Diagnosis of Potato Mop-Top Virus in Soil Using Bait Plant Bioassay and RT-PCR-microplate Hybridization

被引:20
作者
Nakayama, Takato [1 ]
Maoka, Tetsuo [1 ]
Hataya, Tatsuji [2 ]
Shimizu, Motoshige [3 ]
Fuwa, Hideaki [4 ]
Tsuda, Shogo [5 ]
Mori, Motoyuki [5 ]
机构
[1] Natl Agr Res Ctr Hokkaido Reg, Sapporo, Hokkaido 0628555, Japan
[2] Hokkaido Univ, Res Fac Agr, Sapporo, Hokkaido 0608589, Japan
[3] Hokkaido Prefectural Tokachi Agr Expt Stn, Memuro, Hokkaido 0820081, Japan
[4] Natl Ctr Seeds & Seedlings, Hokkaido Chuo Stn, Nishinosato, Kitahiroshima 0611102, Japan
[5] Natl Agr Res Ctr Hokkaido Reg, Memuro Res Stn, Memuro, Hokkaido 0820081, Japan
关键词
Potato mop-top virus; Detection; Bait plant bioassay; RT-PCR-microplate hybridization; Spongospora subterranea; Plasmodiophoraceae; Vector; Pomovirus; Spraing; F-SP SUBTERRANEA; SPONGOSPORA-SUBTERRANEA; POWDERY SCAB; RESTING SPORES; POLYMYXA-BETAE; UNITED-STATES; TRANSMISSION; TUBERS; FUROVIRUS; CYSTOSORUS;
D O I
10.1007/s12230-010-9128-5
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Spraing (brown rings or arcs) of potato caused by Potato mop-top virus (PMTV) occurred in a field of Tokachi, Hokkaido, Japan in 2005. To monitor the expansion of spraing-affected areas, we developed a soil diagnostic method that consisted of a bioassay using tomato as bait plant to trap the vector of PMTV, Spongospora subterranea, the causal agent of powdery scab of potatoes, followed by reverse transcription-polymerase chain reaction-microplate hybridization (RT-PCR-MPH) to detect the virus from roots of bait plants. After incubation of tomato seedlings grown with their roots immersed in a soil suspension at 18A degrees C for 9 days, total RNA extracted from bait roots was analyzed by RT-PCR-MPH using PMTV-specific primers and a digoxigenin (DIG)-labeled probe. Soil diagnosis using the present method in an infested area revealed 137 of 224 fields (61.2%) were infested by PMTV although tubers harvested from only one of these fields had spraing.
引用
收藏
页码:218 / 225
页数:8
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