State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
CAS Center for Excellence in Biotic Interactions, University of Chinese Academy of Sciences, Beijing, China.
PLoS Pathog. 2021 Mar 10;17(3):e1009424. doi: 10.1371/journal.ppat.1009424. eCollection 2021 Mar.
Maintenance of a balance between the levels of viral replication and selective pressure from the immune systems of insect vectors is one of the prerequisites for efficient transmission of insect-borne propagative phytoviruses. The mechanism regulating the adaptation of RNA viruses to insect vectors by genomic variation remains unknown. Our previous study demonstrated an extension of the 3'-untranslated terminal region (UTR) of two genomic segments of rice stripe virus (RSV). In the present study, a reverse genetic system for RSV in human cells and an insect vector, the small brown planthopper Laodelphax striatellus, was used to demonstrate that the 3'-terminal extensions suppressed viral replication in vector insects by inhibiting promoter activity due to structural interference with the panhandle structure formed by viral 3'- and 5'-UTRs. The extension sequence in the viral RNA1 segment was targeted by an endogenous insect microRNA, miR-263a, which decreased the inhibitory effect of the extension sequence on viral promoter activity. Surprisingly, the expression of miR-263a was negatively regulated by RSV infection. This elaborate coordination between terminal variation of the viral genome and endogenous insect microRNAs controls RSV replication in planthopper, thus reflecting a distinct strategy of adaptation of phytoviruses to insect vectors.
维持病毒复制水平与昆虫媒介免疫系统选择压力之间的平衡是高效传播昆虫传播增殖型植病毒的前提之一。调节 RNA 病毒通过基因组变异适应昆虫媒介的机制尚不清楚。我们之前的研究表明,水稻条纹病毒(RSV)两个基因组片段的 3'-非翻译末端区域(UTR)得到了扩展。在本研究中,利用人类细胞和昆虫媒介小褐飞虱(Laodelphax striatellus)中的 RSV 反向遗传系统,证明 3'-末端扩展通过结构干扰病毒 3'-和 5'-UTR 形成的柄状结构来抑制启动子活性,从而抑制了载体昆虫中的病毒复制。病毒 RNA1 片段中的扩展序列被内源性昆虫 microRNA,miR-263a 靶向,该 microRNA 通过降低扩展序列对病毒启动子活性的抑制作用来减少其抑制效果。令人惊讶的是,miR-263a 的表达受 RSV 感染的负调控。这种病毒基因组末端变异与内源性昆虫 microRNA 之间的精细协调控制着 RSV 在飞虱中的复制,从而反映了植病毒适应昆虫媒介的独特策略。