球孢囊线虫对共线性马铃薯抗性qtl GpaVvrn和GpaVspl的适应涉及不同的基因组区域和交叉毒力的缺失。

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Océane Lechevalier, Magali Esquibet, Mathieu Gautier, Rachel Fourdin, Eric Grenier, Sylvain Fournet, Josselin Montarry
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引用次数: 0

摘要

自从欧洲禁止使用化学杀线虫剂以来,使用替代方法控制囊线虫种群的速度加快了。抗性QTL GpaVvrn来自野生物种vernei Solanum,广泛存在于具有抗性的欧洲马铃薯品种中,并对苍白球疫种群提供了强有力的保护,尽管在实验进化研究和田间种群中已经证明了抗性破坏的风险。携带抗性QTL GpaVspl的野生亲缘sparsipilum可能是控制毒力苍白菌的一个有趣的替代抗性来源。本研究的目的是了解线虫对这两个共线性抗性qtl的适应基因组学。从两个自然种群开始,实验进化方法允许在抗性马铃薯基因型上进行10代之后,选择适应每个QTL的独立线虫谱系。通过表型分析和基因组扫描相结合的方法分析了这些毒性谱系。表型分析可以量化毒力水平并确认抗性分解。Pool-Seq全基因组测序和基因组扫描分析确定了选择下的基因组区域,可能涉及对每种抗性因子的适应机制。这些区域内的候选基因提供了对适应的遗传基础的见解,揭示了已知抑制植物免疫的效应物。由于基因组扫描突出了适应这两种抗性因子的不同基因组区域,我们能够预测并从表型上证实在GpaVvrn和GpaVspl上进化的线虫谱系之间不存在交叉毒力。这些发现对设计有效和可持续的耐药性管理策略具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adaptation of the Cyst Nematode Globodera pallida to the Colinear Potato Resistant QTLs GpaVvrn and GpaVspl Involved Distinct Genomic Regions and Absence of Cross-Virulence.

The use of alternative methods to control cyst nematode populations has accelerated since the ban of chemical nematicides in Europe. The resistant QTL GpaVvrn, derived from the wild species Solanum vernei, is widely present in resistant European potato cultivars and provides strong protection against Globodera pallida populations although a risk of resistance breakdown has already been demonstrated in both experimental evolution studies and field populations. The wild relative S. sparsipilum, harbouring the resistant QTL GpaVspl, would be an interesting alternative source of resistance to control virulent G. pallida. The goal of the present study was to understand the genomics of adaptation of the nematode to these two colinear resistant QTLs. Starting with two natural populations, an experimental evolution approach allowed, after 10 generations on resistant potato genotypes, selecting independent nematode lineages adapted to each QTL. These virulent lineages were analysed through a combination of phenotyping and genome scans approaches. Phenotyping enabled the quantification of virulence levels and confirmed resistance breakdowns. Pool-Seq whole genome sequencing followed by genome scan analyses identified genomic regions under selection, potentially involved in the adaptive mechanisms to each resistance factor. Candidate genes within these regions provided insights into the genetic basis of adaptation, revealing effectors known to suppress plant immunity. As genome scans highlighted distinct genomic regions for the adaptation to both resistant factors, we were able to predict and phenotypically confirm the absence of cross-virulence between nematode lineages evolving on GpaVvrn and GpaVspl. These findings have significant implications for the design of effective and sustainable resistance management strategies.

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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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