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Full genome virus detection in fecal samples using sensitive nucleic acid preparation, deep sequencing, and a novel iterative sequence classification algorithm

机译:使用敏感的核酸制备,深度测序和新颖的迭代序列分类算法对粪便样品进行全基因组病毒检测

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摘要

We have developed a full genome virus detection process that combines sensitive nucleic acid preparation optimised for virus identification in fecal material with Illumina MiSeq sequencing and a novel post-sequencing virus identification algorithm. Enriched viral nucleic acid was converted to double-stranded DNA and subjected to Illumina MiSeq sequencing. The resulting short reads were processed with a novel iterative Python algorithm SLIM for the identification of sequences with homology to known viruses. De novo assembly was then used to generate full viral genomes. The sensitivity of this process was demonstrated with a set of fecal samples from HIV-1 infected patients. A quantitative assessment of the mammalian, plant, and bacterial virus content of this compartment was generated and the deep sequencing data were sufficient to assembly 12 complete viral genomes from 6 virus families. The method detected high levels of enteropathic viruses that are normally controlled in healthy adults, but may be involved in the pathogenesis of HIV-1 infection and will provide a powerful tool for virus detection and for analyzing changes in the fecal virome associated with HIV-1 progression and pathogenesis
机译:我们已经开发了一种全基因组病毒检测方法,该方法将针对粪便中的病毒识别进行了优化的敏感核酸制备与Illumina MiSeq测序和新型的测序后病毒识别算法结合在一起。将富集的病毒核酸转化为双链DNA,并进行Illumina MiSeq测序。用新颖的迭代Python算法SLIM处理所得的短读,以鉴定与已知病毒同源的序列。然后使用从头组装产生完整的病毒基因组。一组来自HIV-1感染患者的粪便样本证明了这一过程的敏感性。对该隔室的哺乳动物,植物和细菌病毒含量进行了定量评估,并且深度测序数据足以组装来自6个病毒家族的12个完整病毒基因组。该方法检测到正常情况下在健康成年人中可控制的高水平肠病病毒,但可能与HIV-1感染的发病机制有关,将为病毒检测和分析与HIV-1相关的粪便病毒的变化提供强大的工具进展和发病机理

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