Heo Seong, Kim Hyun Ran, Lee Hee Jae
Apple Research Institute, National Institute of Horticultural and Herbal Science, Rural Development Administration, Gunwi 39000, Korea.
Department of Plant Science, Seoul National University, Seoul 08826, Korea.
Plant Pathol J. 2019 Apr;35(2):164-171. doi: 10.5423/PPJ.OA.10.2018.0206. Epub 2019 Apr 1.
An assay for detecting (ASSVd) was developed based on nucleic acid sequence based amplification (NASBA) in combination with real-time detection during the amplification process using molecular beacon. The ASSVd specific primers for amplification of the viroid RNA and molecular beacon for detecting the viroid were designed based on highly conserved regions of several ASSVd sequences including Korean isolate. The assay had a detection range of 1 × 10 to 1 × 10 ASSVd RNA copies/μl with reproducibility and precision. Following the construction of standard curves based on time to positive (TTP) value for the serial dilutions ranging from 1 × 10 to 1 × 10 copies of the recombinant plasmid, a standard regression line was constructed by plotting the TTP values versus the logarithm of the starting ASSVd RNA copy number of 10-fold dilutions each. Compared to the established RT-PCR methods, our method was more sensitive for detecting ASSVd. The real-time quantitative NASBA method will be fast, sensitive, and reliable for routine diagnosis and selection of viroid-free stock materials. Furthermore, real-time quantitative NASBA may be especially useful for detecting low levels in apple trees with early viroid-infection stage and for monitoring the influence on tree growth.
基于核酸序列扩增技术(NASBA),结合在扩增过程中使用分子信标进行实时检测,开发了一种检测苹果锈果类病毒(ASSVd)的检测方法。用于扩增类病毒RNA的ASSVd特异性引物和用于检测类病毒的分子信标是根据包括韩国分离株在内的多个ASSVd序列的高度保守区域设计的。该检测方法的检测范围为1×10至1×10个ASSVd RNA拷贝/μl,具有重现性和精密度。基于1×10至1×10拷贝重组质粒系列稀释液的阳性时间(TTP)值构建标准曲线后,通过绘制TTP值与每次10倍稀释起始ASSVd RNA拷贝数的对数关系图,构建了标准回归线。与已建立的逆转录聚合酶链反应(RT-PCR)方法相比,我们的方法检测ASSVd更灵敏。实时定量NASBA方法对于类病毒-free砧木材料的常规诊断和选择将是快速、灵敏且可靠的。此外,实时定量NASBA对于检测处于类病毒感染早期阶段的苹果树上的低水平病毒以及监测对树木生长的影响可能特别有用。