Laboratory of Virology, Institute of Virology and Biotechnology, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.
College of Chemistry and Life Science, Zhejiang Normal University, Jinhua, China.
Mol Plant Pathol. 2023 Jan;24(1):59-70. doi: 10.1111/mpp.13277. Epub 2022 Oct 28.
Southern rice black-streaked dwarf virus (SRBSDV; Fijivirus, Reoviridae) has become a threat to cereal production in East Asia in recent years. Our previous cytopathologic studies have suggested that SRBSDV induces a process resembling programmed cell death in infected tissues that results in distinctive growth abnormalities. The viral product responsible for the cell death, however, remains unknown. Here P9-2 protein, but not its RNA, was shown to induce cell death in Escherichia coli and plant cells when expressed either locally with a transient expression vector or systemically using a heterologous virus. Both computer prediction and fluorescent assays indicated that the viral nonstructural protein was targeted to the plasma membrane (PM) and further modification of its subcellular localization abolished its ability to induce cell death, indicating that its PM localization was required for the cell death induction. P9-2 was predicted to harbour two transmembrane helices within its central hydrophobic domain. A series of mutation assays further showed that its central transmembrane hydrophobic domain was crucial for cell death induction and that its conserved F90, Y101, and L103 amino acid residues could play synergistic roles in maintaining its ability to induce cell death. Its homologues in other fijiviruses also induced cell death in plant and bacterial cells, implying that the fijiviral nonstructural protein may trigger cell death by targeting conserved cellular factors or via a highly conserved mechanism.
近年来,南方水稻黑条矮缩病毒(SRBSDV;斐济病毒,呼肠孤病毒科)已成为东亚谷类生产的威胁。我们之前的细胞病理学研究表明,SRBSDV 在感染组织中诱导类似于程序性细胞死亡的过程,导致明显的生长异常。然而,负责细胞死亡的病毒产物仍不清楚。本研究中,当 P9-2 蛋白通过瞬时表达载体在局部或使用异源病毒在系统中表达时,无论是其 RNA 还是蛋白均能诱导大肠杆菌和植物细胞死亡。计算机预测和荧光分析均表明,该病毒非结构蛋白定位于质膜(PM),进一步改变其亚细胞定位会使其丧失诱导细胞死亡的能力,表明其 PM 定位对于诱导细胞死亡是必需的。P9-2 被预测在其中心疏水区内具有两个跨膜螺旋。一系列突变分析进一步表明,其中心跨膜疏水区对于诱导细胞死亡至关重要,其保守的 F90、Y101 和 L103 氨基酸残基可能在维持其诱导细胞死亡的能力方面发挥协同作用。其他斐济病毒的同源物也能在植物和细菌细胞中诱导细胞死亡,这表明斐济病毒的非结构蛋白可能通过靶向保守的细胞因子或通过高度保守的机制触发细胞死亡。