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综合生物信息学分析和系统生物学方法鉴定 COVID-19 与心包炎之间的相互作用。

Comprehensive bioinformatics analysis and systems biology approaches to identify the interplay between COVID-19 and pericarditis.

机构信息

Department of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, China.

Department of Genetics and Cell Biology, Basic Medical College, Qingdao University, Qingdao, China.

出版信息

Front Immunol. 2024 Feb 22;15:1264856. doi: 10.3389/fimmu.2024.1264856. eCollection 2024.

DOI:10.3389/fimmu.2024.1264856
PMID:38455049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10918693/
Abstract

BACKGROUND

Increasing evidence indicating that coronavirus disease 2019 (COVID-19) increased the incidence and related risks of pericarditis and whether COVID-19 vaccine is related to pericarditis has triggered research and discussion. However, mechanisms behind the link between COVID-19 and pericarditis are still unknown. The objective of this study was to further elucidate the molecular mechanisms of COVID-19 with pericarditis at the gene level using bioinformatics analysis.

METHODS

Genes associated with COVID-19 and pericarditis were collected from databases using limited screening criteria and intersected to identify the common genes of COVID-19 and pericarditis. Subsequently, gene ontology, pathway enrichment, protein-protein interaction, and immune infiltration analyses were conducted. Finally, TF-gene, gene-miRNA, gene-disease, protein-chemical, and protein-drug interaction networks were constructed based on hub gene identification.

RESULTS

A total of 313 common genes were selected, and enrichment analyses were performed to determine their biological functions and signaling pathways. Eight hub genes (, , , , , , , and ) were identified using the protein-protein interaction network, and immune infiltration analysis was then carried out to examine the functional relationship between the eight hub genes and immune cells as well as changes in immune cells in disease. Transcription factors, miRNAs, diseases, chemicals, and drugs with high correlation with hub genes were predicted using bioinformatics analysis.

CONCLUSIONS

This study revealed a common gene interaction network between COVID-19 and pericarditis. The screened functional pathways, hub genes, potential compounds, and drugs provided new insights for further research on COVID-19 associated with pericarditis.

摘要

背景

越来越多的证据表明,2019 年冠状病毒病(COVID-19)增加了心包炎的发病率和相关风险,COVID-19 疫苗是否与心包炎有关,这引发了研究和讨论。然而,COVID-19 与心包炎之间的联系机制尚不清楚。本研究旨在通过生物信息学分析,从基因水平上进一步阐明 COVID-19 合并心包炎的分子机制。

方法

使用有限的筛选标准从数据库中收集与 COVID-19 和心包炎相关的基因,并进行交集以确定 COVID-19 和心包炎的共同基因。随后进行基因本体、通路富集、蛋白质-蛋白质相互作用和免疫浸润分析。最后,基于枢纽基因鉴定构建 TF-基因、基因-miRNA、基因-疾病、蛋白质-化学物质和蛋白质-药物相互作用网络。

结果

共筛选出 313 个共同基因,进行富集分析以确定其生物学功能和信号通路。利用蛋白质-蛋白质相互作用网络鉴定出 8 个枢纽基因(、、、、、、和),然后进行免疫浸润分析,以研究这 8 个枢纽基因与免疫细胞以及疾病中免疫细胞变化之间的功能关系。利用生物信息学分析预测与枢纽基因具有高相关性的转录因子、miRNA、疾病、化学物质和药物。

结论

本研究揭示了 COVID-19 与心包炎之间共同的基因相互作用网络。筛选出的功能通路、枢纽基因、潜在化合物和药物为进一步研究 COVID-19 相关心包炎提供了新的思路。

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本文引用的文献

1
Humoral Immune Response after COVID-19 mRNA Vaccination in Patients with Liver Cirrhosis: A Prospective Real-Life Single Center Study.肝硬化患者接种新冠病毒mRNA疫苗后的体液免疫反应:一项前瞻性真实世界单中心研究
Biomedicines. 2023 Apr 28;11(5):1320. doi: 10.3390/biomedicines11051320.
2
COVID-19, Myocarditis and Pericarditis.新型冠状病毒病、心肌炎和心包炎。
Circ Res. 2023 May 12;132(10):1302-1319. doi: 10.1161/CIRCRESAHA.123.321878. Epub 2023 May 11.
3
Autoantibodies against chemokines linked with better disease outcomes in COVID-19.
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Nat Rev Immunol. 2023 Apr;23(4):203. doi: 10.1038/s41577-023-00860-2.
4
Endotoxin tolerance and low activation of TLR-4/NF-κB axis in monocytes of COVID-19 patients.COVID-19 患者单核细胞内内毒素耐受和 TLR-4/NF-κB 轴的低激活。
J Mol Med (Berl). 2023 Feb;101(1-2):183-195. doi: 10.1007/s00109-023-02283-x. Epub 2023 Feb 15.
5
Disentangling the common genetic architecture and causality of rheumatoid arthritis and systemic lupus erythematosus with COVID-19 outcomes: Genome-wide cross trait analysis and bidirectional Mendelian randomization study.解析类风湿关节炎和系统性红斑狼疮与 COVID-19 结局的常见遗传结构和因果关系:全基因组跨表型分析和双向孟德尔随机化研究。
J Med Virol. 2023 Feb;95(2):e28570. doi: 10.1002/jmv.28570.
6
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Brief Bioinform. 2023 Jan 19;24(1). doi: 10.1093/bib/bbac523.
7
Psychiatric symptoms before and after COVID-19 vaccination: A cohort study of hospitalized schizophrenia patients.接种 COVID-19 疫苗前后的精神症状:一项住院精神分裂症患者的队列研究。
Asian J Psychiatr. 2022 Dec;78:103319. doi: 10.1016/j.ajp.2022.103319. Epub 2022 Nov 11.
8
The STRING database in 2023: protein-protein association networks and functional enrichment analyses for any sequenced genome of interest.2023 年的 STRING 数据库:针对任何感兴趣的测序基因组的蛋白质-蛋白质关联网络和功能富集分析。
Nucleic Acids Res. 2023 Jan 6;51(D1):D638-D646. doi: 10.1093/nar/gkac1000.
9
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Int J Mol Sci. 2022 Sep 26;23(19):11338. doi: 10.3390/ijms231911338.
10
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Nucleic Acids Res. 2023 Jan 6;51(D1):D1257-D1262. doi: 10.1093/nar/gkac833.