Chen Yu, Chen Xiao-Yun, Peng Cheng, Xu Jun-Feng, Shen Jie, Li Yue-Ying, Wang Xiao-Fu
tate Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, China.
School of Clinical Medicine, Ningxia Medical University, Yinchuan 750004, China.
Yi Chuan. 2021 Aug 20;43(8):802-812. doi: 10.16288/j.yczz.21-110.
The genetically modified (GM) maize 'Shuangkang'12-5 has good insect resistance and herbicide tolerance, which is one of the first series of GM maizes obtained a safety certificate in China, and it has broad application prospect in the future. This study established an on-site rapid detection method for GM 'Shuangkang'12-5 based on recombinase polymerase amplification (RPA) technology, which primes and probe were designed according to the specific flank sequence. Then the best combination of primers and probe was obtained through a screeing process. The amplification results of fluorescence RPA can be directly visualized under blue light. The results showed that the visual detection system of GM 'Shuangkang'12-5 with high specificity, and the detection sensitivity of the method could reached 10 copies. Further research found that the RPA amplification system had a wide range of temperature (34℃-46℃). According to this property, the common self-heating warm pastes on the market were used replace the traditional heating instruments to stimulate the RPA.The results showed that the self-heating warm paste meets the temperature requirement of the RPA system. Finally, we combined the self-heating warm pastes with the RPA visual detection system to conduct on-site detection of GM 'Shuangkang'12-5, and compared the results with the detection results of qPCR. The detection showed that the results of on-site visual detection method established in this study were consistent with the detection results of the qPCR. Moreover, the visual detection method was more shorter in time and the final detection result was clear and easy to distinguish. The rapid on-site visual detection method for GM 'Shuangkang' 12-5 established in this study has high specificity, high sensitivity and convenience. It not only meets the needs of on-site rapid detection of GM 'Shuangkang'12-5, but also provides highlight for the development of other on-site rapid detection methods.
转基因玉米“双抗”12 - 5具有良好的抗虫性和除草剂耐受性,是我国首批获得安全证书的转基因玉米系列之一,具有广阔的应用前景。本研究基于重组酶聚合酶扩增(RPA)技术建立了转基因“双抗”12 - 5的现场快速检测方法,根据其特异性侧翼序列设计引物和探针。通过筛选过程获得了引物和探针的最佳组合。荧光RPA的扩增结果在蓝光下可直接可视化。结果表明,转基因“双抗”12 - 5的可视化检测系统具有高特异性,该方法的检测灵敏度可达10个拷贝。进一步研究发现,RPA扩增系统具有较宽的温度范围(34℃ - 46℃)。根据这一特性,使用市售常见的自热暖贴代替传统加热仪器来激发RPA。结果表明,自热暖贴满足RPA系统的温度要求。最后,将自热暖贴与RPA可视化检测系统结合,对转基因“双抗”12 - 5进行现场检测,并与qPCR检测结果进行比较。检测表明,本研究建立的现场可视化检测方法的结果与qPCR检测结果一致。而且,可视化检测方法用时更短,最终检测结果清晰易辨。本研究建立的转基因“双抗”12 - 5现场快速可视化检测方法具有高特异性、高灵敏度和便捷性。它不仅满足了转基因“双抗”12 - 5现场快速检测的需求,也为其他现场快速检测方法的发展提供了亮点。