Department of Agricultural Biology, Colorado State University, Fort Collins, CO 80523, USA.
Environ Entomol. 2024 Feb 20;53(1):34-39. doi: 10.1093/ee/nvad060.
Of the many arthropod species affecting hemp (Cannabis sativa L.) cultivation in the United States, one species of particular importance is the hemp russet mite (Aculops cannabicola, HRM). Hemp russet mite is a microscopic arthropod which feeds on all parts of hemp plants. Due to its minute size, HRM can proliferate undetected for a long time, complicating management efforts and causing serious economic losses. DNA sequencing and PCR assays can facilitate accurate identification and early detection of HRM in infested-plants. Therefore, a real-time SYBR Green based species-specific PCR assay (quantitative PCR, qPCR) was developed for the identification of HRM DNA by amplification of a 104 bp Internal Transcribed Spacer 1 (ITS1) sequence. The detection limit was estimated to be approximately 48 copies of the HRM marker gene sequence. The real-time-PCR assay is rapid, detects all life stages of mite under 2 hours. A 10-fold serial dilution of the plasmid DNA containing the ITS1 insert were used as standards in the real-time PCR assay. The quantification cycle (Cq) value of the assay showed a strong linear relationship with HRM DNA with R2 of 0.96. The assay was tested against several commonly found hemp pests including two-spotted spider mite and western flower thrips to determine specificity of the assay and to show that no non-target species DNA was amplified. The outcomes of this research will have important applications for agricultural biosecurity through accurate identification of HRM, early detection and timely deployment of management tactics to manage and prevent pest outbreaks.
在美国,有许多节肢动物物种会影响大麻(Cannabis sativa L.)的种植,其中一种特别重要的物种是大麻锈螨(Aculops cannabicola,HRM)。大麻锈螨是一种微小的节肢动物,以大麻植物的所有部位为食。由于其微小的体型,HRM 可以在很长一段时间内未被察觉地繁殖,从而使管理工作变得复杂,并造成严重的经济损失。DNA 测序和 PCR 检测可以促进对受感染植物中 HRM 的准确识别和早期检测。因此,开发了一种基于实时 SYBR Green 的种特异性 PCR 检测方法(定量 PCR,qPCR),通过扩增 104 bp 内转录间隔区 1(ITS1)序列来鉴定 HRM DNA。检测限估计约为 HRM 标记基因序列的 48 个拷贝。实时 PCR 检测方法快速,可在 2 小时内检测到螨虫的所有生命阶段。将含有 ITS1 插入片段的质粒 DNA 进行 10 倍系列稀释,作为实时 PCR 检测的标准。该检测方法的定量循环(Cq)值与 HRM DNA 具有很强的线性关系,R2 为 0.96。该检测方法还针对包括二斑叶螨和西花蓟马在内的几种常见大麻害虫进行了测试,以确定该检测方法的特异性,并表明没有非目标物种的 DNA 被扩增。这项研究的结果将通过准确识别 HRM、早期检测和及时部署管理策略来管理和预防害虫爆发,对农业生物安全具有重要应用。