RNA干扰介导的缺氧诱导因子1信号通路基因沉默增强了褐腿粒螨的缺氧敏感性。

IF 3.8 1区 农林科学 Q1 AGRONOMY
Yang Zou,Hui Ai,Gang Miao,Yudie Hu,Hejun Liu,Bin Xia,Tianrong Xin,Zhiwen Zou
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引用次数: 0

摘要

背景变态反应原和贮藏害虫卵形异叶蚜(Aleuroglyphus ovatus, Troupeau, 1878)威胁人类健康和食品安全。虽然改良空气具有防治害虫的潜力,但其对该物种的效果尚未得到证实。本研究旨在探讨氮诱导的缺氧对卵圆按蚊死亡率、发育及缺氧反应机制的影响,为制定针对性的防治策略提供科学依据。卵虫死亡率随长时间缺氧暴露和氧浓度降低而增加。缺氧处理1 d后,2% O2条件下孵化率降至60.85%,5% O2条件下孵化率保持稳定。与正常对照组相比,未成熟阶段的发育延迟分别为2.51天(5% O2)和3.12天(2% O2)。缺氧诱导因子1 (HIF1)信号通路——包括HIF1α、HIF1β和HIF1博士——显示出进化上保守的功能,所有三个基因的同步表达模式表明反馈介导的共调控。至关重要的是,针对所有三个基因的RNA干扰分别提高了成人死亡率,与未干扰组相比,在5%和2% O2下分别增加了1.67-2.06倍和2.19-2.88倍。卵子中靶向HIF1α的干扰也导致胚胎发育和孵化受到抑制。结论低氧条件下卵圆按蚊的死亡加速、发育迟缓和途径协同调控,暴露了卵圆按蚊的脆弱性,可用于害虫防治。数据证实,将大气控制与靶向这三种基因中的任何一种的单基因RNAi相结合,可提高致死率。本研究对节肢动物HIF1信号通路的缺氧反应进行了系统的解剖,建立了生态干预与分子沉默相结合的跨学科策略,为害虫的可持续防治提供了理论基础。©2025化学工业协会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA interference-mediated silencing of hypoxia-inducible factor 1 signaling pathway genes enhanced the hypoxia sensitivity in the brown-legged grain mite, Aleuroglyphus ovatus.
BACKGROUND The allergen and storage pest Aleuroglyphus ovatus (Troupeau, 1878) threatens human health and food safety. While modified atmosphere shows pest control potential, its efficacy against this species remains unverified. This study evaluates nitrogen-induced hypoxia effects on A. ovatus mortality, development, and hypoxia-response mechanisms to establish a scientific basis for targeted control strategies. RESULTS A. ovatus mortality increased with prolonged hypoxia exposure and reduced oxygen concentrations. Following 1-day hypoxia treatment, hatchability declined to 60.85% of control levels under 2% O2, whereas it remained stable at 5% O2. Developmental delays of 2.51 days (5% O2) and 3.12 days (2% O2) were observed in total immature stages compared to normoxic controls. The hypoxia-inducible factor 1 (HIF1) signaling pathway-comprising HIF1α, HIF1β, and PHD-demonstrated evolutionarily conserved functionality, with synchronous expression patterns across all three genes suggesting feedback-mediated co-regulation. Crucially, RNA interference respectively targeting all three genes enhanced adult mortality, achieving 1.67-2.06-fold and 2.19-2.88-fold increases at 5% and 2% O2, compared to non-interference groups. Interference targeting HIF1α in eggs also resulted in suppressed embryonic development and hatching. CONCLUSION Mortality acceleration, developmental delays, and pathway co-regulation under hypoxia expose vulnerabilities of A. ovatus exploitable for pest management. Data confirm that combining atmospheric controls with single-gene RNAi targeting any of these three genes enhances lethality. As a systematic dissection of the HIF1 signaling pathway's hypoxic response in arthropods-a rarely explored area-this work established an interdisciplinary strategy integrating ecological interventions and molecular silencing, providing a theoretical basis for sustainable pest control. © 2025 Society of Chemical Industry.
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来源期刊
Pest Management Science
Pest Management Science 农林科学-昆虫学
CiteScore
7.90
自引率
9.80%
发文量
553
审稿时长
4.8 months
期刊介绍: Pest Management Science is the international journal of research and development in crop protection and pest control. Since its launch in 1970, the journal has become the premier forum for papers on the discovery, application, and impact on the environment of products and strategies designed for pest management. Published for SCI by John Wiley & Sons Ltd.
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