To protect global strawberry production, clean plant programs rely on rigorous certification and quarantine testing to prevent the spread of disease. For decades, biological graft indexing has been the "gold standard" for virus detection; however, it often fails to identify viruses that remain latent in single infections or viruses requiring extended periods to induce symptoms. High throughput sequencing (HTS) offers an alternative that identifies all known and emerging viruses independent of the nucleotide sequences of their genomes including those undetected by traditional bioassays. This study compared HTS with graft indexing using 73 virus-infected donor plants, 584 indicator clones, and two replicates to evaluate HTS as a replacement for conventional graft bioassay testing. Donor material was analyzed via HTS and simultaneously grafted onto two replicates of four Fragaria indicator clones (UC-4, UC-5, UC-10, UC-11). Indicator symptoms were monitored weekly over eight weeks and again following natural dormancy. The RT-qPCR/RT-PCR testing for virus transmission was also conducted at eight weeks and after dormancy. HTS identified viral infections in all donor plants, detecting 17 different viruses across eight families, and revealing mixed infections in 75% of plants. In contrast, 83% of indicators developed symptoms within the current standard of eight weeks post graft. Only 61% of the indicator plants displayed symptoms both before and after dormancy, while 7% remained asymptomatic throughout despite receiving grafts from HTS-positive donors. Given the limitations of biological indexing, this research strongly supports the integration of HTS as a frontline detection tool to enhance the reliability and efficiency of certification programs.
Daniel Fager, M. Al Rwahnih, D. Mollov· Plant Disease· 0 citations
Ramu stunt virus (RmSV), a member of the genus Mechlorovirus within the family Phenuiviridae, was previously described as a six-segmented RNA virus infecting sugarcane. In this study, we re-examined type material and additional isolates using high-throughput sequencing and RT-PCR validation, revealing that RmSV possesses a nine-segmented genome, making it the largest reported in the Phenuiviridae. This expanded architecture includes duplicated RNA segments (RNA 2a and RNA 2b) encoding nucleocapsid-like proteins and two novel segments (RNA 7 and RNA 8). Comparative analysis showed that RNA 2a and 2b share about 84% amino acid identity, while RNA 5 encodes a third nucleocapsid homolog, indicating unprecedented domain redundancy. Structural modeling confirmed that all three nucleocapsid proteins maintain a conserved fold despite low sequence identity, with electrostatic mapping suggesting differential RNA-binding potential. Additionally, RNA 6 encodes a hypothetical protein structurally similar to the rice stripe virus disease-specific S-protein, implicating a role in symptom development. Transcript abundance analysis revealed RNA 6 as the most highly expressed segment across isolates. These findings revise the genomic composition of RmSV, highlight mechanisms of genome plasticity and adaptive evolution in plant-infecting bunyaviruses, and underscore practical implications for diagnostic assay design, resistance breeding, and biosecurity surveillance.
Peter Abrahamian, Samuel C. Grinstead, D. Mollov· Virology· 0 citations