Nagpal Kanika, Jasrotia Poonam, Jaglan Maha Singh, Kashyap Prem Lal, Maanju Sunny, Kumar Sudheer
Crop Protection Division, Indian Council of Agricultural Research (ICAR)- Indian Institute of Wheat and Barley Research, Karnal, Haryana, India.
Department of Entomology, College of Agriculture, Chaudhary Charan Singh (CCS) Haryana Agricultural University, Hisar, Haryana, India.
Front Plant Sci. 2025 Aug 18;16:1628692. doi: 10.3389/fpls.2025.1628692. eCollection 2025.
The rice weevil ( L.) is one of the most destructive pests of stored cereal grains, particularly wheat, leading to considerable post-harvest losses and posing serious threats to global food security and international trade. Rapid and accurate identification of infestations is essential for implementing timely pest management strategies and adhering to phytosanitary regulations. In this study, we report the development and validation of a molecular diagnostic assay that is rapid, sensitive, and highly specific for the early detection of in stored wheat grains. Two novel species-specific oligonucleotide primer sets-KNSoCox1F1/KNSoCox1R1 and KNSoCox2F1/KNSoCox2R1-were designed to amplify target regions of the ( and ), generating diagnostic fragments of 176 bp and 248 bp, respectively. Conventional PCR demonstrated high specificity, with no cross-reactivity observed in other non-target insects or uninfested wheat samples. Further, sensitivity assessments using quantitative real-time PCR (qPCR) revealed detection thresholds as low as 1 picogram of genomic DNA, which corresponds to a single insect per 10 kg of grains. The assay easily operates in moderately equipped molecular laboratories and offers quick results with streamlined workflows or automation, making it ideally suited for use in quarantine stations, grain storage facilities, and entomological diagnostic laboratories. Its reliability, speed, and cost-efficiency make it a powerful tool for pest surveillance, ecological studies, and enhancing biosecurity protocols.
米象(Sitophilus oryzae (L.))是储存谷物尤其是小麦中最具破坏性的害虫之一,会导致大量收获后损失,并对全球粮食安全和国际贸易构成严重威胁。快速准确地识别虫害对于及时实施害虫管理策略和遵守植物检疫规定至关重要。在本研究中,我们报告了一种分子诊断检测方法的开发与验证,该方法快速、灵敏且高度特异,可用于早期检测储存小麦中的米象。设计了两组新型物种特异性寡核苷酸引物——KNSoCox1F1/KNSoCox1R1和KNSoCox2F1/KNSoCox2R1——用于扩增米象(Sitophilus oryzae)(细胞色素氧化酶亚基1和细胞色素氧化酶亚基2)的目标区域,分别产生176 bp和248 bp的诊断片段。常规PCR显示出高特异性,在其他非目标昆虫或未受侵染的小麦样品中未观察到交叉反应。此外,使用定量实时PCR(qPCR)进行的灵敏度评估显示检测阈值低至1皮克基因组DNA,相当于每10千克谷物中有一只昆虫。该检测方法在配备中等的分子实验室中易于操作,通过简化的工作流程或自动化可快速得出结果,非常适合在检疫站、粮食储存设施和昆虫学诊断实验室中使用。其可靠性、速度和成本效益使其成为害虫监测、生态研究和加强生物安全协议的有力工具。