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Analysis of chikungunya virus proteins reveals that non-structural proteins nsP2 and nsP3 exhibit RNA interference (RNAi) suppressor activity

机译:基孔肯雅病毒蛋白的分析表明,非结构蛋白nsP2和nsP3表现出RNA干扰(RNAi)抑制活性

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RNAi pathway is an antiviral defence mechanism employed by insects that result in degradation of viral RNA thereby curbing infection. Several viruses including flaviviruses encode viral suppressors of RNAi (VSRs) to counteract the antiviral RNAi pathway. Till date, no VSR has been reported in alphaviruses. The present study was undertaken to evaluate chikungunya virus (CHIKV) proteins for RNAi suppressor activity. We systematically analyzed all nine CHIKV proteins for RNAi suppressor activity using Sf21 RNAi sensor cell line based assay. Two non-structural proteins, namely, nsP2 and nsP3 were found to exhibit RNAi suppressor activity. We further validated the findings in natural hosts, namely in Aedes and in mammalian cell lines and further through EMSA and Agrobacterium infiltration in GFP silenced transgenic tobacco plants. Domains responsible for maximum RNAi suppressor activity were also identified within these proteins. RNA binding motifs in these domains were identified and their participation in RNAi suppression evaluated using site directed mutagenesis. Sequence alignment of these motifs across all species of known alphaviruses revealed conservation of these motifs emphasizing on a similar role of action in other species of alphaviruses as well. Further validation of RNAi suppressor activity of these proteins awaits establishment of specific virus infection models.
机译:RNAi途径是昆虫采用的抗病毒防御机制,可导致病毒RNA降解从而遏制感染。包括黄病毒在内的几种病毒编码RNAi的病毒抑制剂(VSR),以抵消抗病毒RNAi途径。到目前为止,尚无α病毒报告VSR。本研究旨在评估基孔肯雅病毒(CHIKV)蛋白的RNAi抑制活性。我们使用基于Sf21 RNAi传感器细胞系的分析系统分析了所有九种CHIKV蛋白的RNAi抑制活性。发现两种非结构蛋白,即nsP2和nsP3表现出RNAi抑制活性。我们进一步验证了在自然宿主中的发现,即在伊蚊和哺乳动物细胞系中的发现,以及通过EMSA和农杆菌在GFP沉默的转基因烟草植物中的渗透。在这些蛋白质中还鉴定了负责最大RNAi抑制活性的域。鉴定了这些结构域中的RNA结合基序,并使用定点诱变评估了它们在RNAi抑制中的参与。这些基序在所有已知α病毒种中的序列比对揭示了这些基序的保守性,强调了在其他α病毒种中也具有相似的作用。这些蛋白质的RNAi抑制子活性的进一步验证有待建立特定的病毒感染模型。

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