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Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v
African swine fever virus (ASFV), a DNA double-stranded virus with high infectivity and mortality, causing a devastating blow to the pig industry and the world economy. The CD2v protein is an essential immunoprotective protein of ASFV. In this study, we expressed the extracellular region of the CD2v...
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/PMC9716131/ https://www.ncbi.nlm.nih.gov/pubmed/36466651 http://dx.doi.org/10.3389/fmicb.2022.1056117 |
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author | Liu, Siyuan Ding, Peiyang Du, Yongkun Ren, Dongna Chen, Yilan Li, Minghui Sun, Xueke Wang, Siqiao Chang, Zejie Li, Ruiqi Zhang, Gaiping |
author_facet | Liu, Siyuan Ding, Peiyang Du, Yongkun Ren, Dongna Chen, Yilan Li, Minghui Sun, Xueke Wang, Siqiao Chang, Zejie Li, Ruiqi Zhang, Gaiping |
author_sort | Liu, Siyuan |
collection | PubMed |
description | African swine fever virus (ASFV), a DNA double-stranded virus with high infectivity and mortality, causing a devastating blow to the pig industry and the world economy. The CD2v protein is an essential immunoprotective protein of ASFV. In this study, we expressed the extracellular region of the CD2v protein in the 293F expression system to achieve proper glycosylation. Monoclonal antibodies (mAbs) were prepared by immunizing mice with the recombinant CD2v protein. Eventually, four mAbs that target the extracellular region of the ASFV CD2v protein were obtained. All four mAbs responded well to the ASFV HLJ/18 strain and recognized the same linear epitope, (154)SILE(157). The specific shortest amino acid sequence of this epitope has been accurately identified for the first time. Meaningfully, the (154)SILE(157) epitope was highly conformed in the ASFV Chinese epidemic strain and Georgia2008/1 strains according to the analysis of the conservation and have a fair protective effect. These findings contribute to further understanding of the protein function of CD2v and provide potential support for the development of diagnostic tools and vaccines for ASFV. |
format | Online Article Text |
id | pubmed-9716131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97161312022-12-03 Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v Liu, Siyuan Ding, Peiyang Du, Yongkun Ren, Dongna Chen, Yilan Li, Minghui Sun, Xueke Wang, Siqiao Chang, Zejie Li, Ruiqi Zhang, Gaiping Front Microbiol Microbiology African swine fever virus (ASFV), a DNA double-stranded virus with high infectivity and mortality, causing a devastating blow to the pig industry and the world economy. The CD2v protein is an essential immunoprotective protein of ASFV. In this study, we expressed the extracellular region of the CD2v protein in the 293F expression system to achieve proper glycosylation. Monoclonal antibodies (mAbs) were prepared by immunizing mice with the recombinant CD2v protein. Eventually, four mAbs that target the extracellular region of the ASFV CD2v protein were obtained. All four mAbs responded well to the ASFV HLJ/18 strain and recognized the same linear epitope, (154)SILE(157). The specific shortest amino acid sequence of this epitope has been accurately identified for the first time. Meaningfully, the (154)SILE(157) epitope was highly conformed in the ASFV Chinese epidemic strain and Georgia2008/1 strains according to the analysis of the conservation and have a fair protective effect. These findings contribute to further understanding of the protein function of CD2v and provide potential support for the development of diagnostic tools and vaccines for ASFV. Frontiers Media S.A. 2022-11-18 /pmc/articles/PMC9716131/ /pubmed/36466651 http://dx.doi.org/10.3389/fmicb.2022.1056117 Text en Copyright © 2022 Liu, Ding, Du, Ren, Chen, Li, Sun, Wang, Chang, Li and Zhang. 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 | Microbiology Liu, Siyuan Ding, Peiyang Du, Yongkun Ren, Dongna Chen, Yilan Li, Minghui Sun, Xueke Wang, Siqiao Chang, Zejie Li, Ruiqi Zhang, Gaiping Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v |
title | Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v |
title_full | Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v |
title_fullStr | Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v |
title_full_unstemmed | Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v |
title_short | Development and characterization of monoclonal antibodies against the extracellular domain of African swine fever virus structural protein, CD2v |
title_sort | development and characterization of monoclonal antibodies against the extracellular domain of african swine fever virus structural protein, cd2v |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716131/ https://www.ncbi.nlm.nih.gov/pubmed/36466651 http://dx.doi.org/10.3389/fmicb.2022.1056117 |
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