Prediction of Potential Targets of an Emerging Zoonotic Paramyxovirus: An Integrated Bioinformatics Analysis

Q4 Pharmacology, Toxicology and Pharmaceutics Current Pharmacogenomics and Personalized Medicine Pub Date : 2021-03-15 DOI:10.2174/1875692118666210315150037
M. Sai, Viswam Subeesh, S. HemaSreeGN, G. Saraswathy, N. Gouri
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Abstract

Nipah virus (NiV) is a zoonotic paramyxovirus that can cause severe respiratory illness and encephalitis in humans, with no effective targets and treatment. To investigate potential targets involved in the progression of NiV infection by bioinformatics studies. To identify the key gene involved in NiV infection, a microarray dataset (GSE32902) was downloaded from the National Centre of Biotechnology Information (NCBI). The differentially expressed genes were unraveled by using Geo2Enrichr and the functional enrichment analysis was identified by using Database for Annotation, Visualization, and Integrated Discovery (DAVID). Search Tool for the Retrieval of Interacting Genes (STRING) was used to construct the Protein-protein interaction (PPI) network and visualized by using Cytoscape. A total of 500 genes (262 up-regulated and 238 down-regulated) were identified among NiV infected cells. 19 genes were found with a node degree of more than 10. All of them were upregulated genes. MX1, ISG15 and IFIT1 were found to have the highest node degree (degree = 20) followed by RSAD2 and IRF7 with node degree 18 and MX2 and IFIT3 with node degree 17. The above results explicitly demonstrate that the expressed genes attribute to a defensive response against the virus. Henceforth finding agonists for these genes would help in the effective management of Niv infection.
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一种新型人畜共患副粘病毒潜在靶点的预测:综合生物信息学分析
尼帕病毒是一种人畜共患副粘病毒,可引起人类严重呼吸道疾病和脑炎,没有有效的靶点和治疗方法。目的:通过生物信息学研究探讨NiV感染进展的潜在靶点。为了确定与NiV感染相关的关键基因,从国家生物技术信息中心(NCBI)下载了微阵列数据集(GSE32902)。差异表达基因通过geo2enrichment进行解析,功能富集分析通过Database for Annotation, Visualization, and Integrated Discovery (DAVID)进行鉴定。利用相互作用基因检索工具(STRING)构建蛋白-蛋白相互作用(PPI)网络,并利用Cytoscape进行可视化。在NiV感染细胞中共鉴定出500个基因,其中上调262个,下调238个。结度大于10的基因有19个。它们都是上调基因。节点度最高的是MX1、ISG15和IFIT1,节点度为20,其次是RSAD2和IRF7,节点度为18,MX2和IFIT3节点度为17。上述结果明确表明,表达的基因归因于对病毒的防御反应。因此,找到这些基因的激动剂将有助于有效地管理Niv感染。
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来源期刊
Current Pharmacogenomics and Personalized Medicine
Current Pharmacogenomics and Personalized Medicine Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.40
自引率
0.00%
发文量
11
期刊介绍: Current Pharmacogenomics and Personalized Medicine (Formerly ‘Current Pharmacogenomics’) Current Pharmacogenomics and Personalized Medicine (CPPM) is an international peer reviewed biomedical journal that publishes expert reviews, and state of the art analyses on all aspects of pharmacogenomics and personalized medicine under a single cover. The CPPM addresses the complex transdisciplinary challenges and promises emerging from the fusion of knowledge domains in therapeutics and diagnostics (i.e., theragnostics). The journal bears in mind the increasingly globalized nature of health research and services.
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