| Literature DB >> 29803008 |
Min Cui1, Renyong Jia2, Juan Huang1, Xianglong Wu1, Zhiqiang Hu1, Xingcui Zhang1, Mingshu Wang3, Dekang Zhu3, Shun Chen3, Mafeng Liu3, Xinxin Zhao3, Yin Wu3, Qiao Yang3, Shaqiu Zhang3, Yunya Liu3, Ling Zhang3, Zhongqiong Yin4, Bo Jing4, Anchun Cheng5.
Abstract
Duck Tembusu virus (DTMUV), belonging to the Flaviviridae family, is a single-stranded positive-sense RNA virus. Since April 2010, the outbreak of DTMUV in southeast provinces of China has caused great economic losses. MicroRNAs (miRNAs) play important regulatory roles in viral infection through binding to the host target genes or the viral genomes. To better understanding the molecular mechanisms of virus-host interaction, here we identified the miRNA expression profiles in DTMUV-infected and uninfected DEF cells by high-throughput sequencing. A total of 287 known and 63 novel miRNAs were identified. 48 miRNAs, including 26 known miRNAs and 22 novel miRNAs, were differentially expressed in response to DTMUV infection. Among these miRNAs, 37 miRNAs were up-regulated and 11 miRNAs were down-regulated. 9 miRNAs were randomly selected for validation by qRT-PCR experiment. The results of qRT-PCR experiment were consistent with the sequencing data. GO enrichment showed that the predicted targets of these differentially expressed miRNAs were mainly involved in the regulation of immune system, cellular process and metabolic process. KEGG pathways analysis showed that predicted target genes were involved in several signaling pathways such as Wnt signaling pathway, TGF-beta signaling pathway, mTOR signaling pathway and FoxO signaling pathway. This is the first study to evaluate changes of miRNA expression in DEF cells upon DTMUV infection. Our findings provide important clues for better understanding the DTMUV-host interaction.Entities:
Keywords: Duck Tembusu virus; High-throughput sequencing; MicroRNA
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Year: 2018 PMID: 29803008 DOI: 10.1016/j.meegid.2018.05.020
Source DB: PubMed Journal: Infect Genet Evol ISSN: 1567-1348 Impact factor: 3.342