CYP380C12在棉蚜(半翅目:蚜科)中功能的分子分析:计算机和RNAi分析。

Lianjun Zhang, Ziyan Zhuang, Jingang Xie, Wenting Kong, Tingting Li, Shengfei Wang, Xiaoning Liu
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引用次数: 0

摘要

棉蚜是造成重大经济损失的严重害虫,对新烟碱类杀虫剂的抗药性发展迅速,防治难度大。昆虫细胞色素p450在杀虫剂解毒过程中发挥着重要作用。在本研究中,我们旨在了解CYP380C12在棉蚜中的功能。对棉蚜的CYP380C12基因进行了克隆和鉴定,其相对表达量在不同的虫龄间存在差异。吡虫啉(IMI)处理48 h后,CYP380C12的表达量较水组增加48.5%。分子对接预测CYP380C12与IMI的结合自由能为-7.0 kcal/mol,表明在对接的活性位点具有良好的稳定性,并通过分子动力学模拟得到了验证。随后,在24、48和72 h, dsCYP380C12处理组CYP380C12的沉默效率分别达到48.9%、47.0%和40.0%,IMI处理棉蚜的死亡率分别是Water和dsGFP对照组的1.45倍和1.38倍。dsCYP380C12处理的蚜虫繁殖周期(9.67±0.88)显著短于水处理的(13.67±1.20)。综上所述,沉默CYP380C12基因不仅增加了棉蚜对IMI的敏感性,而且缩短了棉蚜的繁殖周期。了解CYP380C12在棉蚜中的功能,可以为制定创新的棉蚜防治策略提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular insights on the function of CYP380C12 in Aphis gossypii Glover (Hemiptera: Aphididae): in silico and RNAi analyses.

Aphis gossypii Glover is a serious pest that causes significant economic losses and is difficult to control due to the rapid development of resistance to neonicotinoids. Insect cytochrome P450s play an important role in detoxification of insecticides. In this study, we aimed to understand the function of CYP380C12 in A. gossypii. The CYP380C12 gene of A. gossypii was cloned and characterized, and its relative expression level differed among instars. The expression of CYP380C12 increased by 48.5% compared with the Water group under imidacloprid (IMI) stress for 48 h. Molecular docking predicted the binding free energy of CYP380C12 and IMI was -7.0 kcal/mol, indicating an excellent stability at the docked active site, which was verified by molecular dynamics simulations. Subsequently, silencing efficiency of CYP380C12 in the dsCYP380C12 treatment group reached 48.9%, 47.0%, and 40.0% at 24, 48, and 72 h, and the mortality of A. gossypii treated with IMI was 1.45- and 1.38-fold that of the Water and dsGFP control groups, respectively. Moreover, the reproductive period of aphids treated with dsCYP380C12 (9.67 ± 0.88) was significantly shorter than that of those sprayed with Water (13.67 ± 1.20). Taken together, these results indicated that silencing CYP380C12 not only increases sensitivity of A. gossypii to IMI but also shortens its reproductive period. Understanding the function of CYP380C12 in A. gossypii can provide new insights for developing innovative strategies to control A. gossypii.

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