Location: National Germplasm Resources Laboratory
Title: Complete genome sequence of rose virus A, the first carlavirus identified in roseAuthor
DIAZ-LARA, ALFREDO - University Of California, Davis | |
Mollov, Dimitre | |
GOLINO, DEBORAH - University Of California, Davis | |
AL RWAHNIH, MAHER - University Of California, Davis |
Submitted to: Archives of Virology
Publication Type: Peer Reviewed Journal Publication Acceptance Date: 10/30/2019 Publication Date: 11/11/2019 Citation: Diaz-Lara, A., Mollov, D.S., Golino, D., Al Rwahnih, M. 2019. Complete genome sequence of rose virus A, the first carlavirus identified in rose. Archives of Virology. https://doi.org/10.1007/s00705-019-04460-1. DOI: https://doi.org/10.1007/s00705-019-04460-1 Interpretive Summary: Roses (Rosa spp.), one of the most popular ornamentals worldwide, are used as both cut flowers and landscape plants. Many viral diseases affect rose production. It is important to detect and eliminate virus infected roses prior to material being propagated and distributed. We report a new virus identified in rose and provisionally named Rose virus A (RVA). The RVA genomic organization and sequence was determined. This study provides information for the proper classification of RVA. The genome sequence facilitates developing reliable detection methods that can be used to screen rose genetic material and develop better viral control measures for trade and production industries. Technical Abstract: A novel virus was discovered in a Rosa wichuraiana Crep. by high throughput sequencing, and tentatively named rose virus A (RVA). Based on sequence identity and phylogenetic analysis, RVA represents a new member of the genus Carlavirus (family Betaflexiviridae). The genome of RVA is 8,849 nucleotides long excluding a poly(A) tail and comprises six open reading frames (ORFs). Predicted ORFs include replicase, coat protein, nucleic acid binding protein and triple gene block (TGB) arranged as it would be in a typical carlavirus. RVA is the first carlavirus identified in rose and has the highest nucleotide identity to poplar mosaic virus. Reverse transcription PCR-based assays were developed to confirm RVA in the original source and to screen additional rose plants. |