Institute of Technology, University of Tartu, Tartu, Estonia.
Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerpen, Belgium.
PLoS Pathog. 2020 Sep 4;16(9):e1008825. doi: 10.1371/journal.ppat.1008825. eCollection 2020 Sep.
Most alphaviruses (family Togaviridae) including Sindbis virus (SINV) and other human pathogens, are transmitted by arthropods. The first open reading frame in their positive strand RNA genome encodes for the non-structural polyprotein, a precursor to four separate subunits of the replicase. The replicase interacts with cis-acting elements located near the intergenic region and at the ends of the viral RNA genome. A trans-replication assay was developed and used to analyse the template requirements for nine alphavirus replicases. Replicases of alphaviruses of the Semliki Forest virus complex were able to cross-utilize each other's templates as well as those of outgroup alphaviruses. Templates of outgroup alphaviruses, including SINV and the mosquito-specific Eilat virus, were promiscuous; in contrast, their replicases displayed a limited capacity to use heterologous templates, especially in mosquito cells. The determinants important for efficient replication of template RNA were mapped to the 5' region of the genome. For SINV these include the extreme 5'- end of the genome and sequences corresponding to the first stem-loop structure in the 5' untranslated region. Mutations introduced in these elements drastically reduced infectivity of recombinant SINV genomes. The trans-replicase tools and approaches developed here can be instrumental in studying alphavirus recombination and evolution, but can also be applied to study other viruses such as picornaviruses, flaviviruses and coronaviruses.
大多数甲病毒(黄病毒科),包括辛德毕斯病毒(SINV)和其他人类病原体,都是由节肢动物传播的。它们的正链 RNA 基因组中的第一个开放阅读框编码非结构多蛋白,这是复制酶四个独立亚基的前体。复制酶与位于基因间区附近和病毒 RNA 基因组末端的顺式作用元件相互作用。开发了一种转复制测定法,并用于分析 9 种甲病毒复制酶的模板要求。森林病毒复合物的甲病毒复制酶能够交叉利用彼此的模板以及外群甲病毒的模板。外群甲病毒的模板,包括 SINV 和蚊子特异性的依拉病毒,是混杂的;相比之下,它们的复制酶显示出有限的利用异源模板的能力,特别是在蚊子细胞中。对模板 RNA 进行有效复制的决定因素被映射到基因组的 5'区域。对于 SINV,这些包括基因组的极端 5'-末端和 5'非翻译区中第一个茎环结构对应的序列。这些元件中的突变极大地降低了重组 SINV 基因组的感染性。这里开发的转复制酶工具和方法可用于研究甲病毒重组和进化,但也可用于研究其他病毒,如小核糖核酸病毒、黄病毒和冠状病毒。