Department of Biology and Microbiology, South Dakota State University, Brookings, SD 57006, USA.
Department of Agronomy, Horticulture, and Plant Science, South Dakota State University, Brookings, SD 57006, USA.
Viruses. 2018 Dec 14;10(12):713. doi: 10.3390/v10120713.
Mycoviruses belonging to the family cause persistent infection of many different host fungi. We previously determined that the white mold fungus, , infected with Sclerotinia sclerotiorum hypovirus 2-L (SsHV2-L) exhibits reduced virulence, delayed/reduced sclerotial formation, and enhanced production of aerial mycelia. To gain better insight into the cellular basis for these changes, we characterized changes in mRNA and small RNA (sRNA) accumulation in to infection by SsHV2-L. A total of 958 mRNAs and 835 sRNA-producing loci were altered after infection by SsHV2-L, among which >100 mRNAs were predicted to encode proteins involved in the metabolism and trafficking of carbohydrates and lipids. Both . endogenous and virus-derived sRNAs were predominantly 22 nt in length suggesting one dicer-like enzyme cleaves both. Novel classes of endogenous small RNAs were predicted, including phasiRNAs and tRNA-derived small RNAs. Moreover, . phasiRNAs, which were derived from noncoding RNAs and have the potential to regulate mRNA abundance in trans, showed differential accumulation due to virus infection. tRNA fragments did not accumulate differentially after hypovirus infection. Hence, in-depth analysis showed that infection of . by a hypovirulence-inducing hypovirus produced selective, large-scale reprogramming of mRNA and sRNA production.
属于真菌病毒科的真菌病毒会导致许多不同宿主真菌的持续性感染。我们之前已经确定,感染了核盘菌慢病毒 2-L(SsHV2-L)的白腐菌,表现出毒力降低、产菌核延迟/减少和气生菌丝增强的特性。为了更深入地了解这些变化的细胞基础,我们对 SsHV2-L 感染后 中的 mRNA 和小 RNA(sRNA)积累变化进行了特征描述。在感染 SsHV2-L 后,共有 958 个 mRNA 和 835 个 sRNA 产生基因座发生改变,其中 >100 个 mRNA 预测编码参与碳水化合物和脂质代谢和运输的蛋白质。 和病毒衍生的 sRNA 主要都是 22nt 长,表明只有一种 Dicer 样酶切割它们。预测了新的内源性小 RNA 类别,包括 phasiRNA 和 tRNA 衍生的小 RNA。此外,由于病毒感染,phasiRNA(来源于非编码 RNA 并具有在转录水平上调节 mRNA 丰度的潜力)的积累也出现了差异。tRNA 片段在感染慢病毒后并没有差异积累。因此,深入分析表明,诱导毒力降低的慢病毒感染会导致 的 mRNA 和 sRNA 产生选择性的大规模重编程。