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首页> 外文期刊>Molecular biology reports >Transcriptome profiling and digital gene expression analysis of Nile tilapia (Oreochromis niloticus) infected by Streptococcus agalactiae
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Transcriptome profiling and digital gene expression analysis of Nile tilapia (Oreochromis niloticus) infected by Streptococcus agalactiae

机译:无乳链球菌感染的尼罗罗非鱼的转录组分析和数字基因表达分析

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Tilapia is an important freshwater aquaculture species worldwide. In recent years, streptococcal diseases have severely threatened development of tilapia aquaculture, while effective prevention and control methods have not yet been established. In order to understand the immunological response of tilapia to infection by Streptococcus agalactiae (S. agalactiae), this study employed Solexa/Illumina RNA-seq and digital gene expression (DGE) technology to investigate changes in the tilapia transcriptome before and after S. agalactiae infection. We obtained 82,799 unigenes (mean size: 618 bp) using de novo assembly. Unigenes were annotated by comparing against databases including Nr, Swissprot, cluster of orthologous groups of proteins, Kyoto encyclopedia of genes and genomes, and gene ontology. Combined with DGE technology, transcriptomic changes in tilapia before and after bacteria challenging were examined. A total of 774 significantly up-regulated and 625 significantly down-regulated unigenes were identified, among which 293 were mapped to 181 signaling pathways including 17 immune-related pathways involving 65 differentially expressed genes. We observed a change in the expression of six genes in the Toll-like receptor signaling pathway, and this was subsequently confirmed via quantitative real-time PCR. This comparative study of the tilapia transcriptome before and after S. agalactiae infection identified important differentially-expressed immune-related genes and signaling pathways that will provide useful insights for further analysis of the mechanisms of tilapia defense against S. agalactiae infection.
机译:罗非鱼是全世界重要的淡水养殖品种。近年来,链球菌病严重威胁罗非鱼养殖的发展,但尚未建立有效的预防和控制方法。为了了解罗非鱼对无乳链球菌感染的免疫反应,本研究采用Solexa / Illumina RNA-seq和数字基因表达(DGE)技术来研究无乳链球菌前后罗非鱼转录组的变化。感染。我们从头获得了82,799个单基因(平均大小:618 bp)。通过与数据库(包括Nr,Swissprot,直系同源蛋白质簇,京都基因和基因组百科全书以及基因本体)进行比较,对单基因进行了注释。结合DGE技术,检查了挑战细菌前后罗非鱼的转录组变化。鉴定出总共774个显着上调的基因和625个显着下调的单基因,其中293个映射到181个信号通路,包括涉及65个差异表达基因的17个免疫相关通路。我们观察到Toll样受体信号通路中六个基因表达的变化,随后通过实时定量PCR证实了这一点。对无乳链球菌感染前后罗非鱼转录组的这项比较研究确定了重要的差异表达的免疫相关基因和信号通路,这将为进一步分析罗非鱼抗无乳链球菌感染的机制提供有用的见识。

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