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鸭流感病毒复制时组织特异性转录组变化。

Tissue Specific Transcriptome Changes Upon Influenza A Virus Replication in the Duck.

机构信息

Department of Biological Sciences, University of Alberta, Edmonton, AB, Canada.

Li Ka Shing Institute of Virology, University of Alberta, Edmonton, AB, Canada.

出版信息

Front Immunol. 2021 Nov 5;12:786205. doi: 10.3389/fimmu.2021.786205. eCollection 2021.

Abstract

Ducks are the natural host and reservoir of influenza A virus (IAV), and as such are permissive to viral replication while being unharmed by most strains. It is not known which mechanisms of viral control are globally regulated during infection, and which are specific to tissues during infection. Here we compare transcript expression from tissues from Pekin ducks infected with a recombinant H5N1 strain A/Vietnam 1203/04 (VN1203) or an H5N2 strain A/British Columbia 500/05 using RNA-sequencing analysis and aligning reads to the NCBI assembly ZJU1.0 of the domestic duck () genome. Highly pathogenic VN1203 replicated in lungs and showed systemic dissemination, while BC500, like most low pathogenic strains, replicated in the intestines. VN1203 infection induced robust differential expression of genes all three days post infection, while BC500 induced the greatest number of differentially expressed genes on day 2 post infection. While there were many genes globally upregulated in response to either VN1203 or BC500, tissue specific gene expression differences were observed. Lungs of ducks infected with VN1203 and intestines of birds infected with BC500, tissues important in influenza replication, showed highest upregulation of pattern recognition receptors and interferon stimulated genes early in the response. These tissues also appear to have specific downregulation of inflammatory components, with downregulation of distinct sets of proinflammatory cytokines in lung, and downregulation of key components of leukocyte recruitment and complement pathways in intestine. Our results suggest that global and tissue specific regulation patterns help the duck control viral replication as well as limit some inflammatory responses in tissues involved in replication to avoid damage.

摘要

鸭子是甲型流感病毒(IAV)的天然宿主和储存库,因此对大多数毒株具有病毒复制的许可性,而不会受到伤害。目前尚不清楚在感染过程中哪些病毒控制机制是全球调节的,哪些是感染过程中组织特异性的。在这里,我们比较了感染重组 H5N1 株 A/Vietnam 1203/04(VN1203)或 H5N2 株 A/British Columbia 500/05 的北京鸭组织的转录表达,使用 RNA-seq 分析并将读取与 NCBI 组装的家鸭基因组 ZJU1.0 对齐()。高致病性 VN1203 在肺部复制并显示全身传播,而 BC500 与大多数低致病性株一样,在肠道中复制。VN1203 感染诱导所有三种感染后 3 天的基因高度差异表达,而 BC500 感染在感染后 2 天诱导最多数量的差异表达基因。虽然有许多基因对 VN1203 或 BC500 都有全球上调,但观察到组织特异性基因表达差异。感染 VN1203 的鸭肺和感染 BC500 的鸟类肠道,这是流感复制的重要组织,在早期反应中显示出模式识别受体和干扰素刺激基因的最高上调。这些组织似乎也具有特定的炎症成分下调,在肺中下调了一组不同的促炎细胞因子,在肠道中下调了白细胞募集和补体途径的关键成分。我们的研究结果表明,全球和组织特异性调节模式有助于鸭子控制病毒复制,并在参与复制的组织中限制某些炎症反应,以避免损伤。

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