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从中国河南省分离鉴定的猪德尔塔冠状病毒 HNZK-02 株及其转录组分析

Isolation, characterization and transcriptome analysis of porcine deltacoronavirus strain HNZK-02 from Henan Province, China.

机构信息

The College of Animal Science and Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450002, PR China.

Key Laboratory for Animal-derived Food Safety of Henan Province, Zhengzhou, 450002, PR China.

出版信息

Mol Immunol. 2021 Jun;134:86-99. doi: 10.1016/j.molimm.2021.03.006. Epub 2021 Mar 16.

Abstract

Porcine deltacoronavirus (PDCoV), an emerging porcine enteropathogenic coronavirus, causes acute watery diarrhea and vomiting in piglets. Here, we isolated a strain of PDCoV from intestinal content of a piglet with severe watery diarrhea on a farm located in Henan Province, named PDCoV strain HNZK-02. Subsequently, the complete genomes of cell-cultured PDCoV HNZK-02 passage 5 and 15 were sequenced and analyzed. There was a continuous 3-nucleotide deletion and 7 amino acid changes in S genes when compared with the other reported PDCoVs. RNA sequencing (RNA-seq)-based transcriptome analysis was used to quantitatively identify differentially expressed genes after PDCoV infection in ST cells. In total, 523 differentially expressed genes (DEGs) were identified, including 62 upregulated genes and 457 downregulated genes. The 62 upregulated genes were associated with TNF signaling pathway, cytokine-cytokine receptor interaction, Toll-like receptor signaling pathway, IL-17 signaling, chemokine signaling pathway and NF-κB signaling pathway. The significant expressing changed genes, including three antiviral genes (Mx1, OASL, OAS1) and three inflammatory chemokine related genes (CCL5, CXCL8, CXCL10) were further validated using quantitative real-time RT-PCR (qRT-PCR) assay. It showed the consistent expression patterns of the candidate genes with those from RNA-seq. Our results demonstrated that PDCoV infection activates NF-κB signaling pathway and leads to the expression of inflammatory factors, which may be related to TLRs but TLR2 is not a critical factor.In general, these results can help us to confirm the molecular regulation mechanism and also provide us a comprehensive resource of PDCoV infection.

摘要

猪德尔塔冠状病毒(PDCoV)是一种新兴的猪肠道致病性冠状病毒,可引起仔猪急性水样腹泻和呕吐。本研究从河南省某猪场发生严重水样腹泻仔猪的肠内容物中分离到一株 PDCoV,命名为 PDCoV 株 HNZK-02。随后,对细胞培养的 PDCoV HNZK-02 第 5 代和第 15 代的全基因组进行了测序和分析。与其他已报道的 PDCoVs 相比,S 基因连续缺失 3 个核苷酸并发生 7 个氨基酸变化。采用基于 RNA 测序(RNA-seq)的转录组分析定量鉴定 PDCoV 感染 ST 细胞后差异表达基因。共鉴定出 523 个差异表达基因(DEGs),包括 62 个上调基因和 457 个下调基因。62 个上调基因与 TNF 信号通路、细胞因子-细胞因子受体相互作用、Toll 样受体信号通路、IL-17 信号通路、趋化因子信号通路和 NF-κB 信号通路有关。使用定量实时 RT-PCR(qRT-PCR)检测进一步验证了显著表达变化的基因,包括三个抗病毒基因(Mx1、OASL、OAS1)和三个炎症趋化因子相关基因(CCL5、CXCL8、CXCL10)。候选基因的表达模式与 RNA-seq 的结果一致。研究结果表明,PDCoV 感染激活 NF-κB 信号通路并导致炎症因子的表达,这可能与 TLRs 有关,但 TLR2 不是关键因素。总之,这些结果可以帮助我们确认分子调控机制,并为 PDCoV 感染提供全面的资源。

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