Rahman Md-Mafizur, Nam Hwayeun, Choi Nakjung, Kim Juil
Agriculture and Life Sciences Research Institute, Kangwon National University, Chuncheon 24341, Republic of Korea.
Department of Biotechnology and Genetic Engineering, Faculty of Biological Science, Islamic University, Kushtia 7003, Bangladesh.
Insects. 2023 Jan 25;14(2):124. doi: 10.3390/insects14020124.
Asian planthoppers (Hemiptera: Delphacidae) that include brown planthoppers (BPH, , Stål), white-backed planthoppers (WBPH, , Horváth), and small brown planthoppers (SBPH, , Fallén) are the primary sucking-type pests of rice. These three insects share morphological and sequence similarities. As insecticide resistance patterns and control strategies vary according to species, the accurate discrimination of these species is important. Here, we developed six species-specific primers based on partial mitochondrial genome sequences. The primers were successfully used in multiplex PCR, loop-mediated isothermal amplification (LAMP) assays, and conventional PCR. Here, we used genomic DNA obtained using the DNA-releasing technique (tissue samples were incubated at 95 °C for 5 min with 30 μL nuclease-free water, and the supernatant was used). We showed that multiplex PCR could analyze the density of each species following a mass collection in the field; the LAMP assay can diagnose the species within 40 min; conventional PCR can be widely applied to a large number of field samples, as well as individuals or mass collections. In conclusion, these results demonstrate the potential of the species-specific primers and DNA-releasing technique for accurate multiplex PCR and LAMP assays, which may assist the intensive field monitoring of integrated management of these species.
包括褐飞虱(Nilaparvata lugens,Stål)、白背飞虱(Sogatella furcifera,Horváth)和灰飞虱(Laodelphax striatellus,Fallén)在内的亚洲飞虱(半翅目:飞虱科)是水稻的主要刺吸式害虫。这三种昆虫在形态和序列上具有相似性。由于杀虫剂抗性模式和防治策略因物种而异,准确鉴别这些物种很重要。在此,我们基于部分线粒体基因组序列开发了六种物种特异性引物。这些引物成功应用于多重PCR、环介导等温扩增(LAMP)检测和常规PCR。在此,我们使用了通过DNA释放技术获得的基因组DNA(将组织样本与30 μL无核酸酶水在95 °C孵育5分钟,取上清液)。我们表明,多重PCR可以在田间大量采集后分析每个物种的密度;LAMP检测可以在40分钟内诊断出物种;常规PCR可以广泛应用于大量田间样本以及个体或大量采集样本。总之,这些结果证明了物种特异性引物和DNA释放技术在准确的多重PCR和LAMP检测中的潜力,这可能有助于对这些物种的综合管理进行密集的田间监测。