Analysis of long noncoding RNAs and messenger RNAs expression profiles in the hearts of mice with acute viral myocarditis

Author:

Xue Yimin1,Ke Jun23,Zhang Jiuyun23,Chen Mingguang1,Zeng Lijuan1,Fan Qiaolian1,Zheng Chunfu45ORCID,Chen Feng23ORCID

Affiliation:

1. Fourth Department of Critical Care Medicine, Shengli Clinical Medical College of Fujian Medical University Fujian Provincial Hospital Fuzhou Fujian China

2. Department of Emergency, Shengli Clinical Medical College of Fujian Medical University Fujian Provincial Hospital Fuzhou Fujian China

3. Fujian Provincial Key Laboratory of Emergency Medicine Fujian Provincial Hospital Fuzhou Fujian China

4. Institute of Animal Health, Guangdong Academy of Agricultural Sciences, Key Laboratory of Livestock Disease Prevention of Guangdong Province, Scientific Observation and Experiment Station of Veterinary Drugs and Diagnostic Techniques of Guangdong Province Ministry of Agriculture and Rural Affairs Guangzhou Guangdong China

5. Department of Microbiology, Immunology, and Infectious Diseases University of Calgary Calgary Alberta Canada

Abstract

AbstractAcute viral myocarditis (AVMC) is a common acute myocardial inflammation caused by viral infections, which can lead to severe cardiac dysfunction. Several long noncoding RNAs (lncRNAs) with aberrant expression have been identified in the pathogenesis of AVMC. However, the expression profiles and functions of lncRNAs in AVMC have not been fully elucidated. In the present study, we constructed AVMC mouse models by intraperitoneal injection of coxsackievirus B3 (CVB3) and performed RNA sequencing (RNA‐seq) on heart tissues to investigate the differences in lncRNAs and messenger RNAs (mRNAs) expression profiles. Based on the cutoff criteria of adjusted p‐values (padj) <0.05 and |log2FoldChange| >1, a total of 1122 differentially expressed lncRNAs (DElncRNAs) and 3186 differentially expressed mRNAs (DEmRNAs) were screened, including 734 upregulated and 388 downregulated lncRNAs, 1821 upregulated and 1365 downregulated mRNAs. RT‐qPCR analysis validated that the expression patterns of 12 randomly selected genes (6 DElncRNAs and 6 DEmRNAs) were highly consistent with those in RNA‐seq, proving the reliability of the RNA‐seq data. Then, Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses revealed that differentially expressed genes were mainly involved in metabolic and immune‐related processes. Furthermore, co‐expression networks between DElncRNAs and DEmRNAs in cytokine‐cytokine receptor interaction, MAPK signaling pathway, and PI3K‐Akt signaling pathway were constructed to study the molecular interactions of these molecules. Our study, for the first time, reveals the expression profiles of lncRNAs and mRNAs associated with AVMC, which may shed light on the roles of lncRNAs in disease pathogenesis and aid in discovering new therapeutic targets.

Funder

Natural Science Foundation of Fujian Province

Publisher

Wiley

Subject

Infectious Diseases,Virology

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