Identifying the Interaction Between Tuberculosis and SARS-CoV-2 Infections via Bioinformatics Analysis and Machine Learning

IF 2.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ze-Min Huang, Jia-Qi Kang, Pei-Zhen Chen, Lin-Fen Deng, Jia-Xin Li, Ying-Xin He, Jie Liang, Nan Huang, Tian-Ye Luo, Qi-Wen Lan, Hao-Kai Chen, Xu-Guang Guo
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引用次数: 0

Abstract

The number of patients with COVID-19 caused by severe acute respiratory syndrome coronavirus 2 is still increasing. In the case of COVID-19 and tuberculosis (TB), the presence of one disease affects the infectious status of the other. Meanwhile, coinfection may result in complications that make treatment more difficult. However, the molecular mechanisms underpinning the interaction between TB and COVID-19 are unclear. Accordingly, transcriptome analysis was used to detect the shared pathways and molecular biomarkers in TB and COVID-19, allowing us to determine the complex relationship between COVID-19 and TB. Two RNA-seq datasets (GSE114192 and GSE163151) from the Gene Expression Omnibus were used to find concerted differentially expressed genes (DEGs) between TB and COVID-19 to identify the common pathogenic mechanisms. A total of 124 common DEGs were detected and used to find shared pathways and drug targets. Several enterprising bioinformatics tools were applied to perform pathway analysis, enrichment analysis and networks analysis. Protein–protein interaction analysis and machine learning was used to identify hub genes (GAS6, OAS3 and PDCD1LG2) and datasets GSE171110, GSE54992 and GSE79362 were used for verification. The mechanism of protein-drug interactions may have reference value in the treatment of coinfection of COVID-19 and TB.

Abstract Image

通过生物信息学分析和机器学习确定结核病和SARS-CoV-2感染之间的相互作用。
由严重急性呼吸综合征冠状病毒2型感染的COVID-19患者人数仍在增加。就COVID-19和结核病而言,一种疾病的存在会影响另一种疾病的感染状况。同时,合并感染可能导致并发症,使治疗更加困难。然而,结核病与COVID-19相互作用的分子机制尚不清楚。因此,利用转录组分析检测TB和COVID-19的共享途径和分子生物标志物,使我们能够确定COVID-19与TB之间的复杂关系。利用基因表达Omnibus的两个RNA-seq数据集(GSE114192和GSE163151)寻找TB和COVID-19之间一致的差异表达基因(DEGs),以确定共同的致病机制。共检测到124个共同的deg,并用于寻找共享途径和药物靶点。应用了几种先进的生物信息学工具进行通路分析、富集分析和网络分析。利用蛋白-蛋白相互作用分析和机器学习技术鉴定中心基因(GAS6、OAS3和PDCD1LG2),并利用数据集GSE171110、GSE54992和GSE79362进行验证。蛋白质-药物相互作用的机制可能对COVID-19合并结核感染的治疗具有参考价值。
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来源期刊
Biochemical Genetics
Biochemical Genetics 生物-生化与分子生物学
CiteScore
3.90
自引率
0.00%
发文量
133
审稿时长
4.8 months
期刊介绍: Biochemical Genetics welcomes original manuscripts that address and test clear scientific hypotheses, are directed to a broad scientific audience, and clearly contribute to the advancement of the field through the use of sound sampling or experimental design, reliable analytical methodologies and robust statistical analyses. Although studies focusing on particular regions and target organisms are welcome, it is not the journal’s goal to publish essentially descriptive studies that provide results with narrow applicability, or are based on very small samples or pseudoreplication. Rather, Biochemical Genetics welcomes review articles that go beyond summarizing previous publications and create added value through the systematic analysis and critique of the current state of knowledge or by conducting meta-analyses. Methodological articles are also within the scope of Biological Genetics, particularly when new laboratory techniques or computational approaches are fully described and thoroughly compared with the existing benchmark methods. Biochemical Genetics welcomes articles on the following topics: Genomics; Proteomics; Population genetics; Phylogenetics; Metagenomics; Microbial genetics; Genetics and evolution of wild and cultivated plants; Animal genetics and evolution; Human genetics and evolution; Genetic disorders; Genetic markers of diseases; Gene technology and therapy; Experimental and analytical methods; Statistical and computational methods.
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