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Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides
Porcine reproductive and respiratory syndrome (PRRS) is a widespread disease with great economic importance in the pig industry. Although vaccines against the PRRS virus (PRRSV) have been employed for more than 20 years, differentiating infected from vaccinated animals remains challenging. In this s...
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/PMC9189411/ https://www.ncbi.nlm.nih.gov/pubmed/35706603 http://dx.doi.org/10.3389/fvets.2022.902822 |
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author | Li, Dong-Yan Cui, Xing-Yang Huang, Xin-Yi Hu, Yue Tian, Xiao-Xiao Wang, Tao Yang, Yong-Bo Wang, Qian Tian, Zhi-Jun Cai, Xue-Hui An, Tong-Qing |
author_facet | Li, Dong-Yan Cui, Xing-Yang Huang, Xin-Yi Hu, Yue Tian, Xiao-Xiao Wang, Tao Yang, Yong-Bo Wang, Qian Tian, Zhi-Jun Cai, Xue-Hui An, Tong-Qing |
author_sort | Li, Dong-Yan |
collection | PubMed |
description | Porcine reproductive and respiratory syndrome (PRRS) is a widespread disease with great economic importance in the pig industry. Although vaccines against the PRRS virus (PRRSV) have been employed for more than 20 years, differentiating infected from vaccinated animals remains challenging. In this study, all 907 non-structural protein 2 (NSP2) full-length sequences of PRRSV-2 available from GenBank were aligned. Two peptides, at positions 562–627 (m1B) and 749–813 (m2B) of NSP2, were selected, and their potential for use in differential diagnosis was assessed. Both m1B and m2B were recognized by PRRSV-positive pig serum in peptide-coated enzyme-linked immunosorbent assays. Further epitope identification yielded five overlapping short peptides for the immunodominant regions of m1B and m2B. Using the infectious clone of PRRSV HuN4-F112 as a template, the deletion mutants, rHuN4-F112-m1B, rHuN4-F112-m2B, and rHuN4-F112-C5-m1B-m2B, were generated and successfully rescued in Marc-145 cells. Growth kinetics revealed that the deletion of m1B and m2B did not significantly affect virus replication. Hence, m1B and m2B show potential as molecular markers for developing a PRRSV vaccine. |
format | Online Article Text |
id | pubmed-9189411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91894112022-06-14 Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides Li, Dong-Yan Cui, Xing-Yang Huang, Xin-Yi Hu, Yue Tian, Xiao-Xiao Wang, Tao Yang, Yong-Bo Wang, Qian Tian, Zhi-Jun Cai, Xue-Hui An, Tong-Qing Front Vet Sci Veterinary Science Porcine reproductive and respiratory syndrome (PRRS) is a widespread disease with great economic importance in the pig industry. Although vaccines against the PRRS virus (PRRSV) have been employed for more than 20 years, differentiating infected from vaccinated animals remains challenging. In this study, all 907 non-structural protein 2 (NSP2) full-length sequences of PRRSV-2 available from GenBank were aligned. Two peptides, at positions 562–627 (m1B) and 749–813 (m2B) of NSP2, were selected, and their potential for use in differential diagnosis was assessed. Both m1B and m2B were recognized by PRRSV-positive pig serum in peptide-coated enzyme-linked immunosorbent assays. Further epitope identification yielded five overlapping short peptides for the immunodominant regions of m1B and m2B. Using the infectious clone of PRRSV HuN4-F112 as a template, the deletion mutants, rHuN4-F112-m1B, rHuN4-F112-m2B, and rHuN4-F112-C5-m1B-m2B, were generated and successfully rescued in Marc-145 cells. Growth kinetics revealed that the deletion of m1B and m2B did not significantly affect virus replication. Hence, m1B and m2B show potential as molecular markers for developing a PRRSV vaccine. Frontiers Media S.A. 2022-05-30 /pmc/articles/PMC9189411/ /pubmed/35706603 http://dx.doi.org/10.3389/fvets.2022.902822 Text en Copyright © 2022 Li, Cui, Huang, Hu, Tian, Wang, Yang, Wang, Tian, Cai and An. 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 | Veterinary Science Li, Dong-Yan Cui, Xing-Yang Huang, Xin-Yi Hu, Yue Tian, Xiao-Xiao Wang, Tao Yang, Yong-Bo Wang, Qian Tian, Zhi-Jun Cai, Xue-Hui An, Tong-Qing Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides |
title | Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides |
title_full | Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides |
title_fullStr | Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides |
title_full_unstemmed | Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides |
title_short | Characterization of Two Immunodominant Antigenic Peptides in NSP2 of PRRSV-2 and Generation of a Marker PRRSV Strain Based on the Peptides |
title_sort | characterization of two immunodominant antigenic peptides in nsp2 of prrsv-2 and generation of a marker prrsv strain based on the peptides |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189411/ https://www.ncbi.nlm.nih.gov/pubmed/35706603 http://dx.doi.org/10.3389/fvets.2022.902822 |
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