Urayama Syun-Ichi, Takaki Yoshihiro, Nunoura Takuro
Research and Development Center for Marine Biosciences, Japan Agency for Marine-Earth Science and Technology (JAMSTEC).
Microbes Environ. 2016;31(1):33-40. doi: 10.1264/jsme2.ME15171. Epub 2016 Feb 13.
Knowledge of the distribution and diversity of RNA viruses is still limited in spite of their possible environmental and epidemiological impacts because RNA virus-specific metagenomic methods have not yet been developed. We herein constructed an effective metagenomic method for RNA viruses by targeting long double-stranded (ds)RNA in cellular organisms, which is a hallmark of infection, or the replication of dsRNA and single-stranded (ss)RNA viruses, except for retroviruses. This novel dsRNA targeting metagenomic method is characterized by an extremely high recovery rate of viral RNA sequences, the retrieval of terminal sequences, and uniform read coverage, which has not previously been reported in other metagenomic methods targeting RNA viruses. This method revealed a previously unidentified viral RNA diversity of more than 20 complete RNA viral genomes including dsRNA and ssRNA viruses associated with an environmental diatom colony. Our approach will be a powerful tool for cataloging RNA viruses associated with organisms of interest.
尽管RNA病毒可能对环境和流行病学产生影响,但由于尚未开发出针对RNA病毒的宏基因组学方法,我们对其分布和多样性的了解仍然有限。我们在此构建了一种有效的针对RNA病毒的宏基因组学方法,该方法通过靶向细胞生物中的长双链(ds)RNA来实现,长双链RNA是感染的标志,或是除逆转录病毒外的dsRNA和单链(ss)RNA病毒复制的标志。这种新型的靶向dsRNA的宏基因组学方法具有病毒RNA序列回收率极高、末端序列可检索以及读数覆盖均匀的特点,而此前在其他针对RNA病毒的宏基因组学方法中尚未有过相关报道。该方法揭示了一个此前未被识别的病毒RNA多样性,其中包括20多个完整的RNA病毒基因组,这些病毒包括与环境硅藻群落相关的dsRNA和ssRNA病毒。我们的方法将成为对与感兴趣的生物体相关的RNA病毒进行编目的有力工具。