We have used high-throughput Illumina sequencing to identify novel recombinants between
deformed wing virus (DWV) and Varroa destructor virus-1 (VDV-1), which accumulate to
higher levels than DWV in both honeybees and Varroa destructor mites. The recombinants,
VDV-1VVD and VDV-1DVD, exhibit crossovers between the 5’-untranslated region (5’-UTR),
and/or the regions encoding the structural (capsid) and non-structural viral proteins. This
implies the genomes are modular and that each region may evolve independently, as
demonstrated in human enteroviruses. Individual honeybee pupae were infected with a
mixture of observed recombinants and DWV. The strong correlation between VDV-1DVD
levels in honeybee pupae and the associated mites was observed, suggesting that this
recombinant, with a DWV-derived 5’-UTR and non-structural protein region flanking VDV-
1-derived capsid encoding region, is better adapted to transmission between V. destructor and
honeybees than the parental DWV or a recombinant bearing the VDV-1-derived 5’-UTR
(VDV-1VVD)