Insecticide-induced sublethal effect in the fall armyworm is mediated by miR-9993/miR-2a-3p - FPPS/JHAMT - JH molecular module

IF 4.2 1区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aiyu Wang , Yuanxue Yang , Yun Zhang , Chao Xue , Yinjie Cheng , Yifei Zhang , Wenjuan Zhang , Ming Zhao , Jianhua Zhang
{"title":"Insecticide-induced sublethal effect in the fall armyworm is mediated by miR-9993/miR-2a-3p - FPPS/JHAMT - JH molecular module","authors":"Aiyu Wang ,&nbsp;Yuanxue Yang ,&nbsp;Yun Zhang ,&nbsp;Chao Xue ,&nbsp;Yinjie Cheng ,&nbsp;Yifei Zhang ,&nbsp;Wenjuan Zhang ,&nbsp;Ming Zhao ,&nbsp;Jianhua Zhang","doi":"10.1016/j.pestbp.2025.106400","DOIUrl":null,"url":null,"abstract":"<div><div>The sublethal effect of insecticides can affect the population dynamics of pests by changing the physiological or behavioral changes, which poses a serious threat to the sustainable control of crop pests in the field. However, the molecular regulation mechanism that mediates the sublethal effect of insecticides on crop pests remains unsolved. Here, we show that the sublethal effect of spinetoram and cyantraniliprole on <em>Spodoptera frugiperda</em> is mediated by the molecular module of microRNA-9993/microRNA-2a-3p - farnesyl diphosphate synthase gene (<em>FPPS</em>)/juvenile hormone (JH) acid methyltransferase gene (<em>JHAMT</em>) - JH. Spinetoram prolonged the duration of larvae and pupae, decreased the weight of pupae, while cyantraniliprole prolonged the duration of larvae and decreased the emergence rate. Similarly, injection of the juvenile hormone analogue (JHA) methoprene significantly prolonged the developmental duration of larvae and pupae, decreased the pupal weight and emergence rate. This sublethal phenotypic change was due to the upregulation of key JH synthesis genes, including <em>FPPS</em> and <em>JHAMT</em>, mediated by spinetoram and cyantraniliprole, resulting in an increase in JH titer. Furthermore, it was confirmed by small RNA sequencing, dual luciferase analysis and agomir-miRNA injection, miR-9993 and miR-2a-3p that it could bind <em>FPPS</em> and <em>JHAMT</em> respectively, and regulated the expression level of <em>FPPS</em> and <em>JHAMT</em> to affect the titer of JH, thus changing the phenotype of <em>S. frugiperda</em>. Collectively, these results provide insights into the mechanism of insecticide regulation of sublethal effects of pests, expand our understanding of development-related miRNAs, and reveal key factors involved in JH signaling pathways that support sublethal effects of insecticides.</div></div>","PeriodicalId":19828,"journal":{"name":"Pesticide Biochemistry and Physiology","volume":"210 ","pages":"Article 106400"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pesticide Biochemistry and Physiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0048357525001130","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The sublethal effect of insecticides can affect the population dynamics of pests by changing the physiological or behavioral changes, which poses a serious threat to the sustainable control of crop pests in the field. However, the molecular regulation mechanism that mediates the sublethal effect of insecticides on crop pests remains unsolved. Here, we show that the sublethal effect of spinetoram and cyantraniliprole on Spodoptera frugiperda is mediated by the molecular module of microRNA-9993/microRNA-2a-3p - farnesyl diphosphate synthase gene (FPPS)/juvenile hormone (JH) acid methyltransferase gene (JHAMT) - JH. Spinetoram prolonged the duration of larvae and pupae, decreased the weight of pupae, while cyantraniliprole prolonged the duration of larvae and decreased the emergence rate. Similarly, injection of the juvenile hormone analogue (JHA) methoprene significantly prolonged the developmental duration of larvae and pupae, decreased the pupal weight and emergence rate. This sublethal phenotypic change was due to the upregulation of key JH synthesis genes, including FPPS and JHAMT, mediated by spinetoram and cyantraniliprole, resulting in an increase in JH titer. Furthermore, it was confirmed by small RNA sequencing, dual luciferase analysis and agomir-miRNA injection, miR-9993 and miR-2a-3p that it could bind FPPS and JHAMT respectively, and regulated the expression level of FPPS and JHAMT to affect the titer of JH, thus changing the phenotype of S. frugiperda. Collectively, these results provide insights into the mechanism of insecticide regulation of sublethal effects of pests, expand our understanding of development-related miRNAs, and reveal key factors involved in JH signaling pathways that support sublethal effects of insecticides.

Abstract Image

杀虫剂的亚致死效应可通过改变害虫的生理或行为变化来影响害虫的种群动态,对田间作物害虫的可持续控制构成严重威胁。然而,介导杀虫剂对农作物害虫亚致死效应的分子调控机制仍未得到解决。在此,我们发现斯派诺胺和氰虫酰胺对鞘翅目害虫的亚致死效应是由 microRNA-9993 / microRNA-2a-3p - 法尼酰二磷酸合成酶基因(FPPS)/幼虫激素(JH)酸甲基转移酶基因(JHAMT) - JH 的分子模块介导的。辛硫磷延长了幼虫和蛹的存活时间,降低了蛹的重量,而氰虫腈延长了幼虫的存活时间,降低了出苗率。同样,注射幼虫激素类似物(JHA)甲氧苄啶可显著延长幼虫和蛹的发育期,降低蛹的重量和出苗率。这种亚致死性表型变化是由于斯皮内酯和氰戊菊酯介导的关键 JH 合成基因(包括 FPPS 和 JHAMT)上调,导致 JH 滴度增加。此外,通过小 RNA 测序、双荧光素酶分析和注射 agomir-miRNA 证实,miR-9993 和 miR-2a-3p 可分别与 FPPS 和 JHAMT 结合,并调控 FPPS 和 JHAMT 的表达水平,从而影响 JH 的滴度,进而改变 S. frugiperda 的表型。总之,这些研究结果为了解杀虫剂调控害虫亚致死效应的机制提供了新的视角,拓展了我们对发育相关miRNAs的认识,并揭示了JH信号通路中支持杀虫剂亚致死效应的关键因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
7.00
自引率
8.50%
发文量
238
审稿时长
4.2 months
期刊介绍: Pesticide Biochemistry and Physiology publishes original scientific articles pertaining to the mode of action of plant protection agents such as insecticides, fungicides, herbicides, and similar compounds, including nonlethal pest control agents, biosynthesis of pheromones, hormones, and plant resistance agents. Manuscripts may include a biochemical, physiological, or molecular study for an understanding of comparative toxicology or selective toxicity of both target and nontarget organisms. Particular interest will be given to studies on the molecular biology of pest control, toxicology, and pesticide resistance. Research Areas Emphasized Include the Biochemistry and Physiology of: • Comparative toxicity • Mode of action • Pathophysiology • Plant growth regulators • Resistance • Other effects of pesticides on both parasites and hosts.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信