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Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing

Japanese encephalitis virus (JEV), a mosquito-borne Flavivirus, causes acute viral encephalitis with high morbidity and mortality in humans and animals. MicroRNAs (miRNAs) are small noncoding RNAs that are important modulators of the intricate host-pathogen interaction networks. However, our knowled...

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Autores principales: Cai, Yuhan, Zhu, Ling, Zhou, Yuanchen, Liu, Xiao, Liu, Xiaowan, Li, Xinqiong, Lang, Qiaoli, Qiao, Xiaogai, Xu, Zhiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307358/
https://www.ncbi.nlm.nih.gov/pubmed/25608654
http://dx.doi.org/10.3390/ijms16012204
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author Cai, Yuhan
Zhu, Ling
Zhou, Yuanchen
Liu, Xiao
Liu, Xiaowan
Li, Xinqiong
Lang, Qiaoli
Qiao, Xiaogai
Xu, Zhiwen
author_facet Cai, Yuhan
Zhu, Ling
Zhou, Yuanchen
Liu, Xiao
Liu, Xiaowan
Li, Xinqiong
Lang, Qiaoli
Qiao, Xiaogai
Xu, Zhiwen
author_sort Cai, Yuhan
collection PubMed
description Japanese encephalitis virus (JEV), a mosquito-borne Flavivirus, causes acute viral encephalitis with high morbidity and mortality in humans and animals. MicroRNAs (miRNAs) are small noncoding RNAs that are important modulators of the intricate host-pathogen interaction networks. However, our knowledge of the changes that occur in miRNAs in host cells after JEV infection is still limited. To understand the molecular pathogenesis of JEV at the level of posttranscriptional regulation, we used Illumina deep sequencing to sequence two small RNA libraries prepared from PK-15 cells before and after JEV infection. We identified 522 and 427 miRNAs in the infected and uninfected cells, respectively. Overall, 132 miRNAs were expressed significantly differently after challenge with JEV: 78 were upregulated and 54 downregulated. The sequencing results for selected miRNAs were confirmed with RT-qPCR. GO analysis of the host target genes revealed that these dysregulated miRNAs are involved in complex cellular pathways, including the metabolic pathway, inflammatory response and immune response. To our knowledge, this is the first report of the comparative expression of miRNAs in PK-15 cells after JEV infection. Our findings will underpin further studies of miRNAs’ roles in JEV replication and identify potential candidates for antiviral therapies against JEV.
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spelling pubmed-43073582015-02-02 Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing Cai, Yuhan Zhu, Ling Zhou, Yuanchen Liu, Xiao Liu, Xiaowan Li, Xinqiong Lang, Qiaoli Qiao, Xiaogai Xu, Zhiwen Int J Mol Sci Article Japanese encephalitis virus (JEV), a mosquito-borne Flavivirus, causes acute viral encephalitis with high morbidity and mortality in humans and animals. MicroRNAs (miRNAs) are small noncoding RNAs that are important modulators of the intricate host-pathogen interaction networks. However, our knowledge of the changes that occur in miRNAs in host cells after JEV infection is still limited. To understand the molecular pathogenesis of JEV at the level of posttranscriptional regulation, we used Illumina deep sequencing to sequence two small RNA libraries prepared from PK-15 cells before and after JEV infection. We identified 522 and 427 miRNAs in the infected and uninfected cells, respectively. Overall, 132 miRNAs were expressed significantly differently after challenge with JEV: 78 were upregulated and 54 downregulated. The sequencing results for selected miRNAs were confirmed with RT-qPCR. GO analysis of the host target genes revealed that these dysregulated miRNAs are involved in complex cellular pathways, including the metabolic pathway, inflammatory response and immune response. To our knowledge, this is the first report of the comparative expression of miRNAs in PK-15 cells after JEV infection. Our findings will underpin further studies of miRNAs’ roles in JEV replication and identify potential candidates for antiviral therapies against JEV. MDPI 2015-01-20 /pmc/articles/PMC4307358/ /pubmed/25608654 http://dx.doi.org/10.3390/ijms16012204 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cai, Yuhan
Zhu, Ling
Zhou, Yuanchen
Liu, Xiao
Liu, Xiaowan
Li, Xinqiong
Lang, Qiaoli
Qiao, Xiaogai
Xu, Zhiwen
Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing
title Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing
title_full Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing
title_fullStr Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing
title_full_unstemmed Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing
title_short Identification and Analysis of Differentially-Expressed microRNAs in Japanese Encephalitis Virus-Infected PK-15 Cells with Deep Sequencing
title_sort identification and analysis of differentially-expressed micrornas in japanese encephalitis virus-infected pk-15 cells with deep sequencing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307358/
https://www.ncbi.nlm.nih.gov/pubmed/25608654
http://dx.doi.org/10.3390/ijms16012204
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