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Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus

Chicken anemia virus (CAV) is an important viral pathogen that causes anemia and severe immunodeficiency syndrome in chickens worldwide. In this study, a potential diagnostic monoclonal antibody against the CAV VP1 protein was developed which can precisely recognize the CAV antigen for diagnostic an...

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Autores principales: Lien, Yi-Yang, Huang, Chi-Hung, Sun, Fang-Chun, Sheu, Shyang-Chwen, Lu, Tsung-Chi, Lee, Meng-Shiunn, Hsueh, Shu-Chin, Chen, Hsi-Jien, Lee, Meng-Shiou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317461/
https://www.ncbi.nlm.nih.gov/pubmed/22437539
http://dx.doi.org/10.4142/jvs.2012.13.1.73
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author Lien, Yi-Yang
Huang, Chi-Hung
Sun, Fang-Chun
Sheu, Shyang-Chwen
Lu, Tsung-Chi
Lee, Meng-Shiunn
Hsueh, Shu-Chin
Chen, Hsi-Jien
Lee, Meng-Shiou
author_facet Lien, Yi-Yang
Huang, Chi-Hung
Sun, Fang-Chun
Sheu, Shyang-Chwen
Lu, Tsung-Chi
Lee, Meng-Shiunn
Hsueh, Shu-Chin
Chen, Hsi-Jien
Lee, Meng-Shiou
author_sort Lien, Yi-Yang
collection PubMed
description Chicken anemia virus (CAV) is an important viral pathogen that causes anemia and severe immunodeficiency syndrome in chickens worldwide. In this study, a potential diagnostic monoclonal antibody against the CAV VP1 protein was developed which can precisely recognize the CAV antigen for diagnostic and virus recovery purposes. The VP1 gene of CAV encoding the N-terminus-deleted VP1 protein, VP1Nd129, was cloned into an Escherichia (E.) coli expression vector. After isopropyl-β-D-thiogalactopyronoside induction, VP1Nd129 protein was shown to be successfully expressed in the E. coli. By performing an enzyme-linked immunoabsorbent assay using two coating antigens, purified VP1Nd129 and CAV-infected liver tissue lysate, E3 monoclonal antibody (mAb) was found to have higher reactivity against VP1 protein than the other positive clones according to the result of limiting dilution method from 64 clones. Using immunohistochemistry, the presence of the VP1-specific mAb, E3, was confirmed using CAV-infected liver and thymus tissues as positive-infected samples. Additionally, CAV particle purification was also performed using an immunoaffinity column containing E3 mAb. The monoclonal E3 mAb developed in this study will not only be very useful for detecting CAV infection and performing histopathology studies of infected chickens, but may also be used to purify CAV particles in the future.
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spelling pubmed-33174612012-04-04 Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus Lien, Yi-Yang Huang, Chi-Hung Sun, Fang-Chun Sheu, Shyang-Chwen Lu, Tsung-Chi Lee, Meng-Shiunn Hsueh, Shu-Chin Chen, Hsi-Jien Lee, Meng-Shiou J Vet Sci Original Article Chicken anemia virus (CAV) is an important viral pathogen that causes anemia and severe immunodeficiency syndrome in chickens worldwide. In this study, a potential diagnostic monoclonal antibody against the CAV VP1 protein was developed which can precisely recognize the CAV antigen for diagnostic and virus recovery purposes. The VP1 gene of CAV encoding the N-terminus-deleted VP1 protein, VP1Nd129, was cloned into an Escherichia (E.) coli expression vector. After isopropyl-β-D-thiogalactopyronoside induction, VP1Nd129 protein was shown to be successfully expressed in the E. coli. By performing an enzyme-linked immunoabsorbent assay using two coating antigens, purified VP1Nd129 and CAV-infected liver tissue lysate, E3 monoclonal antibody (mAb) was found to have higher reactivity against VP1 protein than the other positive clones according to the result of limiting dilution method from 64 clones. Using immunohistochemistry, the presence of the VP1-specific mAb, E3, was confirmed using CAV-infected liver and thymus tissues as positive-infected samples. Additionally, CAV particle purification was also performed using an immunoaffinity column containing E3 mAb. The monoclonal E3 mAb developed in this study will not only be very useful for detecting CAV infection and performing histopathology studies of infected chickens, but may also be used to purify CAV particles in the future. The Korean Society of Veterinary Science 2012-03 2012-03-20 /pmc/articles/PMC3317461/ /pubmed/22437539 http://dx.doi.org/10.4142/jvs.2012.13.1.73 Text en © 2012 The Korean Society of Veterinary Science. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lien, Yi-Yang
Huang, Chi-Hung
Sun, Fang-Chun
Sheu, Shyang-Chwen
Lu, Tsung-Chi
Lee, Meng-Shiunn
Hsueh, Shu-Chin
Chen, Hsi-Jien
Lee, Meng-Shiou
Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus
title Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus
title_full Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus
title_fullStr Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus
title_full_unstemmed Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus
title_short Development and characterization of a potential diagnostic monoclonal antibody against capsid protein VP1 of the chicken anemia virus
title_sort development and characterization of a potential diagnostic monoclonal antibody against capsid protein vp1 of the chicken anemia virus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317461/
https://www.ncbi.nlm.nih.gov/pubmed/22437539
http://dx.doi.org/10.4142/jvs.2012.13.1.73
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