Institute of Microbiology, College of Life Sciences, Zhejiang University, Hangzhou, China.
College of Advanced Agricultural Sciences, Zhejiang A&F University, Hangzhou, China.
Pest Manag Sci. 2022 Jul;78(7):3164-3172. doi: 10.1002/ps.6946. Epub 2022 May 11.
Fungal insecticides are notorious for slow kill action, an intrinsic trait that can be improved by the genetic engineering of an exogenous or endogenous virulence factor. However, transgenic insecticides expressing exogenous toxin and herbicide-resistant marker genes may cause unexpected ecological risks and are hardly permitted for field release due to strict regulatory hurdles. It is necessary to improve biotechnology that can speed up fungal insect-killing action and exclude ecological risk source.
A markerless transformation system of Beauveria bassiana, a main source of wide-spectrum fungal insecticides, was reconstructed based on the fungal uridine auxotrophy (Δura3). The system was applied for overexpression of the small cysteine-free protein (120 amino acids) gene cfp previously characterized as a regulator of the fungal virulence and gene expression. Three cfp-overexpressed strains showed much faster kill action to Galleria mellonella larvae than the parental wild-type via normal cuticle infection but no change in vegetative growth and aerial condition. The faster kill action was achieved due to not only significant increases in conidial adherence to insect cuticle and total activity of secreted cuticle-degrading Pr1 proteases and of antioxidant enzymes crucial for collapse of insect immune defense but acceleration of hemocoel localization, proliferation in vivo and host death from mummification.
The markerless system is free of any foreign DNA fragment as a source of ecologic risk and provides a novel biotechnological approach to enhancing fungal insecticidal activity with non-risky endogenous genes and striding over the regulatory hurdles. © 2022 Society of Chemical Industry.
真菌杀虫剂以缓慢的杀虫作用而臭名昭著,这种内在特性可以通过遗传工程改造外源或内源性毒力因子来改善。然而,表达外源毒素和除草剂抗性标记基因的转基因杀虫剂可能会带来意想不到的生态风险,由于严格的监管障碍,几乎不可能获准野外释放。有必要改进生物技术,以加快真菌杀虫作用并排除生态风险源。
基于真菌尿嘧啶营养缺陷型(Δura3),重建了广谱真菌杀虫剂的主要来源球孢白僵菌的无标记转化系统。该系统用于过表达先前被表征为真菌毒力和基因表达调节剂的小胱氨酸自由蛋白(120 个氨基酸)基因 cfp。与亲本野生型相比,通过正常的表皮感染,三个 cfp 过表达菌株对家蚕幼虫的致死作用明显加快,但营养生长和空气条件没有变化。更快的致死作用不仅归因于分生孢子对昆虫表皮的附着显著增加,以及分泌的表皮降解 Pr1 蛋白酶和对昆虫免疫防御崩溃至关重要的抗氧化酶的总活性显著增加,还归因于血腔定位、体内增殖和宿主因木乃伊化而死亡的加速。
无标记系统不含任何外源 DNA 片段,作为生态风险的来源,为利用非风险内源基因增强真菌杀虫活性提供了一种新的生物技术方法,并跨越了监管障碍。© 2022 化学工业学会。