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An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus

Currently, the outbreak of serotype 4 fowl adenovirus (FAdV-4) has spread worldwide and caused tremendous economic loss to the poultry industry. Although inactivated vaccines have been licensed against FAdV-4 in China, a rapid and efficient serological method for measuring the titer of neutralizing...

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Autores principales: Guo, Yiwen, Xie, Songhua, Xu, Zhenqi, Xie, Quan, Wang, Weikang, Wan, Zhimin, Li, Tuofan, Qin, Aijian, Shao, Hongxia, Ye, Jianqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019121/
https://www.ncbi.nlm.nih.gov/pubmed/35464358
http://dx.doi.org/10.3389/fvets.2022.867697
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author Guo, Yiwen
Xie, Songhua
Xu, Zhenqi
Xie, Quan
Wang, Weikang
Wan, Zhimin
Li, Tuofan
Qin, Aijian
Shao, Hongxia
Ye, Jianqiang
author_facet Guo, Yiwen
Xie, Songhua
Xu, Zhenqi
Xie, Quan
Wang, Weikang
Wan, Zhimin
Li, Tuofan
Qin, Aijian
Shao, Hongxia
Ye, Jianqiang
author_sort Guo, Yiwen
collection PubMed
description Currently, the outbreak of serotype 4 fowl adenovirus (FAdV-4) has spread worldwide and caused tremendous economic loss to the poultry industry. Although inactivated vaccines have been licensed against FAdV-4 in China, a rapid and efficient serological method for measuring the titer of neutralizing antibodies (NAbs) specific for FAdV-4 post-infection or vaccination is rarely reported. Classical virus neutralization test (VNT) is superior in sensitivity and specificity for detecting NAbs but is either time-consuming or laborious. In this study, a recombinant virus FA4-EGFP expressing EGFP-fiber-2 fusion protein, rather than wild type (WT) FAdV-4 was used to develop a novel VNT for detecting FAdV-4 NAbs. Specificity analysis showed that the approach only reacted with the sera against FAdV-4, not with the sera against other avian pathogens tested. The novel VNT was effective in the detection of NAbs against FAdV-4 in sera from both experimentally infected and clinically vaccinated chickens, and had good linear correlation with the classical VNT. Moreover, the novel VNT not only significantly simplifies the procedure for detection of NAbs, but also shortens the timeline to 24 h in comparison with the classical VNT with 3-4 d. All these data demonstrate that the FA4-EGFP based VNT developed here provides an efficient diagnostic method for monitoring the immunological state of the vaccination or diagnosing the clinical infection of FAdV-4 in a quick and funding-saving manner.
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spelling pubmed-90191212022-04-21 An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus Guo, Yiwen Xie, Songhua Xu, Zhenqi Xie, Quan Wang, Weikang Wan, Zhimin Li, Tuofan Qin, Aijian Shao, Hongxia Ye, Jianqiang Front Vet Sci Veterinary Science Currently, the outbreak of serotype 4 fowl adenovirus (FAdV-4) has spread worldwide and caused tremendous economic loss to the poultry industry. Although inactivated vaccines have been licensed against FAdV-4 in China, a rapid and efficient serological method for measuring the titer of neutralizing antibodies (NAbs) specific for FAdV-4 post-infection or vaccination is rarely reported. Classical virus neutralization test (VNT) is superior in sensitivity and specificity for detecting NAbs but is either time-consuming or laborious. In this study, a recombinant virus FA4-EGFP expressing EGFP-fiber-2 fusion protein, rather than wild type (WT) FAdV-4 was used to develop a novel VNT for detecting FAdV-4 NAbs. Specificity analysis showed that the approach only reacted with the sera against FAdV-4, not with the sera against other avian pathogens tested. The novel VNT was effective in the detection of NAbs against FAdV-4 in sera from both experimentally infected and clinically vaccinated chickens, and had good linear correlation with the classical VNT. Moreover, the novel VNT not only significantly simplifies the procedure for detection of NAbs, but also shortens the timeline to 24 h in comparison with the classical VNT with 3-4 d. All these data demonstrate that the FA4-EGFP based VNT developed here provides an efficient diagnostic method for monitoring the immunological state of the vaccination or diagnosing the clinical infection of FAdV-4 in a quick and funding-saving manner. Frontiers Media S.A. 2022-04-06 /pmc/articles/PMC9019121/ /pubmed/35464358 http://dx.doi.org/10.3389/fvets.2022.867697 Text en Copyright © 2022 Guo, Xie, Xu, Xie, Wang, Wan, Li, Qin, Shao 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
Guo, Yiwen
Xie, Songhua
Xu, Zhenqi
Xie, Quan
Wang, Weikang
Wan, Zhimin
Li, Tuofan
Qin, Aijian
Shao, Hongxia
Ye, Jianqiang
An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus
title An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus
title_full An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus
title_fullStr An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus
title_full_unstemmed An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus
title_short An Efficient and Rapid Assay for Detecting Neutralizing Antibodies Against Serotype 4 Fowl Adenovirus
title_sort efficient and rapid assay for detecting neutralizing antibodies against serotype 4 fowl adenovirus
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019121/
https://www.ncbi.nlm.nih.gov/pubmed/35464358
http://dx.doi.org/10.3389/fvets.2022.867697
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