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转录组分析与卡帕羊中小反刍病毒感染相关的基因。

Transcriptome Analysis for Genes Associated with Small Ruminant Lentiviruses Infection in Goats of Carpathian Breed.

机构信息

Department of Biochemistry, National Veterinary Research Institute, 24-100 Pulawy, Poland.

Department of Animal Molecular Biology, National Research Institute of Animal Production, Krakowska 1, 32-083 Kraków, Poland.

出版信息

Viruses. 2021 Oct 13;13(10):2054. doi: 10.3390/v13102054.

DOI:10.3390/v13102054
PMID:34696484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8538975/
Abstract

Small ruminant lentiviruses (SRLV) are economically important viral pathogens of sheep and goats. SRLV infection may interfere in the innate and adaptive immunity of the host, and genes associated with resistance or susceptibility to infection with SRLV have not been fully recognized. The presence of animals with relatively high and low proviral load suggests that some host factors are involved in the control of virus replication. To better understand the role of the genes involved in the host response to SRLV infection, RNA sequencing (RNA-seq) method was used to compare whole gene expression profiles in goats carrying both a high (HPL) and low (LPL) proviral load of SRLV and uninfected animals. Data enabled the identification of 1130 significant differentially expressed genes (DEGs) between control and LPL groups: 411 between control and HPL groups and 1434 DEGs between HPL and LPL groups. DEGs detected between the control group and groups with a proviral load were found to be significantly enriched in several gene ontology (GO) terms, including an integral component of membrane, extracellular region, response to growth factor, inflammatory and innate immune response, transmembrane signaling receptor activity, myeloid differentiation primary response gene 88 (MyD88)-dependent toll-like receptor signaling pathway as well as regulation of cytokine secretion. Our results also demonstrated significant deregulation of selected pathways in response to viral infection. The presence of SRLV proviral load in blood resulted in the modification of gene expression belonging to the toll-like receptor signaling pathway, the tumor necrosis factor (TNF) signaling pathway, the cytokine-cytokine receptor interaction, the phagosome, the Ras signaling pathway, the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT) (PI3K-Akt) signaling pathway and rheumatoid arthritis. It is worth mentioning that the most predominant in all pathways were genes represented by toll-like receptors, tubulins, growth factors as well as interferon gamma receptors. DEGs detected between LPL and HPL groups were found to have significantly enriched regulation of signaling receptor activity, the response to toxic substances, nicotinamide adenine dinucleotide (NADH) dehydrogenase complex assembly, cytokine production, vesicle, and vacuole organization. In turn, the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway tool classified DEGs that enrich molecular processes such as B and T-cell receptor signaling pathways, natural killer cell-mediated cytotoxicity, Fc gamma R-mediated phagocytosis, toll-like receptor signaling pathways, TNF, mammalian target of rapamycin (mTOR) signaling and forkhead box O (Foxo) signaling pathways, etc. Our data indicate that changes in SRLV proviral load induced altered expression of genes related to different biological processes such as immune response, inflammation, cell locomotion, and cytokine production. These findings provide significant insights into defense mechanisms against SRLV infection. Furthermore, these data can be useful to develop strategies against SRLV infection by selection of animals with reduced SRLV proviral concentration that may lead to a reduction in the spread of the virus.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/669f6dcee999/viruses-13-02054-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/fcfb6c7dfefa/viruses-13-02054-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/cf5103b62251/viruses-13-02054-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/d433a87ed55d/viruses-13-02054-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/1efc22c85026/viruses-13-02054-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/5e867aed602c/viruses-13-02054-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/669f6dcee999/viruses-13-02054-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/fcfb6c7dfefa/viruses-13-02054-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/cf5103b62251/viruses-13-02054-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/d433a87ed55d/viruses-13-02054-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/1efc22c85026/viruses-13-02054-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/5e867aed602c/viruses-13-02054-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e26/8538975/669f6dcee999/viruses-13-02054-g006.jpg
摘要

小反刍兽疫病毒(SRLV)是绵羊和山羊的重要经济病毒病原体。SRLV 感染可能会干扰宿主的先天和适应性免疫,而与 SRLV 感染的抗性或易感性相关的基因尚未完全被识别。存在具有相对高和低前病毒载量的动物表明,一些宿主因素参与了病毒复制的控制。为了更好地了解宿主对 SRLV 感染反应中涉及的基因的作用,使用 RNA 测序(RNA-seq)方法比较了携带高(HPL)和低(LPL)SRLV 前病毒载量的山羊与未感染动物的全基因表达谱。数据鉴定了对照组和 LPL 组之间的 1130 个显著差异表达基因(DEGs):对照组和 HPL 组之间的 411 个,HPL 和 LPL 组之间的 1434 个 DEGs。在对照组和前病毒载量组之间检测到的 DEGs 在几个基因本体论(GO)术语中显著富集,包括膜的整体成分、细胞外区、生长因子反应、炎症和先天免疫反应、跨膜信号受体活性、髓样分化初级反应基因 88(MyD88)依赖性 Toll 样受体信号通路以及细胞因子分泌的调节。我们的结果还表明,病毒感染后一些选定途径的表达明显失调。血液中存在 SRLV 前病毒载量会导致属于 Toll 样受体信号通路、肿瘤坏死因子(TNF)信号通路、细胞因子-细胞因子受体相互作用、吞噬体、Ras 信号通路、磷酸肌醇 3-激酶(PI3K)/蛋白激酶 B(AKT)(PI3K-Akt)信号通路和类风湿关节炎的基因表达发生改变。值得一提的是,在所有途径中,最主要的是 Toll 样受体、微管蛋白、生长因子以及干扰素 γ 受体代表的基因。在 LPL 和 HPL 组之间检测到的 DEGs 被发现显著富集了信号受体活性的调节、对有毒物质的反应、烟酰胺腺嘌呤二核苷酸(NADH)脱氢酶复合物组装、细胞因子产生、囊泡和液泡组织。反过来,京都基因与基因组百科全书(KEGG)途径工具将 DEGs 分类为与 B 和 T 细胞受体信号通路、自然杀伤细胞介导的细胞毒性、Fc 受体γ介导的吞噬作用、Toll 样受体信号通路、TNF、哺乳动物雷帕霉素靶蛋白(mTOR)信号和叉头框 O(Foxo)信号通路等分子过程相关的基因。我们的数据表明,SRLV 前病毒载量的变化诱导了与不同生物学过程相关的基因表达改变,如免疫反应、炎症、细胞运动和细胞因子产生。这些发现为针对 SRLV 感染的防御机制提供了重要的见解。此外,这些数据可以通过选择前病毒浓度降低的动物来开发针对 SRLV 感染的策略,这可能导致病毒传播减少。

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