Li Cheng-Jin, Sun Hui-Quan, Zhao Wen-Xia, Wang Xiao-Yi, Lin Ruo-Zhu, Yao Yan-Xia
Key Laboratory of Forest Protection of the National Forestry and Grassland Administration, Ecology and Nature Conservation Institute, Chinese Academy of Forestry, Beijing 100091, China.
J Econ Entomol. 2023 Dec 11;116(6):1969-1981. doi: 10.1093/jee/toad189.
Agrilus mali stands as a significant wood-boring pest prevalent in Northeast Asia. Identifying this pest beetle is often hindered by insufficient efficient, rapid, on-site discrimination methods beyond examining adult morphological features. As a result, an urgent need arises for developing and implementing a rapid and accurate molecular technique to distinguish and manage the beetle. This study presents a straightforward, swift, highly specific, and sensitive method built upon recombinase polymerase amplification combined with a lateral flow dipstick (RPA-LFD). This method demonstrates the capability to promptly identify the beetle, even during its larval stage. RPA primers and probes were designed using the internal transcribed spacer 1 region. Through probe optimization, false-positive signals were successfully eliminated, with an accompanying discussion on the underlying causes of such signals. The RPA-LFD assays exhibited remarkable specificity and sensitivity, requiring as little as 10-3 ng of purified DNA. Furthermore, the extraction of crude DNA was achieved through immersion in sterile distilled water, thus streamlining the assay process. Achievable at temperatures ranging from 30 to 50 °C, the RPA-LFD assay can be executed manually without specialized equipment. By merging the RPA-LFD assay with DNA coarse extraction, A. mali can be detected within just 30 min. This current study effectively demonstrates the immense potential of RPA-LFD in quarantine and pest management. Additionally, it presents a universal technique for the rapid on-site diagnosis of insects, showcasing the wide applicability of this method.
苹果小吉丁虫是一种在东北亚地区普遍存在的重要蛀干害虫。除了检查成虫形态特征外,由于缺乏高效、快速的现场鉴别方法,对这种害虫甲虫的鉴定常常受到阻碍。因此,迫切需要开发和应用一种快速准确的分子技术来鉴别和管理这种甲虫。本研究提出了一种基于重组酶聚合酶扩增结合侧向流动试纸条(RPA-LFD)的简单、快速、高度特异且灵敏的方法。该方法证明了即使在幼虫阶段也能迅速鉴定出这种甲虫的能力。利用内部转录间隔区1区域设计了RPA引物和探针。通过探针优化,成功消除了假阳性信号,并对这些信号产生的潜在原因进行了讨论。RPA-LFD检测表现出显著的特异性和灵敏度,仅需10-3 ng纯化DNA。此外,通过浸入无菌蒸馏水中即可实现粗DNA的提取,从而简化了检测过程。RPA-LFD检测在30至50°C的温度范围内均可进行,无需专门设备即可手动操作。通过将RPA-LFD检测与DNA粗提取相结合,仅需30分钟即可检测出苹果小吉丁虫。本研究有效地证明了RPA-LFD在检疫和害虫管理中的巨大潜力。此外,它还提出了一种用于昆虫快速现场诊断的通用技术,展示了该方法的广泛适用性。