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Root galls possibly caused by Spongospora subterranea were observed on hairy nightshade (Solanum sarrachoide; HNS). HNS galls and galls from potato were used to artificially inoculate potato and HNS. Eighty-three and 52% potato and HNS plants inoculated with potato inoculum had root galls, respectively. Ten and 31% potato and HNS plants inoculated with HNS inoculum had root galls, respectively. A S. subterranea-specific PCR significantly correlated (P < 0.0001, Phi Coefficient = 0.69) with visual assessment of gall incidence in 34 of 40 samples. Five of 40 samples had no galls, but gave positive PCRs. One of 40 samples had root galls, but gave a negative PCR. More sporosori were produced on potato than on HNS. Therefore, the root galls on HNS were caused by S. subterranea that is able to complete its life cycle on HNS and produce new generations of sporosori that are infectious on potato.

Hairy nightshade is a common weed in potato rotations in the western United States. As a close relative of potato, hairy nightshade can host numerous potato nematodes, diseases, and insect pests. Hairy nightshade hosts three common parasitic nematodes of potato, Columbia and northern root-knot nematodes, and stubby root nematode. Tubers of a potato breeding line with roots that are resistant to Columbia root-knot nematode—race 1, were damaged when grown in the presence of hairy nightshade. The weed provided an alternate host for the nematode, which then allowed the nematode to infect susceptible tubers. Stubby root nematodes transmit tobacco rattle virus (TRV), the causal agent for corky ringspot disease (CRS) of potato. CRS disease was maintained in soil when hairy nightshade was present in rotation crops of alfalfa or Scotch spearmint that otherwise eliminated the disease. Hairy nightshade also is a host of potato leaf roll virus (PLRV), which is transmitted by green peach aphids (GPA). GPA pre...

Tobacco rattle virus (TRV), the causal agent of corky ringspot disease of potato (CRS), was detected by reverse transcription-polymerase chain reaction (RT-PCR) in root tissues of field- and greenhouse-grown wheat (two) and corn (10) cultivars. TRV was also detected in some of the same samples by enzyme-linked immunosorbent assay (ELISA), but in a low frequency. Compared to ‘Samsun NN’ tobacco, wheat and corn appeared to be poorer hosts of TRV. However, these crops served as inoculum reservoirs of TRV. A nonviruliferous population of the nematodeParatrichodorus allius, the vector of TRV, acquired the virus from infected wheat and corn roots, and transmitted it to potato. ‘Russet Norkotah’ potatoes grown following TRV-infected corn and wheat, were blemished with arcs, concentric rings and diffuse browning, characteristic symptoms of CRS. The observations presented here suggest that wheat and corn as rotational crops will sustain TRV in a CRS problem field and the virus may cause severe damage on subsequent potato crops.

Soil samples from corky ringspot (CRS) problem fields of potato in the states of Washington and Oregon were collected and planted withNicotiana tabacum ‘Samsun NN’ tobacco to bait tobacco rattle virus (TRV) and to increaseParatrichodorus allius populations, the vector of TRV. Pathogenicity of three isolates of TRV was assessed on Russet Burbank and Russet Norkotah plants usingP. allius as the vector. The most severe CRS tuber symptoms were with TRV from Pasco, WA, followed by Umatilla, OR, and Mattawa, WA, indicating a distinct variation in virulence among virus isolates. The lowest number ofP. allius that transmitted TRV resulting in CRS symptoms on Russet Norkotah was three nematodes per 250 cm3 soil. When potato plants were exposed toP. allius at different times in their growth, tubers on older plants were more resistant than younger tubers to CRS. Severity of CRS tuber symptoms was correlated with age of potato plants in pot culture. Reproduction ofP. allius on potato roots did not influence the incidence and severity of tubers symptoms. Under similar conditions, Bintje, a variety known to be resistant to CRS, served as a host forP. allius, yet remained asymptomatic. The protocol employed in these studies is appropriate for testing potato germplasm for resistance to CRS.

Experiments were conducted to determine whether the beet leafhopper, Circulifer tenellus (Baker) (Hemiptera: Cicadellidae), transmits the purple top phytoplasma to potato, Solanum tuberosum L.; beets, Beta vulgaris L.; and selected weed hosts. The beet leafhopper-transmitted virescence agent (BLTVA) phytoplasma was identified as the causal agent of the potato purple top disease outbreaks that recently occurred in the Columbia Basin of Washington and Oregon. The phytoplasma previously was found to be associated almost exclusively with the beet leafhopper, suggesting that this insect is the probable vector of BLTVA in this important potato-growing region. Eight potato cultivars, including 'Russet Burbank', 'Ranger Russet', 'Shepody', 'Umatilla Russet', 'Atlantic', 'FL-1879', 'FL-1867', and 'FL-1833', were exposed for a week to BLTVA-infected beet leafhoppers. After exposure, the plants were maintained outdoors in large cages and then tested for BLTVA by using polymerase chain reaction after 6 to 7 wk. The leafhoppers transmitted BLTVA to seven of the eight exposed potato cultivars. Sixty-four percent of the exposed plants tested positive for the phytoplasma. In addition, 81% of the BLTVA-infected potato plants developed distinct potato purple top disease symptoms. Beet leafhoppers also transmitted BLTVA to beets and several weeds, including groundsel, Senecio vulgaris L.; shepherd's purse, Capsella bursa-pastoris (L.) Medik); kochia, Kochia scoparia (L.) Schrad; and Russian thistle, Salsola kali L. This is the first report of transmission of BLTVA to potatoes, beets, and the above-mentioned four weed species. Results of the current study prove that the beet leafhopper is a vector of the potato purple top disease.

At least 16 taxa of cicadellids and delphacids were tested by polymerase chain reaction (PCR) for the presence of a phytoplasma in the clover proliferation group, designated 16SrVI. Nucleic acid extracts from individual insects or groups of 5-10 were tested using PCR primers designed from the DNA sequence of 16S-23S rRNA or ribosomal protein genes of the pathogen. The beet leafhopper, Circulifer tenellus (Baker), was most often associated with the phytoplasma, with approximately 16% of the insects testing positive. The phytoplasma was occasionally found associated with Ceratagallia spp. Leafhopper species that were not associated with the phytoplasma included Macrosteles spp., Dikraneura spp., Colladonus montanus (Van Duzee), Circulifer geminatus (Van Duzee), Ballana spp., Amplysellus spp., Paraphlepsius spp., Texananus spp., Balclutha spp., Latalus spp., Erythroneura spp., Exitianus exitiosus (Uhler), and unidentified delphacids. The detected phytoplasma was similar to, or synonymous with, the beet leafhopper-transmitted virescence agent that is associated with the potato purple top disease in the Columbia Basin region of Washington and Oregon. This is in contrast to the phytoplasma associated with potato purple top disease in Mexico that is related to aster yellows (group 16SrI). The association of the group 16SrVI phytoplasma almost exclusively with the beet leafhopper suggests that this insect is the major vector of the phytoplasma in this region.