Key Laboratory of Plant Immunity, Department of Plant Pathology, Nanjing Agricultural University, Nanjing, P. R. China.
Financial Department, Nanjing Agricultural University, Nanjing, P. R. China.
PLoS Pathog. 2021 Jul 28;17(7):e1009757. doi: 10.1371/journal.ppat.1009757. eCollection 2021 Jul.
Antiviral RNA silencing/interference (RNAi) of negative-strand (-) RNA plant viruses (NSVs) has been studied less than for single-stranded, positive-sense (+)RNA plant viruses. From the latter, genomic and subgenomic mRNA molecules are targeted by RNAi. However, genomic RNA strands from plant NSVs are generally wrapped tightly within viral nucleocapsid (N) protein to form ribonucleoproteins (RNPs), the core unit for viral replication, transcription and movement. In this study, the targeting of the NSV tospoviral genomic RNA and mRNA molecules by antiviral RNA-induced silencing complexes (RISC) was investigated, in vitro and in planta. RISC fractions isolated from tospovirus-infected N. benthamiana plants specifically cleaved naked, purified tospoviral genomic RNAs in vitro, but not genomic RNAs complexed with viral N protein. In planta RISC complexes, activated by a tobacco rattle virus (TRV) carrying tospovirus NSs or Gn gene fragments, mainly targeted the corresponding viral mRNAs and hardly genomic (viral and viral-complementary strands) RNA assembled into RNPs. In contrast, for the (+)ssRNA cucumber mosaic virus (CMV), RISC complexes, activated by TRV carrying CMV 2a or 2b gene fragments, targeted CMV genomic RNA. Altogether, the results indicated that antiviral RNAi primarily targets tospoviral mRNAs whilst their genomic RNA is well protected in RNPs against RISC-mediated cleavage. Considering the important role of RNPs in the replication cycle of all NSVs, the findings made in this study are likely applicable to all viruses belonging to this group.
抗病毒 RNA 沉默/干扰(RNAi)的负链(-)RNA 植物病毒(NSVs)比单链、正链(+)RNA 植物病毒研究得少。在后一种情况下,基因组和亚基因组 mRNA 分子是 RNAi 的靶标。然而,植物 NSV 的基因组 RNA 链通常紧密包裹在病毒核衣壳(N)蛋白内,形成核糖核蛋白(RNP),这是病毒复制、转录和运动的核心单元。在这项研究中,抗病毒 RNA 诱导的沉默复合物(RISC)在体外和体内靶向 NSV tovirus 基因组 RNA 和 mRNA 分子的情况进行了研究。从感染 tospovirus 的 N. benthamiana 植物中分离的 RISC 分数特异性地在体外切割裸露的、纯化的 tospovirus 基因组 RNA,但不切割与病毒 N 蛋白复合的基因组 RNA。在体内,由携带 tospovirus NSs 或 Gn 基因片段的烟草脆裂病毒(TRV)激活的 RISC 复合物主要靶向相应的病毒 mRNA,几乎不靶向组装成 RNP 的基因组(病毒和病毒互补链)RNA。相比之下,对于(+)ssRNA 黄瓜花叶病毒(CMV),由携带 CMV 2a 或 2b 基因片段的 TRV 激活的 RISC 复合物靶向 CMV 基因组 RNA。总的来说,结果表明抗病毒 RNAi 主要靶向 tospovirus mRNA,而其基因组 RNA 在 RNP 中很好地免受 RISC 介导的切割。考虑到 RNP 在所有 NSV 复制周期中的重要作用,本研究中的发现可能适用于属于该组的所有病毒。