Anouk C van Westerhoven, Jelmer Dijkstra, Jose L Aznar Palop, Kyran Wissink, Jasper Bell, Gert H J Kema, Michael F Seidl
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Here, we construct, to our knowledge, the first fungal pan-mitogenome graph of nearly 500 <i>F</i>. <i>oxysporum</i> mitogenome assemblies to uncover the variation and evolution. In general, the gene order of fungal mitogenomes is not well conserved, yet the mitogenome of <i>F. oxysporum</i> and related species are highly colinear. We observed two strikingly contrasting regions in the <i>F. oxysporum</i> pan-mitogenome, comprising a highly conserved core mitogenome and a long variable region (6-16 kb in size), of which we identified three distinct types. The pan-mitogenome graph reveals that only five intron insertions occurred in the core mitogenome and that the long variable regions drive the difference between mitogenomes. Moreover, we observed that their evolution is neither concurrent with the core mitogenome nor with the nuclear genome. Our large-scale analysis of long variable regions uncovers frequent recombination between mitogenomes, even between strains that belong to different taxonomic clades. This challenges the common assumption of incompatibility between genetically diverse <i>F. oxysporum</i> strains and provides new insights into the evolution of this fungal species.IMPORTANCEInsights into plant pathogen evolution is essential for the understanding and management of disease. <i>Fusarium oxysporum</i> is a major fungal pathogen that can infect many economically important crops. Pathogenicity can be transferred between strains by the horizontal transfer of pathogenicity chromosomes. The fungus has been thought to evolve clonally, yet recent evidence suggests active sexual recombination between related isolates, which could at least partially explain the horizontal transfer of pathogenicity chromosomes. By constructing a pan-genome graph of nearly 500 mitochondrial genomes, we describe the genetic variation of mitochondria in unprecedented detail and demonstrate frequent mitochondrial recombination. Importantly, recombination can occur between genetically diverse isolates from distinct taxonomic clades and thus can shed light on genetic exchange between fungal strains.</p>","PeriodicalId":18315,"journal":{"name":"mBio","volume":" ","pages":"e0275824"},"PeriodicalIF":5.1000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Frequent genetic exchanges revealed by a pan-mitogenome graph of a fungal plant pathogen.\",\"authors\":\"Anouk C van Westerhoven, Jelmer Dijkstra, Jose L Aznar Palop, Kyran Wissink, Jasper Bell, Gert H J Kema, Michael F Seidl\",\"doi\":\"10.1128/mbio.02758-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Mitochondria are present in almost all eukaryotic lineages. The mitochondrial genomes (mitogenomes) evolve separately from nuclear genomes, and they can therefore provide relevant insights into the evolution of their host species. <i>Fusarium oxysporum</i> is a major fungal plant pathogen that is assumed to reproduce clonally. However, horizontal chromosome transfer between strains can occur through heterokaryon formation, and recently, signs of sexual recombination have been observed. Similarly, signs of recombination in <i>F. oxysporum</i> mitogenomes challenged the prevailing assumption of clonal reproduction in this species. Here, we construct, to our knowledge, the first fungal pan-mitogenome graph of nearly 500 <i>F</i>. <i>oxysporum</i> mitogenome assemblies to uncover the variation and evolution. In general, the gene order of fungal mitogenomes is not well conserved, yet the mitogenome of <i>F. oxysporum</i> and related species are highly colinear. We observed two strikingly contrasting regions in the <i>F. oxysporum</i> pan-mitogenome, comprising a highly conserved core mitogenome and a long variable region (6-16 kb in size), of which we identified three distinct types. The pan-mitogenome graph reveals that only five intron insertions occurred in the core mitogenome and that the long variable regions drive the difference between mitogenomes. Moreover, we observed that their evolution is neither concurrent with the core mitogenome nor with the nuclear genome. Our large-scale analysis of long variable regions uncovers frequent recombination between mitogenomes, even between strains that belong to different taxonomic clades. 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引用次数: 0
摘要
线粒体存在于几乎所有真核生物系中。线粒体基因组(有丝分裂基因组)的进化与核基因组的进化是分开的,因此它们可以为宿主物种的进化提供相关信息。Fusarium oxysporum 是一种主要的植物真菌病原体,被认为会进行克隆繁殖。然而,菌株间的水平染色体转移可通过异核子的形成而发生,最近还观察到了有性重组的迹象。同样,在 F. oxysporum 有丝分裂基因组中出现的重组迹象也对该物种克隆繁殖的普遍假设提出了挑战。据我们所知,我们在这里构建了第一个真菌泛有丝分裂基因组图谱,包含了近 500 个有丝分裂真菌有丝分裂基因组,以揭示其变异和进化。一般来说,真菌有丝分裂基因组的基因顺序并不十分保守,然而牛孢镰刀菌和相关物种的有丝分裂基因组却具有高度的共线性。我们在 F. oxysporum 泛有丝分裂基因组中观察到了两个截然不同的区域,包括一个高度保守的核心有丝分裂基因组和一个长的可变区域(大小为 6-16 kb),其中我们发现了三种不同的类型。泛有丝分裂基因组图显示,核心有丝分裂基因组中只有五个内含子插入,而长可变区则导致了有丝分裂基因组之间的差异。此外,我们观察到它们的进化既不与核心有丝分裂基因组同步,也不与核基因组同步。我们对长可变区的大规模分析发现了有丝分裂基因组之间频繁的重组,甚至在属于不同分类支系的菌株之间也是如此。这挑战了基因不同的 F. oxysporum 菌株之间不相容的普遍假设,并为这一真菌物种的进化提供了新的见解。重要意义了解植物病原体的进化对于理解和管理疾病至关重要。Fusarium oxysporum 是一种主要的真菌病原体,可感染多种具有重要经济价值的作物。致病性可通过致病性染色体的水平转移在菌株之间传递。该真菌一直被认为是克隆进化的,但最近的证据表明,相关分离株之间存在活跃的有性重组,这至少可以部分解释致病性染色体的水平转移。通过构建近 500 个线粒体基因组的泛基因组图谱,我们前所未有地详细描述了线粒体的遗传变异,并证明了线粒体重组的频繁发生。重要的是,重组可能发生在不同分类支系的不同基因分离物之间,因此可以揭示真菌菌株之间的基因交换。
Frequent genetic exchanges revealed by a pan-mitogenome graph of a fungal plant pathogen.
Mitochondria are present in almost all eukaryotic lineages. The mitochondrial genomes (mitogenomes) evolve separately from nuclear genomes, and they can therefore provide relevant insights into the evolution of their host species. Fusarium oxysporum is a major fungal plant pathogen that is assumed to reproduce clonally. However, horizontal chromosome transfer between strains can occur through heterokaryon formation, and recently, signs of sexual recombination have been observed. Similarly, signs of recombination in F. oxysporum mitogenomes challenged the prevailing assumption of clonal reproduction in this species. Here, we construct, to our knowledge, the first fungal pan-mitogenome graph of nearly 500 F. oxysporum mitogenome assemblies to uncover the variation and evolution. In general, the gene order of fungal mitogenomes is not well conserved, yet the mitogenome of F. oxysporum and related species are highly colinear. We observed two strikingly contrasting regions in the F. oxysporum pan-mitogenome, comprising a highly conserved core mitogenome and a long variable region (6-16 kb in size), of which we identified three distinct types. The pan-mitogenome graph reveals that only five intron insertions occurred in the core mitogenome and that the long variable regions drive the difference between mitogenomes. Moreover, we observed that their evolution is neither concurrent with the core mitogenome nor with the nuclear genome. Our large-scale analysis of long variable regions uncovers frequent recombination between mitogenomes, even between strains that belong to different taxonomic clades. This challenges the common assumption of incompatibility between genetically diverse F. oxysporum strains and provides new insights into the evolution of this fungal species.IMPORTANCEInsights into plant pathogen evolution is essential for the understanding and management of disease. Fusarium oxysporum is a major fungal pathogen that can infect many economically important crops. Pathogenicity can be transferred between strains by the horizontal transfer of pathogenicity chromosomes. The fungus has been thought to evolve clonally, yet recent evidence suggests active sexual recombination between related isolates, which could at least partially explain the horizontal transfer of pathogenicity chromosomes. By constructing a pan-genome graph of nearly 500 mitochondrial genomes, we describe the genetic variation of mitochondria in unprecedented detail and demonstrate frequent mitochondrial recombination. Importantly, recombination can occur between genetically diverse isolates from distinct taxonomic clades and thus can shed light on genetic exchange between fungal strains.
期刊介绍:
mBio® is ASM''s first broad-scope, online-only, open access journal. mBio offers streamlined review and publication of the best research in microbiology and allied fields.