首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Comparative analysis of putative novel microRNA expression profiles induced by enterovirus 71 and coxsackievirus A16 infections in human umbilical vein endothelial cells using high-throughput sequencing
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Comparative analysis of putative novel microRNA expression profiles induced by enterovirus 71 and coxsackievirus A16 infections in human umbilical vein endothelial cells using high-throughput sequencing

机译:利用高通量测序,肠道病毒71和Coxsackievirus A16感染诱导的推定新微瘤表达谱的比较分析

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摘要

Hand, foot and mouth disease (HFMD) is mainly caused by human enterovirus 71 (EV71) and coxsackievirus A16 (CA16), which circulate alternatively or together in epidemic areas. Although the two viruses exhibit genetic homology, their clinical manifestations have some discrepancies. However, the factors underlying these differences remain unclear. Herein, we mainly focused on the alterations and roles of putative novel miRNAs in human umbilical vein endothelial cells (HUVECs) following EV71 and CA16 infections using high-throughput sequencing. The results identified 247 putative novel, differentially expressed miRNAs, of which only 11 miRNAs presented an opposite trend between the EV71- and CA16-infected samples and were used for target prediction. Gene ontology (GO) and pathway enrichment analysis of the predicted targets displayed the top 15 significant biological processes, molecular functions, cell components and pathways. Subsequently, regulatory miRNA-predicted targets and miRNA-GO and miRNA-pathway networks were constructed to further reveal the complex regulatory mechanisms of the miRNAs during infection. Therefore, our data provide useful insights that will help elucidate the different host-pathogen interactions following EV71 and CA16 infections and may offer novel therapeutic targets for these infections.
机译:手,脚和口腔疾病(HFMD)主要由人肠病毒71(EV71)和CoxSackeigirus A16(CA16)引起,其可选地或在流行区域中循环。虽然两种病毒表现出遗传同源性,但它们的临床表现有一些差异。然而,这些差异的因素仍然不清楚。在此,我们主要专注于使用高通量测序在EV71和Ca16感染之后推定的新型miRNA在人脐静脉内皮细胞(Huvecs)中的改变和角色。结果鉴定了247名推定新型差异表达的miRNA,其中11 miRNA仅介绍了EV71-和CA16感染样品之间的相反趋势,并用于靶预测。预测目标的基因本体(GO)和途径浓缩分析显示出前15个重要的生物过程,分子函数,细胞成分和途径。随后,构建了调节miRNA预测的靶和miRNA-Go和miRNA-Patway网络,以进一步揭示感染期间miRNA的复杂调节机制。因此,我们的数据提供了有用的见解,这将有助于阐明EV71和Ca16感染后的不同宿主病原体相互作用,并且可以为这些感染提供新的治疗靶标。

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