A Replicating Viral Vector Greatly Enhances Accumulation of Helical Virus-Like Particles in Plants
Eva C. Thuenemann,
Matthew J. Byrne,
Hadrien Peyret,
Keith Saunders,
Roger Castells-Graells,
Inmaculada Ferriol,
Mattia Santoni,
John F. C. Steele,
Neil A. Ranson,
Linda Avesani,
Juan Jose Lopez-Moya,
George P. Lomonossoff
Affiliations
Eva C. Thuenemann
John Innes Centre, Department of Biochemistry and Metabolism, Norwich Research Park, Norwich NR4 7UH, UK
Matthew J. Byrne
Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK
Hadrien Peyret
John Innes Centre, Department of Biochemistry and Metabolism, Norwich Research Park, Norwich NR4 7UH, UK
Keith Saunders
John Innes Centre, Department of Biochemistry and Metabolism, Norwich Research Park, Norwich NR4 7UH, UK
Roger Castells-Graells
John Innes Centre, Department of Biochemistry and Metabolism, Norwich Research Park, Norwich NR4 7UH, UK
Inmaculada Ferriol
Centre for Research in Agricultural Genomics (CRAG, CSIC-IRTA-UAB-UB), 08193 Cerdanyola del Vallès, Spain
Mattia Santoni
Diamante srl. Strada Le Grazie, 15, 37134 Verona, Italy
John F. C. Steele
John Innes Centre, Department of Biochemistry and Metabolism, Norwich Research Park, Norwich NR4 7UH, UK
Neil A. Ranson
Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK
Linda Avesani
Department of Biotechnology, University of Verona, Strada Le Grazie, 15, 37134 Verona, Italy
Juan Jose Lopez-Moya
Centre for Research in Agricultural Genomics (CRAG, CSIC-IRTA-UAB-UB), 08193 Cerdanyola del Vallès, Spain
George P. Lomonossoff
John Innes Centre, Department of Biochemistry and Metabolism, Norwich Research Park, Norwich NR4 7UH, UK
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-HT). 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.