首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Enriching pathogen transcripts from infected samples: A capture-based approach to enhanced host-pathogen RNA sequencing
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Enriching pathogen transcripts from infected samples: A capture-based approach to enhanced host-pathogen RNA sequencing

机译:从感染样品中富集病原体转录本:一种基于捕获的方法来增强宿主-病原体RNA测序

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摘要

To fully understand the interactions of a pathogen with its host, it is necessary to analyze the RNA transcripts of both the host and pathogen throughout the course of an infection. Although this can be accomplished relatively easily on the host side, the analysis of pathogen transcripts is complicated by the overwhelming amount of host RNA isolated from an infected sample. Even with the read depth provided by second-generation sequencing, it is extremely difficult to get enough pathogen reads for an effective gene-level analysis. In this study, we describe a novel capture-based technique and device that considerably enriches for pathogen transcripts from infected samples. This versatile method can, in principle, enrich for any pathogen in any infected sample. To test the technique's efficacy, we performed time course tissue culture infections using Rift Valley fever virus and Francisella tularensis. At each time point, RNA sequencing (RNA-Seq) was performed and the results of the treated samples were compared with untreated controls. The capture of pathogen transcripts, in all cases, led to more than an order of magnitude enrichment of pathogen reads, greatly increasing the number of genes hit, the coverage of those genes, and the depth at which each transcript was sequenced.
机译:为了充分了解病原体与其宿主之间的相互作用,有必要在整个感染过程中分析宿主和病原体的RNA转录本。尽管这可以在宿主方面相对容易地实现,但是病原体转录本的分析由于从受感染样品中分离出的大量宿主RNA而变得复杂。即使使用第二代测序提供的读取深度,也很难获得足够的病原体读数以进行有效的基因水平分析。在这项研究中,我们描述了一种新颖的基于捕获的技术和设备,该技术和设备可大大丰富感染样本中的病原体转录本。原则上,这种通用方法可以富集任何感染样品中的任何病原体。为了测试该技术的有效性,我们使用了裂谷热病毒和弗朗西斯菌tularensis进行了时程组织培养感染。在每个时间点,进行RNA测序(RNA-Seq),并将处理后的样品的结果与未处理的对照进行比较。在所有情况下,病原体转录本的捕获导致病原体读数的富集超过一个数量级,大大增加了命中基因的数量,这些基因的覆盖范围以及每个转录本的测序深度。

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