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奶牛山羊感染伪结核棒状杆菌脾脏的转录组分析。

Transcriptome analysis of Corynebacterium pseudotuberculosis-infected spleen of dairy goats.

机构信息

College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi, 712100, China.

College of Animal Medicine, Xinjiang Agricultural University, Urumqi, 830000, China.

出版信息

Microb Pathog. 2020 Oct;147:104370. doi: 10.1016/j.micpath.2020.104370. Epub 2020 Jul 9.

Abstract

Caseous lymphadenitis is a chronic disease of goats caused by Corynebacterium pseudotuberculosis (C.pseudotuberculosis) which causes great harm to the dairy goats industry. In order to obtain detailed information about the pathogenesis and host immune response in C.pseudotuberculosis-infected goats, in this study, the gene expression difference of spleen tissue after infection with C.pseudotuberculosis was analyzed by high-throughput sequencing. Transcripts obtained over 412 700 462 clean reads after reassembly were 21 343 genes detected, of which 14 720 were known genes and 7623 new genes were predicted. There were 448 up-regulated and 519 down-regulated differentially expressed genes (DEGs). Gene Ontology (GO) analysis indicated that all of the DEGs were annotated into biological process, cellular component and molecular function. Most of these unigenes are annotated in cellular processes, the cell and binding. KEGG analysis of the DEGs showed that a total of 8733 DEGs unigenes were annotated into 459 pathways classified into 6 main categories. Most of these annotated unigenes were related to immune system response to the infectious diseases pathways. In addition, 14 DEGs were verified by quantitative real-time PCR. As the first, in vivo, RNAseq analysis of dairy goats and C.pseudotuberculosis infection, this study provides knowledge about the transcriptomics of spleen in C.pseudotuberculosis-infected goats, from which a complex molecular pathways and immune response mechanism are involved in C.pseudotuberculosis infection.

摘要

干酪性淋巴结炎是一种由假结核棒状杆菌(C.pseudotuberculosis)引起的山羊慢性疾病,对奶山羊产业造成了极大的危害。为了获得假结核棒状杆菌感染山羊发病机制和宿主免疫反应的详细信息,本研究通过高通量测序分析了感染后山羊脾脏组织的基因表达差异。组装后获得超过 412700462 条清洁读段,检测到 21343 个基因,其中 14720 个为已知基因,预测到 7623 个新基因。有 448 个上调和 519 个下调差异表达基因(DEGs)。基因本体论(GO)分析表明,所有 DEGs 都被注释到生物过程、细胞成分和分子功能。这些基因大部分被注释到细胞过程、细胞和结合中。KEGG 分析 DEGs 表明,共注释到 459 条通路的 8733 个 DEGs 基因分为 6 个主要类别。这些注释的基因大部分与免疫系统对传染病的反应途径有关。此外,通过定量实时 PCR 验证了 14 个 DEGs。作为首例对奶山羊和假结核棒状杆菌感染的体内 RNAseq 分析,本研究提供了假结核棒状杆菌感染山羊脾脏转录组学的知识,其中涉及复杂的分子途径和免疫反应机制。

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