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microRNA profiling in the zoonotic parasite Echinococcus canadensis using a high-throughput approach

机译:使用高通量方法在人畜共患病的加拿大棘球E虫中进行microRNA分析

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Background microRNAs (miRNAs), a class of small non-coding RNAs, are key regulators of gene expression at post-transcriptional level and play essential roles in fundamental biological processes such as development and metabolism. The particular developmental and metabolic characteristics of cestode parasites highlight the importance of studying miRNA gene regulation in these organisms. Here, we perform a comprehensive analysis of miRNAs in the parasitic cestode Echinococcus canadensis G7, one of the causative agents of the neglected zoonotic disease cystic echinococcosis. Methods Small RNA libraries from protoscoleces and cyst walls of E. canadensis G7 and protoscoleces of E. granulosus sensu stricto G1 were sequenced using Illumina technology. For miRNA prediction, miRDeep2 core algorithm was used. The output list of candidate precursors was manually curated to generate a high confidence set of miRNAs. Differential expression analysis of miRNAs between stages or species was estimated with DESeq. Expression levels of selected miRNAs were validated using poly-A RT-qPCR. Results In this study we used a high-throughput approach and found transcriptional evidence of 37 miRNAs thus expanding the miRNA repertoire of E. canadensis G7. Differential expression analysis showed highly regulated miRNAs between life cycle stages, suggesting a role in maintaining the features of each developmental stage or in the regulation of developmental timing. In this work we characterize conserved and novel Echinococcus miRNAs which represent 30 unique miRNA families. Here we confirmed the remarkable loss of conserved miRNA families in E. canadensis, reflecting their low morphological complexity and high adaptation to parasitism. Conclusions We performed the first in-depth study profiling of small RNAs in the zoonotic parasite E. canadensis G7. We found that miRNAs are the preponderant small RNA silencing molecules, suggesting that these small RNAs could be an essential mechanism of gene regulation in this species. We also identified both parasite specific and divergent miRNAs which are potential biomarkers of infection. This study will provide valuable information for better understanding of the complex biology of this parasite and could help to find new potential targets for therapy and/or diagnosis.
机译:背景microRNA(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。 est虫寄生虫的特殊发育和代谢特征突出了研究这些生物中miRNA基因调控的重要性。在这里,我们对寄生的尾est加拿大棘球EG7(被忽视的人畜共患病囊性棘球co病的病原体之一)中的miRNA进行了全面分析。方法采用Illumina技术对加拿大E. canadensis G7原球藻和囊壁以及E. granulosus sensu stricto G1原球藻的小RNA文库进行测序。对于miRNA预测,使用了miRDeep2核心算法。手动选择了候选前体的输出列表,以生成高可信度的miRNA集。使用DESeq评估阶段或物种之间miRNA的差异表达分析。使用poly-A RT-qPCR验证所选miRNA的表达水平。结果在这项研究中,我们使用了高通量方法,发现了37种miRNA的转录证据,从而扩展了加拿大大肠杆菌G7的miRNA库。差异表达分析显示,生命周期各阶段之间的miRNA受高度调节,表明在维持每个发育阶段的特征或调节发育时机中的作用。在这项工作中,我们表征了代表30个独特miRNA家族的保守且新颖的棘球mi miRNA。在这里,我们证实了加拿大大肠埃希菌中保守的miRNA家族的显着丧失,反映了它们低形态复杂性和对寄生虫的高度适应性。结论我们对人畜共患病的加拿大大肠杆菌E.canadensis G7中的小RNA进行了首次深入研究。我们发现,miRNA是主要的小RNA沉默分子,这表明这些小RNA可能是该物种中基因调控的重要机制。我们还确定了寄生虫特异性和发散性miRNAs,它们是感染的潜在生物标记。这项研究将提供有价值的信息,以更好地了解该寄生虫的复杂生物学,并有助于寻找治疗和/或诊断的新潜在靶标。

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