Cargando…
Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes
Recently, the outbreak of the infection of Duck adenovirus 3 (DAdV-3) characterized by swelling and hemorrhagic liver and kidney has caused huge economic losses to duck industry since 2014 in China. To date, the B cell epitopes in the Fiber-1 protein and the underlying infection mechanism of DAdV-3...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597451/ https://www.ncbi.nlm.nih.gov/pubmed/36311658 http://dx.doi.org/10.3389/fvets.2022.1003262 |
_version_ | 1784816094113955840 |
---|---|
author | Shao, Hongxia Zhang, Wenyuan Lin, Yun Xie, Jing Ren, Dan Xie, Quan Li, Tuofan Wan, Zhimin Qin, Aijian Ye, Jianqiang |
author_facet | Shao, Hongxia Zhang, Wenyuan Lin, Yun Xie, Jing Ren, Dan Xie, Quan Li, Tuofan Wan, Zhimin Qin, Aijian Ye, Jianqiang |
author_sort | Shao, Hongxia |
collection | PubMed |
description | Recently, the outbreak of the infection of Duck adenovirus 3 (DAdV-3) characterized by swelling and hemorrhagic liver and kidney has caused huge economic losses to duck industry since 2014 in China. To date, the B cell epitopes in the Fiber-1 protein and the underlying infection mechanism of DAdV-3 have not been investigated. In this study, the recombinant Fiber-1 protein was first expressed in E. coli and six novel monoclonal antibodies (mAbs) against Fiber-1 were generated, designated as 1D8, 1E6, 3G6, 4G1, 4G2, and 6F10, respectively. Moreover, mAbs 3G6 and 6F10 could efficiently immunoprecipitate the Fiber-1 in LMH cells infected with DAdV-3 or transfected with pcDNA3.1-Fiber-1. Notably, mAbs 3G6 and 4G2 also showed certain neutralizing activity against DAdV-3 infection in vitro. Epitopes mapping revealed that the B cell epitope recognized by 6F10, 3G6, 4G1, 1D8, 4G2, and 1E6 was located in 34-66aa, 67-99aa, 64-296aa, 297-329aa, 330-362aa, and 363-395aa, respectively. Sequence alignments further found that the six epitopes recognized by these mAbs were highly conserved among different DAdV-3 isolates. The generated mAbs specific to Fiber-1 and their defined epitopes provide powerful tools for establishing rapid and efficient diagnostics for the detection of DAdV-3 and pave the way for further studying on the critical role of Fiber-1 in mediating the infection of DAdV-3. |
format | Online Article Text |
id | pubmed-9597451 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95974512022-10-27 Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes Shao, Hongxia Zhang, Wenyuan Lin, Yun Xie, Jing Ren, Dan Xie, Quan Li, Tuofan Wan, Zhimin Qin, Aijian Ye, Jianqiang Front Vet Sci Veterinary Science Recently, the outbreak of the infection of Duck adenovirus 3 (DAdV-3) characterized by swelling and hemorrhagic liver and kidney has caused huge economic losses to duck industry since 2014 in China. To date, the B cell epitopes in the Fiber-1 protein and the underlying infection mechanism of DAdV-3 have not been investigated. In this study, the recombinant Fiber-1 protein was first expressed in E. coli and six novel monoclonal antibodies (mAbs) against Fiber-1 were generated, designated as 1D8, 1E6, 3G6, 4G1, 4G2, and 6F10, respectively. Moreover, mAbs 3G6 and 6F10 could efficiently immunoprecipitate the Fiber-1 in LMH cells infected with DAdV-3 or transfected with pcDNA3.1-Fiber-1. Notably, mAbs 3G6 and 4G2 also showed certain neutralizing activity against DAdV-3 infection in vitro. Epitopes mapping revealed that the B cell epitope recognized by 6F10, 3G6, 4G1, 1D8, 4G2, and 1E6 was located in 34-66aa, 67-99aa, 64-296aa, 297-329aa, 330-362aa, and 363-395aa, respectively. Sequence alignments further found that the six epitopes recognized by these mAbs were highly conserved among different DAdV-3 isolates. The generated mAbs specific to Fiber-1 and their defined epitopes provide powerful tools for establishing rapid and efficient diagnostics for the detection of DAdV-3 and pave the way for further studying on the critical role of Fiber-1 in mediating the infection of DAdV-3. Frontiers Media S.A. 2022-10-12 /pmc/articles/PMC9597451/ /pubmed/36311658 http://dx.doi.org/10.3389/fvets.2022.1003262 Text en Copyright © 2022 Shao, Zhang, Lin, Xie, Ren, Xie, Li, Wan, Qin and Ye. 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 Shao, Hongxia Zhang, Wenyuan Lin, Yun Xie, Jing Ren, Dan Xie, Quan Li, Tuofan Wan, Zhimin Qin, Aijian Ye, Jianqiang Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes |
title | Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes |
title_full | Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes |
title_fullStr | Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes |
title_full_unstemmed | Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes |
title_short | Novel monoclonal antibodies against Fiber-1 of duck adenovirus 3 and their B cell epitopes |
title_sort | novel monoclonal antibodies against fiber-1 of duck adenovirus 3 and their b cell epitopes |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9597451/ https://www.ncbi.nlm.nih.gov/pubmed/36311658 http://dx.doi.org/10.3389/fvets.2022.1003262 |
work_keys_str_mv | AT shaohongxia novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT zhangwenyuan novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT linyun novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT xiejing novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT rendan novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT xiequan novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT lituofan novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT wanzhimin novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT qinaijian novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes AT yejianqiang novelmonoclonalantibodiesagainstfiber1ofduckadenovirus3andtheirbcellepitopes |