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首页> 外文期刊>Fish & Shellfish Immunology >Transcriptomic profiles of striped snakehead cells (SSN-1) infected with snakehead vesiculovirus (SHVV) identifying IFI35 as a positive factor for SHVV replication
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Transcriptomic profiles of striped snakehead cells (SSN-1) infected with snakehead vesiculovirus (SHVV) identifying IFI35 as a positive factor for SHVV replication

机译:用SnakeHead Vesiculovirus(SHVV)感染的条纹蛇头细胞(SSN-1)的转录组谱鉴定IFI35作为SHVV复制的正因素

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摘要

Snakehead vesiculovirus (SHVV) has caused great economic loss in snakehead fish culture in China. However, there is no effective strategy to prevent the epidemic of the virus. Understanding the host factors in response to virus infection is the basis for the prevention of viral disease. In this study, the transcriptomic profiles of SHVV-infected and mock-infected SSN-1 cells (derived from striped snakehead, Channa striatus) at 3 and 24 h (h) post of infection (poi) were obtained using high-throughput sequencing technique. A total of 93,372 unigenes were obtained. The differently expressed genes (DEGs) of SSN-1 cells upon SHVV infection were thereby identified, including 3668 and 3536 DEGs at 3 and 24 h poi, respectively. These DEGs were involved in many pathways of viral pathogenesis, including retinoic acid-inducible gene I (RIG-I) like receptors pathway, Toll-like receptor signaling pathway, NF-kappa B signaling pathway, PI3K-Akt signaling pathway and MAPK signaling pathway. Therefore, several immune-related DEGs were randomly selected and confirmed by quantitative real-time PCR (qRT-PCR). In addition, the effects of the interferon inducible protein 35 (IFI35) on SHVV replication were further investigated. Over-expression or inhibition of IFI35 significantly promoted or reduced SHVV replication at the level of viral gene expression, which indicated that IFI35 might be a positive factor for SHVV replication in SSN-1 cells. Our findings presented some valuable information, which will benefit for future study on SHVV-host interactions.
机译:Snakehead Vesiculovirus(Shvv)在中国蛇麦鱼类文化引起了巨大的经济损失。然而,没有有效的策略来防止病毒的流行病。了解宿主因子响应病毒感染是预防病毒疾病的基础。在该研究中,使用高通量测序技术获得3和24h(h)感染的Shvv感染和衍生自旋转蛇头,通道纹状体)的转录组谱(衍生自条纹蛇头,通道)(POI) 。获得总共93,372个unigenes。由此鉴定了SHVV感染时SSN-1细胞的不同表达基因(DEGS),包括3668和3536℃,分别为3和24小时POI。这些DEG涉及许多病毒发病机构的途径,包括视黄酸 - 诱导基因I(RIG-I),如受体途径,可收费的受体信号传导途径,NF-Kappa信号通路,PI3K-AKT信号通路和MAPK信号通路。因此,通过定量实时PCR(QRT-PCR)随机选择并确认几个免疫相关的次数。此外,进一步研究了干扰素诱导蛋白35(IFI35)对SHVV复制的影响。 IFI35的过度表达或抑制在病毒基因表达水平下显着促进或降低了SHVV复制,这表明IFI35可能是SSN-1细胞中SHVV复制的正因素。我们的调查结果提出了一些有价值的信息,这将有利于对SHVV-or互动的互动研究。

著录项

  • 来源
    《Fish & Shellfish Immunology》 |2019年第2019期|共7页
  • 作者单位

    Yangzhou Univ Coll Anim Sci &

    Technol Yangzhou 225009 Jiangsu Peoples R China;

    Zhongkai Univ Agr &

    Engn Guangdong Prov Water Environm &

    Aquat Prod Secur Guangzhou Key Lab Aquat Anim Dis &

    Waterfowl Bree Guangdong Prov Key Lab Waterfowl Hlth Breeding Co Guangzhou 510225 Guangdong Peoples R China;

    Zhongkai Univ Agr &

    Engn Guangdong Prov Water Environm &

    Aquat Prod Secur Guangzhou Key Lab Aquat Anim Dis &

    Waterfowl Bree Guangdong Prov Key Lab Waterfowl Hlth Breeding Co Guangzhou 510225 Guangdong Peoples R China;

    Zhongkai Univ Agr &

    Engn Guangdong Prov Water Environm &

    Aquat Prod Secur Guangzhou Key Lab Aquat Anim Dis &

    Waterfowl Bree Guangdong Prov Key Lab Waterfowl Hlth Breeding Co Guangzhou 510225 Guangdong Peoples R China;

    Lake Super State Univ Sch Biol Sci Sault Ste Marie MI 49783 USA;

    Yangzhou Univ Coll Anim Sci &

    Technol Yangzhou 225009 Jiangsu Peoples R China;

    Zhongkai Univ Agr &

    Engn Guangdong Prov Water Environm &

    Aquat Prod Secur Guangzhou Key Lab Aquat Anim Dis &

    Waterfowl Bree Guangdong Prov Key Lab Waterfowl Hlth Breeding Co Guangzhou 510225 Guangdong Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 水产、渔业;
  • 关键词

    Transcriptomic sequence; SSN-1; SHVV; Differentially expressed genes; IFI35;

    机译:转录组序列;SSN-1;SHVV;差异表达基因;IFI35;

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