Song Baifen, Huang Yanmei, Ma Jinzhu, Yu Liquan, Yu Yongzhong, Peng Chen, Wu Wenxue
Key Laboratory of Animal Epidemiology and Zoonosis, College of Veterinary Medicine, China Agricultural University, Beijing, People's Republic of China.
The College of Life Science and Technology, Heilongjiang Bayi Agricultural University, Daqing, People's Republic of China.
Infect Drug Resist. 2023 Aug 31;16:5729-5740. doi: 10.2147/IDR.S411034. eCollection 2023.
Virus infection can cause the changes of lncRNA expression levels to regulate the interaction between virus and host, but the relationship between BHV-1 infection and lncRNA has not been reported.
In this study, in order to reveal the molecular mechanism of RNA in BoHV-1 infection, the Madin-Darby bovine kidney (MDBK) cells were infected with BoHV-1, transcriptome sequencing were performed by next-generation sequencing at 18 h or 24 h or 33 h of viral infection and then based on the competitive endogenous RNA (ceRNA) theory, lncRNA-miRNA-mRNA networks were constructed using these high-throughput sequencing data. The network analysis, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were performed for functional annotation and exploration of ncRNA ceRNAs in BoHV-1 infection.
The results showed that 48 lncRNAs, 123 mRNAs and 20 miRNAs as differentially expressed genes, and the mitogen activated protein kinase (MAPK) pathway and calcium signaling pathway were significantly enriched in the ceRNA network. Some differentially expressed lncRNA genes were randomly selected for verification by RT-qPCR, and the results showed that their expression trend was consistent with the results of transcriptome sequencing data.
This study revealed that BoHV-1 infection can affect the expression of RNAs in MDBK cells and the regulation of ceRNA network to carry out corresponding biological functions in the host, but further experimental studies are still necessary to prove the hub genes function in ceRNA network and the molecular mechanism in BoHV-1 infection.
病毒感染可导致长链非编码RNA(lncRNA)表达水平发生变化,从而调节病毒与宿主之间的相互作用,但牛疱疹病毒1型(BHV-1)感染与lncRNA之间的关系尚未见报道。
在本研究中,为揭示RNA在牛疱疹病毒1型(BoHV-1)感染中的分子机制,用BoHV-1感染马-达二氏牛肾(MDBK)细胞,在病毒感染18小时、24小时或33小时时通过新一代测序进行转录组测序,然后基于竞争性内源RNA(ceRNA)理论,利用这些高通量测序数据构建lncRNA- miRNA- mRNA网络。对该网络进行分析、基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路分析,以对BoHV-1感染中的非编码RNA的ceRNAs进行功能注释和探索。
结果显示,有48个lncRNAs、123个mRNAs和20个miRNAs作为差异表达基因,丝裂原活化蛋白激酶(MAPK)通路和钙信号通路在ceRNA网络中显著富集。随机选择一些差异表达的lncRNA基因通过RT-qPCR进行验证,结果表明它们的表达趋势与转录组测序数据的结果一致。
本研究揭示了BoHV-1感染可影响MDBK细胞中RNA的表达以及ceRNA网络的调控,从而在宿主中发挥相应的生物学功能,但仍需进一步的实验研究来证明ceRNA网络中的枢纽基因功能以及BoHV-1感染中的分子机制。