Channappa Manjunatha, Thiruvengadam Venkatesan, Shivakumar Nanditha, Thammayya Shivakumara K, Nayyar Nishtha, Muthugounder Mohan, Ramasamy Gandhi G, Syamala Ramya R, Kukreti Aditya, Karthik Chikkabidare M, Selvamani Selvababu, Pathak Jyoti, Jha Girish K, Sushil Satya N
Division of Genomic Resources, ICAR-National Bureau of Agricultural Insect Resources, Bengaluru, 560 024, India.
ICAR-Indian Agricultural Statistical Research Institute, New Delhi, 110 012, India.
Sci Rep. 2025 May 23;15(1):18026. doi: 10.1038/s41598-025-02399-9.
The fall armyworm, Spodoptera frugiperda, is an invasive, polyphagous pest that threatens approximately 353 plant species across 72 families worldwide. Due to morphological similarities with other noctuid pests during the early larval, pupal, and adult stages, traditional identification methods are labour-intensive and require specialist expertise. Rapid, reliable detection is essential given the pest's potential for widespread destruction. Through genome-wide in-silico analysis, this study identified a unique region within a signal peptide gene of S. frugiperda, which served as the basis for developing PCR, LAMP, and RPA-based assays for detection. The PCR assay produced a specific 550 bp amplicon for S. frugiperda, showing no cross-reactivity with negative controls. In the LAMP assay, positive samples exhibited a sky-blue colour, while negative samples turned violet when hydroxynaphthol blue dye was used. The RPA assay, with SYBR green dye, displayed bright green in positive samples and brick-red in negatives. Sensitivity tests demonstrated that PCR detected as low as 1 pg/µL, while LAMP and RPA achieved a higher sensitivity of 100 fg/µL. This study introduces the first RPA colorimetric assay for S. frugiperda, providing a time-efficient, cost-effective option that requires minimal equipment, ideal for field detection, thereby supporting timely pest monitoring and management.
草地贪夜蛾,即草地贪夜蛾(Spodoptera frugiperda),是一种具有入侵性的多食性害虫,威胁着全球72个科的约353种植物。由于在幼虫早期、蛹期和成虫期与其他夜蛾科害虫在形态上相似,传统的鉴定方法劳动强度大,需要专业知识。鉴于这种害虫具有广泛破坏的可能性,快速、可靠的检测至关重要。通过全基因组的电子分析,本研究在草地贪夜蛾信号肽基因内鉴定出一个独特区域,以此为基础开发了基于PCR、LAMP和RPA的检测方法。PCR检测法为草地贪夜蛾产生了一个550 bp的特异性扩增子,与阴性对照无交叉反应。在LAMP检测中,使用羟基萘酚蓝染料时,阳性样本呈现天蓝色,而阴性样本变为紫色。使用SYBR绿染料的RPA检测中,阳性样本显示亮绿色,阴性样本显示砖红色。敏感性测试表明,PCR检测低至1 pg/µL,而LAMP和RPA的敏感性更高,达到100 fg/µL。本研究介绍了首个针对草地贪夜蛾的RPA比色检测法,提供了一种省时、经济高效的选择,所需设备最少,非常适合现场检测,从而支持及时的害虫监测和管理。