Knockout of chitin synthase gene confers resistance to Bt toxin Vip3Aa in Helicoverpa zea.
IF 3.8
1区 农林科学
Q1 AGRONOMY
Chan C Heu,Inana X Schutze,Dannialle M LeRoy,Yu-Hui Wang,Ben A DeGain,Dawson D Kerns,Heba Abdelgaffar,Juan Luis Jurat-Fuentes,Luciano M Matzkin,Yves Carrière,Bruce E Tabashnik,Jeffrey A Fabrick
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Abstract
BACKGROUND
Genetically engineered crops that produce insecticidal proteins from Bacillus thuringiensis (Bt) have many benefits and are used globally to manage key insect pests, including Helicoverpa zea (Lepidoptera: Noctuidae), a major pest of crops in the Americas. However, pests of at least 11 species, including H. zea, have evolved resistance to Bt crops, diminishing their effectiveness and benefits. For H. zea in the United States, practical resistance to Bt corn and cotton producing crystalline (Cry) Bt proteins is widespread and early warning of resistance to the vegetative insecticidal protein Vip3Aa has been reported. Thus, a better understanding of the genetic basis of resistance to Vip3Aa is needed to monitor, manage and counter resistance. In some strains of lepidopteran pests, resistance to Vip3Aa is associated with disruptive mutations in the chitin synthase 2 (CHS2) gene but this association had not been investigated previously in H. zea.
RESULTS
Here, we show that mutations introduced by CRISPR/Cas9 editing of the CHS2 gene can cause resistance to Vip3A in H. zea. Disruptive mutations in CHS2 facilitated the creation of strain CHS2-KO that had 29 000-fold resistance to Vip3Aa relative to its unedited parental susceptible strain. Resistance to Vip3Aa in CHS2-KO was autosomal, recessive, and did not cause cross-resistance to Cry1Ac or Cry2Ab.
CONCLUSION
Results of this study indicate that CHS2 plays an important role in Vip3Aa intoxication in H. zea. It will be important to determine if mutations in CHS2 contribute to field-evolved resistance to Vip3Aa in H. zea and other pests. © 2025 Society of Chemical Industry. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.
敲除几丁质合成酶基因使玉米对Bt毒素Vip3Aa产生抗性。
从苏云金芽孢杆菌(Bt)中产生杀虫蛋白的基因工程作物有许多好处,并在全球范围内用于控制主要害虫,包括美洲作物的主要害虫玉米螺旋虫(鳞翅目:夜蛾科)。然而,至少有11种害虫,包括玉米蚜,已经进化出对Bt作物的抗性,降低了它们的有效性和效益。在美国,对Bt玉米和棉花产生结晶Bt蛋白的玉米和棉花的实际抗性普遍存在,并且已经报道了对营养杀虫蛋白Vip3Aa产生抗性的早期预警。因此,需要更好地了解对Vip3Aa抗性的遗传基础,以监测、管理和对抗抗性。在鳞翅目害虫的某些品系中,对Vip3Aa的抗性与几丁质合成酶2 (CHS2)基因的破坏性突变有关,但这种关联先前未在玉米玉米中研究过。结果通过CRISPR/Cas9编辑CHS2基因引入的突变可引起玉米h.s zea对Vip3A的抗性。CHS2的破坏性突变促进了菌株CHS2- ko的产生,该菌株对Vip3Aa的抗性是未经编辑的亲本易感菌株的29000倍。CHS2-KO对Vip3Aa的抗性是常染色体隐性的,不引起对Cry1Ac或Cry2Ab的交叉抗性。结论CHS2在玉米Vip3Aa中毒过程中起重要作用。确定CHS2突变是否有助于玉米和其他害虫对Vip3Aa的田间进化抗性将是重要的。©2025化学工业协会。这篇文章是由美国政府雇员贡献的,他们的工作在美国属于公有领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。