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{"title":"Comparative Pangenomic Insights into the Distinct Evolution of Virulence Factors Among Grapevine Trunk Pathogens.","authors":"Jadran F Garcia, Abraham Morales-Cruz, Noé Cochetel, Andrea Minio, Rosa Figueroa-Balderas, Philippe E Rolshausen, Kendra Baumgartner, Dario Cantu","doi":"10.1094/MPMI-09-23-0129-R","DOIUrl":null,"url":null,"abstract":"<p><p>The permanent organs of grapevines (<i>Vitis vinifera</i> L.), like those of other woody perennials, are colonized by various unrelated pathogenic ascomycete fungi secreting cell wall-degrading enzymes and phytotoxic secondary metabolites that contribute to host damage and disease symptoms. Trunk pathogens differ in the symptoms they induce and the extent and speed of damage. Isolates of the same species often display a wide virulence range, even within the same vineyard. This study focuses on <i>Eutypa lata</i>, <i>Neofusicoccum parvum</i>, and <i>Phaeoacremonium minimum</i>, causal agents of Eutypa dieback, Botryosphaeria dieback, and Esca, respectively. We sequenced 50 isolates from viticulture regions worldwide and built nucleotide-level, reference-free pangenomes for each species. Through examination of genomic diversity and pangenome structure, we analyzed intraspecific conservation and variability of putative virulence factors, focusing on functions under positive selection and recent gene family dynamics of contraction and expansion. Our findings reveal contrasting distributions of putative virulence factors in the core, dispensable, and private genomes of each pangenome. For example, carbohydrate active enzymes (CAZymes) were prevalent in the core genomes of each pangenome, whereas biosynthetic gene clusters were prevalent in the dispensable genomes of <i>E. lata</i> and <i>P. minimum</i>. The dispensable fractions were also enriched in Gypsy transposable elements and virulence factors under positive selection (polyketide synthase genes in <i>E. lata</i> and <i>P. minimum</i>, glycosyltransferases in <i>N. parvum</i>). Our findings underscore the complexity of the genomic architecture in each species and provide insights into their adaptive strategies, enhancing our understanding of the underlying mechanisms of virulence. [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.</p>","PeriodicalId":19009,"journal":{"name":"Molecular Plant-microbe Interactions","volume":" ","pages":"127-142"},"PeriodicalIF":3.4000,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant-microbe Interactions","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1094/MPMI-09-23-0129-R","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/2/21 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
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Abstract
The permanent organs of grapevines (Vitis vinifera L.), like those of other woody perennials, are colonized by various unrelated pathogenic ascomycete fungi secreting cell wall-degrading enzymes and phytotoxic secondary metabolites that contribute to host damage and disease symptoms. Trunk pathogens differ in the symptoms they induce and the extent and speed of damage. Isolates of the same species often display a wide virulence range, even within the same vineyard. This study focuses on Eutypa lata , Neofusicoccum parvum , and Phaeoacremonium minimum , causal agents of Eutypa dieback, Botryosphaeria dieback, and Esca, respectively. We sequenced 50 isolates from viticulture regions worldwide and built nucleotide-level, reference-free pangenomes for each species. Through examination of genomic diversity and pangenome structure, we analyzed intraspecific conservation and variability of putative virulence factors, focusing on functions under positive selection and recent gene family dynamics of contraction and expansion. Our findings reveal contrasting distributions of putative virulence factors in the core, dispensable, and private genomes of each pangenome. For example, carbohydrate active enzymes (CAZymes) were prevalent in the core genomes of each pangenome, whereas biosynthetic gene clusters were prevalent in the dispensable genomes of E. lata and P. minimum . The dispensable fractions were also enriched in Gypsy transposable elements and virulence factors under positive selection (polyketide synthase genes in E. lata and P. minimum , glycosyltransferases in N. parvum ). Our findings underscore the complexity of the genomic architecture in each species and provide insights into their adaptive strategies, enhancing our understanding of the underlying mechanisms of virulence. [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.
葡萄树干病原体毒力因子不同进化的比较泛基因组学见解。
葡萄藤(V.vinifera L.)的永久器官与其他木本多年生植物一样,被各种不相关的致病子囊菌定殖,分泌细胞壁降解酶和植物毒性次级代谢产物,导致宿主损伤和疾病症状。主干病原体在其诱发的症状以及损伤的程度和速度上各不相同。同一物种的分离株通常表现出广泛的毒力范围,即使在同一葡萄园内也是如此。本研究的重点是分别引起扁尾蠊、球孢杆菌和Esca的致病因子——宽尾蠊(Eutypa lata)、小新梭形球虫(Neofusicoccum parvum)和最小Phaeoacremonium。我们对来自世界各地葡萄栽培区的50个分离株进行了测序,并为每个物种构建了核苷酸水平的、无参考的泛基因组。通过检查基因组多样性和泛基因组结构,我们分析了假定毒力因子的种内保守性和变异性,重点关注正选择下的功能,以及最近收缩和扩张的基因家族动力学。我们的发现揭示了假定毒力因子在每个泛基因组的核心、可有可无和私有基因组中的对比分布。例如,CAZymes在每个泛基因组的核心基因组中普遍存在,而生物合成基因簇在E.lata和P.minimum的可有可无的基因组中普遍。在阳性选择下,可有可无的组分还富含Gypsy转座元件和毒力因子(E.lata中的聚酮合酶基因和N.parvum中的P.minimum糖基转移酶)。我们的发现强调了每个物种基因组结构的复杂性,并深入了解了它们的适应策略,增强了我们对毒力潜在机制的理解。
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