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Pfcyp51 exclusively determines reduced sensitivity to 14α-demethylase inhibitor fungicides in the banana black Sigatoka pathogen Pseudocercospora fijiensis

机译:Pfcyp51专门确定香蕉黑色Sigatoka病原体假晶孢菌菌的14α-脱甲基酶抑制剂杀菌剂的敏感性降低

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摘要

The haploid fungus Pseudocercospora fijiensis causes black Sigatoka in banana and is chiefly controlled by extensive fungicide applications, threatening occupational health and the environment. The 14α-Demethylase Inhibitors (DMIs) are important disease control fungicides, but they lose sensitivity in a rather gradual fashion, suggesting an underlying polygenic genetic mechanism. In spite of this, evidence found thus far suggests that P. fijiensis cyp51 gene mutations are the main responsible factor for sensitivity loss in the field. To better understand the mechanisms involved in DMI resistance, in this study we constructed a genetic map using DArTseq markers on two F1 populations generated by crossing two different DMI resistant strains with a sensitive strain. Analysis of the inheritance of DMI resistance in the F1 populations revealed two major and discrete DMI-sensitivity groups. This is an indicative of a single major responsible gene. Using the DMI-sensitivity scorings of both F1 populations and the generation of genetic linkage maps, the sensitivity causal factor was located in a single genetic region. Full agreement was found for genetic markers in either population, underlining the robustness of the approach. The two maps indicated a similar genetic region where the Pfcyp51 gene is found. Sequence analyses of the Pfcyp51 gene of the F1 populations also revealed a matching bimodal distribution with the DMI resistant. Amino acid substitutions in P. fijiensis CYP51 enzyme of the resistant progeny were previously correlated with the loss of DMI sensitivity. In addition, the resistant progeny inherited a Pfcyp51 gene promoter insertion, composed of a repeat element with a palindromic core, also previously correlated with increased gene expression. This genetic approach confirms that Pfcyp51 is the single explanatory gene for reduced sensitivity to DMI fungicides in the analysed P. fijiensis strains. Our study is the first genetic analysis to map the underlying genetic factors for reduced DMI efficacy.
机译:单倍体真菌假晶孢子孢子会导致香蕉中的黑色信号,主要由广泛的杀菌剂应用控制,威胁职业健康和环境。 14α-脱甲基酶抑制剂(DMIS)是重要的疾病控制杀菌剂,但它们以相当渐进的方式失去敏感性,表明潜在的多种子基遗传机制。尽管如此,迄今为止发现的证据表明,P.Fijiensis Cyp51基因突变是该领域敏感性损失的主要负责因素。为了更好地了解患DMI抗性的机制,在本研究中,我们在通过用敏感菌株交叉两种不同的DMI抗性菌株产生的两个F1群体上使用Dartseq标记构建了遗传图。分析F1群体中DMI抗性的遗传揭示了两个主要和离散的DMI敏感性组。这是一个单一主要负责基因的指示。使用F1群体的DMI敏感度和遗传联系地图的产生,敏感性因果因子位于单个遗传区域中。发现任何人口中的遗传标记都有完全协议,强调了这种方法的稳健性。这两张地图表明了发现pfcyp51基因的类似遗传区域。 F1群体的PFCYP51基因的序列分析还揭示了与DMI抗性的匹配双峰分布。抗抗性后代的P.Fijiensis Cyp51中的氨基酸取代与DMI敏感性的损失相关。此外,抗性后代遗传的PFCYP51基因启动子插入插入,其由具有回复元件的重复元素组成,其先前与增加的基因表达相关。该遗传方法证实,PFCYP51是单一解释基因,用于降低分析的P.Fijiensis菌株的DMI杀菌剂的敏感性。我们的研究是第一个映射潜在的遗传因素来降低DMI疗效的遗传分析。

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