L G Nagy, P J Vonk, M Künzler, C Földi, M Virágh, R A Ohm, F Hennicke, B Bálint, Á Csernetics, B Hegedüs, Z Hou, X B Liu, S Nan, M Pareek, N Sahu, B Szathmári, T Varga, H Wu, X Yang, Z Merényi
<p><p>Fruiting bodies (sporocarps, sporophores or basidiomata) of mushroom-forming fungi (<i>Agaricomycetes</i>) are among the most complex structures produced by fungi. Unlike vegetative hyphae, fruiting bodies grow determinately and follow a genetically encoded developmental program that orchestrates their growth, tissue differentiation and sexual sporulation. In spite of more than a century of research, our understanding of the molecular details of fruiting body morphogenesis is still limited and a general synthesis on the genetics of this complex process is lacking. In this paper, we aim at a comprehensive identification of conserved genes related to fruiting body morphogenesis and distil novel functional hypotheses for functionally poorly characterised ones. As a result of this analysis, we report 921 conserved developmentally expressed gene families, only a few dozens of which have previously been reported to be involved in fruiting body development. Based on literature data, conserved expression patterns and functional annotations, we provide hypotheses on the potential role of these gene families in fruiting body development, yielding the most complete description of molecular processes in fruiting body morphogenesis to date. We discuss genes related to the initiation of fruiting, differentiation, growth, cell surface and cell wall, defence, transcriptional regulation as well as signal transduction. Based on these data we derive a general model of fruiting body development, which includes an early, proliferative phase that is mostly concerned with laying out the mushroom body plan (via cell division and differentiation), and a second phase of growth via cell expansion as well as meiotic events and sporulation. Altogether, our discussions cover 1 480 genes of <i>Coprinopsis cinerea</i>, and their orthologs in <i>Agaricus bisporus, Cyclocybe aegerita, Armillaria ostoyae, Auriculariopsis ampla, Laccaria bicolor, Lentinula edodes, Lentinus tigrinus, Mycena kentingensis, Phanerochaete chrysosporium, Pleurotus ostreatus</i>, and <i>Schizophyllum commune</i>, providing functional hypotheses for ~10 % of genes in the genomes of these species. Although experimental evidence for the role of these genes will need to be established in the future, our data provide a roadmap for guiding functional analyses of fruiting related genes in the <i>Agaricomycetes</i>. We anticipate that the gene compendium presented here, combined with developments in functional genomics approaches will contribute to uncovering the genetic bases of one of the most spectacular multicellular developmental processes in fungi. <b>Citation:</b> Nagy LG, Vonk PJ, Künzler M, Földi C, Virágh M, Ohm RA, Hennicke F, Bálint B, Csernetics Á, Hegedüs B, Hou Z, Liu XB, Nan S, M. Pareek M, Sahu N, Szathmári B, Varga T, Wu W, Yang X, Merényi Z (2023). Lessons on fruiting body morphogenesis from genomes and transcriptomes of <i>Agaricomycetes. Studies in Mycology</i> <b>104</b>: 1-85. doi: 10
成菇真菌的子实体(孢子囊、孢子或担子瘤)是真菌产生的最复杂的结构之一。与营养菌丝不同,子实体的生长是决定性的,并遵循遗传编码的发育程序,协调它们的生长、组织分化和性孢子形成。尽管经过一个多世纪的研究,我们对子实体形态发生的分子细节的了解仍然有限,缺乏对这一复杂过程的遗传学综合。在本文中,我们旨在全面鉴定与子实体形态发生有关的保守基因,并对功能不明确的基因提出新的功能假设。根据这一分析结果,我们报道了921个保守的发育表达基因家族,其中只有几十个先前被报道参与子实体发育。基于文献数据、保守表达模式和功能注释,我们对这些基因家族在子实体发育中的潜在作用提出了假设,得到了迄今为止最完整的子实体形态发生分子过程描述。我们讨论了与结果、分化、生长、细胞表面和细胞壁、防御、转录调控以及信号转导有关的基因。基于这些数据,我们得出了子实体发育的一般模型,其中包括早期的增殖阶段,主要涉及制定蘑菇体计划(通过细胞分裂和分化),以及通过细胞扩增以及减数分裂事件和产孢的第二阶段生长。我们总共讨论了1 480个铜opsis cinerea的基因,以及它们在双孢蘑菇(Agaricus bisporus)、绿环菌(Cyclocybe aegerita)、蜜环菌(Armillaria ostoyae)、耳虫(Auriculariopsis ampla)、双色乳酸菌(Laccaria bicolor)、香菇(Lentinula edodes)、香菇(lentus tigrinus)、肯特菌(Mycena kentingensis)、黄孢平革菌(Phanerochaete chrysporium)、平菇(Pleurotus ostreatus)和裂叶菌(Schizophyllum commune)中的同源基因,为这些物种基因组中约10%的基因提供了功能假设。虽然这些基因作用的实验证据需要在未来建立,但我们的数据为指导真菌中结果相关基因的功能分析提供了路线图。我们预计,这里提出的基因纲要,结合功能基因组学方法的发展,将有助于揭示真菌中最壮观的多细胞发育过程之一的遗传基础。引用本文:Nagy LG, Vonk PJ, k zler M, Földi C, Virágh M, Ohm RA, Hennicke F, Bálint B, csertics Á, heged S B,侯志,刘小斌,Nan S, M. Pareek M, Sahu N, Szathmári B, Varga T,吴伟,杨旭,mersamnyi Z(2023)。菌丝体基因组和转录组对子实体形态发生的启示。真菌学研究104:1-85。doi: 10.3114 / sim.2022.104.01。
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Pub Date : 2023-06-01Epub Date: 2023-05-25DOI: 10.3114/sim.2023.105.01
M Groenewald, C T Hittinger, K Bensch, D A Opulente, X-X Shen, Y Li, C Liu, A L LaBella, X Zhou, S Limtong, S Jindamorakot, P Gonçalves, V Robert, K H Wolfe, C A Rosa, T Boekhout, N Čadež, G Éter, J P Sampaio, M-A Lachance, A M Yurkov, H-M Daniel, M Takashima, K Boundy-Mills, D Libkind, K Aoki, T Sugita, A Rokas
<p><p>The subphylum <i>Saccharomycotina</i> is a lineage in the fungal phylum <i>Ascomycota</i> that exhibits levels of genomic diversity similar to those of plants and animals. The <i>Saccharomycotina</i> consist of more than 1 200 known species currently divided into 16 families, one order, and one class. Species in this subphylum are ecologically and metabolically diverse and include important opportunistic human pathogens, as well as species important in biotechnological applications. Many traits of biotechnological interest are found in closely related species and often restricted to single phylogenetic clades. However, the biotechnological potential of most yeast species remains unexplored. Although the subphylum <i>Saccharomycotina</i> has much higher rates of genome sequence evolution than its sister subphylum, <i>Pezizomycotina</i>, it contains only one class compared to the 16 classes in <i>Pezizomycotina</i>. The third subphylum of <i>Ascomycota</i>, the <i>Taphrinomycotina</i>, consists of six classes and has approximately 10 times fewer species than the <i>Saccharomycotina</i>. These data indicate that the current classification of all these yeasts into a single class and a single order is an underappreciation of their diversity. Our previous genome-scale phylogenetic analyses showed that the <i>Saccharomycotina</i> contains 12 major and robustly supported phylogenetic clades; seven of these are current families (<i>Lipomycetaceae, Trigonopsidaceae, Alloascoideaceae, Pichiaceae, Phaffomycetaceae, Saccharomycodaceae</i>, and <i>Saccharomycetaceae</i>), one comprises two current families (<i>Dipodascaceae</i> and <i>Trichomonascaceae</i>), one represents the genus <i>Sporopachydermia</i>, and three represent lineages that differ in their translation of the CUG codon (CUG-Ala, CUG-Ser1, and CUG-Ser2). Using these analyses in combination with relative evolutionary divergence and genome content analyses, we propose an updated classification for the <i>Saccharomycotina</i>, including seven classes and 12 orders that can be diagnosed by genome content. This updated classification is consistent with the high levels of genomic diversity within this subphylum and is necessary to make the higher rank classification of the <i>Saccharomycotina</i> more comparable to that of other fungi, as well as to communicate efficiently on lineages that are not yet formally named. <b>Taxonomic novelties: New classes:</b> <i>Alloascoideomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Dipodascomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Lipomycetes</i> M. Groenew., Hittinger, Opulente, A. Rokas, <i>Pichiomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Sporopachydermiomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Trigonopsidomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas. <b>New orders:</b> <i><b>Alloascoideomycetes:</b></i> <i>Alloascoideales</i> M. Groenew., Hittinger, Opulente & A. Rokas; <i><b>Di
酵母菌亚门(subphylum Saccharomycotina)是真菌门(Ascomycota)中的一个分支,其基因组多样性水平与动植物相似。酵母菌亚门目前有 1200 多个已知物种,分为 16 科、1 目和 1 类。该亚门中的物种在生态和新陈代谢方面具有多样性,包括重要的人类机会性病原体以及在生物技术应用中非常重要的物种。许多具有生物技术意义的性状都存在于近缘物种中,而且往往局限于单一的系统发育支系。然而,大多数酵母物种的生物技术潜力仍有待开发。虽然酵母亚门的基因组序列进化速度远高于其姊妹亚门 Pezizomycotina,但与 Pezizomycotina 的 16 个类别相比,酵母亚门只包含一个类别。Ascomycota 的第三个亚门,Taphrinomycotina,包括 6 个类别,其物种数量大约是 Saccharomycotina 的 10 倍。这些数据表明,目前将所有这些酵母菌分为一个类和一个目是对其多样性的低估。我们之前进行的基因组规模的系统发育分析表明,酵母菌纲包含 12 个主要的、得到强有力支持的系统发育支系;其中 7 个是现存的科(唇形科、三叉科、藻类学科、藻类学科、藻类学科、酵母菌科和酵母菌科)、一个代表目前的两个科(Dipodascaceae 和 Trichomonascaceae),一个代表 Sporopachydermia 属,三个代表在翻译 CUG 密码子(CUG-Ala、CUG-Ser1 和 CUG-Ser2)时不同的品系。通过这些分析以及相对进化差异和基因组含量分析,我们提出了酵母菌纲的最新分类方法,包括可通过基因组含量进行诊断的 7 类和 12 目。这一更新的分类与该亚门中基因组的高度多样性相一致,而且对于使酵母菌亚门的高等级分类与其他真菌的高等级分类更具有可比性,以及对尚未正式命名的世系进行有效交流是必要的。新分类法:新类别:Alloascoideomycetes M. Groenew.Rokas, Dipodascomycetes M. Groenew.Rokas, Lipomycetes M. Groenew.Rokas, Sporopachydermiomycetes M. Groenew.Rokas, Trigonopsidomycetes M. Groenew.Rokas.New orders:Alloascoideomycetes:Alloascoideales M. Groenew.Rokas; Dipodascomycetes:Dipodascales M. Groenew.Rokas; Lipomycetes:Groenew., Hittinger, Opulente & A. Rokas; Lipomycetes: Lipomycetales M. Groenew.Rokas; Pichiomycetes:Alaninales M. Groenew.Groenew., Hittinger, Opulente & A. Rokas; Pichiomycetes: Alaninales M. Groenew.Rokas, Serinales M. Groenew.Rokas; Saccharomycetes:M.Groenew.、Hittinger、Opulente & A. Rokas;Saccharomycetes: Phaffomycetales M. Groenew.Groenew., Hittinger, Opulente & A. Rokas; Saccharomycetes: Phaffomycetales M. Groenew.Rokas; Sporopachydermiomycetes:Sporopachydermiales M. Groenew.Rokas; Trigonopsidomycetes:Groenew., Hittinger, Opulente & A. Rokas; Trigonopsidomycetes: Trigonopsidales M. Groenew.Rokas.New families:Alaninales:新科:Alaninales: Pachysolenaceae M. Groenew.Rokas; Pichiales:Pichiaceae M. Groenew.Rokas; Sporopachydermiales:Groenew., Hittinger, Opulente & A. Rokas; Sporopachydermiales: Sporopachydermiaceae M. Groenew.Rokas.引用:Groenewald M, Hittinger CT, Bensch K, Opulente DA, Shen X-X, Li Y, Liu C, LaBella AL, Zhou X, Limtong S, Jindamorakot S, Gonçalves P, Robert V, Wolfe KH, Rosa CA、Boekhout T, Čadež N, Péter G, Sampaio JP, Lachance M-A, Yurkov AM, Daniel H-M, Takashima M, Boundy-Mills K, Libkind D, Aoki K, Sugita T, Rokas A (2023).具有重要生物技术价值的真菌亚门酵母菌的基因组信息高等级分类。Doi: 10.3114/sim.2023.105.01 本研究献给酵母分类学先驱 Cletus P. Kurtzman(1938-2017 年)。
{"title":"A genome-informed higher rank classification of the biotechnologically important fungal subphylum <i>Saccharomycotina</i>.","authors":"M Groenewald, C T Hittinger, K Bensch, D A Opulente, X-X Shen, Y Li, C Liu, A L LaBella, X Zhou, S Limtong, S Jindamorakot, P Gonçalves, V Robert, K H Wolfe, C A Rosa, T Boekhout, N Čadež, G Éter, J P Sampaio, M-A Lachance, A M Yurkov, H-M Daniel, M Takashima, K Boundy-Mills, D Libkind, K Aoki, T Sugita, A Rokas","doi":"10.3114/sim.2023.105.01","DOIUrl":"10.3114/sim.2023.105.01","url":null,"abstract":"<p><p>The subphylum <i>Saccharomycotina</i> is a lineage in the fungal phylum <i>Ascomycota</i> that exhibits levels of genomic diversity similar to those of plants and animals. The <i>Saccharomycotina</i> consist of more than 1 200 known species currently divided into 16 families, one order, and one class. Species in this subphylum are ecologically and metabolically diverse and include important opportunistic human pathogens, as well as species important in biotechnological applications. Many traits of biotechnological interest are found in closely related species and often restricted to single phylogenetic clades. However, the biotechnological potential of most yeast species remains unexplored. Although the subphylum <i>Saccharomycotina</i> has much higher rates of genome sequence evolution than its sister subphylum, <i>Pezizomycotina</i>, it contains only one class compared to the 16 classes in <i>Pezizomycotina</i>. The third subphylum of <i>Ascomycota</i>, the <i>Taphrinomycotina</i>, consists of six classes and has approximately 10 times fewer species than the <i>Saccharomycotina</i>. These data indicate that the current classification of all these yeasts into a single class and a single order is an underappreciation of their diversity. Our previous genome-scale phylogenetic analyses showed that the <i>Saccharomycotina</i> contains 12 major and robustly supported phylogenetic clades; seven of these are current families (<i>Lipomycetaceae, Trigonopsidaceae, Alloascoideaceae, Pichiaceae, Phaffomycetaceae, Saccharomycodaceae</i>, and <i>Saccharomycetaceae</i>), one comprises two current families (<i>Dipodascaceae</i> and <i>Trichomonascaceae</i>), one represents the genus <i>Sporopachydermia</i>, and three represent lineages that differ in their translation of the CUG codon (CUG-Ala, CUG-Ser1, and CUG-Ser2). Using these analyses in combination with relative evolutionary divergence and genome content analyses, we propose an updated classification for the <i>Saccharomycotina</i>, including seven classes and 12 orders that can be diagnosed by genome content. This updated classification is consistent with the high levels of genomic diversity within this subphylum and is necessary to make the higher rank classification of the <i>Saccharomycotina</i> more comparable to that of other fungi, as well as to communicate efficiently on lineages that are not yet formally named. <b>Taxonomic novelties: New classes:</b> <i>Alloascoideomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Dipodascomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Lipomycetes</i> M. Groenew., Hittinger, Opulente, A. Rokas, <i>Pichiomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Sporopachydermiomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas, <i>Trigonopsidomycetes</i> M. Groenew., Hittinger, Opulente & A. Rokas. <b>New orders:</b> <i><b>Alloascoideomycetes:</b></i> <i>Alloascoideales</i> M. Groenew., Hittinger, Opulente & A. Rokas; <i><b>Di","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"1 1","pages":"1-22"},"PeriodicalIF":14.1,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11182611/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69600543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-06-01Epub Date: 2023-06-12DOI: 10.3114/sim.2023.105.03
L Zhao, J Z Groenewald, M Hernández-Restrepo, H-J Schroers, P W Crous
<p><p><i>Clonostachys</i> (<i>Bionectriaceae</i>, <i>Hypocreales</i>) species are common soil-borne fungi, endophytes, epiphytes, and saprotrophs. Sexual morphs of <i>Clonostachys</i> spp<i>.</i> were placed in the genus <i>Bionectria</i>, which was further segregated into the six subgenera <i>Astromata</i>, <i>Bionectria</i>, <i>Epiphloea</i>, <i>Myronectria</i>, <i>Uniparietina</i>, and <i>Zebrinella</i>. However, with the end of dual nomenclature, <i>Clonostachys</i> became the single depository for sexual and asexual morph-typified species. Species of <i>Clonostachys</i> are typically characterised by penicillate, sporodochial, and, in many cases, dimorphic conidiophores (primary and secondary conidiophores). Primary conidiophores are mononematous, either verticillium-like or narrowly penicillate. The secondary conidiophores generally form imbricate conidial chains that can collapse to slimy masses, particularly on sporodochia. In the present study, we investigated the species diversity within a collection of 420 strains of <i>Clonostachys</i> from the culture collection of, and personal collections at, the Westerdijk Fungal Biodiversity Institute in Utrecht, the Netherlands. Strains were analysed based on their morphological characters and molecular phylogeny. The latter used DNA sequence data of the nuclear ribosomal internal transcribed spacer regions and intervening 5.8S nrDNA (ITS) and partial 28S large subunit (LSU) nrDNA and partial protein encoding genes including the RNA polymerase II second largest subunit (<i>RPB2</i>), translation elongation factor 1-alpha (<i>TEF1</i>) and β-tubulin (<i>TUB2</i>). Based on these results, the subgenera <i>Astromata</i>, <i>Bionectria</i>, <i>Myronectria</i> and <i>Zebrinella</i> are supported within <i>Clonostachys</i>. Furthermore, the genus <i>Sesquicillium</i> is resurrected to accommodate the former subgenera <i>Epiphloea</i> and <i>Uniparietina</i>. The close relationship of <i>Clonostachys</i> and <i>Sesquicillium</i> is strongly supported as both are inferred phylogenetically as sister-genera. New taxa include 24 new species and 10 new combinations. Recognition of <i>Sesquicillium</i> distinguishes species typically forming a reduced perithecial stroma superficially on plant tissue from species in <i>Clonostachys</i> often forming well-developed, through bark erumpent stromata. The patterns of observed perithecial wall anatomies, perithecial wall and stroma interfaces, and asexual morph diversifications described in a previously compiled monograph are used for interpreting ancestral state reconstructions. It is inferred that the common ancestor of <i>Clonostachys</i> and <i>Sesquicillium</i> may have formed perithecia superficially on leaves, possessed a perithecial wall consisting of a single region, and formed intercalary phialides in penicilli of conidiophores. Character interpretation may also allow hypothesising that diversification of morphs occurred then in the two genera independent
Luo & W.Y. Zhuang)Z.Q. Zeng & W.Y. Zhuang.Epitypes (basionyms):Fusidium buxi J.C. Schmidt ex Link, Verticillium candelabrum Bonord.引用:Zhao L, Groenewald JZ, Hernández-Restrepo M, Schroers H-J, Crous PW (2023).Revising Clonostachys and allied genera in Bionectriaceae.Doi: 10.3114/sim.2023.105.03.
{"title":"Revising <i>Clonostachys</i> and allied genera in <i>Bionectriaceae</i>.","authors":"L Zhao, J Z Groenewald, M Hernández-Restrepo, H-J Schroers, P W Crous","doi":"10.3114/sim.2023.105.03","DOIUrl":"10.3114/sim.2023.105.03","url":null,"abstract":"<p><p><i>Clonostachys</i> (<i>Bionectriaceae</i>, <i>Hypocreales</i>) species are common soil-borne fungi, endophytes, epiphytes, and saprotrophs. Sexual morphs of <i>Clonostachys</i> spp<i>.</i> were placed in the genus <i>Bionectria</i>, which was further segregated into the six subgenera <i>Astromata</i>, <i>Bionectria</i>, <i>Epiphloea</i>, <i>Myronectria</i>, <i>Uniparietina</i>, and <i>Zebrinella</i>. However, with the end of dual nomenclature, <i>Clonostachys</i> became the single depository for sexual and asexual morph-typified species. Species of <i>Clonostachys</i> are typically characterised by penicillate, sporodochial, and, in many cases, dimorphic conidiophores (primary and secondary conidiophores). Primary conidiophores are mononematous, either verticillium-like or narrowly penicillate. The secondary conidiophores generally form imbricate conidial chains that can collapse to slimy masses, particularly on sporodochia. In the present study, we investigated the species diversity within a collection of 420 strains of <i>Clonostachys</i> from the culture collection of, and personal collections at, the Westerdijk Fungal Biodiversity Institute in Utrecht, the Netherlands. Strains were analysed based on their morphological characters and molecular phylogeny. The latter used DNA sequence data of the nuclear ribosomal internal transcribed spacer regions and intervening 5.8S nrDNA (ITS) and partial 28S large subunit (LSU) nrDNA and partial protein encoding genes including the RNA polymerase II second largest subunit (<i>RPB2</i>), translation elongation factor 1-alpha (<i>TEF1</i>) and β-tubulin (<i>TUB2</i>). Based on these results, the subgenera <i>Astromata</i>, <i>Bionectria</i>, <i>Myronectria</i> and <i>Zebrinella</i> are supported within <i>Clonostachys</i>. Furthermore, the genus <i>Sesquicillium</i> is resurrected to accommodate the former subgenera <i>Epiphloea</i> and <i>Uniparietina</i>. The close relationship of <i>Clonostachys</i> and <i>Sesquicillium</i> is strongly supported as both are inferred phylogenetically as sister-genera. New taxa include 24 new species and 10 new combinations. Recognition of <i>Sesquicillium</i> distinguishes species typically forming a reduced perithecial stroma superficially on plant tissue from species in <i>Clonostachys</i> often forming well-developed, through bark erumpent stromata. The patterns of observed perithecial wall anatomies, perithecial wall and stroma interfaces, and asexual morph diversifications described in a previously compiled monograph are used for interpreting ancestral state reconstructions. It is inferred that the common ancestor of <i>Clonostachys</i> and <i>Sesquicillium</i> may have formed perithecia superficially on leaves, possessed a perithecial wall consisting of a single region, and formed intercalary phialides in penicilli of conidiophores. Character interpretation may also allow hypothesising that diversification of morphs occurred then in the two genera independent","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"1 1","pages":"205-266"},"PeriodicalIF":16.5,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11182609/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69601202","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-06-01Epub Date: 2023-06-02DOI: 10.3114/sim.2023.105.02
L W Hou, A Giraldo, J Z Groenewald, T Rämä, R C Summerbell, G Z Huang, L Cai, P W Crous
<p><p><i>Acremonium</i> is acknowledged as a highly ubiquitous genus including saprobic, parasitic, or endophytic fungi that inhabit a variety of environments. Species of this genus are extensively exploited in industrial, commercial, pharmaceutical, and biocontrol applications, and proved to be a rich source of novel and bioactive secondary metabolites. <i>Acremonium</i> has been recognised as a taxonomically difficult group of ascomycetes, due to the reduced and high plasticity of morphological characters, wide ecological distribution and substrate range. Recent advances in molecular phylogenies, revealed that <i>Acremonium</i> is highly polyphyletic and members of <i>Acremonium</i> <i>s. lat.</i> belong to at least three distinct orders of <i>Sordariomycetes</i>, of which numerous orders, families and genera with acremonium-like morphs remain undefined. To infer the phylogenetic relationships and establish a natural classification for acremonium-like taxa, systematic analyses were conducted based on a large number of cultures with a global distribution and varied substrates. A total of 633 cultures with acremonium-like morphology, including 261 ex-type cultures from 89 countries and a variety of substrates including soil, plants, fungi, humans, insects, air, and water were examined. An overview phylogenetic tree based on three loci (ITS, LSU, <i>rpb2</i>) was generated to delimit the orders and families. Separate trees based on a combined analysis of four loci (ITS, LSU, <i>rpb2</i>, <i>tef-1α</i>) were used to delimit species at generic and family levels. Combined with the morphological features, host associations and ecological analyses, acremonium-like species evaluated in the present study are currently assigned to 63 genera, and 14 families in <i>Cephalothecales,</i> <i>Glomerellales</i> and <i>Hypocreales</i>, mainly in the families <i>Bionectriaceae</i>, <i>Plectosphaerellaceae</i> and <i>Sarocladiaceae</i> and five new hypocrealean families, namely <i>Chrysonectriaceae</i>, <i>Neoacremoniaceae</i>, <i>Nothoacremoniaceae</i>, <i>Pseudoniessliaceae</i> and <i>Valsonectriaceae</i>. Among them, 17 new genera and 63 new combinations are proposed, with descriptions of 65 new species. Furthermore, one epitype and one neotype are designated to stabilise the taxonomy and use of older names. Results of this study demonstrated that most species of <i>Acremonium</i> <i>s. lat.</i> grouped in genera of <i>Bionectriaceae</i>, including the type <i>A</i>. <i>alternatum</i>. A phylogenetic backbone tree is provided for <i>Bionectriaceae</i>, in which 183 species are recognised and 39 well-supported genera are resolved, including 10 new genera. Additionally, <i>rpb2</i> and <i>tef-1α</i> are proposed as potential DNA barcodes for the identification of taxa in <i>Bionectriaceae</i>. <b>Taxonomic novelties: New families:</b> <i>Chrysonectriaceae</i> L.W. Hou, L. Cai & Crous, <i>Neoacremoniaceae</i> L.W. Hou, L. Cai & Crous, <i>Nothoacremoniaceae</i> L.W.
Cai & Crous, Protocreopsis finnmarkica L.W. Hou, L. Cai, Rämä & Crous, Proxiovicillium lepidopterorum L.W. Hou, L. Cai & Crous, Ramosiphorum echinoporiae L.W. Hou, L. Cai & Crous, R. polyporicola L.W. Hou, L. Cai & Crous, R. thailandicum L.W. Hou, L. Cai & Crous, Verruciconidia erythroxyli L.W. Hou, L. Cai & Crous, Ve. infuscata L.W. Hou, L. Cai & Crous.thailandicum L.W. Hou, L. Cai & Crous, Verruciconidia erythroxyli L.W. Hou, L. Cai & Crous, Ve. infuscata L.W. Hou, L. Cai & Crous, Ve. quercina L.W. Hou, L. Cai & Crous, Ve. siccicapita L.W. Hou, L. Cai & Crous, Ve. unguis L.W. Hou, L. Cai & Crous, Waltergis L.W. Hou, L. Cai & Crous.Cai & Crous, Waltergamsia alkalina L.W. Hou, L. Cai & Crous, W. catenata L.W. Hou, L. Cai & Crous, W. moroccensis L.W. Hou, L. Cai & Crous, W. obpyriformis L.W. Hou, L. Cai & Crous; Chrysonectriaceae: Chrysonectria crystallifera L.W. Hou, L. Cai & Crous; Nectectriaceae: Chrysonectria crystallifera L.W. Hou, L. Cai & Crous.Cai & Crous; Nectriaceae: Xenoacremonium allantoideum L.W. Hou, L. Cai & Crous; Neoacremoniaceae: Neoacremonium distortum L.W. Hou, L. Cai & Crous, N. flavum L.W. Hou, L. Cai & Crous; Nothoacremoniaceae: Nothoacremonium subcylindricum L. W. Hou, L. Cai & Crous; Nothoacremoniaceae: Nothoacremonium subcylindricum L. W. Hou, L. Cai & Crous.W. Hou, L. Cai & Crous, No. vesiculophorum L.W. Hou, L. Cai & Crous; Myrotheciomycetaceae: Trichothecium hongkongense L.W. Hou, L. Cai & Crous; Plectosphaerellaceae: Brunneomyces polyphialidus L.W. Hou, L. Cai & Crous, Parafuscohypha proliferata L. W. Hou, L. Cai & Crous.Sarocladiaceae: Chlamydocillium acaciae L.W. Hou, L. Cai & Crous, C. antarcticum L.W. Hou, L. Cai & Crous, C. guttulatum L.W. Hou, L. Cai & Crous, C. lolii L.W. Hou, L. Cai & Crous, C. soli L.W. Hou, L. Cai & Crous.Hou, L. Cai & Crous, C. terrestre L.W. Hou, L. Cai & Crous, Parasarocladium chondroidum L.W. Hou, L. Cai & Crous, Polyphialocladium fusisporum L.W. Hou, L. Cai & Crous, Sarocladium agarici L.W. Hou, L. Cai & Crous, S. citri L.W. Hou, L. Cai & Crous, S. citri L.W. Hou, L. Cai & Crous, S. citri L.W. Hou, L. Cai & Crous, S. citri L.W. Hou, L. Cai & Crous.Cai & Crous,S. ferrugineum L.W.Hou,L. Cai & Crous,S. fuscum L.W.Hou,L. Cai & Crous,S. theobromae L.W.Hou,L. Cai & Crous;Valsonectriaceae:Valsonectria crystalligena L.W.Hou,L. Cai & Crous,V. hilaris L.W.Hou,L. Cai & Crous。New combinations: Bionectriaceae: Acremonium purpurascens (Sukapure & Thirum.) L.W. Hou, L. Cai & Crous, Bulbithecium arxii (Malloch) L.W. Hou, L. Cai & Crous, Bu.Borodinense (Tad. Ito et al.) L.W. Hou, L. Cai & Crous, Bulbithecium arxii (Malloch) L.W. Hou, L. Cai & Crous, Bu.L.W. Hou, L. Cai & Crous, Emericellopsis exuviara (Sigler et al.) L.W. Hou, L. Cai & Crous, E. fimetaria (Pers.) L.W.
{"title":"Redisposition of acremonium-like fungi in <i>Hypocreales</i>.","authors":"L W Hou, A Giraldo, J Z Groenewald, T Rämä, R C Summerbell, G Z Huang, L Cai, P W Crous","doi":"10.3114/sim.2023.105.02","DOIUrl":"10.3114/sim.2023.105.02","url":null,"abstract":"<p><p><i>Acremonium</i> is acknowledged as a highly ubiquitous genus including saprobic, parasitic, or endophytic fungi that inhabit a variety of environments. Species of this genus are extensively exploited in industrial, commercial, pharmaceutical, and biocontrol applications, and proved to be a rich source of novel and bioactive secondary metabolites. <i>Acremonium</i> has been recognised as a taxonomically difficult group of ascomycetes, due to the reduced and high plasticity of morphological characters, wide ecological distribution and substrate range. Recent advances in molecular phylogenies, revealed that <i>Acremonium</i> is highly polyphyletic and members of <i>Acremonium</i> <i>s. lat.</i> belong to at least three distinct orders of <i>Sordariomycetes</i>, of which numerous orders, families and genera with acremonium-like morphs remain undefined. To infer the phylogenetic relationships and establish a natural classification for acremonium-like taxa, systematic analyses were conducted based on a large number of cultures with a global distribution and varied substrates. A total of 633 cultures with acremonium-like morphology, including 261 ex-type cultures from 89 countries and a variety of substrates including soil, plants, fungi, humans, insects, air, and water were examined. An overview phylogenetic tree based on three loci (ITS, LSU, <i>rpb2</i>) was generated to delimit the orders and families. Separate trees based on a combined analysis of four loci (ITS, LSU, <i>rpb2</i>, <i>tef-1α</i>) were used to delimit species at generic and family levels. Combined with the morphological features, host associations and ecological analyses, acremonium-like species evaluated in the present study are currently assigned to 63 genera, and 14 families in <i>Cephalothecales,</i> <i>Glomerellales</i> and <i>Hypocreales</i>, mainly in the families <i>Bionectriaceae</i>, <i>Plectosphaerellaceae</i> and <i>Sarocladiaceae</i> and five new hypocrealean families, namely <i>Chrysonectriaceae</i>, <i>Neoacremoniaceae</i>, <i>Nothoacremoniaceae</i>, <i>Pseudoniessliaceae</i> and <i>Valsonectriaceae</i>. Among them, 17 new genera and 63 new combinations are proposed, with descriptions of 65 new species. Furthermore, one epitype and one neotype are designated to stabilise the taxonomy and use of older names. Results of this study demonstrated that most species of <i>Acremonium</i> <i>s. lat.</i> grouped in genera of <i>Bionectriaceae</i>, including the type <i>A</i>. <i>alternatum</i>. A phylogenetic backbone tree is provided for <i>Bionectriaceae</i>, in which 183 species are recognised and 39 well-supported genera are resolved, including 10 new genera. Additionally, <i>rpb2</i> and <i>tef-1α</i> are proposed as potential DNA barcodes for the identification of taxa in <i>Bionectriaceae</i>. <b>Taxonomic novelties: New families:</b> <i>Chrysonectriaceae</i> L.W. Hou, L. Cai & Crous, <i>Neoacremoniaceae</i> L.W. Hou, L. Cai & Crous, <i>Nothoacremoniaceae</i> L.W.","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"1 1","pages":"23-203"},"PeriodicalIF":16.5,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11182610/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69601162","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
E. Tanaka, K. Tanada, T. Hosoe, B. Shrestha, M. Kolařík, M. Liu
Claviceps (Clavicipitaceae, Hypocreales) was erected in 1853, although ergotism had been well-known for a much longer time. By 2000, about 70 taxa had been described in Claviceps, of which eight species and six varieties were based on Japanese type or authentic specimens. Most of these Japanese Claviceps taxa are based on lost specimens or have invalid names, which means many species practically exist only in the scientific literature. The ambiguous identities of these species have hindered taxonomic resolution of the genus Claviceps. Consequently, we sought and collected more than 300 fresh specimens in search of the lost Japanese ergots. Multilocus phylogenetic analyses based on DNA sequences from LSU, TEF-1α, TUB2, Mcm7, and RPB2 revealed the phylogenetic relationships between the Japanese specimens and known Claviceps spp., as well as the presence of biogeographic patterns. Based on the phylogenetic analysis, host range and morphology, we re-evaluated Japanese Claviceps and recognised at least 21 species in Japan. Here we characterised 14 previously described taxa and designated neo-, lecto- and epi-types for C. bothriochloae, C. imperatae, C. litoralis, C. microspora, C. panicoidearum and C. yanagawaensis. Two varieties were elevated to species rank with designated neotypes, i.e. C. agropyri and C. kawatanii. Six new species, C. miscanthicola, C. oplismeni, C. palustris, C. phragmitis, C. sasae and C. tandae were proposed and described.
{"title":"In search of lost ergots: phylogenetic re-evaluation of Claviceps species in Japan and their biogeographic patterns revealed","authors":"E. Tanaka, K. Tanada, T. Hosoe, B. Shrestha, M. Kolařík, M. Liu","doi":"10.3114/sim.2022.106.01","DOIUrl":"https://doi.org/10.3114/sim.2022.106.01","url":null,"abstract":"Claviceps (Clavicipitaceae, Hypocreales) was erected in 1853, although ergotism had been well-known for a much longer time. By 2000, about 70 taxa had been described in Claviceps, of which eight species and six varieties were based on Japanese type or authentic specimens. Most of these Japanese Claviceps taxa are based on lost specimens or have invalid names, which means many species practically exist only in the scientific literature. The ambiguous identities of these species have hindered taxonomic resolution of the genus Claviceps. Consequently, we sought and collected more than 300 fresh specimens in search of the lost Japanese ergots. Multilocus phylogenetic analyses based on DNA sequences from LSU, TEF-1α, TUB2, Mcm7, and RPB2 revealed the phylogenetic relationships between the Japanese specimens and known Claviceps spp., as well as the presence of biogeographic patterns. Based on the phylogenetic analysis, host range and morphology, we re-evaluated Japanese Claviceps and recognised at least 21 species in Japan. Here we characterised 14 previously described taxa and designated neo-, lecto- and epi-types for C. bothriochloae, C. imperatae, C. litoralis, C. microspora, C. panicoidearum and C. yanagawaensis. Two varieties were elevated to species rank with designated neotypes, i.e. C. agropyri and C. kawatanii. Six new species, C. miscanthicola, C. oplismeni, C. palustris, C. phragmitis, C. sasae and C. tandae were proposed and described.","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"1 1","pages":""},"PeriodicalIF":16.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69600421","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Escovopsis is a symbiont of fungus-growing ant colonies. Unstandardised taxonomy prevented the evaluation of the morphological diversity of Escovopsis for more than a century. The aim of this study is to create a standardised taxonomic framework to assess the morphological and phylogenetic diversity of Escovopsis . Therefore, to set the foundation for Escovopsis taxonomy and allow interspecific comparisons within the genus, we redescribe the ex-type cultures of Escovopsis aspergilloides , E. clavata , E. lentecrescens , E. microspora , E. moelleri , E. multiformis , and E. weberi . Thus, based on the parameters adopted in this study combined with phylogenetic analyses using five molecular markers, we synonymize E. microspora with E. weberi , and introduce 13 new species isolated from attine nests collected in Argentina, Brazil, Costa Rica, Mexico, and Panama: E. breviramosa , E. chlamydosporosa , E. diminuta , E. elongatistipitata , E. gracilis , E. maculosa , E. papillata , E. peniculiformis , E. phialicopiosa , E. pseudocylindrica , E. rectangula , E. rosisimilis , and E. spicaticlavata . Our results revealed a great interspecific morphological diversity throughout Escovopsis . Notwithstanding, colony growth rates at different temperatures, as well as vesicle shape, appear to be the most outstanding features distinguishing species in the genus. This study fills an important gap in the systematics of Escovopsis that will allow future researchers to unravel the genetic and morphological diversity and species diversification of these attine ant symbionts.
Escovopsis是真菌生长蚁群的共生体。一个多世纪以来,未标准化的分类方法阻碍了对蛇尾草形态多样性的评估。本研究的目的是建立一个标准化的分类框架,以评估Escovopsis的形态和系统发育多样性。因此,为了为Escovopsis分类奠定基础,并允许在属内进行种间比较,我们重新描述了Escovopsis aspergilloides, E. clavata, E. lentecrescens, E. microspora, E. moelleri, E. multiformis和E. weberi的前型培养。因此,基于本研究所采用的参数,结合5个分子标记的系统发育分析,我们将小孢子e与weberi进行了同义化,并引入了从阿根廷、巴西、哥斯达黎加、墨西哥和巴拿马采集的阿丁巢中分离的13个新种:e . breviramosa e . chlamydosporosa e . diminuta e . elongatistipitata e .股薄肌e . maculosa e . papillata e . peniculiformis e . phialicopiosa e . pseudocylindrica e . rectangula大肠rosisimilis,大肠spicaticlavata。我们的研究结果揭示了整个Escovopsis的巨大种间形态多样性。尽管如此,不同温度下的菌落生长速度以及囊泡形状似乎是该属中区分物种的最显著特征。这项研究填补了蚁群系统学的重要空白,为未来的研究人员揭示这些蚁群共生体的遗传和形态多样性以及物种多样性提供了基础。
{"title":"Taxonomy and systematics of the fungus-growing ant associate Escovopsis (Hypocreaceae)","authors":"Q.V. Montoya, M.J.S. Martiarena, A. Rodrigues","doi":"10.3114/sim.2023.106.06","DOIUrl":"https://doi.org/10.3114/sim.2023.106.06","url":null,"abstract":"Escovopsis is a symbiont of fungus-growing ant colonies. Unstandardised taxonomy prevented the evaluation of the morphological diversity of Escovopsis for more than a century. The aim of this study is to create a standardised taxonomic framework to assess the morphological and phylogenetic diversity of Escovopsis . Therefore, to set the foundation for Escovopsis taxonomy and allow interspecific comparisons within the genus, we redescribe the ex-type cultures of Escovopsis aspergilloides , E. clavata , E. lentecrescens , E. microspora , E. moelleri , E. multiformis , and E. weberi . Thus, based on the parameters adopted in this study combined with phylogenetic analyses using five molecular markers, we synonymize E. microspora with E. weberi , and introduce 13 new species isolated from attine nests collected in Argentina, Brazil, Costa Rica, Mexico, and Panama: E. breviramosa , E. chlamydosporosa , E. diminuta , E. elongatistipitata , E. gracilis , E. maculosa , E. papillata , E. peniculiformis , E. phialicopiosa , E. pseudocylindrica , E. rectangula , E. rosisimilis , and E. spicaticlavata . Our results revealed a great interspecific morphological diversity throughout Escovopsis . Notwithstanding, colony growth rates at different temperatures, as well as vesicle shape, appear to be the most outstanding features distinguishing species in the genus. This study fills an important gap in the systematics of Escovopsis that will allow future researchers to unravel the genetic and morphological diversity and species diversification of these attine ant symbionts.","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135758459","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Z.G. Abad, T.I. Burgess, T. Bourret, K. Bensch, S.O. Cacciola, B. Scanu, R. Mathew, B. Kasiborski, S. Srivastava, K. Kageyama, J.C. Bienapfl, G. Verkleij, K. Broders, L. Schena, A.J. Redford
Many members of the Oomycota genus Phytophthora cause economic and environmental impact diseases in nurseries, horticulture, forest, and natural ecosystems and many are of regulatory concern around the world. At present, there are 223 described species, including eight unculturable and three lost species. Twenty-eight species need to be redescribed or validated. A lectotype, epitype or neotype was selected for 20 species, and a redescription based on the morphological/molecular characters and phylogenetic placement is provided. In addition, the names of five species are validated: P. cajani , P. honggalleglyana (Synonym: P. hydropathica ), P. megakarya , P. pisi and P. pseudopolonica for which morphology and phylogeny are given. Two species, P. ×multiformis and P. uniformis are presented as new combinations. Phytophthora palmivora is treated with a representative strain as both lecto- and epitypification are pending. This manuscript provides the updated multigene phylogeny and molecular toolbox with seven genes (ITS rDNA, β-tub , COI , EF1α , HSP90 , L10 , and YPT1 ) generated from the type specimens of 212 validly published, and culturable species (including nine hybrid taxa). The genome information of 23 types published to date is also included. Several aspects of the taxonomic revision and phylogenetic re-evaluation of the genus including species concepts, concept and position of the phylogenetic clades recognized within Phytophthora are discussed. Some of the contents of this manuscript, including factsheets for the 212 species, are associated with the “ IDphy : molecular and morphological identification of Phytophthora based on the types” online resource (https://idtools.org/tools/1056/index.cfm). The first version of the IDphy online resource released to the public in September 2019 contained 161 species. In conjunction with this publication, we are updating the IDphy online resource to version 2 to include the 51 species recently described. The current status of the 223 described species is provided along with information on type specimens with details of the host (substrate), location, year of collection and publications. Additional information is provided regarding the ex-type culture(s) for the 212 valid culturable species and the diagnostic molecular toolbox with seven genes that includes the two metabarcoding genes (ITS and COI ) that are important for Sanger sequencing and also very valuable Molecular Operational Taxonomic Units (MOTU) for second and third generation metabarcoding High-throughput sequencing (HTS) technologies. The IDphy online resource will continue to be updated annually to include new descriptions. This manuscript in conjunction with IDphy represents a monographic study and the most updated revision of the taxonomy and phylogeny of Phytophthora , widely considered one of the most important genera of plant pathogens.
疫霉菌属的许多成员在苗圃、园艺、森林和自然生态系统中引起经济和环境影响疾病,许多成员在世界范围内受到监管关注。目前,有223个被描述的物种,包括8个不可培养的物种和3个消失的物种。28个物种需要重新描述或验证。对20个种进行了选型、表型和新型分析,并根据形态/分子特征和系统发育定位对其进行了重新描述。此外,还验证了五个物种的名称:P. cajani, P. honggalleglyana(同义:P. hydropathica), P. megakarya, P. pisi和P. pseudopolonica,并给出了形态和系统发育。P. ×multiformis和P. uniformis作为新组合提出。棕榈疫霉用一种有代表性的菌株进行处理,因为两者的凝集和典型化都有待解决。本文提供了更新的多基因系统发育和分子工具箱,其中包括从212个有效发表的模式标本和可培养物种(包括9个杂交分类群)中生成的7个基因(ITS rDNA, β-tub, COI, EF1α, HSP90, L10和YPT1)。还包括迄今已发表的23种类型的基因组信息。本文讨论了该属的分类修订和系统发育重新评价的几个方面,包括种概念、在疫霉菌中发现的系统发育分支的概念和位置。该手稿的部分内容,包括212个物种的情况说明书,与“IDphy:基于类型的疫霉分子和形态学鉴定”在线资源(https://idtools.org/tools/1056/index.cfm)有关。2019年9月向公众发布的第一版IDphy在线资源包含161个物种。与此同时,我们正在将IDphy在线资源更新到第2版,以包括最近描述的51个物种。所描述的223个物种的现状以及模式标本的信息,包括宿主(基质)、地点、收集年份和出版物的详细信息。本文还提供了关于212个有效可培养物种的前型培养和包含7个基因的诊断分子工具箱的附加信息,其中包括两个元条形码基因(ITS和COI),这两个基因对Sanger测序很重要,也是第二代和第三代元条形码高通量测序(HTS)技术非常有价值的分子操作分类单元(MOTU)。IDphy在线资源将继续每年更新,以包括新的描述。该手稿与IDphy一起代表了对疫霉的分类和系统发育的一项专题研究和最新修订,疫霉被广泛认为是植物病原体中最重要的属之一。
{"title":"Phytophthora: taxonomic and phylogenetic revision of the genus","authors":"Z.G. Abad, T.I. Burgess, T. Bourret, K. Bensch, S.O. Cacciola, B. Scanu, R. Mathew, B. Kasiborski, S. Srivastava, K. Kageyama, J.C. Bienapfl, G. Verkleij, K. Broders, L. Schena, A.J. Redford","doi":"10.3114/sim.2023.106.05","DOIUrl":"https://doi.org/10.3114/sim.2023.106.05","url":null,"abstract":"Many members of the Oomycota genus Phytophthora cause economic and environmental impact diseases in nurseries, horticulture, forest, and natural ecosystems and many are of regulatory concern around the world. At present, there are 223 described species, including eight unculturable and three lost species. Twenty-eight species need to be redescribed or validated. A lectotype, epitype or neotype was selected for 20 species, and a redescription based on the morphological/molecular characters and phylogenetic placement is provided. In addition, the names of five species are validated: P. cajani , P. honggalleglyana (Synonym: P. hydropathica ), P. megakarya , P. pisi and P. pseudopolonica for which morphology and phylogeny are given. Two species, P. ×multiformis and P. uniformis are presented as new combinations. Phytophthora palmivora is treated with a representative strain as both lecto- and epitypification are pending. This manuscript provides the updated multigene phylogeny and molecular toolbox with seven genes (ITS rDNA, β-tub , COI , EF1α , HSP90 , L10 , and YPT1 ) generated from the type specimens of 212 validly published, and culturable species (including nine hybrid taxa). The genome information of 23 types published to date is also included. Several aspects of the taxonomic revision and phylogenetic re-evaluation of the genus including species concepts, concept and position of the phylogenetic clades recognized within Phytophthora are discussed. Some of the contents of this manuscript, including factsheets for the 212 species, are associated with the “ IDphy : molecular and morphological identification of Phytophthora based on the types” online resource (https://idtools.org/tools/1056/index.cfm). The first version of the IDphy online resource released to the public in September 2019 contained 161 species. In conjunction with this publication, we are updating the IDphy online resource to version 2 to include the 51 species recently described. The current status of the 223 described species is provided along with information on type specimens with details of the host (substrate), location, year of collection and publications. Additional information is provided regarding the ex-type culture(s) for the 212 valid culturable species and the diagnostic molecular toolbox with seven genes that includes the two metabarcoding genes (ITS and COI ) that are important for Sanger sequencing and also very valuable Molecular Operational Taxonomic Units (MOTU) for second and third generation metabarcoding High-throughput sequencing (HTS) technologies. The IDphy online resource will continue to be updated annually to include new descriptions. This manuscript in conjunction with IDphy represents a monographic study and the most updated revision of the taxonomy and phylogeny of Phytophthora , widely considered one of the most important genera of plant pathogens.","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"19 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136008335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
R. Xue, X. Zhang, C. Xu, H. Xie, L.L. Wu, Y. Wang, L. Tang, Y. Hao, K. Zhao, S. Jiang, Y. Li, Y.Y. Yang, Z. Li, Z. Liang, N. Zeng
Xerocomoideae is an ecologically and economically important Boletaceae subfamily (Boletales) comprising 10 genera. Although many studies have focused on Xerocomoideae in China, the diversity, taxonomy and molecular phylogeny still remained incompletely understood. In the present study, taxonomic and phylogenetic studies on Chinese species of Xerocomoideae were carried out by morphological examinations and molecular phylogenetic analyses. Eight genera in Xerocomoideae, viz. Aureoboletus, Boletellus, Heimioporus, Hemileccinum, Hourangia, Phylloporus, Pulchroboletus, and Xerocomus were confirmed to be distributed in China; 97 species of the subfamily were accepted as being distributed in China; one ambiguous taxon was tentatively named Bol. aff. putuoensis; two synonyms, viz. A. marroninus and P. dimorphus were defined. Among the Chinese accepted species, 13 were newly described, viz. A. albipes, A. conicus, A. ornatipes, Bol. erythrolepis, Bol. rubidus, Bol. sinochrysenteroides, Bol. subglobosus, Bol. zenghuoxingii, H. squamipes, P. hainanensis, Pul. erubescens, X. albotomentosus, and X. fuscatus, 36 known species were redescribed, and the other 48 species were reviewed. Keys to accepted species of Aureoboletus, Boletellus, Heimioporus, Hemileccinum, Hourangia, Phylloporus, and Xerocomus in China were also provided.
{"title":"The subfamily Xerocomoideae (Boletaceae, Boletales) in China","authors":"R. Xue, X. Zhang, C. Xu, H. Xie, L.L. Wu, Y. Wang, L. Tang, Y. Hao, K. Zhao, S. Jiang, Y. Li, Y.Y. Yang, Z. Li, Z. Liang, N. Zeng","doi":"10.3114/sim.2022.106.03","DOIUrl":"https://doi.org/10.3114/sim.2022.106.03","url":null,"abstract":"Xerocomoideae is an ecologically and economically important Boletaceae subfamily (Boletales) comprising 10 genera. Although many studies have focused on Xerocomoideae in China, the diversity, taxonomy and molecular phylogeny still remained incompletely understood. In the present study, taxonomic and phylogenetic studies on Chinese species of Xerocomoideae were carried out by morphological examinations and molecular phylogenetic analyses. Eight genera in Xerocomoideae, viz. Aureoboletus, Boletellus, Heimioporus, Hemileccinum, Hourangia, Phylloporus, Pulchroboletus, and Xerocomus were confirmed to be distributed in China; 97 species of the subfamily were accepted as being distributed in China; one ambiguous taxon was tentatively named Bol. aff. putuoensis; two synonyms, viz. A. marroninus and P. dimorphus were defined. Among the Chinese accepted species, 13 were newly described, viz. A. albipes, A. conicus, A. ornatipes, Bol. erythrolepis, Bol. rubidus, Bol. sinochrysenteroides, Bol. subglobosus, Bol. zenghuoxingii, H. squamipes, P. hainanensis, Pul. erubescens, X. albotomentosus, and X. fuscatus, 36 known species were redescribed, and the other 48 species were reviewed. Keys to accepted species of Aureoboletus, Boletellus, Heimioporus, Hemileccinum, Hourangia, Phylloporus, and Xerocomus in China were also provided.","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"1 1","pages":""},"PeriodicalIF":16.5,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"69600489","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A genome-informed higher rank classification of the biotechnologically important fungal subphylum Saccharomycotina-Supplementary files","authors":"M. Groenewald","doi":"10.3114/sim.2023.105.01_supp","DOIUrl":"https://doi.org/10.3114/sim.2023.105.01_supp","url":null,"abstract":"Lv:0:53:http://www.w3.org/1999/02/22-rdf-syntax-ns#XMLLiteral<xhtml:span xmlns:xhtml=\"http://www.w3.org/1999/xhtml\" xml:lang=\"en\">Supplementary files to this article: Fig S1, Tables S1-S3.</xhtml:span>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"28 1-2 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136092822","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2022-12-01Epub Date: 2022-11-16DOI: 10.3114/sim.2022.102.02
F Sklenář, K Glässnerová, Ž Jurjević, J Houbraken, R A Samson, C M Visagie, N Yilmaz, J Gené, J Cano, A J Chen, A Nováková, T Yaguchi, M Kolařík, V Hubka
<p><p><i>Aspergillus</i> series <i>Versicolores</i> members occur in a wide range of environments and substrates such as indoor environments, food, clinical materials, soil, caves, marine or hypersaline ecosystems. The taxonomy of the series has undergone numerous re-arrangements including a drastic reduction in the number of species and subsequent recovery to 17 species in the last decade. The identification to species level is however problematic or impossible in some isolates even using DNA sequencing or MALDI-TOF mass spectrometry indicating a problem in the definition of species boundaries. To revise the species limits, we assembled a large dataset of 518 strains. From these, a total of 213 strains were selected for the final analysis according to their calmodulin (<i>CaM</i>) genotype, substrate and geography. This set was used for phylogenetic analysis based on five loci (<i>benA</i>, <i>CaM</i>, <i>RPB2</i>, <i>Mcm7</i>, <i>Tsr1</i>). Apart from the classical phylogenetic methods, we used multispecies coalescence (MSC) model-based methods, including one multilocus method (STACEY) and five single-locus methods (GMYC, bGMYC, PTP, bPTP, ABGD). Almost all species delimitation methods suggested a broad species concept with only four species consistently supported. We also demonstrated that the currently applied concept of species is not sustainable as there are incongruences between single-gene phylogenies resulting in different species identifications when using different gene regions. Morphological and physiological data showed overall lack of good, taxonomically informative characters, which could be used for identification of such a large number of existing species. The characters expressed either low variability across species or significant intraspecific variability exceeding interspecific variability. Based on the above-mentioned results, we reduce series <i>Versicolores</i> to four species, namely <i>A.</i> <i>versicolor, A. creber</i>, <i>A. sydowii</i> and <i>A. subversicolor</i>, and the remaining species are synonymized with either <i>A. versicolor</i> or <i>A. creber</i>. The revised descriptions of the four accepted species are provided. They can all be identified by any of the five genes used in this study. Despite the large reduction in species number, identification based on phenotypic characters remains challenging, because the variation in phenotypic characters is high and overlapping among species, especially between <i>A. versicolor</i> and <i>A. creber</i>. Similar to the 17 narrowly defined species, the four broadly defined species do not have a specific ecology and are distributed worldwide. We expect that the application of comparable methodology with extensive sampling could lead to a similar reduction in the number of cryptic species in other extensively studied <i>Aspergillus</i> species complexes and other fungal genera. <b>Citation:</b> Sklenář F, Glässnerová K, Jurjević Ž, Houbraken J, Samson RA, Visagie CM, Yilm
曲霉系列 Versicolores 成员广泛存在于各种环境和基质中,如室内环境、食品、临床材料、土壤、洞穴、海洋或高盐度生态系统。该系列的分类经历了多次重新排列,包括物种数量的急剧减少,以及在过去十年中恢复到 17 个物种。然而,即使使用 DNA 测序法或 MALDI-TOF 质谱法,也很难或无法对某些分离物进行物种鉴定,这表明物种界限的界定存在问题。为了修订物种界限,我们收集了一个包含 518 株菌株的大型数据集。根据钙调蛋白(CaM)的基因型、底物和地理位置,我们从中挑选出 213 株菌株进行最终分析。这组菌株被用于基于五个基因位点(benA、CaM、RPB2、Mcm7、Tsr1)的系统进化分析。除了经典的系统发生学方法外,我们还使用了基于多物种凝聚(MSC)模型的方法,包括一种多焦点方法(STACEY)和五种单焦点方法(GMYC、bGMYC、PTP、bPTP、ABGD)。几乎所有的物种划分方法都提出了一个宽泛的物种概念,只有四个物种得到了一致支持。我们还证明,目前使用的物种概念是不可持续的,因为在使用不同基因区域时,单基因系统发育之间存在不一致,导致物种鉴定结果不同。形态学和生理学数据表明,总体上缺乏良好的、分类信息丰富的特征,而这些特征可用来识别如此众多的现有物种。这些特征要么在不同物种之间的变异性较低,要么种内变异性明显超过种间变异性。基于上述结果,我们将 Versicolores 系列减少为 4 个种,即 A. versicolor、A. creber、A. sydowii 和 A. subversicolor,其余种与 A. versicolor 或 A. creber 同名。提供了四个已接受种的修订描述。它们都可以通过本研究中使用的五种基因中的任何一种进行鉴定。尽管物种数量大幅减少,但基于表型特征的鉴定仍具有挑战性,因为表型特征的变异很大,且物种间存在重叠,尤其是 A. versicolor 和 A. creber 之间。与 17 个狭义种类似,4 个广义种也没有特定的生态学特征,分布于世界各地。我们预计,在广泛采样的情况下应用可比方法,可使其他被广泛研究的曲霉菌种群和其他真菌属中的隐蔽种数量减少。引用:Sklenář F, Glässnerová K, Jurjević Ž, Houbraken J, Samson RA, Visagie CM, Yilmaz N, Gené J, Cano J, Chen AJ, Nováková A, Yaguchi T, Kolařík M, Hubka V (2022)。Aspergillus series Versicolores 的分类学:物种减少和种内变异的经验教训。Doi: 10.3114/sim.2022.102.02.
{"title":"Taxonomy of <i>Aspergillus</i> series <i>Versicolores</i>: species reduction and lessons learned about intraspecific variability.","authors":"F Sklenář, K Glässnerová, Ž Jurjević, J Houbraken, R A Samson, C M Visagie, N Yilmaz, J Gené, J Cano, A J Chen, A Nováková, T Yaguchi, M Kolařík, V Hubka","doi":"10.3114/sim.2022.102.02","DOIUrl":"10.3114/sim.2022.102.02","url":null,"abstract":"<p><p><i>Aspergillus</i> series <i>Versicolores</i> members occur in a wide range of environments and substrates such as indoor environments, food, clinical materials, soil, caves, marine or hypersaline ecosystems. The taxonomy of the series has undergone numerous re-arrangements including a drastic reduction in the number of species and subsequent recovery to 17 species in the last decade. The identification to species level is however problematic or impossible in some isolates even using DNA sequencing or MALDI-TOF mass spectrometry indicating a problem in the definition of species boundaries. To revise the species limits, we assembled a large dataset of 518 strains. From these, a total of 213 strains were selected for the final analysis according to their calmodulin (<i>CaM</i>) genotype, substrate and geography. This set was used for phylogenetic analysis based on five loci (<i>benA</i>, <i>CaM</i>, <i>RPB2</i>, <i>Mcm7</i>, <i>Tsr1</i>). Apart from the classical phylogenetic methods, we used multispecies coalescence (MSC) model-based methods, including one multilocus method (STACEY) and five single-locus methods (GMYC, bGMYC, PTP, bPTP, ABGD). Almost all species delimitation methods suggested a broad species concept with only four species consistently supported. We also demonstrated that the currently applied concept of species is not sustainable as there are incongruences between single-gene phylogenies resulting in different species identifications when using different gene regions. Morphological and physiological data showed overall lack of good, taxonomically informative characters, which could be used for identification of such a large number of existing species. The characters expressed either low variability across species or significant intraspecific variability exceeding interspecific variability. Based on the above-mentioned results, we reduce series <i>Versicolores</i> to four species, namely <i>A.</i> <i>versicolor, A. creber</i>, <i>A. sydowii</i> and <i>A. subversicolor</i>, and the remaining species are synonymized with either <i>A. versicolor</i> or <i>A. creber</i>. The revised descriptions of the four accepted species are provided. They can all be identified by any of the five genes used in this study. Despite the large reduction in species number, identification based on phenotypic characters remains challenging, because the variation in phenotypic characters is high and overlapping among species, especially between <i>A. versicolor</i> and <i>A. creber</i>. Similar to the 17 narrowly defined species, the four broadly defined species do not have a specific ecology and are distributed worldwide. We expect that the application of comparable methodology with extensive sampling could lead to a similar reduction in the number of cryptic species in other extensively studied <i>Aspergillus</i> species complexes and other fungal genera. <b>Citation:</b> Sklenář F, Glässnerová K, Jurjević Ž, Houbraken J, Samson RA, Visagie CM, Yilm","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"102 ","pages":"53-93"},"PeriodicalIF":14.1,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9903908/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9240641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}