MRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, UK.
Institute of Technology, University of Tartu, Nooruse 1, Tartu 50411, Estonia.
Viruses. 2018 Feb 18;10(2):88. doi: 10.3390/v10020088.
Mosquitoes transmit several human- and animal-pathogenic alphaviruses ( family). In alphavirus-infected mosquito cells two different types of virus-specific small RNAs are produced as part of the RNA interference response: short-interfering (si)RNAs and PIWI-interacting (pi)RNAs. The siRNA pathway is generally thought to be the main antiviral pathway. Although an antiviral activity has been suggested for the piRNA pathway its role in host defences is not clear. Knock down of key proteins of the piRNA pathway (Ago3 and Piwi5) in -derived cells reduced the production of alphavirus chikungunya virus (CHIKV)-specific piRNAs but had no effect on virus replication. In contrast, knock down of the siRNA pathway key protein Ago2 resulted in an increase in virus replication. Similar results were obtained when expression of Piwi4 was silenced. Knock down of the helicase Spindle-E (SpnE), an essential co-factor of the piRNA pathway in , resulted in increased virus replication indicating that SpnE acts as an antiviral against alphaviruses such as CHIKV and the related Semliki Forest virus (SFV). Surprisingly, this effect was found to be independent of the siRNA and piRNA pathways in cells and specific for alphaviruses. This suggests a small RNA-independent antiviral function for this protein in mosquitoes.
蚊子传播几种人类和动物致病性的甲病毒(family)。在感染甲病毒的蚊子细胞中,作为 RNA 干扰反应的一部分,会产生两种不同类型的病毒特异性小 RNA:短干扰 (si)RNA 和 PIWI 相互作用 (pi)RNA。通常认为 siRNA 途径是主要的抗病毒途径。尽管已经提出了 piRNA 途径具有抗病毒活性,但它在宿主防御中的作用尚不清楚。在 -derived 细胞中敲低 piRNA 途径的关键蛋白 (Ago3 和 Piwi5) 会减少甲病毒基孔肯雅病毒 (CHIKV) 特异性 piRNA 的产生,但对病毒复制没有影响。相比之下,siRNA 途径关键蛋白 Ago2 的敲低会导致病毒复制增加。当沉默 Piwi4 的表达时,也会得到类似的结果。敲低螺旋酶 Spindle-E (SpnE),piRNA 途径在 中的必需辅助因子,会导致病毒复制增加,表明 SpnE 作为抗病毒因子,可抵抗甲病毒,如 CHIKV 和相关的 Semliki Forest 病毒 (SFV)。令人惊讶的是,这种效应在 细胞中独立于 siRNA 和 piRNA 途径,并且对甲病毒具有特异性。这表明该蛋白在蚊子中具有小 RNA 非依赖性的抗病毒功能。