Zhang Yubao, Xie Zhongkui, Fletcher John D, Wang Yajun, Wang Ruoyu, Guo Zhihong, He Yuhui
Northwest Institute of Eco-Environment and Resources, Chinese Academy of Sciences, Lanzhou 730000, China.
The New Zealand Institute for Plant and Food Research, PB 4704 Christchurch, New Zealand.
Plant Pathol J. 2020 Feb;36(1):76-86. doi: 10.5423/PPJ.OA.12.2019.0298. Epub 2020 Feb 1.
Cucumber mosaic virus (CMV) is damaging to the growth and quality of lettuce crops in Lanzhou, China. Recently, however, for the first time an isolate of lettuce necrotic yellows virus (LNYV) has been detected in lettuce crops in China, and there is concern that this virus may also pose a threat to lettuce production in China. Consequently, there is a need to develop a rapid and efficient detection method to accurately identify LNYV and CMV infections and help limit their spread. Reverse transcription loop-mediated isothermal amplification (RT-LAMP) assays were developed to detect the nucleoprotein (N) and coat protein (CP) genes of LNYV and CMV, respectively. RT-LAMP amplification products were visually assessed in reaction tubes separately using green fluorescence and gel electrophoresis. The assays successfully detected both viruses in infected plants without cross reactivity recorded from either CMV or LNYV or four other related plant viruses. Optimum LAMP reactions were conducted in betaine-free media with 6 mM Mg at 65°C for LNYV and 60°C for 60 min for CMV, respectively. The detection limit was 3.5 pg/ml and 20 fg/ml using RT-LAMP for LNYV and CMV plasmids, respectively. Detection sensitivity for both RT-LAMP assays was greater by a factor of 100 compared to the conventional reverse transcription polymerase chain reaction assays. This rapid, specific, and sensitive technique should be more widely applied due to its low cost and minimal equipment requirements.
黄瓜花叶病毒(CMV)对中国兰州生菜作物的生长和品质造成损害。然而,最近首次在中国生菜作物中检测到生菜坏死黄化病毒(LNYV)的一个分离株,人们担心这种病毒也可能对中国的生菜生产构成威胁。因此,需要开发一种快速有效的检测方法,以准确识别LNYV和CMV感染,并有助于限制它们的传播。分别开发了逆转录环介导等温扩增(RT-LAMP)检测方法来检测LNYV和CMV的核蛋白(N)和衣壳蛋白(CP)基因。RT-LAMP扩增产物分别在反应管中使用绿色荧光和凝胶电泳进行视觉评估。这些检测方法成功地检测到了受感染植物中的两种病毒,未记录到CMV、LNYV或其他四种相关植物病毒的交叉反应。最佳LAMP反应分别在不含甜菜碱的培养基中进行,LNYV在65°C下反应60分钟,CMV在60°C下反应60分钟,镁离子浓度为6 mM。使用RT-LAMP检测LNYV和CMV质粒的检测限分别为3.5 pg/ml和20 fg/ml。与传统的逆转录聚合酶链反应检测方法相比,两种RT-LAMP检测方法的检测灵敏度都提高了100倍。由于成本低且设备要求最少,这种快速、特异且灵敏的技术应得到更广泛的应用。