Institute of Plant Protection, Jiangsu Academy of Agricultural Sciences, Jiangsu Technical Service Center of Diagnosis and Detection for Plant Virus Diseases, Nanjing, China.
College of Life Sciences, Nanjing Normal University, Nanjing, China.
J Basic Microbiol. 2018 Mar;58(3):227-237. doi: 10.1002/jobm.201700325. Epub 2017 Dec 7.
RNA interference (RNAi) is a conserved mechanism against viruses in plants and animals. It is thought to inactivate the viral genome by producing virus-derived small interfering RNAs (vsiRNAs). Rice black-streaked dwarf virus (RBSDV) is transmitted to plants by the small brown planthopper (Laodelphax striatellus), and seriously threatens production of rice in East Asia, particularly Oryza sativa japonica subspecies. Through deep sequencing, genome-wide comparisons of RBSDV-derived vsiRNAs were made between the japonica variety Nipponbare, and the indica variety 9311. Four small RNA libraries were constructed from the leaves and shoots of each variety. We found 659,756 unique vsiRNAs in the four samples, and only 43,485 reads were commonly shared. The size distributions of vsiRNAs were mostly 21- and 22-nt long, and A/U bias (66-68%) existed at the first nucleotide of vsiRNAs. Additionally, vsiRNAs were continuously but heterogeneously distributed along S1-S10 segments of the RBSDV genome. Distribution profiles of vsiRNA hotspots were similar in different hosts and tissues, and the 5'- and 3'-terminal regions of S4, S5, and S8 had more hotspots. Distribution and abundance of RBSDV vsiRNAs could be useful in designing efficient targets for exploiting RNA interference for virus resistance. Degradome analysis found 25 and 11 host genes appeared to be targeted by vsiRNAs in 9311 and Nipponbare. We report for the first time vsiRNAs derived from RBSDV-infected rice.
RNA 干扰(RNAi)是动植物中一种针对病毒的保守机制。它被认为通过产生病毒衍生的小干扰 RNA(vsiRNA)来使病毒基因组失活。水稻黑条矮缩病毒(RBSDV)通过小灰飞虱(Laodelphax striatellus)传播给植物,并严重威胁东亚,特别是粳稻亚种的水稻生产。通过深度测序,对粳稻品种 Nipponbare 和籼稻品种 9311 中 RBSDV 衍生的 vsiRNA 进行了全基因组比较。从每个品种的叶片和茎部构建了四个小 RNA 文库。我们在四个样本中发现了 659756 个独特的 vsiRNA,只有 43485 个读取序列是共同共享的。vsiRNA 的大小分布主要为 21- 和 22-nt 长,并且在 vsiRNA 的第一个核苷酸存在 A/U 偏向(66-68%)。此外,vsiRNA 沿着 RBSDV 基因组的 S1-S10 片段连续但不均匀地分布。不同宿主和组织中 vsiRNA 热点的分布模式相似,S4、S5 和 S8 的 5'和 3'末端区域具有更多的热点。RBSDV vsiRNA 的分布和丰度可用于设计有效的 RNA 干扰靶点以抵抗病毒。降解组分析发现,在 9311 和 Nipponbare 中有 25 和 11 个宿主基因似乎被 vsiRNA 靶向。我们首次报道了源自 RBSDV 感染水稻的 vsiRNA。