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新型中肠胰蛋白酶原激活基因表达量降低与(L.)实验室选择品系对 Cry1Ac 抗性相关。

Reduced Expression of a Novel Midgut Trypsin Gene Involved in Protoxin Activation Correlates with Cry1Ac Resistance in a Laboratory-Selected Strain of (L.).

机构信息

College of Plant Protection, Hunan Agricultural University, Changsha 410125, China.

Department of Plant Protection, Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

出版信息

Toxins (Basel). 2020 Jan 23;12(2):76. doi: 10.3390/toxins12020076.

Abstract

(Bt) produce diverse insecticidal proteins to kill insect pests. Nevertheless, evolution of resistance to Bt toxins hampers the sustainable use of this technology. Previously, we identified down-regulation of a trypsin-like serine protease gene in the midgut transcriptome and RNA-Seq data of a laboratory-selected Cry1Ac-resistant strain, SZ-R. We show here that reduced PxTryp_SPc1 expression significantly reduced caseinolytic and trypsin protease activities affecting Cry1Ac protoxin activation, thereby conferring higher resistance to Cry1Ac protoxin than activated toxin in SZ-R strain. Herein, the full-length cDNA sequence of gene was cloned, and we found that it was mainly expressed in midgut tissue in all larval instars. Subsequently, we confirmed that the gene was significantly decreased in SZ-R larval midgut and was further reduced when selected with high dose of Cry1Ac protoxin. Moreover, down-regulation of the gene was genetically linked to resistance to Cry1Ac in the SZ-R strain. Finally, RNAi-mediated silencing of gene expression decreased larval susceptibility to Cry1Ac protoxin in the susceptible DBM1Ac-S strain, supporting that low expression of gene is involved in Cry1Ac resistance in . These findings contribute to understanding the role of midgut proteases in the mechanisms underlying insect resistance to Bt toxins.

摘要

苏云金芽孢杆菌(Bt)产生多种杀虫蛋白以杀死害虫。然而,对 Bt 毒素的抗性进化阻碍了这项技术的可持续使用。此前,我们在实验室选择的 Cry1Ac 抗性品系 SZ-R 的中肠转录组和 RNA-Seq 数据中发现一种胰蛋白酶样丝氨酸蛋白酶基因的下调。我们在这里表明,PxTryp_SPc1 表达的减少显著降低了酪蛋白水解和胰蛋白酶活性,从而影响 Cry1Ac 原毒素的激活,因此与 SZ-R 菌株中的激活毒素相比,该品系对 Cry1Ac 原毒素具有更高的抗性。在此,克隆了基因的全长 cDNA 序列,我们发现它在所有幼虫龄期的中肠组织中主要表达。随后,我们证实该基因在 SZ-R 幼虫中肠组织中显著下调,当用高剂量的 Cry1Ac 原毒素选择时,其表达进一步降低。此外,基因的下调与 SZ-R 品系对 Cry1Ac 的抗性遗传相关。最后,RNAi 介导的基因表达沉默降低了敏感的 DBM1Ac-S 品系幼虫对 Cry1Ac 原毒素的敏感性,这表明基因的低表达参与了 对 Cry1Ac 的抗性。这些发现有助于理解中肠蛋白酶在昆虫对 Bt 毒素抗性机制中的作用。

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