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In depth analysis of genes and pathways of the mammary gland involved in the pathogenesis of bovine Escherichia coli-mastitis

机译:深入分析涉及牛大肠杆菌-乳腺炎发病机理的乳腺基因和途径

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Background Bovine mastitis is one of the most costly and prevalent diseases affecting dairy cows worldwide. In order to develop new strategies to prevent Escherichia coli-induced mastitis, a detailed understanding of the molecular mechanisms underlying the host immune response to an E. coli infection is necessary. To this end, we performed a global gene-expression analysis of mammary gland tissue collected from dairy cows that had been exposed to a controlled E. coli infection. Biopsy samples of healthy and infected utter tissue were collected at T = 24 h post-infection (p.i.) and at T = 192 h p.i. to represent the acute phase response (APR) and chronic stage, respectively. Differentially expressed (DE) genes for each stage were analyzed and the DE genes detected at T = 24 h were also compared to data collected from two previous E. coli mastitis studies that were carried out on post mortem tissue. Results Nine-hundred-eighty-two transcripts were found to be differentially expressed in infected tissue at T = 24 (P E. coli mastitis studies revealed 248 were common and mainly involved immune response functions. KEGG pathway analysis indicated that these genes were involved in 12 pathways related to the pro-inflammatory response and APR, but also identified significant representation of two unexpected pathways: natural killer cell-mediated cytotoxicity pathway (KEGG04650) and the Rig-I-like receptor signalling pathway (KEGG04622). Conclusions In E. coli-induced mastitis, infected mammary gland tissue was found to significantly up-regulate expression of genes related to the immune response and down-regulate genes related to fat metabolism. Up to 25% of the DE immune response genes common to the three E. coli mastitis studies at T = 24 h were independent of E. coli strain and dose, cow lactation stage and number, tissue collection method and gene analysis method used. Hence, these DE genes likely represent important mediators of the local APR against E. coli in the mammary gland.
机译:背景技术牛乳腺炎是影响全世界奶牛的最昂贵,最流行的疾病之一。为了制定预防大肠埃希氏菌引起的乳腺炎的新策略,对宿主对大肠埃希氏菌感染的免疫反应的分子机制有详细的了解是必要的。为此,我们对收集自暴露于受控大肠杆菌感染的奶牛的乳腺组织进行了全局基因表达分析。在感染后24 h(p.i.)和T = 192 h p.i时收集健康和感染的子宫组织的活检样品。分别代表急性期反应(APR)和慢性期。分析每个阶段的差异表达(DE)基因,并将在T = 24 h检测到的DE基因与从先前两个在尸体组织上进行的大肠杆菌乳腺炎研究中收集的数据进行比较。结果在T = 24时,有942个转录物在受感染组织中差异表达(大肠杆菌乳腺炎研究显示248个常见,主要涉及免疫应答功能,KEGG途径分析表明这些基因与与促炎反应和APR相关的12条途径,还确定了两种意想不到的途径的重要代表:天然杀伤细胞介导的细胞毒性途径(KEGG04650)和Rig-1样受体信号传导途径(KEGG04622)。大肠杆菌引起的乳腺炎,被感染的乳腺组织被发现显着上调与免疫反应相关的基因的表达,而下调与脂肪代谢相关的基因,这多达三个E共有的DE免疫反应基因的25%。 T = 24 h时的大乳腺炎研究与大肠埃希菌的菌株和剂量,泌乳阶段和数量,组织收集方法和基因分析方法无关。这些基因可能代表了乳腺中针对大肠杆菌的局部APR的重要介体。

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