Cotton plants overexpressing the Bacillus thuringiensis Cry23Aa and Cry37Aa binary-like toxins exhibit high resistance to the cotton boll weevil (Anthonomus grandis)

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Thuanne Pires Ribeiro , Diogo Martins-de-Sa , Leonardo Lima Pepino Macedo , Isabela Tristan Lourenço-Tessutti , Gustavo Caseca Ruffo , João Pedro Abreu Sousa , Julia Moura do Rósario Santana , Osmundo Brilhante Oliveira-Neto , Stéfanie Menezes Moura , Maria Cristina Mattar Silva , Carolina Vianna Morgante , Nelson Geraldo Oliveira , Marcos Fernando Basso , Maria Fatima Grossi-de-Sa
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引用次数: 0

Abstract

The cotton boll weevil (CBW, Anthonomus grandis) stands as one of the most significant threats to cotton crops (Gossypium hirsutum). Despite substantial efforts, the development of a commercially viable transgenic cotton event for effective open-field control of CBW has remained elusive. This study describes a detailed characterization of the insecticidal toxins Cry23Aa and Cry37Aa against CBW. Our findings reveal that CBW larvae fed on artificial diets supplemented exclusively with Cry23Aa decreased larval survival by roughly by 69%, while supplementation with Cry37Aa alone displayed no statistical difference compared to the control. However, the combined provision of both toxins in the artificial diet led to mortality rates approaching 100% among CBW larvae (LC50 equal to 0.26 PPM). Additionally, we engineered transgenic cotton plants by introducing cry23Aa and cry37Aa genes under control of the flower bud-specific pGhFS4 and pGhFS1 promoters, respectively. Seven transgenic cotton events expressing high levels of Cry23Aa and Cry37Aa toxins in flower buds were selected for greenhouse bioassays, and the mortality rate of CBW larvae feeding on their T0 and T1 generations ranged from 75% to 100%. Our in silico analyses unveiled that Cry23Aa displays all the hallmark characteristics of β-pore-forming toxins (β-PFTs) that bind to sugar moieties in glycoproteins. Intriguingly, we also discovered a distinctive zinc-binding site within Cry23Aa, which appears to be involved in protein-protein interactions. Finally, we discuss the major structural features of Cry23Aa that likely play a role in the toxin’s mechanism of action. In view of the low LC50 for CBW larvae and the significant accumulation of these toxins in the flower buds of both T0 and T1 plants, we anticipate that through successive generations of these transgenic lines, cotton plants engineered to overexpress cry23Aa and cry37Aa hold promise for effectively managing CBW infestations in cotton crops.

Abstract Image

过表达苏云金芽孢杆菌 Cry23Aa 和 Cry37Aa 双元样毒素的棉花植株对棉铃象鼻虫表现出很强的抗性
棉铃象鼻虫(CBW,Anthonomus grandis)是棉花作物(Gossypium hirsutum)最主要的威胁之一。尽管付出了巨大努力,但开发出商业上可行的转基因棉花以有效控制棉铃象甲的工作仍然遥遥无期。本研究描述了 Cry23Aa 和 Cry37Aa 对 CBW 杀虫毒素的详细特征。我们的研究结果表明,用完全添加 Cry23Aa 的人工饲料喂养 CBW 幼虫,幼虫存活率大约下降了 69%,而单独添加 Cry37Aa 与对照相比没有统计学差异。然而,在人工饲料中同时添加两种毒素会导致 CBW 幼虫的死亡率接近 100%(半数致死浓度为 0.26 PPM)。此外,我们还在花蕾特异性 pGhFS4 和 pGhFS1 启动子的控制下分别导入了 cry23Aa 和 cry37Aa 基因,从而构建了转基因棉花植株。在温室生物测定中筛选出了 7 个在花蕾中表达高水平 Cry23Aa 和 Cry37Aa 毒素的转基因棉花,CBW 幼虫取食其 T0 和 T1 代的死亡率从 75% 到 100% 不等。我们的硅学分析发现,Cry23Aa 具有与糖蛋白中的糖分子结合的β-孔形成毒素(β-PFTs)的所有标志性特征。有趣的是,我们还在 Cry23Aa 中发现了一个独特的锌结合位点,它似乎参与了蛋白质与蛋白质之间的相互作用。最后,我们讨论了 Cry23Aa 的主要结构特征,这些特征可能在该毒素的作用机制中发挥作用。鉴于 CBW 幼虫的半数致死浓度较低,以及这些毒素在 T0 和 T1 植株花蕾中的大量积累,我们预计通过这些转基因品系的连续世代,过量表达 cry23Aa 和 cry37Aa 的棉花植株有望有效控制棉花作物中的 CBW 虫害。
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来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
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