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大豆疫霉菌无毒基因的判别单倍型导致了一种预测表型的分子检测方法。

Discriminant haplotypes of avirulence genes of Phytophthora sojae lead to a molecular assay to predict phenotypes.

机构信息

Department of Phytology, Université Laval, Québec, QC, Canada.

National Agri-Food Biotechnology Institute (NABI), Mohali, India.

出版信息

Mol Plant Pathol. 2020 Mar;21(3):318-329. doi: 10.1111/mpp.12898. Epub 2020 Jan 7.

Abstract

The soybean-Phytophthora sojae interaction operates on a gene-for-gene relationship, where the product of a resistance gene (Rps) in the host recognizes that of an avirulence gene (Avr) in the pathogen to generate an incompatible reaction. To exploit this form of resistance, one must match with precision the appropriate Rps gene with the corresponding Avr gene. Currently, this association is evaluated by phenotyping assays that are labour-intensive and often imprecise. To circumvent this limitation, we sought to develop a molecular assay that would reveal the avirulence allele of the seven main Avr genes (Avr1a, Avr1b, Avr1c, Avr1d, Avr1k, Avr3a, and Avr6) in order to diagnose with precision the pathotypes of P. sojae isolates. For this purpose, we analysed the genomic regions of these Avr genes in 31 recently sequenced isolates with different virulence profiles and identified discriminant mutations between avirulence and virulence alleles. Specific primers were designed to generate amplicons of a distinct size, and polymerase chain reaction conditions were optimized in a final assay of two parallel runs. When tested on the 31 isolates of known virulence, the assay accurately revealed all avirulence alleles. The test was further assessed and compared to a phenotyping assay on 25 isolates of unknown virulence. The two assays matched in 97% (170/175) of the interactions studied. Interestingly, the sole cases of discrepancy were obtained with Avr3a, which suggests a possible imperfect interaction with Rps3a. This molecular assay offers a powerful and reliable tool to exploit and study with greater precision soybean resistance against P. sojae.

摘要

大豆与大豆疫霉的互作遵循基因对基因关系,宿主中抗性基因(Rps)的产物识别病原体中无毒基因(Avr)的产物,从而产生不亲和反应。为了利用这种形式的抗性,必须精确匹配适当的 Rps 基因与相应的 Avr 基因。目前,这种关联是通过费力且往往不准确的表型分析来评估的。为了克服这一限制,我们试图开发一种分子分析方法,以准确揭示七个主要 Avr 基因(Avr1a、Avr1b、Avr1c、Avr1d、Avr1k、Avr3a 和 Avr6)的无毒等位基因,从而精确诊断大豆疫霉菌株的致病型。为此,我们分析了 31 个具有不同毒力谱的最近测序分离株中这些 Avr 基因的基因组区域,并鉴定了无毒和毒性等位基因之间的区分突变。设计了特异性引物来产生大小不同的扩增子,并在最终的双平行运行的聚合酶链反应条件下进行了优化。在对已知毒力的 31 个分离株进行测试时,该检测方法准确地揭示了所有无毒等位基因。进一步对该检测方法进行了评估,并与 25 个未知毒力的分离株的表型分析进行了比较。两种检测方法在 97%(170/175)的研究互作中匹配。有趣的是,仅在 Avr3a 中出现了不一致的情况,这表明可能与 Rps3a 存在不完全的互作。这种分子检测方法为利用和更精确地研究大豆对大豆疫霉的抗性提供了一种强大而可靠的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e98e/7036360/f43946fc45a9/MPP-21-318-g001.jpg

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