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Genome-wide profiling of chicken dendritic cell response to infectious bursal disease

BACKGROUND: Avian infectious bursal disease virus (IBDV) is a highly contagious, immunosuppressive disease of young chickens, which causes high mortality rates and large economic losses in the poultry industry. Dendritic cells (DCs), which are antigen-presenting cells, have the unique ability to ind...

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Autores principales: Lin, Jian, Xia, Jing, Zhang, Keyun, Yang, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097849/
https://www.ncbi.nlm.nih.gov/pubmed/27816055
http://dx.doi.org/10.1186/s12864-016-3157-5
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author Lin, Jian
Xia, Jing
Zhang, Keyun
Yang, Qian
author_facet Lin, Jian
Xia, Jing
Zhang, Keyun
Yang, Qian
author_sort Lin, Jian
collection PubMed
description BACKGROUND: Avian infectious bursal disease virus (IBDV) is a highly contagious, immunosuppressive disease of young chickens, which causes high mortality rates and large economic losses in the poultry industry. Dendritic cells (DCs), which are antigen-presenting cells, have the unique ability to induce both innate and acquired immune responses and may significantly influence virus pathogenicity. To understand the interaction between IBDV and DCs, a microarray was used to analyse the response of DCs infected by IBDV. RESULTS: IBDV infection induced 479 upregulated and 466 downregulated mRNAs in chicken DCs. Analysis of Gene Ontology suggested that transcription from the RNA polymerase II promoter and the RNA biosynthetic process were enriched, and pathway analyses suggested that oxidative phosphorylation, as well as the T cell receptor and Interleukin-17 (IL-17) signalling pathways might be activated by IBDV infection. Moreover, microRNA (miRNA) and long non-coding RNA (lncRNA) alterations in IBDV-infected chicken DCs were observed. A total of 18 significantly upregulated or downregulated miRNAs and 441 significantly upregulated or downregulated lncRNAs were identified in IBDV-stimulated DCs. We constructed 42 transcription factor (TF)–miRNA–mRNA interactions involving 1 TF, 3 miRNAs, and 42 mRNAs in IBDV-stimulated DCs. Finally, we predicted the target genes of differentially expressed lncRNAs, and constructed lncRNA-mRNA regulatory networks. CONCLUSIONS: The results of this study suggest a mechanism to explain how IBDV infection triggers an effective immune response in chicken DCs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3157-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-50978492016-11-08 Genome-wide profiling of chicken dendritic cell response to infectious bursal disease Lin, Jian Xia, Jing Zhang, Keyun Yang, Qian BMC Genomics Research Article BACKGROUND: Avian infectious bursal disease virus (IBDV) is a highly contagious, immunosuppressive disease of young chickens, which causes high mortality rates and large economic losses in the poultry industry. Dendritic cells (DCs), which are antigen-presenting cells, have the unique ability to induce both innate and acquired immune responses and may significantly influence virus pathogenicity. To understand the interaction between IBDV and DCs, a microarray was used to analyse the response of DCs infected by IBDV. RESULTS: IBDV infection induced 479 upregulated and 466 downregulated mRNAs in chicken DCs. Analysis of Gene Ontology suggested that transcription from the RNA polymerase II promoter and the RNA biosynthetic process were enriched, and pathway analyses suggested that oxidative phosphorylation, as well as the T cell receptor and Interleukin-17 (IL-17) signalling pathways might be activated by IBDV infection. Moreover, microRNA (miRNA) and long non-coding RNA (lncRNA) alterations in IBDV-infected chicken DCs were observed. A total of 18 significantly upregulated or downregulated miRNAs and 441 significantly upregulated or downregulated lncRNAs were identified in IBDV-stimulated DCs. We constructed 42 transcription factor (TF)–miRNA–mRNA interactions involving 1 TF, 3 miRNAs, and 42 mRNAs in IBDV-stimulated DCs. Finally, we predicted the target genes of differentially expressed lncRNAs, and constructed lncRNA-mRNA regulatory networks. CONCLUSIONS: The results of this study suggest a mechanism to explain how IBDV infection triggers an effective immune response in chicken DCs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3157-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-05 /pmc/articles/PMC5097849/ /pubmed/27816055 http://dx.doi.org/10.1186/s12864-016-3157-5 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Lin, Jian
Xia, Jing
Zhang, Keyun
Yang, Qian
Genome-wide profiling of chicken dendritic cell response to infectious bursal disease
title Genome-wide profiling of chicken dendritic cell response to infectious bursal disease
title_full Genome-wide profiling of chicken dendritic cell response to infectious bursal disease
title_fullStr Genome-wide profiling of chicken dendritic cell response to infectious bursal disease
title_full_unstemmed Genome-wide profiling of chicken dendritic cell response to infectious bursal disease
title_short Genome-wide profiling of chicken dendritic cell response to infectious bursal disease
title_sort genome-wide profiling of chicken dendritic cell response to infectious bursal disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097849/
https://www.ncbi.nlm.nih.gov/pubmed/27816055
http://dx.doi.org/10.1186/s12864-016-3157-5
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