Beet Western Yellows Luteovirus in Western Oregon Pathosystem Relationships in a Vegetable–Sugar Beet Seed Production Region
نویسنده
چکیده
uring the 1980s, crisphead lettuce, butterhead lettuce, and spinach crops in western Oregon (Fig. 1) became increasingly damaged by beet western yellows luteovirus (BWYV) (5,8) infection (15), a previously insignificant problem in this area. Utilizing double antibody sandwich enzyme-linked immunosorbent assay (DASELISA) methodology (2), we identified potential BWYV inoculum sources in vicinities of affected lettuce and spinach fields (15) based on the known host range of BWYV (5–9) and prior agroecosystem investigations of BWYV in the Pacific Northwest (20,29,30,32–34,37,38). In current and prior (14,15) studies, we identified three principal subreservoirs of BWYV inoculum in the Willamette Valley: multiseasonal plantings of vegetable crops, biennial plantings of sugar beet seed fields (21), and numerous BWYV-susceptible weed species prevalent in this agroecosystem (14), including native, introduced, and escaped annual and perennial species. We also endeavored to understand beet western yellows (BWY) disease-cycle components in western Oregon and to document the presence and determine the effects of BWYV in representative western Oregon sugar beet seed fields (17). The incidence of potential aphid vectors on one or more of 30 western Oregon plant species or forms commonly infected by BWYV was also separately examined (16). The purpose of this paper is to present interactions within the BWY pathosystem that cause risks to BWYV-susceptible crops in western Oregon.
منابع مشابه
The satellite RNA of barley yellow dwarf virus-RPV is supported by beet western yellows virus in dicotyledonous protoplasts and plants.
The subgroup II luteovirus barley yellow dwarf virus-RPV (BYDV-RPV) acts as a helper virus for a satellite RNA (satRPV RNA). The subgroup II luteovirus beet western yellows virus (BWYV) and the ST9-associated RNA (ST9a RNA), a BWYV-associated RNA that encodes a polymerase similar to those of subgroup I luteoviruses, were assayed for their ability to support replication of satRPV RNA. SatRPV RNA...
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