以祖先基因组扩增和水平基因转移为证据的 Botryosphaeriaceae 的生活方式变化

IF 24.5 1区 生物学 Q1 MYCOLOGY Fungal Diversity Pub Date : 2023-12-11 DOI:10.1007/s13225-023-00530-7
Xuncheng Wang, Wei Zhang, Junbo Peng, Ishara S. Manawasinghe, Linna Wu, Yonghua Li, Qikai Xing, Xinghong Li, Jiye Yan
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引用次数: 0

摘要

Botryosphaeriaceae (Botryosphaeriales,Dothideomycetes,Ascomycota)包括常见的机会性病原体,可导致木本植物茎干溃疡。Botryosphaeriaceae 物种的生活方式可以作为内生菌、病原体和吸液菌而变化,一个物种可以有一种或多种生活方式。因此,该科是研究生活方式和生活方式变化之间关系的极佳对象。据推测,该科植物的祖先是树液生物,而它们从非病原体祖先进化为木本病原体的机制尚不清楚。在此,我们对 18 个 Botryosphaeriaceae 基因组进行了分析,其中包括 4 个新生成的高质量 Botryosphaeriaceae 菌株基因组。我们将 Botryosphaeriaceae 基因组与系统发育上密切相关的 Dothideomycetes 类群(包括植物病原菌和树腐菌)进行了比较,发现 Botryosphaeriaceae 中的基因家族有显著的净扩展。这种基因扩增在 Botryosphaeriaceae 属分化之前的早期祖先中十分突出。这种扩展影响了致病性相关基因和解毒基因。此外,我们还分析了水平基因转移(一种非亲子关系生物之间遗传物质的转移机制),并在该家族中发现了广泛的推定王国内部水平基因转移事件。大部分基因是在现代菌属分化之前,在 Botryosphaeriaceae 的远古祖先进化过程中转移的,并且富含致病性相关基因和解毒基因。此外,对Botryosphaeriaceae物种Lasiodiplodia theobromae的RNA测序分析表明,与致病性相关的基因和解毒基因,包括通过基因家族扩展和水平基因转移获得的基因,在感染植物宿主后而不是在感染前被显著诱导。这些发现揭示了基因家族扩增和水平基因转移在 Botryosphaeriaceae 感染木本植物的进化适应过程中的关键作用。我们推测 Botryosphaeriaceae 物种的致病生活方式是在该科早期分化过程中从吸附生活方式或内生生活方式演变而来的。然而,与 Botryosphaeriaceae 关系密切的内生菌基因组很少,因此有必要开展进一步研究,以明确内生菌的进化关系。
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Lifestyle changes in Botryosphaeriaceae as evidenced by ancestral genome expansion and horizontal gene transfer

Botryosphaeriaceae (Botryosphaeriales, Dothideomycetes, Ascomycota) encompasses commonly encountered opportunistic pathogens that cause stem cankers on woody plants. Lifestyles of Botryosphaeriaceae species could vary as endophytes, pathogens and saprobes and one species can have one or more lifestyles. Therefore, this family is an excellent candidate to study the relationships among lifestyles and lifestyle changes. It is postulated that this family has saprobic ancestors, and the mechanisms by which they evolved from nonpathogenic ancestors to woody pathogens remain unclear. Here, we present an analysis of 18 Botryosphaeriaceae genomes, including four newly generated high-quality genomes of Botryosphaeriaceae strains. We compared Botryosphaeriaceae genomes with phylogenetically closely related Dothideomycetes taxa including plant pathogens and saprobes which revealed significant net gene family expansion in Botryosphaeriaceae. This gene expansion is prominent in the early ancestors before the divergence of genera of Botryosphaeriaceae. This expansion affected the pathogenicity-related genes and detoxification genes. Furthermore, we analysed horizontal gene transfer, which is a mechanism of transfer to genetic material between organisms that are not in a parent–offspring relationship and identified widespread putative intra-kingdom horizontal gene transfer events in this family. Most were transferred during the evolution of ancient ancestors of Botryosphaeriaceae, before the divergence of the modern genera and were enriched in pathogenicity-related genes and detoxification genes. Furthermore, The RNA sequencing analysis of the Botryosphaeriaceae species Lasiodiplodia theobromae revealed that pathogenicity-related genes and detoxification genes, including those obtained through gene family expansion and horizontal gene transfers, were significantly induced after the infection of plant hosts rather than before infection. These insights reveal critical roles for gene family expansion and horizontal gene transfers in the evolutionary adaptation of Botryosphaeriaceae in the infection of woody plants. We postulate that the pathogenic lifestyle of Botryosphaeriaceae species evolved from saprobic or endophytic lifestyles in the early divergence of this family. However, there are few endophytic genomes available for closely related species of Botryosphaeriaceae, thus further studies are necessary to clarify the evolutionary relationships of the endophytes.

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来源期刊
Fungal Diversity
Fungal Diversity 生物-真菌学
CiteScore
44.80
自引率
9.90%
发文量
17
审稿时长
6 months
期刊介绍: Fungal Diversity, the official journal of the Kunming Institute of Botany of the Chinese Academy of Sciences, is an international, peer-reviewed journal covering all aspects of mycology. It prioritizes papers on biodiversity, systematic, and molecular phylogeny. While it welcomes novel research and review articles, authors aiming to publish checklists are advised to seek regional journals, and the introduction of new species and genera should generally be supported by molecular data. Published articles undergo peer review and are accessible online first with a permanent DOI, making them citable as the official Version of Record according to NISO RP-8-2008 standards. Any necessary corrections after online publication require the publication of an Erratum.
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