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Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection

BACKGROUND: Infectious bronchitis virus (IBV), a prototype of the Coronaviridae family, is an economically important causative agent of infectious bronchitis in chickens and causes an acute and highly contagious upper respiratory tract infections that may lead to nephritis. However, the molecular an...

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Autores principales: Cong, Feng, Liu, Xiaoli, Han, Zongxi, Shao, Yuhao, Kong, Xiangang, Liu, Shengwang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870970/
https://www.ncbi.nlm.nih.gov/pubmed/24168272
http://dx.doi.org/10.1186/1471-2164-14-743
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author Cong, Feng
Liu, Xiaoli
Han, Zongxi
Shao, Yuhao
Kong, Xiangang
Liu, Shengwang
author_facet Cong, Feng
Liu, Xiaoli
Han, Zongxi
Shao, Yuhao
Kong, Xiangang
Liu, Shengwang
author_sort Cong, Feng
collection PubMed
description BACKGROUND: Infectious bronchitis virus (IBV), a prototype of the Coronaviridae family, is an economically important causative agent of infectious bronchitis in chickens and causes an acute and highly contagious upper respiratory tract infections that may lead to nephritis. However, the molecular antiviral mechanisms of chickens to IBV infection remain poorly understood. In this study, we conducted global gene expression profiling of chicken kidney tissue after nephropathogenic IBV infection to better understand the interactions between host and virus. RESULTS: IBV infection contributed to differential expression of 1777 genes, of which 876 were up-regulated and 901 down-regulated in the kidney compared to those of control chickens and 103 associated with immune and inflammatory responses may play important roles in the host defense response during IBV infection. Twelve of the altered immune-related genes were confirmed by real-time RT-PCR. Gene ontology category, KEGG pathway, and gene interaction networks (STRING analysis) were analyzed to identify relationships among differentially expressed genes involved in signal transduction, cell adhesion, immune responses, apoptosis regulation, positive regulation of the I-kappaB kinase/NF-kappaB cascade and response to cytokine stimulus. Most of these genes were related and formed a large network, in which IL6, STAT1, MYD88, IRF1 and NFKB2 were key genes. CONCLUSIONS: Our results provided comprehensive knowledge regarding the host transcriptional response to IBV infection in chicken kidney tissues, thereby providing insight into IBV pathogenesis, particularly the involvement of innate immune pathway genes associated with IBV infection.
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spelling pubmed-38709702013-12-25 Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection Cong, Feng Liu, Xiaoli Han, Zongxi Shao, Yuhao Kong, Xiangang Liu, Shengwang BMC Genomics Research Article BACKGROUND: Infectious bronchitis virus (IBV), a prototype of the Coronaviridae family, is an economically important causative agent of infectious bronchitis in chickens and causes an acute and highly contagious upper respiratory tract infections that may lead to nephritis. However, the molecular antiviral mechanisms of chickens to IBV infection remain poorly understood. In this study, we conducted global gene expression profiling of chicken kidney tissue after nephropathogenic IBV infection to better understand the interactions between host and virus. RESULTS: IBV infection contributed to differential expression of 1777 genes, of which 876 were up-regulated and 901 down-regulated in the kidney compared to those of control chickens and 103 associated with immune and inflammatory responses may play important roles in the host defense response during IBV infection. Twelve of the altered immune-related genes were confirmed by real-time RT-PCR. Gene ontology category, KEGG pathway, and gene interaction networks (STRING analysis) were analyzed to identify relationships among differentially expressed genes involved in signal transduction, cell adhesion, immune responses, apoptosis regulation, positive regulation of the I-kappaB kinase/NF-kappaB cascade and response to cytokine stimulus. Most of these genes were related and formed a large network, in which IL6, STAT1, MYD88, IRF1 and NFKB2 were key genes. CONCLUSIONS: Our results provided comprehensive knowledge regarding the host transcriptional response to IBV infection in chicken kidney tissues, thereby providing insight into IBV pathogenesis, particularly the involvement of innate immune pathway genes associated with IBV infection. BioMed Central 2013-10-30 /pmc/articles/PMC3870970/ /pubmed/24168272 http://dx.doi.org/10.1186/1471-2164-14-743 Text en Copyright © 2013 Cong et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Cong, Feng
Liu, Xiaoli
Han, Zongxi
Shao, Yuhao
Kong, Xiangang
Liu, Shengwang
Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection
title Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection
title_full Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection
title_fullStr Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection
title_full_unstemmed Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection
title_short Transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection
title_sort transcriptome analysis of chicken kidney tissues following coronavirus avian infectious bronchitis virus infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870970/
https://www.ncbi.nlm.nih.gov/pubmed/24168272
http://dx.doi.org/10.1186/1471-2164-14-743
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