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

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
{"title":"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","authors":"M. Sai, Viswam Subeesh, S. HemaSreeGN, G. Saraswathy, N. Gouri","doi":"10.2174/1875692118666210315150037","DOIUrl":null,"url":null,"abstract":"\n\n Nipah virus (NiV) is a zoonotic paramyxovirus that can cause severe respiratory illness and encephalitis in humans, with no effective targets and treatment.\n\n\n\n\nTo investigate potential targets involved in the progression of NiV infection by bioinformatics studies.\n\n\n\n\nTo 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. \n\n\n\n\nA 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. \n\n\n\n\nThe 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. \n\n","PeriodicalId":11056,"journal":{"name":"Current Pharmacogenomics and Personalized Medicine","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prediction of Potential Targets of an Emerging Zoonotic Paramyxovirus: An Integrated Bioinformatics Analysis\",\"authors\":\"M. Sai, Viswam Subeesh, S. HemaSreeGN, G. Saraswathy, N. Gouri\",\"doi\":\"10.2174/1875692118666210315150037\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\n Nipah virus (NiV) is a zoonotic paramyxovirus that can cause severe respiratory illness and encephalitis in humans, with no effective targets and treatment.\\n\\n\\n\\n\\nTo investigate potential targets involved in the progression of NiV infection by bioinformatics studies.\\n\\n\\n\\n\\nTo 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. \\n\\n\\n\\n\\nA 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. \\n\\n\\n\\n\\nThe 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. \\n\\n\",\"PeriodicalId\":11056,\"journal\":{\"name\":\"Current Pharmacogenomics and Personalized Medicine\",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-03-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Pharmacogenomics and Personalized Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/1875692118666210315150037\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Pharmacogenomics and Personalized Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1875692118666210315150037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Prediction of Potential Targets of an Emerging Zoonotic Paramyxovirus: An Integrated Bioinformatics Analysis
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.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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.
期刊最新文献
Association Study between rs10486567, rs13149290, rs1545985 and rs6983267 with Incidence of Prostate Adenocarcinoma Among Iranians Clinical Trial Participant's Perspectives on Genetic Research Data Re-uses for Future Research Exosome and Other Extracellular Vesicles in Gene Therapy and Personalized Care Generalized Analysis of Open Genetic Databases Reveals New Associations with Migraine Prediction Of Deleterious Non-Synonymous Single Nucleotide Polymorphism Of Cathelicidin
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1