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Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV)
BACKGROUD: Encephalomyocarditis virus (EMCV) has been discovered on pig farms worldwide and can cause myocarditis in piglets and reproductive failure in sows. However, little is known about the host transcriptional responses to infection and host-pathogen interactions. METHODS: In this study, transc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336634/ https://www.ncbi.nlm.nih.gov/pubmed/28259172 http://dx.doi.org/10.1186/s12985-017-0718-4 |
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author | Wei, Jia Zhang, Haixia Li, Xiangrong Li, Qiongyi Ma, Zhongren Bai, Jialin Qiao, Zilin Feng, Ruofei |
author_facet | Wei, Jia Zhang, Haixia Li, Xiangrong Li, Qiongyi Ma, Zhongren Bai, Jialin Qiao, Zilin Feng, Ruofei |
author_sort | Wei, Jia |
collection | PubMed |
description | BACKGROUD: Encephalomyocarditis virus (EMCV) has been discovered on pig farms worldwide and can cause myocarditis in piglets and reproductive failure in sows. However, little is known about the host transcriptional responses to infection and host-pathogen interactions. METHODS: In this study, transcription profiling was performed by Illumina RNA-Sequencing (RNA-seq) to identify EMCV induced differentially expressed genes in BHK-21 cells at serial time points (12, 24, and 30 h post infection (hpi)), using mock infected cells as control. RESULTS: We identified 237, 241, and 207 differentially expressed genes (DEGs) respectively, majority of which were up-regulated. A large number of DEGs clustered into host defense, cellular signaling and metabolism categories. Moreover, short time series expression analysis revealed that 12 hpi was an important time point for expression change, indicating host virus resistance. CONCLUSIONS: This RNA-seq analysis provides the first data for understanding the network of virus host interactions under EMCV infection in vitro, and for identifying host components which involved in the virus infection course. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-017-0718-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5336634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53366342017-03-07 Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV) Wei, Jia Zhang, Haixia Li, Xiangrong Li, Qiongyi Ma, Zhongren Bai, Jialin Qiao, Zilin Feng, Ruofei Virol J Short Report BACKGROUD: Encephalomyocarditis virus (EMCV) has been discovered on pig farms worldwide and can cause myocarditis in piglets and reproductive failure in sows. However, little is known about the host transcriptional responses to infection and host-pathogen interactions. METHODS: In this study, transcription profiling was performed by Illumina RNA-Sequencing (RNA-seq) to identify EMCV induced differentially expressed genes in BHK-21 cells at serial time points (12, 24, and 30 h post infection (hpi)), using mock infected cells as control. RESULTS: We identified 237, 241, and 207 differentially expressed genes (DEGs) respectively, majority of which were up-regulated. A large number of DEGs clustered into host defense, cellular signaling and metabolism categories. Moreover, short time series expression analysis revealed that 12 hpi was an important time point for expression change, indicating host virus resistance. CONCLUSIONS: This RNA-seq analysis provides the first data for understanding the network of virus host interactions under EMCV infection in vitro, and for identifying host components which involved in the virus infection course. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12985-017-0718-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-04 /pmc/articles/PMC5336634/ /pubmed/28259172 http://dx.doi.org/10.1186/s12985-017-0718-4 Text en © The Author(s). 2017 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 | Short Report Wei, Jia Zhang, Haixia Li, Xiangrong Li, Qiongyi Ma, Zhongren Bai, Jialin Qiao, Zilin Feng, Ruofei Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV) |
title | Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV) |
title_full | Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV) |
title_fullStr | Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV) |
title_full_unstemmed | Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV) |
title_short | Transcriptional profiling of host cell responses to encephalomyocarditis virus (EMCV) |
title_sort | transcriptional profiling of host cell responses to encephalomyocarditis virus (emcv) |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5336634/ https://www.ncbi.nlm.nih.gov/pubmed/28259172 http://dx.doi.org/10.1186/s12985-017-0718-4 |
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