Yoon June-Sun, Ahn Seung-Joon, Choi Man-Yeon
USDA Agricultural Research Service, Horticultural Crops Research Unit, Corvallis, OR 97331, USA.
Department of Agricultural Convergence Technology, Jeonbuk National University, Jeonju 54596, Republic of Korea.
Insects. 2023 Jan 12;14(1):76. doi: 10.3390/insects14010076.
Spotted-wing drosophila (SWD), , is a destructive and invasive pest that attacks most small fruits and cherries. The current management for SWD involves the use of conventional insecticides. In an effort to develop a biologically based control option, the application of RNA interference (RNAi) has been investigated. To develop an RNAi approach, suitable targets must be identified, and an efficient delivery method must be developed for introducing the double-stranded RNA (dsRNA) in the midgut. In , we previously found that dsRNA nucleases actively degrade dsRNA molecules in the midgut. In this study, we focused on identifying biological targets focused on the midgut membrane. The profile of midgut-specific genes was analyzed and compared with the genes expressed in the whole-body using transcriptome analysis. Differential gene expression analysis revealed that 1921 contigs were upregulated and 1834 contigs were downregulated in the midgut when compared to genes from other body tissues. We chose ten midgut-specifically upregulated genes and empirically confirmed their expressions. We are particularly interested in the midgut membrane proteins, including G protein-coupled receptors (GPCRs) such as diuretic hormone 31 (DH31) receptor, neuropeptide F (NPF) recepror, toll-9, adhesion receptors, methuselah (mth), and gustatory receptor, because insect GPCRs have been offered great potential for next-generation pest management.
斑翅果蝇是一种具有破坏性的入侵害虫,会侵害大多数小浆果和樱桃。目前对斑翅果蝇的防治措施包括使用传统杀虫剂。为了开发一种基于生物学的防治方法,人们对RNA干扰(RNAi)的应用进行了研究。要开发一种RNAi方法,必须确定合适的靶点,并且必须开发一种有效的递送方法,以便将双链RNA(dsRNA)引入中肠。在之前的研究中,我们发现dsRNA核酸酶会在中肠中主动降解dsRNA分子。在本研究中,我们专注于确定以中肠膜为靶点的生物学目标。利用转录组分析,对中肠特异性基因的图谱进行了分析,并与全身表达的基因进行了比较。差异基因表达分析显示,与其他身体组织的基因相比,中肠中有1921个重叠群上调,1834个重叠群下调。我们选择了10个中肠特异性上调基因,并通过实验证实了它们的表达。我们对中肠膜蛋白特别感兴趣,包括G蛋白偶联受体(GPCRs),如利尿激素31(DH31)受体、神经肽F(NPF)受体、Toll-9、黏附受体、玛士撒拉(mth)和味觉受体,因为昆虫GPCRs在下一代害虫管理方面具有巨大潜力。