Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing, China.
Academy of Agricultural Sciences, Southwest University, Chongqing, China.
Pest Manag Sci. 2021 Feb;77(2):677-685. doi: 10.1002/ps.6143. Epub 2020 Nov 2.
The Asian citrus psyllid Diaphorina citri has developed high levels of resistance to many insecticides, and understanding its resistance mechanism will aid in the chemical control of this species. Nicotinamide adenine dinucleotide phosphate (NADPH)-cytochrome P450 reductase (CPR) is crucial in cytochrome P450 function, and in some insects CPR knockdown has increased their susceptibility to insecticides. However, the CPR from D. citri has not been characterized and its function is undescribed.
The CPR gene of D. citri (DcCPR) was cloned and sequenced. The expression level of DcCPR, determined by reverse-transcription quantitative polymerase chain reaction (RT-qPCR) analysis, was highest in the midgut and in nymphs. After feeding on double-stranded RNA for 72 h, the DcCPR messenger RNA level in D. citri adults decreased by 68.4%, and the susceptibility of D. citri to imidacloprid and thiamethoxam significantly increased. Meanwhile, after DcCPR silencing, the specific activities of DcCPR protein and P450s were significantly reduced by 41.6% and 44.7%, respectively. The subsequent western blot analysis and quantification of band intensity also showed that DcCPR content significantly decreased, consistent with the results of the specific activity test. In a eukaryotic expression assay, the viability of cells expressing DcCPR was significantly higher than the viability of cells expressing green fluorescent protein (GFP) when cells were exposed to imidacloprid or thiamethoxam.
These results indicate that DcCPR contributes to D. citri susceptibility to imidacloprid and thiamethoxam.
亚洲柑橘木虱 Diaphorina citri 对许多杀虫剂产生了高水平的抗性,了解其抗性机制将有助于该物种的化学防治。烟酰胺腺嘌呤二核苷酸磷酸(NADPH)-细胞色素 P450 还原酶(CPR)在细胞色素 P450 功能中至关重要,在一些昆虫中 CPR 敲低会增加它们对杀虫剂的敏感性。然而,D. citri 的 CPR 尚未被表征,其功能尚未描述。
克隆并测序了 D. citri 的 CPR 基因。通过反转录定量聚合酶链反应(RT-qPCR)分析确定的 DcCPR 表达水平在中肠和若虫中最高。在用双链 RNA 喂养 72 小时后,D. citri 成虫的 DcCPR 信使 RNA 水平下降了 68.4%,对吡虫啉和噻虫嗪的敏感性显著增加。同时,DcCPR 沉默后,DcCPR 蛋白和 P450s 的比活性分别显著降低了 41.6%和 44.7%。随后的 Western blot 分析和条带强度的定量也表明 DcCPR 含量显著降低,与比活性测试结果一致。在真核表达测定中,当细胞暴露于吡虫啉或噻虫嗪时,表达 DcCPR 的细胞的活力明显高于表达绿色荧光蛋白(GFP)的细胞的活力。
这些结果表明 DcCPR 有助于 D. citri 对吡虫啉和噻虫嗪的敏感性。