Zong Xiaojuan, Wang Wenwen, Wei Hairong, Wang Jiawei, Chen Xin, Xu Li, Zhu Dongzi, Tan Yue, Liu Qingzhong
Key Laboratory for Fruit Biotechnology Breeding of Shandong Province, Shandong Institute of Pomology, Shandong Academy of Agricultural Sciences, Taian 271000, China.
Key Laboratory for Fruit Biotechnology Breeding of Shandong Province, Shandong Institute of Pomology, Shandong Academy of Agricultural Sciences, Taian 271000, China.
J Virol Methods. 2014 Nov;208:85-9. doi: 10.1016/j.jviromet.2014.07.033. Epub 2014 Aug 7.
Prunus necrotic ringspot virus (PNRSV) has seriously reduced the yield of Prunus species worldwide. In this study, a highly efficient and specific two-step reverse transcription loop-mediated isothermal amplification (RT-LAMP) was developed to detect PNRSV. Total RNA was extracted from sweet cherry leaf samples using a commercial kit based on a magnetic nanoparticle technique. Transcripts were used as the templates for the assay. The results of this assay can be detected using agarose gel electrophoresis or by assessing in-tube fluorescence after adding SYBR Green I. The assay is highly specific for PNRSV, and it is more sensitive than reverse-transcription polymerase chain reaction (RT-PCR). Restriction enzyme digestion verified further the reliability of this RT-LAMP assay. To our knowledge, this is the first report of the application of RT-LAMP to PNRSV detection in Prunus species.
李坏死环斑病毒(PNRSV)已严重降低了全球李属植物的产量。在本研究中,开发了一种高效且特异的两步逆转录环介导等温扩增(RT-LAMP)方法来检测PNRSV。使用基于磁性纳米颗粒技术的商业试剂盒从甜樱桃叶片样本中提取总RNA。转录本用作检测的模板。该检测结果可通过琼脂糖凝胶电泳或添加SYBR Green I后评估管内荧光来检测。该检测方法对PNRSV具有高度特异性,并且比逆转录聚合酶链反应(RT-PCR)更灵敏。限制性酶切进一步验证了该RT-LAMP检测方法的可靠性。据我们所知,这是RT-LAMP应用于李属植物中PNRSV检测的首次报道。