Cargando…
LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies
Geese, as aquatic birds, are an important natural reservoir of avian influenza virus (AIV). To characterize the innate antiviral immune response against AIV H9N2 strain infection in geese as well as the probable relationship between the expression of immune-related genes and the distribution of vira...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756125/ https://www.ncbi.nlm.nih.gov/pubmed/26925041 http://dx.doi.org/10.3389/fmicb.2016.00166 |
_version_ | 1782416272947937280 |
---|---|
author | Zhou, Hao Chen, Shun Yan, Bing Chen, Hongjun 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 Yan, Bing Chen, Hongjun 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 | Geese, as aquatic birds, are an important natural reservoir of avian influenza virus (AIV). To characterize the innate antiviral immune response against AIV H9N2 strain infection in geese as well as the probable relationship between the expression of immune-related genes and the distribution of viral antigens, we investigated the levels of immune-related gene transcription both in AIV H9N2 strain-infected geese and in vitro. The patterns of viral location and the tissue distribution of CD4- and CD8α-positive cells were concurrently detected by immunohistochemical staining, which revealed respiratory and digestive organs as the primary sites of antigen-positive signals. Average AIV H9N2 viral loads were detected in the feces, Harderian gland (HG), and trachea, where higher copy numbers were detected compared with the rectum. Our results suggested the strong induction of proinflammatory cytokine expression compared with interferons (IFNs). Notably, in most tissues from the AIV H9N2 strain-infected birds, IFNα and IFNγ gene transcripts were differentially expressed. However, inverse changes in IFNα and IFNγ expression after AIV H9N2 strain infection were observed in vitro. Taken together, the results suggest that AIV H9N2 is widely distributed in multiple tissues, efficiently induces inflammatory cytokines in the HG and spleen of goslings and inversely influences type I and II IFN expression both in vivo and in vitro. The findings of this study further our understanding of host defense mechanisms and the pathogenesis of the H9N2 influenza virus in geese. |
format | Online Article Text |
id | pubmed-4756125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47561252016-02-26 LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies Zhou, Hao Chen, Shun Yan, Bing Chen, Hongjun Wang, Mingshu Jia, Renyong Zhu, Dekang Liu, Mafeng Liu, Fei Yang, Qiao Wu, Ying Sun, Kunfeng Chen, Xiaoyue Jing, Bo Cheng, Anchun Front Microbiol Microbiology Geese, as aquatic birds, are an important natural reservoir of avian influenza virus (AIV). To characterize the innate antiviral immune response against AIV H9N2 strain infection in geese as well as the probable relationship between the expression of immune-related genes and the distribution of viral antigens, we investigated the levels of immune-related gene transcription both in AIV H9N2 strain-infected geese and in vitro. The patterns of viral location and the tissue distribution of CD4- and CD8α-positive cells were concurrently detected by immunohistochemical staining, which revealed respiratory and digestive organs as the primary sites of antigen-positive signals. Average AIV H9N2 viral loads were detected in the feces, Harderian gland (HG), and trachea, where higher copy numbers were detected compared with the rectum. Our results suggested the strong induction of proinflammatory cytokine expression compared with interferons (IFNs). Notably, in most tissues from the AIV H9N2 strain-infected birds, IFNα and IFNγ gene transcripts were differentially expressed. However, inverse changes in IFNα and IFNγ expression after AIV H9N2 strain infection were observed in vitro. Taken together, the results suggest that AIV H9N2 is widely distributed in multiple tissues, efficiently induces inflammatory cytokines in the HG and spleen of goslings and inversely influences type I and II IFN expression both in vivo and in vitro. The findings of this study further our understanding of host defense mechanisms and the pathogenesis of the H9N2 influenza virus in geese. Frontiers Media S.A. 2016-02-17 /pmc/articles/PMC4756125/ /pubmed/26925041 http://dx.doi.org/10.3389/fmicb.2016.00166 Text en Copyright © 2016 Zhou, Chen, Yan, Chen, Wang, Jia, Zhu, Liu, Liu, Yang, Wu, Sun, Chen, Jing and Cheng. http://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) or licensor 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 | Microbiology Zhou, Hao Chen, Shun Yan, Bing Chen, Hongjun Wang, Mingshu Jia, Renyong Zhu, Dekang Liu, Mafeng Liu, Fei Yang, Qiao Wu, Ying Sun, Kunfeng Chen, Xiaoyue Jing, Bo Cheng, Anchun LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies |
title | LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies |
title_full | LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies |
title_fullStr | LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies |
title_full_unstemmed | LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies |
title_short | LPAIV H9N2 Drives the Differential Expression of Goose Interferons and Proinflammatory Cytokines in Both In Vitro and In Vivo Studies |
title_sort | lpaiv h9n2 drives the differential expression of goose interferons and proinflammatory cytokines in both in vitro and in vivo studies |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756125/ https://www.ncbi.nlm.nih.gov/pubmed/26925041 http://dx.doi.org/10.3389/fmicb.2016.00166 |
work_keys_str_mv | AT zhouhao lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT chenshun lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT yanbing lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT chenhongjun lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT wangmingshu lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT jiarenyong lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT zhudekang lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT liumafeng lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT liufei lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT yangqiao lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT wuying lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT sunkunfeng lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT chenxiaoyue lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT jingbo lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies AT chenganchun lpaivh9n2drivesthedifferentialexpressionofgooseinterferonsandproinflammatorycytokinesinbothinvitroandinvivostudies |