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Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells
BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is a causative agent of serious viral enteric disease in suckling pigs. Such diseases cause considerable economic losses in the global swine industry. Enhancing our knowledge of PEDV-induced transcriptomic responses in host cells is imperative to un...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734901/ https://www.ncbi.nlm.nih.gov/pubmed/33317444 http://dx.doi.org/10.1186/s12864-020-07306-2 |
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author | Hu, Zhengzheng Li, Yuchen Du, Heng Ren, Junxiao Zheng, Xianrui Wei, Kejian Liu, Jianfeng |
author_facet | Hu, Zhengzheng Li, Yuchen Du, Heng Ren, Junxiao Zheng, Xianrui Wei, Kejian Liu, Jianfeng |
author_sort | Hu, Zhengzheng |
collection | PubMed |
description | BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is a causative agent of serious viral enteric disease in suckling pigs. Such diseases cause considerable economic losses in the global swine industry. Enhancing our knowledge of PEDV-induced transcriptomic responses in host cells is imperative to understanding the molecular mechanisms involved in the immune response. Here, we analyzed the transcriptomic profile of intestinal porcine epithelial cell line J2 (IPEC-J2) after infection with a classical strain of PEDV to explore the host response. RESULTS: In total, 854 genes were significantly differentially expressed after PEDV infection, including 716 upregulated and 138 downregulated genes. Functional annotation analysis revealed that the differentially expressed genes were mainly enriched in the influenza A, TNF signaling, inflammatory response, cytokine receptor interaction, and other immune-related pathways. Next, the putative promoter regions of the 854 differentially expressed genes were examined for the presence of transcription factor binding sites using the MEME tool. As a result, 504 sequences (59.02%) were identified as possessing at least one binding site of signal transducer and activator of transcription (STAT), and five STAT transcription factors were significantly induced by PEDV infection. Furthermore, we revealed the regulatory network induced by STAT members in the process of PEDV infection. CONCLUSION: Our transcriptomic analysis described the host genetic response to PEDV infection in detail in IPEC-J2 cells, and suggested that STAT transcription factors may serve as key regulators in the response to PEDV infection. These results further our understanding of the pathogenesis of PEDV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07306-2. |
format | Online Article Text |
id | pubmed-7734901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77349012020-12-14 Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells Hu, Zhengzheng Li, Yuchen Du, Heng Ren, Junxiao Zheng, Xianrui Wei, Kejian Liu, Jianfeng BMC Genomics Research Article BACKGROUND: Porcine epidemic diarrhea virus (PEDV) is a causative agent of serious viral enteric disease in suckling pigs. Such diseases cause considerable economic losses in the global swine industry. Enhancing our knowledge of PEDV-induced transcriptomic responses in host cells is imperative to understanding the molecular mechanisms involved in the immune response. Here, we analyzed the transcriptomic profile of intestinal porcine epithelial cell line J2 (IPEC-J2) after infection with a classical strain of PEDV to explore the host response. RESULTS: In total, 854 genes were significantly differentially expressed after PEDV infection, including 716 upregulated and 138 downregulated genes. Functional annotation analysis revealed that the differentially expressed genes were mainly enriched in the influenza A, TNF signaling, inflammatory response, cytokine receptor interaction, and other immune-related pathways. Next, the putative promoter regions of the 854 differentially expressed genes were examined for the presence of transcription factor binding sites using the MEME tool. As a result, 504 sequences (59.02%) were identified as possessing at least one binding site of signal transducer and activator of transcription (STAT), and five STAT transcription factors were significantly induced by PEDV infection. Furthermore, we revealed the regulatory network induced by STAT members in the process of PEDV infection. CONCLUSION: Our transcriptomic analysis described the host genetic response to PEDV infection in detail in IPEC-J2 cells, and suggested that STAT transcription factors may serve as key regulators in the response to PEDV infection. These results further our understanding of the pathogenesis of PEDV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-020-07306-2. BioMed Central 2020-12-14 /pmc/articles/PMC7734901/ /pubmed/33317444 http://dx.doi.org/10.1186/s12864-020-07306-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Hu, Zhengzheng Li, Yuchen Du, Heng Ren, Junxiao Zheng, Xianrui Wei, Kejian Liu, Jianfeng Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells |
title | Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells |
title_full | Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells |
title_fullStr | Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells |
title_full_unstemmed | Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells |
title_short | Transcriptome analysis reveals modulation of the STAT family in PEDV-infected IPEC-J2 cells |
title_sort | transcriptome analysis reveals modulation of the stat family in pedv-infected ipec-j2 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734901/ https://www.ncbi.nlm.nih.gov/pubmed/33317444 http://dx.doi.org/10.1186/s12864-020-07306-2 |
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