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High Plains wheat mosaic virus (HPWMoV) causes a serious disease in major wheat-growing regions worldwide. We report here the complete or partial genomic sequences of five HPWMoV isolates from Australian wheat samples. Phylogenetic analysis of the nucleotide sequences of the eight genomic segments of these five isolates together with others from Genbank found all eight genes formed two lineages, L1 and L2. L1 contained a single isolate from Colorado in the North American Great Plains Region (GPR), and L2 had two unresolved clusters, A and B, of isolates from Australia and the GPR. A quarter of the L2B isolate sequences of the nucleocapsid gene (RNA3) were recombinant, which is unexpected as little evidence of recombination exists in viruses with negative single-stranded RNA genomes. Phylogenies calculated from the amino acid sequences of HPWMoV's RNA-dependent RNA-polymerase (RNA1), glycoprotein (RNA2), and nucleocapsid protein (RNA3) showed they were closest to those of Palo Verde broom virus. However, its movement protein (RNA4) was closer to those of Ti ringspot-associated and common oak ringspot-associated viruses, indicating the RNA4 segments of their ancestors reassorted to produce the current emaraviruses. To avoid increased yield losses from co-infection, biosecurity measures are advised to avoid HPWMoV introduction to countries where wheat streak mosaic virus already occurs. [ABSTRACT FROM AUTHOR]

Tomato black ring virus (TBRV) and beet ringspot virus (BRSV) are closely related but distinct members of subgroup B of the genus Nepovirus. Both viruses have broad host ranges and are transmitted by seed, pollen, and ectoparasitic nematodes. Although 13 TBRV and 3 BRSV genome sequences were already available, no attempt has been made to link sequence data from these recent sequences with those of historical isolates studied in the pre‐sequencing era. High‐throughput sequencing was used to generate eight new TBRV and BRSV genome sequences from three historical >60‐year‐old and two >30‐year‐old isolates, and three more recent isolates. These eight isolates were from the Czech Republic, Germany, and the UK. We compared these with all genomes sequenced previously. Intraspecies recombination (three of four TBRV and two of four BRSV isolates) was frequent amongst the eight new genomes. Interspecies recombination was also present within the RNA1 of TBRV isolates BRSV‐3393 SG GB and BRSV‐9888 ST GB. No satellite RNAs were associated with the eight new genomes. Two commercial enzyme‐linked immunosorbent assay (ELISA) kits used to detect TBRV during routine testing differed in that one detected only TBRV and the other only BRSV, so they are likely to provide incorrect but potentially complementary virus occurrence information. We suggest both ELISA kits, or appropriate molecular tests, be used by biosecurity authorities to avoid this problem. This study illustrates the value of sequencing historical isolates preserved from the pre‐sequencing era. [ABSTRACT FROM AUTHOR]

Many laboratories maintain historical collections of preserved plant virus isolates that store a wealth of untapped data, including original type isolates, studied in the pre‐sequencing era. Currently, many recently recognized virus species exist with no supporting reference sequences. Also, many virus sequences appear new when compared to available sequences, but, on sequencing pre‐sequencing era isolates, they may coincide. Such linkages allow access to data from previously determined biological and other parameters from pre‐sequencing era studies. These linkages are increasingly being found using high‐throughput sequencing, helping clarify virus taxonomy and improving understanding of virus ecology and evolution. Thus, mistakes can be avoided in naming viruses and in combining or separating them, as well as enabling identification of unknown viruses preserved long ago. With well‐established viruses, success in dating and other evolutionary studies, and discovery of changes in regional virus populations, both depend upon comparisons between recent and old isolate sequences covering the greatest possible time periods. Such studies help reveal the extent that human activities have influenced virus evolution and changed virus populations on a global scale. Sequencing virus genomes from herbarium specimens, archaeological specimens, or living plant collections can provide complementary data. By bringing context to newly detected viruses and supporting plant pest risk analyses, linking new virus discoveries to previously generated disease symptom, host range, virus transmission, and geographical distribution data has important implications for plant health regulation. Also, historical isolates can provide an invaluable resource facilitating biosecurity investigations involving virus introductions, entry pathways, and baseline surveillance. [ABSTRACT FROM AUTHOR]