首页> 美国卫生研究院文献>The Journal of Veterinary Medical Science >Leader gene of Corynebacterium pseudotuberculosis may beuseful in vaccines against caseous lymphadenitis of goats: a bioinformaticsapproach
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Leader gene of Corynebacterium pseudotuberculosis may beuseful in vaccines against caseous lymphadenitis of goats: a bioinformaticsapproach

机译:假性棒状杆菌的前导基因可能是在针对山羊干酪性淋巴结炎的疫苗中有用:一种生物信息学方法

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摘要

We conducted an in silico analysis to search for important genes in the pathogenesis of Caseous Lymphadenitis (CL), with prospects for use in formulating effective vaccines against this disease. For this, we performed a survey of proteins expressed by Corynebacterium pseudotuberculosis, using protein sequences collected from the NCBI GenPept database and the keywords “caseous lymphadenitis” and “Corynebacterium pseudotuberculosis” and “goats”. A network was developed using the STRING 10 database, with a confidence score of 0.900. For every gene interaction identified, we summed the interaction score of each gene, generating a combined association score to obtain a single score named weighted number of links (WNL). Genes with the highest WNL were named “leader genes”. Ontological analysis was extracted from the STRING database through Kyoto Encyclopedia of Genes and Genomes (KEGG) database. A search in the GenPept database revealed 2,124 proteins. By using and plotting with STRING 10, we then developed an in silico network model comprised of 1,243 genes/proteins interconnecting through 3,330 interactions. The highest WNL values were identified in the rplB gene, which was named the leader gene. Our ontological analysis shows that this protein acts effectively mainly on Metabolic pathways and Biosynthesis of secondary metabolites. In conclusion, the in silico analyses showed thatrplB has good potential for vaccine development. However, functionalassays are needed to make sure that this protein can potentially induce both humoral andcellular immune responses against C. pseudotuberculosis in goats.
机译:我们进行了计算机分析,以寻找干酪性淋巴结炎(CL)发病机理中的重要基因,并有望用于配制针对这种疾病的有效疫苗。为此,我们使用从NCBI GenPept数据库收集的蛋白质序列以及关键词“干酪样淋巴结炎”和“假结核杆菌”和“山羊”对假结核杆菌表达的蛋白质进行了调查。使用STRING 10数据库开发了一个网络,置信度为0.900。对于确定的每个基因相互作用,我们将每个基因的相互作用得分相加,生成组合的关联得分,以获得一个名为加权链接数(WNL)的单个得分。 WNL最高的基因被称为“前导基因”。通过《京都基因与基因组百科全书》(KEGG)数据库从STRING数据库中提取了本体分析。 GenPept数据库中的搜索显示2,124种蛋白质。通过使用STRING 10并进行绘图,我们然后开发了一个计算机网络模型,该模型包含1,243个基因/蛋白质,通过3,330个相互作用相互连接。在rplB基因(称为前导基因)中鉴定出最高的WNL值。我们的本体分析表明,该蛋白主要在代谢途径和次生代谢产物的生物合成中有效发挥作用。总之,计算机分析表明rplB具有开发疫苗的良好潜力。但是,功能需要进行测定,以确保该蛋白质可以潜在地诱导体液和体液。抗山羊假结核梭菌的细胞免疫反应。

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