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HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells
BACKGROUND: Infectious bursal disease (IBD) is a highly contagious infectious disease that causes severe immunosuppression and damage to the bursa of Fabricius in chickens. Several proteins involved in IBD virus (IBDV) infection, such as surface immunoglobulin M, integrin, annexin A2 and chicken hea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201719/ https://www.ncbi.nlm.nih.gov/pubmed/32375812 http://dx.doi.org/10.1186/s12985-020-01333-x |
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author | Chen, Chunbo Qin, Ying Qian, Kun Shao, Hongxia Ye, Jianqiang Qin, Aijian |
author_facet | Chen, Chunbo Qin, Ying Qian, Kun Shao, Hongxia Ye, Jianqiang Qin, Aijian |
author_sort | Chen, Chunbo |
collection | PubMed |
description | BACKGROUND: Infectious bursal disease (IBD) is a highly contagious infectious disease that causes severe immunosuppression and damage to the bursa of Fabricius in chickens. Several proteins involved in IBD virus (IBDV) infection, such as surface immunoglobulin M, integrin, annexin A2 and chicken heat shock protein 90, have been identified. However, the main protein that plays key roles in virus infection has not yet been confirmed. METHODS: DF-1 cell line was transfected with the pcDNA-VP2 plasmid and analyzed by immunofluorescence assay. The proteins reacted with VP2 of IBDV in DF-1 cells were pulldown with the monoclonal antibody and identified by mass spectrometry. Heat shock cognate protein 70 (HSC70), one of these proteins, was selected to be investigated in the function in IBDV infection by specific antibody and its inhibitor. RESULTS: The DF-1 cell line was transfected with the pcDNA-VP2 plasmid, and expression of IBDV VP2 in DF-1 cells was confirmed by immunofluorescence assays. Heat shock cognate protein 70 (HSC70) was one of the proteins identified by coimmunoprecipitation using a monoclonal antibody (2H11) against VP2 and mass spectrometry analysis. IBDV infection in DF-1 cells was strongly inhibited by both an anti-HSC70 antibody and a HSC70 inhibitor (VER155008). CONCLUSION: These results suggest that HSC70 may be an essential factor for IBDV infection. |
format | Online Article Text |
id | pubmed-7201719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72017192020-05-08 HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells Chen, Chunbo Qin, Ying Qian, Kun Shao, Hongxia Ye, Jianqiang Qin, Aijian Virol J Research BACKGROUND: Infectious bursal disease (IBD) is a highly contagious infectious disease that causes severe immunosuppression and damage to the bursa of Fabricius in chickens. Several proteins involved in IBD virus (IBDV) infection, such as surface immunoglobulin M, integrin, annexin A2 and chicken heat shock protein 90, have been identified. However, the main protein that plays key roles in virus infection has not yet been confirmed. METHODS: DF-1 cell line was transfected with the pcDNA-VP2 plasmid and analyzed by immunofluorescence assay. The proteins reacted with VP2 of IBDV in DF-1 cells were pulldown with the monoclonal antibody and identified by mass spectrometry. Heat shock cognate protein 70 (HSC70), one of these proteins, was selected to be investigated in the function in IBDV infection by specific antibody and its inhibitor. RESULTS: The DF-1 cell line was transfected with the pcDNA-VP2 plasmid, and expression of IBDV VP2 in DF-1 cells was confirmed by immunofluorescence assays. Heat shock cognate protein 70 (HSC70) was one of the proteins identified by coimmunoprecipitation using a monoclonal antibody (2H11) against VP2 and mass spectrometry analysis. IBDV infection in DF-1 cells was strongly inhibited by both an anti-HSC70 antibody and a HSC70 inhibitor (VER155008). CONCLUSION: These results suggest that HSC70 may be an essential factor for IBDV infection. BioMed Central 2020-05-06 /pmc/articles/PMC7201719/ /pubmed/32375812 http://dx.doi.org/10.1186/s12985-020-01333-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Chen, Chunbo Qin, Ying Qian, Kun Shao, Hongxia Ye, Jianqiang Qin, Aijian HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells |
title | HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells |
title_full | HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells |
title_fullStr | HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells |
title_full_unstemmed | HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells |
title_short | HSC70 is required for infectious bursal disease virus (IBDV) infection in DF-1 cells |
title_sort | hsc70 is required for infectious bursal disease virus (ibdv) infection in df-1 cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7201719/ https://www.ncbi.nlm.nih.gov/pubmed/32375812 http://dx.doi.org/10.1186/s12985-020-01333-x |
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