Todd Ciche, William Moar, Aqeel Ahmad, David Bowen, Catherine Chay, Arlene Howe, Uma Kesanapalli, Jennifer Lutke, Gregory Bean, Jason Milligan, Michael Pleau, Yong Yin, Waseem Akbar, Marty Heppler, Cara Griffith, Kimberly Morrell, Katherine Dunkmann, Heather Anderson, Jeffrey Ahrens, Pacifica Sommers, E Sethe Burgie, Fred Zinnel, Meiying Zheng, James Fitzpatrick, Michael Rau, Timothy Rydel, Tommi White, David Kerns, James Roberts
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We hypothesized that diversifying our search for proteins into non-Bt organisms, such as those related to <i>Paenibacillus popilliae,</i> used to control Japanese beetle <i>Popillia japonica</i>, could yield proteins with new insecticidal activities against Lepidoptera. Here, we identified Vip3Cb1 and Vip3Cc1 with broad lepidopteran activity, the first Vip3 proteins discovered from strains in the <i>P. popilliae-</i>containing clade. Vip3Cb1 protected plants against cotton bollworm, <i>Helicoverpa zea</i> and tobacco budworm<i>, Chloridea virescens</i> and <i>H. zea,</i> fall armyworm, <i>Spodoptera frugiperda</i>, and Southwestern corn borer, <i>Diatraea grandiosella</i>, in cotton and maize, respectively, like commercial Vip3Aa. Distinct from Vip3Aa, Vip3Cb1 also protected maize against European corn borer, <i>Ostrinia nubilalis</i>, the primary maize pest in the United States, with recent reports of resistance to Bt proteins. Consistent with previous reports, insects resistant to Vip3Aa were cross-resistant to Vip3Cb1. Cryo-electron microscopy demonstrated that Vip3Cb1 formed a pore-shaped tetramer upon proteolytic activation, in agreement with the pore-forming mechanism of action of Vip3Aa. Thus, diversifying the search beyond Bt has led to the discovery of the first Vip3 proteins from <i>Paenibacillus</i> spp. with different activity spectra from Vip3Aa, providing additional tools to control pests, including those currently resistant to Bt Cry proteins.IMPORTANCENew insecticidal proteins are needed for controlling insect pests that can devastate crop yield if left uncontrolled. Diversifying our search for new insecticidal proteins in <i>Paenibacillus</i> spp. resulted in the discovery of Vip3Cb1 and Vip3Cc1 insecticidal proteins active against lepidopteran crop pests. Structure and cross-resistance studies indicate overlap in the mechanism of action between Vip3Cb1 and commercial Vip3Aa. 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引用次数: 0
摘要
需要新的蛋白质来控制不受苏云金芽孢杆菌(Bt)作物控制的昆虫,以及那些对Bt作物产生抗性的昆虫。越来越多的报道称,这些蛋白质来自非bt生物,用于控制抗bt昆虫。然而,这些蛋白主要控制玉米根虫,Diabrotica spp.(鞘翅目),而大多数抗bt昆虫是鳞翅目。我们假设,将我们的蛋白质搜索多样化到非bt生物中,例如与用于控制日本甲虫Popillia japonica的popilliae Paenibacillus相关的蛋白质,可以产生具有新的杀虫活性的鳞翅目蛋白质。在这里,我们鉴定了具有广泛鳞翅目活性的Vip3Cb1和Vip3Cc1,这是在含有P. popilliae的分支中发现的第一个Vip3蛋白。Vip3Cb1与商品Vip3Aa一样,分别对棉花和玉米的棉铃虫、玉米Helicoverpa and tobacco budworm、绿绿绿蝇clidea and H. zea、秋粘虫Spodoptera frugiperda和西南玉米螟Diatraea granosella具有保护作用。与Vip3Aa不同的是,Vip3Cb1还保护玉米免受欧洲玉米螟(Ostrinia nubilalis)的侵害,这是美国的主要玉米害虫,最近有报道称对Bt蛋白具有抗性。与先前的报道一致,对Vip3Aa具有抗性的昆虫对Vip3Cb1具有交叉抗性。低温电镜显示,Vip3Cb1在蛋白水解激活后形成了一个孔型四聚体,这与Vip3Aa的成孔机制一致。因此,除了Bt之外,多样化的搜索已经导致从Paenibacillus sp.中发现了第一个与Vip3Aa具有不同活性谱的Vip3蛋白,为控制害虫提供了额外的工具,包括那些目前对Bt Cry蛋白具有抗性的害虫。重要的是,需要新的杀虫蛋白来控制害虫,如果不加以控制,害虫会破坏作物产量。我们在拟芽孢杆菌中寻找新的杀虫蛋白,结果发现了对鳞翅目作物害虫有活性的Vip3Cb1和Vip3Cc1杀虫蛋白。结构和交叉抗性研究表明Vip3Cb1和商业Vip3Aa在作用机制上有重叠。然而,新的活动,如控制欧洲玉米螟,使这些蛋白质成为昆虫控制工具箱中的重要新工具。
Vip3C proteins from Paenibacillus spp. for controlling lepidopteran crop pests.
New proteins are needed to control insects not controlled with Bacillus thuringiensis (Bt) crops, and those evolving resistance to Bt crops. These proteins are increasingly being reported from non-Bt organisms to control Bt-resistant insects. However, these proteins mostly control the corn rootworm, Diabrotica spp. (Coleoptera), whereas most Bt-resistant insects are lepidopteran. We hypothesized that diversifying our search for proteins into non-Bt organisms, such as those related to Paenibacillus popilliae, used to control Japanese beetle Popillia japonica, could yield proteins with new insecticidal activities against Lepidoptera. Here, we identified Vip3Cb1 and Vip3Cc1 with broad lepidopteran activity, the first Vip3 proteins discovered from strains in the P. popilliae-containing clade. Vip3Cb1 protected plants against cotton bollworm, Helicoverpa zea and tobacco budworm, Chloridea virescens and H. zea, fall armyworm, Spodoptera frugiperda, and Southwestern corn borer, Diatraea grandiosella, in cotton and maize, respectively, like commercial Vip3Aa. Distinct from Vip3Aa, Vip3Cb1 also protected maize against European corn borer, Ostrinia nubilalis, the primary maize pest in the United States, with recent reports of resistance to Bt proteins. Consistent with previous reports, insects resistant to Vip3Aa were cross-resistant to Vip3Cb1. Cryo-electron microscopy demonstrated that Vip3Cb1 formed a pore-shaped tetramer upon proteolytic activation, in agreement with the pore-forming mechanism of action of Vip3Aa. Thus, diversifying the search beyond Bt has led to the discovery of the first Vip3 proteins from Paenibacillus spp. with different activity spectra from Vip3Aa, providing additional tools to control pests, including those currently resistant to Bt Cry proteins.IMPORTANCENew insecticidal proteins are needed for controlling insect pests that can devastate crop yield if left uncontrolled. Diversifying our search for new insecticidal proteins in Paenibacillus spp. resulted in the discovery of Vip3Cb1 and Vip3Cc1 insecticidal proteins active against lepidopteran crop pests. Structure and cross-resistance studies indicate overlap in the mechanism of action between Vip3Cb1 and commercial Vip3Aa. However, new activities, such as controlling European corn borer, make these proteins important new tools in the insect control toolbox.
期刊介绍:
Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.