Zheng Li, Lu Xia, Liang Xiaofei, Jiang Shuchang, Zhao Jing, Zhan Gangming, Liu Peng, Wu Jianhui, Kang Zhensheng
State Key Laboratory of Crop Stress Biology for Arid Areas and College of Plant Protection, Northwest A&F University, Yangling, China.
Front Microbiol. 2017 Oct 10;8:1960. doi: 10.3389/fmicb.2017.01960. eCollection 2017.
Characterization of newly isolated mycoviruses may contribute to understanding of the evolution and diversity of viruses. Here, a deep sequencing approach was used to analyze the double-stranded RNA (dsRNA) mycoviruses isolated from field-collected samples in China. Database searches showed the presence of at least four totivirus-like sequences, termed virus 1 to 4 (PsV1 to 4). All of these identified sequences contained two overlapping open reading frames (ORFs) which encode a putative coat protein (CP) and an RNA-dependent RNA polymerase (RdRp) showing similar structures to members of the genus . Each PsV contained a -1 ribosomal frameshifting region with a slippery site and a pseudoknot structure in the overlapped regions of these ORFs, indicating that the RdRp is translated as a CP-RdRp fusion. Phylogenetic analyses based on RdRp and CP suggested that these novel viruses belong to the genus in the family . The presences of these PsVs were further validated by transmission electron microscope (TEM) and RT-PCR. Taken together, our results demonstrate the presence of diverse, novel totiviruses in the field populations.
新分离的真菌病毒的特性分析可能有助于理解病毒的进化和多样性。在此,采用深度测序方法分析从中国野外采集的样本中分离出的双链RNA(dsRNA)真菌病毒。数据库搜索显示存在至少四个类全病毒序列,命名为病毒1至4(PsV1至4)。所有这些已鉴定的序列都包含两个重叠的开放阅读框(ORF),它们编码一个假定的衣壳蛋白(CP)和一个依赖RNA的RNA聚合酶(RdRp),其结构与该属的成员相似。每个PsV在这些ORF的重叠区域都含有一个具有滑码位点和假结结构的-1核糖体移码区域,这表明RdRp是以CP-RdRp融合蛋白的形式翻译的。基于RdRp和CP的系统发育分析表明,这些新型病毒属于该科的该属。通过透射电子显微镜(TEM)和逆转录-聚合酶链反应(RT-PCR)进一步验证了这些PsV的存在。综上所述,我们的结果证明了在野外种群中存在多种新型全病毒。