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MicroRNA profiling of the intestinal tissue of Kazakh sheep after experimental Echinococcus granulosus infection, using a high-throughput approach

机译:使用高通量方法对实验性 Echinococcus granulosus 感染后的哈萨克绵羊肠道组织进行MicroRNA分析

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Cystic echinococcosis (CE), caused by infection with the larval stage of the cestode Echinococcus granulosus , is a chronic zoonosis, to which sheep are highly susceptible. Previously, we found that Kazakh sheep with different MHC haplotypes differed in CE infection. Sheep with haplotype MHC Mva Ibc- Sac IIab- Hin 1Iab were resistant to CE infection, while their counterparts without this haplotype were not. MicroRNAs (miRNAs), a class of small non-coding RNAs, are key regulators of gene expression at the post-transcriptional level and play essential roles in fundamental biological processes such as development and metabolism. To identify microRNA controlling resistance to CE in the early stage of infection, microRNA profiling was conducted in the intestinal tissue of sheep with resistant and non-resistant MHC haplotypes after peroral infection with E. granulosus eggs. A total of 351 known and 186 novel miRNAs were detected in the resistant group, against 353 known and 129 novel miRNAs in the non-resistant group. Among these miRNAs, 83 known miRNAs were significantly differentially expressed, including 75 up-regulated and 8 down-regulated miRNAs. Among these known microRNAs, miR-21-3p, miR-542-5p, miR-671, miR-134-5p, miR-26b, and miR-27a showed a significantly higher expression in CE-resistant sheep compared to the CE-non-resistant library, with the FC?>?3. Functional analysis showed that they were NF-kB pathway-responsive miRNAs, which are involved in the inflammation process. The results suggest that these microRNAs may play important roles in the response of intestinal tissue to E. granulosus .
机译:囊性棘球co虫病(CE)是由est虫细小棘球E幼虫期感染引起的,是一种慢性人畜共患病,绵羊非常容易受到感染。以前,我们发现具有不同MHC单倍型的哈萨克羊在CE感染方面有所不同。单体型为MHC Mva Ibc- Sac IIab- Hin 1Iab的绵羊对CE感染具有抗性,而没有这种单体型的绵羊则没有。微小RNA(miRNA)是一类小的非编码RNA,是转录后水平上基因表达的关键调节剂,并且在基本的生物学过程(例如发育和代谢)中发挥重要作用。为了确定在感染早期控制CE对microRNA的抵抗力,对经E. granulosus卵经口感染的MHC单倍型和非耐药MHC单倍型绵羊的肠道组织进行了microRNA分析。在抗药性组中共检测到351个已知miRNA和186个新miRNA,而在非抗药性组中检测到353个已知miRNA和129个新miRNA。在这些miRNA中,有83种已知的miRNA显着差异表达,包括75种上调的miRNA和8种下调的miRNA。在这些已知的microRNA中,miR-21-3p,miR-542-5p,miR-671,miR-134-5p,miR-26b和miR-27a与CE-非抗性库,带有FC?>?3。功能分析表明它们是NF-kB通路反应性miRNA,参与炎症过程。结果表明,这些microRNA可能在肠组织对颗粒大肠杆菌的反应中起重要作用。

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