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Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ
Both Tembusu virus (TMUV) and goose parvovirus (GPV) are causative agents of goose disease. However, the host immune response of the goose against these two different categories of virus has not been well documented. Here, we compared the clinical symptoms and pathological characteristics, antigen d...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858762/ https://www.ncbi.nlm.nih.gov/pubmed/27150912 http://dx.doi.org/10.1038/srep25545 |
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author | Zhou, Hao Chen, Shun Wang, Mingshu Jia, Renyong Zhu, Dekang Liu, Mafeng Liu, Fei Yang, Qiao Wu, Ying Sun, Kunfeng Chen, Xiaoyue Jing, Bo Cheng, Anchun |
author_facet | Zhou, Hao Chen, Shun Wang, Mingshu Jia, Renyong Zhu, Dekang Liu, Mafeng Liu, Fei Yang, Qiao Wu, Ying Sun, Kunfeng Chen, Xiaoyue Jing, Bo Cheng, Anchun |
author_sort | Zhou, Hao |
collection | PubMed |
description | Both Tembusu virus (TMUV) and goose parvovirus (GPV) are causative agents of goose disease. However, the host immune response of the goose against these two different categories of virus has not been well documented. Here, we compared the clinical symptoms and pathological characteristics, antigen distribution and intensity, and expression of immune-related genes in TMUV- and GPV- infected goose. The immunohistochemistry analysis demonstrated that GPV was primarily located in the liver, lung, small intestine, and rectum, while TMUV was situated in the liver, brain, spleen, and small intestine. The induction of IFNγ and proinflammatory cytokines is highly associated with the distribution profiles of antigen and CD8α+ molecules. The effector function of CD8 T cells may be accomplished by the secretion of IFNγ together with high expression of proinflammatory cytokines such as IL1 and IL6. Remarkably, significant increases in the transcription of immune genes were observed after infection, which suggested that both GPV and TMUV can effectively induce immune response in goose PMBCs. This study will provide fundamental information for goose molecular immunology in defending against pandemic viruses. |
format | Online Article Text |
id | pubmed-4858762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48587622016-05-20 Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ Zhou, Hao Chen, Shun Wang, Mingshu Jia, Renyong Zhu, Dekang Liu, Mafeng Liu, Fei Yang, Qiao Wu, Ying Sun, Kunfeng Chen, Xiaoyue Jing, Bo Cheng, Anchun Sci Rep Article Both Tembusu virus (TMUV) and goose parvovirus (GPV) are causative agents of goose disease. However, the host immune response of the goose against these two different categories of virus has not been well documented. Here, we compared the clinical symptoms and pathological characteristics, antigen distribution and intensity, and expression of immune-related genes in TMUV- and GPV- infected goose. The immunohistochemistry analysis demonstrated that GPV was primarily located in the liver, lung, small intestine, and rectum, while TMUV was situated in the liver, brain, spleen, and small intestine. The induction of IFNγ and proinflammatory cytokines is highly associated with the distribution profiles of antigen and CD8α+ molecules. The effector function of CD8 T cells may be accomplished by the secretion of IFNγ together with high expression of proinflammatory cytokines such as IL1 and IL6. Remarkably, significant increases in the transcription of immune genes were observed after infection, which suggested that both GPV and TMUV can effectively induce immune response in goose PMBCs. This study will provide fundamental information for goose molecular immunology in defending against pandemic viruses. Nature Publishing Group 2016-05-06 /pmc/articles/PMC4858762/ /pubmed/27150912 http://dx.doi.org/10.1038/srep25545 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhou, Hao Chen, Shun Wang, Mingshu Jia, Renyong Zhu, Dekang Liu, Mafeng Liu, Fei Yang, Qiao Wu, Ying Sun, Kunfeng Chen, Xiaoyue Jing, Bo Cheng, Anchun Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ |
title | Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ |
title_full | Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ |
title_fullStr | Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ |
title_full_unstemmed | Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ |
title_short | Antigen distribution of TMUV and GPV are coincident with the expression profiles of CD8α-positive cells and goose IFNγ |
title_sort | antigen distribution of tmuv and gpv are coincident with the expression profiles of cd8α-positive cells and goose ifnγ |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4858762/ https://www.ncbi.nlm.nih.gov/pubmed/27150912 http://dx.doi.org/10.1038/srep25545 |
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