昆虫学报 ›› 2025, Vol. 68 ›› Issue (6): 728-735.doi: 10.16380/j.kcxb.2025.06.004

• 研究论文 • 上一篇    下一篇

纳米载体递送系统介导的豌豆蚜四个基因RNA干涉条件筛选

张琨1, 郭士刚1, 常美玲1, 余明玉1, 阚云超1,2, 李丹丹1,*   

  1. (1. 南阳师范学院, 河南省伏牛山昆虫生物学重点实验室, 河南省昆虫生物学国际联合实验室, 南阳 473061; 2. 河南科技学院, 新乡 453003)
  • 出版日期:2025-06-20 发布日期:2025-07-31

RNA interference condition screening on four genes of the pea aphid, Acyrthosiphon pisum (Hemiptera: Aphididae) through the nanocarrier-delivery system

ZHANG Kun1, GUO Shi-Gang1, CHANG Mei-Ling1, YU Ming-Yu1, KAN Yun-Chao1,2, LI Dan-Dan1,*   

  1.  (1. Henan Key Laboratory of Insect Biology in Funiu Mountain, The International Joint Laboratory of Insect Biology in Henan Province, Nanyang Normal University, Nanyang 473061, China; 2. Henan Institute of Science and Technology, Xinxiang 453003, China)
  • Online:2025-06-20 Published:2025-07-31

摘要: 【目的】评估纳米载体递送系统介导豌豆蚜Acyrthosiphon pisum基因的RNA干涉条件。【方法】选择豌豆蚜表皮发育相关基因几丁质合成酶2(chitin synthase 2, CHS2)基因,代谢相关酶液泡型H+-ATP酶AC39(vacuolar H+ ATPase AC39,VhaAC39)基因、水通道蛋白(water-specific aquaporin,Wsa)基因和N6-甲基腺苷(N6 methyladenosine,m6A)修饰关键酶甲基转移酶样蛋白14(methyltransferase-like protein 14,METTL14)基因作为研究对象,通过纳米载体递送系统在豌豆蚜4龄若蚜中分别注射上述4个基因不同浓度(10~5 000 ng/μL, 5~250 ng/头)的dsRNA,注射后48 h时利用qRT-PCR检测这上述4个基因的表达量,筛选dsRNA最适浓度;将这4个基因的dsRNA以最适浓度通过纳米载体递送系统注射豌豆蚜4龄若蚜后12, 24, 36, 48, 60和72 h时qRT-PCR检测这4个基因的表达量,筛选纳米载体递送系统介导RNA干涉的最佳时间。【结果】与注射dsEGFP的对照组相比,豌豆蚜4龄若蚜注射50 ng/μL(25 ng/头) dsCHS2后48 h时,CHS2表达量显著下降47.5%;豌豆蚜4龄若蚜注射50~200 ng/μL(25~100 ng/头) dsMETTL14后48 h时METTL14的表达量显著下降,呈剂量依赖效应;豌豆蚜4 龄若蚜注射50 ng/μL(25 ng/头)dsVhaAC39后48 h时VhaAC39表达量显著下降53.4%,而注射dsWsa后48 h时Wsa的表达量没有显著变化。与注射dsEGFP的对照组相比,CHS2, METTL14和VhaAC39表达量均在注射靶基因dsRNA后48 h时下降最显著,Wsa在注射dsWsa后60 h时下降最显著。【结论】对豌豆蚜使用纳米载体介导的RNA干涉的dsRNA的最佳浓度约为50 ng/μL (25 ng/头),干涉效果较好的时间段为处理后48-60 h时,该研究为使用纳米递送系统实现蚜虫RNA干涉提供了参考。

关键词: 豌豆蚜, dsRNA, RNA 干涉, 纳米载体递送系统; RNA农药

Abstract: 【Aim】To assess the conditions of gene RNA interference mediated by the nanocarrier-delivery system in the pea aphid (Acyrthosiphon pisum). 【Methods】The cuticle development-related gene chitin synthase 2 (CHS2) gene, the metabolism-related enzyme vacuolar H+ATPase AC39 (VhaAC39) gene, the water-specific aquaporin (Wsa) gene and the key enzyme of N6 methyladenosine (m6A) modification methyltransferase-like protein 14 (METTL14) gene of A. pisum were selected. Different concentrations (10-5 000 ng/μL, 5-250 ng/individual) of dsRNAs of the above four genes were injected into the 4th instar nymphs of A. pisum through the nanocarrier-delivery system, and the expression levels of the above four genes at 48 h after injection were determined by qRT-PCR, to screen the optimal concentration of dsRNA. qRT-PCR was used to detect the expression levels of the above four genes at 12, 24, 36, 48, 60 and 72 h after injecting the dsRNAs of the above four genes at the optimal concentration into the 4th instar nymphs of A. pisum through the nanocarrier-delivery system, to screen the optimal time for RNA interference mediated by the nanocarrier-delivery system.【Results】The expression level of CHS2 was significantly decreased by 47.5% at 48 h after injecting 50 ng/μL (25 ng/individual) of dsCHS2 into the 4th instar nymph of A. pisum as compared to that of the control group injected with dsEGFP. The expression levels of METTL14 decreased significantly after injecting 50-500 ng/μL (25-100 ng/individual) of dsMETTL14 into the 4th instar nymphs of A. pisum as compared to that of the control group injected with dsEGFP, exhibiting a dose-dependent effect. The expression level of VhaAC39 decreased significantly by 53.4% at 48 h after injecting 50 ng/μL (25 ng/individual) of dsVhaAC39 into the 4th instar nymph of A. pisum as compared to that of the control group injected with dsEGFP, while the expression level of Wsa showed no significant change at 48 h after dsWsa injection. The expression levels of CHS2, METTL14 and VhaAC39 all decreased most significantly at 48 h after injection of dsRNAs of target genes, while the expression level of Wsa decreased most significantly at 60 h after injection of dsWsa, as compared to those in the control group injected with dsEGFP.【Conclusion】 The optimal concentration of dsRNA in RNA interference mediated by nanocarrier-delivery system is 50 ng/μL (25 ng/individual), and higher RNA interference efficiency appears at 48-60 h after treatment. This study provides new clues for aphid RNA interference with nanocarrier-delivery system.

Key words: Acyrthosiphon pisum, dsRNA, RNA interference, nanocarrier-delivery system, RNA-based pesticides