beneficial immune outcomes. This study provides an alternative vaccine to protect pigs from PRRSV. Frontiers Media S.A. 2022-10-06 /pmc/articles/PMC9582230/ /pubmed/36275018 http://dx.doi.org/10.3389/fcimb.2022.1016897 Text en Copyright © 2022 Zhao, Zhang, Sun, Xie, Zhang, Gao, Wen, Ha, Nan, Zhu, Feng, Cao, Zhang, Zhu, Jin and Lu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Zhao, Guanyu Zhang, Jiaqi Sun, Wenchao Xie, Changzhan Zhang, He Gao, Yan Wen, Shubo Ha, Zhuo Nan, Fulong Zhu, Xiangyu Feng, Sheng Cao, Xinyu Zhang, Ying Zhu, Yanzhu Jin, Ningyi Lu, Huijun Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo |
title | Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo
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title_full | Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo
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title_fullStr | Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo
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title_full_unstemmed | Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo
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title_short | Immunological evaluation of recombination PRRSV GP3 and GP5 DNA vaccines in vivo
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title_sort | immunological evaluation of recombination prrsv gp3 and gp5 dna vaccines in vivo |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582230/ https://www.ncbi.nlm.nih.gov/pubmed/36275018 http://dx.doi.org/10.3389/fcimb.2022.1016897 |
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