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网斑病病原菌的内吸性杀菌剂和局部杀菌剂抗性检测工作流程。

Workflows for detecting fungicide resistance in net form and spot form net blotch pathogens.

机构信息

Centre for Crop and Disease Management, School of Molecular and Life Sciences, Curtin University, Bentley, Australia.

出版信息

Pest Manag Sci. 2024 Apr;80(4):2131-2140. doi: 10.1002/ps.7951. Epub 2024 Jan 19.

Abstract

BACKGROUND

Fungicide resistance in Pyrenophora teres f. maculata and P. teres f. teres has become an important disease management issue. Control of the associated barley foliar diseases, spot form and net form net blotch, respectively, relies on three major groups of fungicides, demethylation inhibitors (DMIs), succinate dehydrogenase inhibitors (SDHIs) and quinone outside inhibitors (QoIs). However, resistance has been reported for the DMI and SDHI fungicides in Australia. To enhance detection of different resistance levels, phenotyping and genotyping workflows were designed.

RESULTS

The phenotyping workflow generated cultures directly from lesions and compared growth on discriminatory doses of tebuconazole (DMI) and fluxapyroxad (SDHI). Genotyping real-time polymerase chain reaction (PCR) assays were based on alleles associated with sensitivity or resistance to the DMI and SDHI fungicides. These workflows were applied to spot form and net form net blotch collections from 2019 consisting predominantly of P. teres f. teres from South Australia and P. teres f. maculata from Western Australia. For South Australia the Cyp51A L489-3 and SdhC-R134 alleles, associated with resistance to tebuconazole and fluxapyroxad, respectively, were the most prevalent. These alleles were frequently found in single isolates with dual resistance. This study also reports the first detection of a 134 base pair insertion located at position-66 (PtTi-6) in the Cyp51A promoter of P. teres f. maculata from South Australia. For Western Australia, the PtTi-1 insertion was the most common allele associated with resistance to tebuconazole.

CONCLUSION

The workflow and PCR assays designed in this study have been demonstrated to efficiently screen P. teres collections for both phenotypic and genetic resistance to DMI and SDHI fungicides. The distribution of reduced sensitivity and resistance to DMI and SDHI fungicides varied between regions in south-western Australia, suggesting the emergence of resistance was impacted by both local pathogen populations and disease management programmes. The knowledge of fungicide resistance in regional P. teres collections will be important for informing appropriate management strategies. © 2023 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

摘要

背景

层出镰刀菌(Pyrenophora teres f. maculata 和 P. teres f. teres)中的杀菌剂抗性已成为一个重要的病害管理问题。分别针对大麦叶部病害——斑点病和网斑病的防治,依赖于三大类杀菌剂:脱甲基抑制剂(DMIs)、琥珀酸脱氢酶抑制剂(SDHIs)和醌外抑制剂(QoIs)。然而,在澳大利亚已报道了 DMIs 和 SDHIs 类杀菌剂的抗性。为了提高对不同抗性水平的检测能力,设计了表型和基因型工作流程。

结果

表型工作流程直接从病斑中培养病原菌,并比较了在不同剂量特丁唑(DMI)和氟环唑(SDHI)下的生长情况。基于与 DMI 和 SDHI 类杀菌剂敏感性或抗性相关的等位基因,设计了实时聚合酶链反应(PCR)基因型检测方法。这些工作流程应用于 2019 年收集的斑点病和网斑病样本,主要来自南澳大利亚的层出镰刀菌 f. teres 和西澳大利亚的层出镰刀菌 f. maculata。在南澳大利亚,与特丁唑和氟环唑抗性相关的 Cyp51A L489-3 和 SdhC-R134 等位基因最为普遍。这些等位基因经常在具有双重抗性的单一分离物中发现。本研究还首次报道了在南澳大利亚的层出镰刀菌 f. maculata 中发现了位于 Cyp51A 启动子位置-66(PtTi-6)的 134 碱基对插入(PtTi-6)。在西澳大利亚,PtTi-1 插入是与特丁唑抗性相关的最常见等位基因。

结论

本研究设计的工作流程和 PCR 检测方法已被证明能够有效地筛选出对 DMI 和 SDHI 类杀菌剂具有表型和遗传抗性的层出镰刀菌。在澳大利亚西南部的不同地区,DMI 和 SDHI 类杀菌剂敏感性降低和抗性的分布存在差异,表明抗性的出现既受到当地病原菌种群的影响,也受到病害管理计划的影响。了解区域性层出镰刀菌种群中的杀菌剂抗性对于制定适当的管理策略非常重要。

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