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A microRNA, PC-5p-30_205949, regulates triflumezopyrim susceptibility in Laodelphax striatellus (Fallen) by targeting CYP419A1 and ABCG23

文献类型： 外文期刊

作者： Wang, Aiyu 1 ; Yang, Yuanxue 1 ; Zhou, Yun 1 ; Zhang, Yun 1 ; Xue, Chao 1 ; Zhao, Yongxin 3 ; Zhao, Ming 1 ; Zhang, Jianhua 1 ;

作者机构： 1.Shandong Acad Agr Sci, Inst Ind Crops, Jinan 250100, Peoples R China

2.Shandong Acad Agr Sci, Yellow River Delta Modern Agr Res Inst, Dongying, Peoples R China

3.Shandong Prov Yuncheng Cty Agr & Rural Bur, Yuncheng, Peoples R China

关键词： Laodelphax striatellus; Triflumezopyrim; PC-5p-30_205949; ABCG23

期刊名称：PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY （ 影响因子：4.7； 五年影响因子：4.7 ）

ISSN： 0048-3575

年卷期： 2023 年 192 卷

页码：

收录情况： SCI

摘要： MicroRNAs (miRNAs) are known to be important post-transcriptional regulators of gene expression and have been shown to be associated with insecticide resistance in insects. In this research, we show that a miRNA, PC-5p30_205949, is involved in triflumezopyrim susceptibility via regulating expressive abundance of cytochrome P450 CYP419A1 and ATP-binding cassette transporters ABCG23 in the small brown planthopper (SBPH), Laodelphax striatellus (Falle & PRIME;n). Triflumezopyrim treatment significantly reduced the abundance of PC-5p-30_205949, feeding of agomir-PC-5p-30_205949 significantly increased the sensitivity of SBPH to triflumezopyrim, and its spatiotemporal expression profiles showed that PC-5p-30_205949 were expressed at all developmental stages and were highly expressed in head tissue. By software prediction and dual luciferase reporter assay, the target genes of PC-5p-30_205949 were identified as two detoxification metabolism genes CYP419A1 and ABCG23. The relative expressions of CYP419A1 and ABCG23 were significantly up-regulated after 24 h, 48 h and 72 h with triflumezopyrim exposure. CYP419A1 was highly expressed in the 4th-instar nymphs and male adults, with the highest expression level in fat body. ABCG23 was highly expressed in female adults, and had the highest expression in head. Furthermore, silencing of CYP419A1 and ABCG23 by RNA interference significantly increased the mortality of SBPH to triflumezopyrim, and molecular docking showed that CYP419A1 and ABCG23 could stably bind to triflumezopyrim with binding free energies of -171.5622 and - 103.3402 kcal mol-1, respectively. These results suggest that SBPH has a strategy to enhance the resistance to triflumezopyrim by attenuating the expression of PC-5P-30_205949, thereby activating the detoxification metabolic pathway by targeting CYP419A1 and ABCG23.

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