John Innes Centre, Department of Biochemistry and Metabolism, Norwich Research Park, Norwich NR4 7UH, UK.
Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.
Viruses. 2021 May 11;13(5):885. doi: 10.3390/v13050885.
The production of plant helical virus-like particles (VLPs) via plant-based expression has been problematic with previous studies suggesting that an RNA scaffold may be necessary for their efficient production. To examine this, we compared the accumulation of VLPs from two potexviruses, papaya mosaic virus and alternanthera mosaic virus (AltMV), when the coat proteins were expressed from a replicating potato virus X- based vector (pEff) and a non-replicating vector (pEAQ-). Significantly greater quantities of VLPs could be purified when pEff was used. The pEff system was also very efficient at producing VLPs of helical viruses from different virus families. Examination of the RNA content of AltMV and tobacco mosaic virus VLPs produced from pEff revealed the presence of vector-derived RNA sequences, suggesting that the replicating RNA acts as a scaffold for VLP assembly. Cryo-EM analysis of the AltMV VLPs showed they had a structure very similar to that of authentic potexvirus particles. Thus, we conclude that vectors generating replicating forms of RNA, such as pEff, are very efficient for producing helical VLPs.
通过植物表达生产植物螺旋病毒样颗粒(VLPs)一直存在问题,先前的研究表明,其高效生产可能需要 RNA 支架。为了研究这个问题,我们比较了两种 Potexvirus(木瓜花叶病毒和Alternanthera 花叶病毒(AltMV))的 VLPs 积累情况,当外壳蛋白由复制型马铃薯 X 病毒(pEff)和非复制型载体(pEAQ-)表达时。当使用 pEff 时,可以更有效地纯化 VLPs。pEff 系统也非常有效地生产来自不同病毒科的螺旋病毒的 VLPs。对 pEff 产生的 AltMV 和烟草花叶病毒 VLPs 的 RNA 含量进行检测,发现了载体衍生的 RNA 序列的存在,表明复制 RNA 充当了 VLP 组装的支架。对 AltMV VLPs 的冷冻电镜分析表明,它们的结构与真实的 Potexvirus 颗粒非常相似。因此,我们得出结论,产生复制 RNA 的载体,如 pEff,非常有效地产生螺旋 VLPs。