草履虫通过 nhr-31 转录因子和液泡型 ATPase 途径对 Cry14A 系列苏云金芽孢杆菌晶体蛋白产生抗性。

IF 5.5 1区 医学 Q1 MICROBIOLOGY
PLoS Pathogens Pub Date : 2024-10-18 eCollection Date: 2024-10-01 DOI:10.1371/journal.ppat.1012611
Youmie Kim, Thanh-Thanh Nguyen, Daniel J Durning, Takao Ishidate, Ozkan Aydemir, Craig C Mello, Yan Hu, Theodore W Kahn, Raffi V Aroian
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引用次数: 0

摘要

苏云金芽孢杆菌(Bt)用于害虫的生物防治已有 60 多年的商业历史。自 1996 年以来,表达 Bt 晶体(Cry)蛋白的转基因植物已用于商业用途,为捕食玉米和棉花的昆虫提供保护。最近,又发现了针对线虫的 Bt Cry 蛋白。其中一种 Cry14Ab 已在转基因大豆植株中表达,并发现它能显著抵御大豆胞囊线虫 Heterodera glycines。然而,迄今为止还没有关于线虫对任何 Cry14A 家族蛋白具有高水平抗性的描述。在此,我们介绍了利用线虫秀丽隐杆线虫(Caenorhabditis elegans)进行正向遗传筛选以确定此类突变体的方法。虽然非条件筛选未能发现高抗性秀丽隐杆线虫,但条件(温度敏感)遗传筛选发现了一个突变体 bre-6(ye123)(表示对 Bt 蛋白抗性),它对 Cry14Aa 和 Cry14Ab 都具有高抗性。bre-6(ye123)雌雄同体对铜中毒的抗性很弱,这表明该突变体并非对所有损伤都有很强的抗性。通过回交-全基因组测序,确定了 ye123 突变的基因为核激素受体 nhr-31。RNAi、DNA挽救和CRISPR分析证实,bre-6(ye123)对Cry14Aa中毒的抗性是由于nhr-31的突变,并将其更名为nhr-31(ye123)。正如对该基因突变的预测,nhr-31(ye123)动物表现出明显的秀丽隐杆线虫液泡 ATPase(vATPase)大部分亚基表达减少。vATPase 亚基 unc-32 和 vha-7 的突变体也表现出对 Cry14Aa 和/或 Cry14Ab 的抗性。这些数据表明,nhr-31 和 vATPase 在 Cry14A 家族蛋白对秀丽隐杆线虫的毒害中起着重要作用,vATPase 水平的降低会导致秀丽隐杆线虫对 Cry14A 家族蛋白的高度抗性,而这种抗性是以较高的适应性为代价的。基于寻找抗性突变体的相对难度以及与 vATPase 途径相关的适应性成本,我们的数据表明,转基因 Cry14Ab 植物可以很好地抵抗线虫寄生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resistance to Cry14A family Bacillus thuringiensis crystal proteins in Caenornabditis elegans operates via the nhr-31 transcription factor and vacuolar-type ATPase pathway.

Bacillus thuringiensis (Bt) has been successfully used commercially for more than 60 years for biocontrol of insect pests. Since 1996, transgenic plants expressing Bt crystal (Cry) proteins have been used commercially to provide protection against insects that predate on corn and cotton. More recently, Bt Cry proteins that target nematodes have been discovered. One of these, Cry14Ab, has been expressed in transgenic soybean plants and found to provide significant protection against the soybean cyst nematode, Heterodera glycines. However, to date there has been no description of high-level resistance to any Cry14A family protein in nematodes. Here, we describe forward genetic screens to identify such mutants using the nematode Caenorhabditis elegans. Although non-conditional screens failed to identify highly resistant C. elegans, a conditional (temperature-sensitive) genetic screen identified one mutant, bre-6(ye123) (for Bt protein resistant), highly resistant to both Cry14Aa and Cry14Ab. The mutant comes at a high fitness cost, showing significant delays in growth and development and reduced fecundity. bre-6(ye123) hermaphrodites are only weakly resistant to copper intoxication, indicating that the mutant is not highly resistant to all insults. Backcrossing-whole genome sequencing was used to identify the gene mutated in ye123 as the nuclear hormone receptor nhr-31. RNAi, DNA rescue, and CRISPR analyses confirm that resistance to Cry14Aa intoxication in bre-6(ye123) is due to mutation of nhr-31 and was renamed nhr-31(ye123). As predicted for a mutation in this gene, nhr-31(ye123) animals showed significantly reduced expression of most of the subunits of the C. elegans vacuolar ATPase (vATPase). Mutants in the vATPase subunits unc-32 and vha-7 also show resistance to Cry14Aa and/or Cry14Ab. These data demonstrate that nhr-31 and the vATPase play a significant role in the intoxication of C. elegans by Cry14A family proteins, that reduction in vATPase levels result in high resistance to Cry14A family proteins, and that such resistance comes at a high fitness cost. Based on the relative difficulty of finding resistant mutants and the fitness cost associated with the vATPase pathway, our data suggest that transgenic Cry14Ab plants may hold up well to resistance by nematode parasites.

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来源期刊
PLoS Pathogens
PLoS Pathogens MICROBIOLOGY-PARASITOLOGY
自引率
3.00%
发文量
598
期刊介绍: Bacteria, fungi, parasites, prions and viruses cause a plethora of diseases that have important medical, agricultural, and economic consequences. Moreover, the study of microbes continues to provide novel insights into such fundamental processes as the molecular basis of cellular and organismal function.
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