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Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate
The oral mucosal vaccine has great potential in preventing a series of diseases caused by porcine circovirus type 2 (PCV2) infection. This study constructed a recombinant Bacillus subtilis RB with PCV2 Capsid protein (Cap) on its spore surface and cotB as a fusion partner. The immune properties of 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/PMC9520567/ https://www.ncbi.nlm.nih.gov/pubmed/36189301 http://dx.doi.org/10.3389/fimmu.2022.1007202 |
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author | Li, Weijie Li, Jianzhen Dai, Xixi Liu, Minggang Khalique, Abdul Wang, Zhenghua Zeng, Yan Zhang, Dongmei Ni, Xueqin Zeng, Dong Jing, Bo Pan, Kangcheng |
author_facet | Li, Weijie Li, Jianzhen Dai, Xixi Liu, Minggang Khalique, Abdul Wang, Zhenghua Zeng, Yan Zhang, Dongmei Ni, Xueqin Zeng, Dong Jing, Bo Pan, Kangcheng |
author_sort | Li, Weijie |
collection | PubMed |
description | The oral mucosal vaccine has great potential in preventing a series of diseases caused by porcine circovirus type 2 (PCV2) infection. This study constructed a recombinant Bacillus subtilis RB with PCV2 Capsid protein (Cap) on its spore surface and cotB as a fusion partner. The immune properties of the recombinant strain were evaluated in a mouse model. IgA in intestinal contents and IgG in serum were detected by enzyme-linked immunosorbent assay (ELISA). The results demonstrated that recombinant spores could activate strong specific mucosal and humoral immune responses. In addition, spores showed good mucosal immune adjuvant function, promoting the proliferation of CD3+, CD4+ and CD8+ T cells and other immune cells. We also found that the relative expression of inflammatory cytokines such as IL-1β, IL-6, IL-10, TNF-α and IFN in the small intestinal mucosa was significantly up-regulated under the stimulation of recombinant bacteriophage. These effects are important for the balance of Th1/Th2-like responses. In summary, our results suggest that recombinant B. subtilis RB as a feed additive provides a new strategy for the development of novel and safe PCV2 mucosal subunit vaccines. |
format | Online Article Text |
id | pubmed-9520567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95205672022-09-30 Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate Li, Weijie Li, Jianzhen Dai, Xixi Liu, Minggang Khalique, Abdul Wang, Zhenghua Zeng, Yan Zhang, Dongmei Ni, Xueqin Zeng, Dong Jing, Bo Pan, Kangcheng Front Immunol Immunology The oral mucosal vaccine has great potential in preventing a series of diseases caused by porcine circovirus type 2 (PCV2) infection. This study constructed a recombinant Bacillus subtilis RB with PCV2 Capsid protein (Cap) on its spore surface and cotB as a fusion partner. The immune properties of the recombinant strain were evaluated in a mouse model. IgA in intestinal contents and IgG in serum were detected by enzyme-linked immunosorbent assay (ELISA). The results demonstrated that recombinant spores could activate strong specific mucosal and humoral immune responses. In addition, spores showed good mucosal immune adjuvant function, promoting the proliferation of CD3+, CD4+ and CD8+ T cells and other immune cells. We also found that the relative expression of inflammatory cytokines such as IL-1β, IL-6, IL-10, TNF-α and IFN in the small intestinal mucosa was significantly up-regulated under the stimulation of recombinant bacteriophage. These effects are important for the balance of Th1/Th2-like responses. In summary, our results suggest that recombinant B. subtilis RB as a feed additive provides a new strategy for the development of novel and safe PCV2 mucosal subunit vaccines. Frontiers Media S.A. 2022-09-15 /pmc/articles/PMC9520567/ /pubmed/36189301 http://dx.doi.org/10.3389/fimmu.2022.1007202 Text en Copyright © 2022 Li, Li, Dai, Liu, Khalique, Wang, Zeng, Zhang, Ni, Zeng, Jing and Pan 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 | Immunology Li, Weijie Li, Jianzhen Dai, Xixi Liu, Minggang Khalique, Abdul Wang, Zhenghua Zeng, Yan Zhang, Dongmei Ni, Xueqin Zeng, Dong Jing, Bo Pan, Kangcheng Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate |
title | Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate |
title_full | Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate |
title_fullStr | Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate |
title_full_unstemmed | Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate |
title_short | Surface Display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: An effective mucosal vaccine candidate |
title_sort | surface display of porcine circovirus type 2 antigen protein cap on the spores of bacillus subtilis 168: an effective mucosal vaccine candidate |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520567/ https://www.ncbi.nlm.nih.gov/pubmed/36189301 http://dx.doi.org/10.3389/fimmu.2022.1007202 |
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