Zeta class glutathione S-transferase is involved in phoxim tolerance and is potentially regulated by the transcription factor CncC in Agrotis ipsilon (Lepidoptera: Noctuidae)

IF 4.2 1区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pesticide Biochemistry and Physiology Pub Date : 2024-09-01 DOI:10.1016/j.pestbp.2024.106106
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Abstract

The black cutworm, Agrotis ipsilon (Lepidoptera: Noctuidae), is an important agricultural pest. Phoxim is an organophosphate insecticide that has been widely used to control A. ipsilon. The extensive application of phoxim has resulted in a reduction in phoxim susceptibility in A. ipsilon. However, the molecular mechanisms underlying phoxim tolerance in A. ipsilon remain unclear. In this work, we report the involvement of AiGSTz1, a zeta class glutathione S-transferase, in phoxim tolerance in A. ipsilon. Exposure to a sublethal concentration (LC50) of phoxim dramatically upregulated the transcription level of the AiGSTz1 gene in A. ipsilon larvae, and this upregulation might be caused by phoxim-induced oxidative stress. The recombinant AiGSTz1 protein expressed in Escherichia coli was able to metabolize phoxim. Furthermore, AiGSTz1 displayed antioxidant activity to protect against oxidative stress. Knockdown of AiGSTz1 by RNA interference significantly increased the mortality rate of A. ipsilon larvae in response to phoxim. In addition, the transcription factor AiCncC can bind to the cap ‘n’ collar isoform C: muscle aponeurosis fibromatosis (CncC:Maf) binding site in the putative promoter of the AiGSTz1 gene. Silencing of AiCncC resulted in a dramatic downregulation of AiGSTz1. These results indicated that AiGSTz1 is involved in phoxim tolerance and is potentially regulated by AiCncC. These findings provide valuable insights into the defense mechanisms used by A. ipsilon against phoxim.

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Zeta 类谷胱甘肽 S 转移酶参与辛硫磷耐受性,并可能受 Agrotis ipsilon(鳞翅目:夜蛾科)转录因子 CncC 的调控
黑节虫(鳞翅目:夜蛾科)是一种重要的农业害虫。辛硫磷是一种有机磷杀虫剂,已被广泛用于控制黑刺蛾。辛硫磷的广泛应用降低了同翅目蚜虫对辛硫磷的敏感性。然而,同翅目蚜虫对辛硫磷耐受性的分子机制仍不清楚。在这项工作中,我们报告了 AiGSTz1(一种 zeta 类谷胱甘肽 S 转移酶)参与了 A. ipsilon 对辛硫磷耐受性的研究。暴露于亚致死浓度(LC50)的辛硫磷会显著上调 A. ipsilon 幼虫体内 AiGSTz1 基因的转录水平,而这种上调可能是由辛硫磷诱导的氧化应激引起的。在大肠杆菌中表达的重组 AiGSTz1 蛋白能够代谢辛硫磷。此外,AiGSTz1 还具有抗氧化活性,可抵御氧化应激。通过 RNA 干扰敲除 AiGSTz1 能显著提高 A. ipsilon 幼虫对辛硫磷的死亡率。此外,转录因子 AiCncC 可与 AiGSTz1 基因推定启动子中的帽'n'领异构体 C:肌腱膜纤维瘤病(CncC:Maf)结合位点结合。沉默 AiCncC 会导致 AiGSTz1 的显著下调。这些结果表明,AiGSTz1 参与了辛硫磷耐受性的作用,并可能受 AiCncC 的调控。这些发现为了解 A. ipsilon 对辛硫磷的防御机制提供了宝贵的信息。
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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.
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