Analysis of the genetic diversity of the soybean rust pathogen Phakopsora pachyrhizi reveals two major evolutionary lineages

IF 2.4 3区 生物学 Q3 GENETICS & HEREDITY
Vinicius Delgado da Rocha , Everton Geraldo Capote Ferreira , Fernanda Machado Castanho , Marcia Kamogae Kuwahara , Cláudia Vieira Godoy , Maurício Conrado Meyer , Kerry F. Pedley , Ralf T. Voegele , Anna Lipzen , Kerrie Barry , Igor V. Grigoriev , Marco Loehrer , Ulrich Schaffrath , Catherine Sirven , Sebastien Duplessis , Francismar Corrêa Marcelino-Guimarães
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Abstract

Phakopsora pachyrhizi, an obligate biotrophic rust fungus, is the causal agent of Asian Soybean Rust (ASR) disease. Here, we utilized whole-genome data to explore the evolutionary patterns and population structure across 45 P. pachyrhizi isolates collected from 1972 to 2017 from diverse geographic regions worldwide. We also characterized in-silico mating-type (MAT) genes of P. pachyrhizi, in the predicted proteome of three isolates, to investigate the sexual compatibility system. Our molecular phylogenetic analysis in P. pachyrhizi inferred two distinct evolutionary lineages structured on a temporal scale, with lineage Pp1 grouping isolates obtained from 1972 to 1994, while more recently collected isolates formed a second lineage, Pp2. We found higher levels of genetic diversity in lineage Pp1, whereas lineage Pp2 exhibited a strong clonal genetic structure, with a significant lower diversity. The widespread propagation of P. pachyrhizi clonal spores across soybean-growing regions likely explains the absence of a large-scale spatial genetic structure within each lineage. Two independent isolates (TW72–1 and AU79–1) showed moderate levels of genetic admixture, suggesting potential somatic hybridization between the two P. pachyrhizi lineages. We observed no clear congruence between virulence levels of P. pachyrhizi isolates and their phylogenetic patterns. Our findings support a probable tetrapolar mating system in P. pachyrhizi. Taken together, our study offers new insights into the evolutionary history of P. pachyrhizi and demonstrates that multiple MAT genes are highly expressed during the later stages of soybean infection, suggesting their potential role in the formation of urediniospores within the life cycle of P. pachyrhizi.

Abstract Image

大豆锈病病原菌厚根Phakopsora pachyrhizi的遗传多样性分析揭示了两大进化谱系
厚根Phakopsora pachyrhizi是一种专性生物营养锈菌,是亚洲大豆锈病(ASR)的病原。在这里,我们利用全基因组数据探索了1972年至2017年从全球不同地理区域收集的45株肿根假单胞菌的进化模式和种群结构。在预测的3个分离株蛋白质组中,我们还对肿根假单胞菌的硅化交配型(MAT)基因进行了分析,以探讨其性相容性系统。我们对肿根菌的分子系统发育分析推断出在时间尺度上有两个不同的进化谱系,谱系Pp1组分离株于1972年至1994年获得,而最近收集的分离株形成了第二个谱系Pp2。我们发现Pp1谱系的遗传多样性水平较高,而Pp2谱系表现出较强的克隆遗传结构,多样性明显较低。肿根假单胞菌克隆孢子在大豆种植区的广泛繁殖可能解释了每个谱系中缺乏大规模空间遗传结构的原因。两个独立的分离株(TW72-1和AU79-1)显示出中等水平的遗传混合,表明两个肿根麻系之间可能存在体细胞杂交。我们观察到肿根假单胞菌分离株的毒力水平与其系统发育模式之间没有明确的一致性。我们的发现支持了一种可能的四极交配系统。综上所述,我们的研究为肿根霉的进化史提供了新的见解,并证明了多个MAT基因在大豆感染的后期高度表达,表明它们在肿根霉生命周期中形成uredinio孢子的潜在作用。
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来源期刊
Fungal Genetics and Biology
Fungal Genetics and Biology 生物-遗传学
CiteScore
6.20
自引率
3.30%
发文量
66
审稿时长
85 days
期刊介绍: Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny. Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists. Research Areas include: • Biochemistry • Cytology • Developmental biology • Evolutionary biology • Genetics • Molecular biology • Phylogeny • Physiology.
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