Development of reverse transcription loop-mediated isothermal amplification assay for rapid detection of an emerging potyvirus: Tomato necrotic stunt virus

被引:15
|
作者
Li, Rugang [1 ]
Ling, Kai-Shu [1 ]
机构
[1] USDA ARS, US Vegetable Lab, Charleston, SC 29414 USA
基金
美国食品与农业研究所;
关键词
Solanum lycopersicum; qRT-PCR; LAMP assay; Field disease diagnosis; LEAF CURL VIRUS; MOSAIC-VIRUS; RT-PCR; PLANTS;
D O I
10.1016/j.jviromet.2014.01.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Tomato necrotic stunt virus (ToNStV) is an emerging potyvirus that causes severe stunting to infected tomato plants. A reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was developed for sensitive detection of ToNStV. The sensitivity of RT-LAMP was comparable to that of conventional RT-PCR, with detection of ToNStV in a reaction containing only 8 pg of total tomato RNA or with 1:20,000 dilution of crude tissue extract. This assay was able to detect ToNStV in a broad range of solanaceous plant species. The RT-LAMP for ToNStV was specific with no cross-reactivity to other potyviruses (i.e. Potato virus Y and Tobacco etch virus), as well as several other common tomato viruses. RT-LAMP should complement RT-PCR and real-time RT-PCR assays reported previously, with a potential to provide a simple, rapid, and sensitive field diagnostic method for ToNStV. Published by Elsevier B.V.
引用
收藏
页码:35 / 40
页数:6
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