Genome-Enabled Analysis of Population Dynamics and Virulence-Associated Loci in the Oat Crown Rust Fungus Puccinia coronata f. sp. avenae.

IF 3.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Plant-microbe Interactions Pub Date : 2024-03-01 Epub Date: 2024-03-21 DOI:10.1094/MPMI-09-23-0126-FI
Tim C Hewitt, Eva C Henningsen, Danilo Pereira, Kerensa McElroy, Eric S Nazareno, Sheshanka Dugyala, Hoa Nguyen-Phuc, Feng Li, Marisa E Miller, Botma Visser, Zacharias A Pretorius, Willem H P Boshoff, Jana Sperschneider, Eva H Stukenbrock, Shahryar F Kianian, Peter N Dodds, Melania Figueroa
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Abstract

Puccinia coronata f. sp. avenae (Pca) is an important fungal pathogen causing crown rust that impacts oat production worldwide. Genetic resistance for crop protection against Pca is often overcome by the rapid virulence evolution of the pathogen. This study investigated the factors shaping adaptive evolution of Pca using pathogen populations from distinct geographic regions within the United States and South Africa. Phenotypic and genome-wide sequencing data of these diverse Pca collections, including 217 isolates, uncovered phylogenetic relationships and established distinct genetic composition between populations from northern and southern regions from the United States and South Africa. The population dynamics of Pca involve a bidirectional movement of inoculum between northern and southern regions of the United States and contributions from clonality and sexuality. The population from South Africa is solely clonal. A genome-wide association study (GWAS) employing a haplotype-resolved Pca reference genome was used to define 11 virulence-associated loci corresponding to 25 oat differential lines. These regions were screened to determine candidate Avr effector genes. Overall, the GWAS results allowed us to identify the underlying genetic factors controlling pathogen recognition in an oat differential set used in the United States to assign pathogen races (pathotypes). Key GWAS findings support complex genetic interactions in several oat lines, suggesting allelism among resistance genes or redundancy of genes included in the differential set, multiple resistance genes recognizing genetically linked Avr effector genes, or potentially epistatic relationships. A careful evaluation of the composition of the oat differential set accompanied by the development or implementation of molecular markers is recommended. [Formula: see text] Copyright © 2024 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.

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燕麦冠锈菌群体动态和毒力相关位点的基因组分析。
冠锈病(Puccinia coronata f. sp. avenae, Pca)是影响世界范围内燕麦生产的重要病原菌。作物保护对Pca的遗传抗性通常被病原体的快速毒力进化所克服。本研究利用美国和南非(SA)不同地理区域的病原菌种群,研究了影响Pca适应性进化的因素。这些不同的Pca集合(包括217个分离株)的表型和全基因组测序数据揭示了美国和南非北部和南部地区种群之间的系统发育关系,并建立了不同的遗传组成。Pca的种群动态涉及美国南北地区之间接种量的双向运动以及克隆性和性的贡献。来自SA的群体为单克隆。采用单倍型解析Pca参考基因组的全基因组关联研究(GWAS)确定了25个燕麦差异系对应的11个毒力相关位点。筛选这些区域以确定候选Avr效应基因。总体而言,GWAS结果使我们能够在美国用于分配病原体种族(病原型)的燕麦鉴别集中确定控制病原体识别的潜在遗传因素。关键的GWAS发现支持几种燕麦系中复杂的遗传相互作用,表明抗性基因之间存在等位基因或差异组中包含的基因冗余,多个抗性基因识别遗传关联的Avr效应基因,或潜在的上位性关系。建议对燕麦鉴别集的组成进行仔细的评估,同时开发或实施分子标记。
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来源期刊
Molecular Plant-microbe Interactions
Molecular Plant-microbe Interactions 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
250
审稿时长
3 months
期刊介绍: Molecular Plant-Microbe Interactions® (MPMI) publishes fundamental and advanced applied research on the genetics, genomics, molecular biology, biochemistry, and biophysics of pathological, symbiotic, and associative interactions of microbes, insects, nematodes, or parasitic plants with plants.
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