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The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection

Circular RNAs (circRNAs) are a new class of noncoding RNAs that have gained increased attention. DNA virus infections have been reported to induce modifications in cellular circRNA transcriptomes and express viral circRNAs. However, the identification and expression of cellular and viral circRNAs ar...

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Autores principales: Yao, Wenxia, Pan, Jinghui, Liu, Zhaoyu, Dong, Zhijie, Liang, Min, Xia, Shu, Xiao, Yao, Cai, Xiaodan, Peng, Tao, Zhou, Xinke, Cai, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649777/
https://www.ncbi.nlm.nih.gov/pubmed/34872355
http://dx.doi.org/10.1128/mBio.03075-21
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author Yao, Wenxia
Pan, Jinghui
Liu, Zhaoyu
Dong, Zhijie
Liang, Min
Xia, Shu
Xiao, Yao
Cai, Xiaodan
Peng, Tao
Zhou, Xinke
Cai, Hua
author_facet Yao, Wenxia
Pan, Jinghui
Liu, Zhaoyu
Dong, Zhijie
Liang, Min
Xia, Shu
Xiao, Yao
Cai, Xiaodan
Peng, Tao
Zhou, Xinke
Cai, Hua
author_sort Yao, Wenxia
collection PubMed
description Circular RNAs (circRNAs) are a new class of noncoding RNAs that have gained increased attention. DNA virus infections have been reported to induce modifications in cellular circRNA transcriptomes and express viral circRNAs. However, the identification and expression of cellular and viral circRNAs are unknown in the context of respiratory syncytial virus (RSV), a human RNA virus with no effective treatments or vaccines. Here, we report a comprehensive identification of the cellular and viral circRNAs induced by RSV infection in A549 cells with high-throughput sequencing. In total, 53,719 cellular circRNAs and 2,280 differentially expressed cellular circRNAs were identified. Trend analysis further identified three significant expression pattern clusters, which were related to the antiviral immune response according to gene enrichment analysis. Subsequent results showed that not only RSV infection but also poly(I·C) treatment and another RNA virus infection induced the upregulation of the top 10 circRNAs from the focused cluster. The top 10 circRNAs generally inhibit RSV replication in turn. Moreover, 1,254 viral circRNAs were identified by the same circRNA sequencing. The induced expression of viral circRNAs by RSV infection was found not only in A549 cells but also in HEp-2 cells. Additionally, we profiled the general characteristics of both cellular and viral circRNAs such as back-splicing signals, etc. Collectively, RSV infection induced the differential expression of cellular circRNAs, some of which affected RSV infection, and RSV also expressed viral circRNAs. Our study reveals novel layers of host-RSV interactions and identifies cellular or viral circRNAs that may be novel therapeutic targets or biomarkers.
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spelling pubmed-86497772021-12-16 The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection Yao, Wenxia Pan, Jinghui Liu, Zhaoyu Dong, Zhijie Liang, Min Xia, Shu Xiao, Yao Cai, Xiaodan Peng, Tao Zhou, Xinke Cai, Hua mBio Research Article Circular RNAs (circRNAs) are a new class of noncoding RNAs that have gained increased attention. DNA virus infections have been reported to induce modifications in cellular circRNA transcriptomes and express viral circRNAs. However, the identification and expression of cellular and viral circRNAs are unknown in the context of respiratory syncytial virus (RSV), a human RNA virus with no effective treatments or vaccines. Here, we report a comprehensive identification of the cellular and viral circRNAs induced by RSV infection in A549 cells with high-throughput sequencing. In total, 53,719 cellular circRNAs and 2,280 differentially expressed cellular circRNAs were identified. Trend analysis further identified three significant expression pattern clusters, which were related to the antiviral immune response according to gene enrichment analysis. Subsequent results showed that not only RSV infection but also poly(I·C) treatment and another RNA virus infection induced the upregulation of the top 10 circRNAs from the focused cluster. The top 10 circRNAs generally inhibit RSV replication in turn. Moreover, 1,254 viral circRNAs were identified by the same circRNA sequencing. The induced expression of viral circRNAs by RSV infection was found not only in A549 cells but also in HEp-2 cells. Additionally, we profiled the general characteristics of both cellular and viral circRNAs such as back-splicing signals, etc. Collectively, RSV infection induced the differential expression of cellular circRNAs, some of which affected RSV infection, and RSV also expressed viral circRNAs. Our study reveals novel layers of host-RSV interactions and identifies cellular or viral circRNAs that may be novel therapeutic targets or biomarkers. American Society for Microbiology 2021-12-07 /pmc/articles/PMC8649777/ /pubmed/34872355 http://dx.doi.org/10.1128/mBio.03075-21 Text en Copyright © 2021 Yao et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Yao, Wenxia
Pan, Jinghui
Liu, Zhaoyu
Dong, Zhijie
Liang, Min
Xia, Shu
Xiao, Yao
Cai, Xiaodan
Peng, Tao
Zhou, Xinke
Cai, Hua
The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection
title The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection
title_full The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection
title_fullStr The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection
title_full_unstemmed The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection
title_short The Cellular and Viral circRNAome Induced by Respiratory Syncytial Virus Infection
title_sort cellular and viral circrnaome induced by respiratory syncytial virus infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8649777/
https://www.ncbi.nlm.nih.gov/pubmed/34872355
http://dx.doi.org/10.1128/mBio.03075-21
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