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Zeta 类谷胱甘肽 S-转移酶参与了辛硫磷的耐受,并且可能受到 CncC 转录因子在斜纹夜蛾(鳞翅目:夜蛾科)中的调控。

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

机构信息

Key Laboratory of Agri-products Quality and Biosafety, Ministry of Education, Anhui Provincial Key Laboratory of Integrated Pest Management on Crops, School of Plant Protection, Anhui Agricultural University, Hefei 230036, China.

Liangshan Branch of Sichuan Tobacco Corporation, Xichang 646600, China.

出版信息

Pestic Biochem Physiol. 2024 Sep;204:106106. doi: 10.1016/j.pestbp.2024.106106. Epub 2024 Aug 30.

DOI:10.1016/j.pestbp.2024.106106
PMID:39277410
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 (LC) 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.

摘要

黑光灯夜蛾(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,已被广泛用于防治 A. ipsilon。辛硫磷的广泛应用导致 A. ipsilon 对辛硫磷的敏感性降低。然而,A. ipsilon 对辛硫磷耐受性的分子机制尚不清楚。在这项工作中,我们报告了 AiGSTz1(一种 ζ 类谷胱甘肽 S-转移酶)参与了 A. ipsilon 对辛硫磷的耐受性。暴露于亚致死浓度(LC)的辛硫磷会显著上调 A. ipsilon 幼虫中 AiGSTz1 基因的转录水平,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 表现出抗氧化活性,以保护其免受氧化应激。通过 RNA 干扰敲低 AiGSTz1 会显著增加 A. ipsilon 幼虫对辛硫磷的死亡率。此外,转录因子 AiCncC 可以与假定的 AiGSTz1 基因启动子中的“帽和领”同种型 C:肌肉腱膜纤维瘤形成(CncC:Maf)结合位点结合。AiCncC 的沉默导致 AiGSTz1 的转录水平显著下调。这些结果表明 AiGSTz1 参与了辛硫磷的耐受性,并且可能受到 AiCncC 的调节。这些发现为 A. ipsilon 对辛硫磷的防御机制提供了有价值的见解。

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