Grybchuk Danyil, Kostygov Alexei Yu, Yurchenko Vyacheslav
Life Science Research Centre, Faculty of Science, University of Ostrava, Ostrava, Czechia.
Central European Institute of Technology, Masaryk University, Brno, Czechia.
Methods Mol Biol. 2025;2893:151-167. doi: 10.1007/978-1-0716-4338-9_12.
Over the last decade, considerable progress has been made in unraveling RNA virus diversity. This has contributed to our understanding of the evolution of these viruses, which include emerging zoonotic human pathogens. Current success has been greatly facilitated by the development of next-generation sequencing platforms instrumental for meta-transcriptomic studies. However, due to the rapid evolution of RNA viruses, there are numerous "blind spots" waiting to be explored; one of those is the RNA virome of unicellular eukaryotes. Here, we present the pipeline, which has been successfully used to characterize various types of RNA viruses, including Leishbuviridae (Bunyaviricetes, Hareavirales) in the parasitic flagellates of the family Trypanosomatidae. The pipeline relies on axenic in vitro cell culture and double-stranded RNA enrichment, followed by direct RNA-sequencing. A detailed procedure description starting from the initial total RNA preparation to the final assembly of the viral segments is provided.
在过去十年中,我们在解析RNA病毒多样性方面取得了显著进展。这有助于我们理解这些病毒的进化,其中包括新出现的人畜共患人类病原体。下一代测序平台的发展极大地推动了元转录组学研究,从而促成了目前的成功。然而,由于RNA病毒的快速进化,仍有许多“盲点”有待探索;其中之一就是单细胞真核生物的RNA病毒组。在此,我们展示了一套流程,该流程已成功用于鉴定各种类型的RNA病毒,包括锥虫科寄生鞭毛虫中的利什布病毒科(布尼亚病毒目,沙粒病毒科)。该流程依赖于无菌体外细胞培养和双链RNA富集,然后进行直接RNA测序。本文提供了从最初的总RNA制备到病毒片段最终组装的详细步骤描述。