Pub Date : 2020-06-01DOI: 10.1016/j.simyco.2020.01.003
S. Haridas , R. Albert , M. Binder , J. Bloem , K. LaButti , A. Salamov , B. Andreopoulos , S.E. Baker , K. Barry , G. Bills , B.H. Bluhm , C. Cannon , R. Castanera , D.E. Culley , C. Daum , D. Ezra , J.B. González , B. Henrissat , A. Kuo , C. Liang , I.V. Grigoriev
Dothideomycetes is the largest class of kingdom Fungi and comprises an incredible diversity of lifestyles, many of which have evolved multiple times. Plant pathogens represent a major ecological niche of the class Dothideomycetes and they are known to infect most major food crops and feedstocks for biomass and biofuel production. Studying the ecology and evolution of Dothideomycetes has significant implications for our fundamental understanding of fungal evolution, their adaptation to stress and host specificity, and practical implications with regard to the effects of climate change and on the food, feed, and livestock elements of the agro-economy. In this study, we present the first large-scale, whole-genome comparison of 101 Dothideomycetes introducing 55 newly sequenced species. The availability of whole-genome data produced a high-confidence phylogeny leading to reclassification of 25 organisms, provided a clearer picture of the relationships among the various families, and indicated that pathogenicity evolved multiple times within this class. We also identified gene family expansions and contractions across the Dothideomycetes phylogeny linked to ecological niches providing insights into genome evolution and adaptation across this group. Using machine-learning methods we classified fungi into lifestyle classes with >95 % accuracy and identified a small number of gene families that positively correlated with these distinctions. This can become a valuable tool for genome-based prediction of species lifestyle, especially for rarely seen and poorly studied species.
{"title":"101 Dothideomycetes genomes: A test case for predicting lifestyles and emergence of pathogens","authors":"S. Haridas , R. Albert , M. Binder , J. Bloem , K. LaButti , A. Salamov , B. Andreopoulos , S.E. Baker , K. Barry , G. Bills , B.H. Bluhm , C. Cannon , R. Castanera , D.E. Culley , C. Daum , D. Ezra , J.B. González , B. Henrissat , A. Kuo , C. Liang , I.V. Grigoriev","doi":"10.1016/j.simyco.2020.01.003","DOIUrl":"10.1016/j.simyco.2020.01.003","url":null,"abstract":"<div><p><em>Dothideomycetes</em> is the largest class of kingdom Fungi and comprises an incredible diversity of lifestyles, many of which have evolved multiple times. Plant pathogens represent a major ecological niche of the class <em>Dothideomycetes</em> and they are known to infect most major food crops and feedstocks for biomass and biofuel production. Studying the ecology and evolution of <em>Dothideomycetes</em> has significant implications for our fundamental understanding of fungal evolution, their adaptation to stress and host specificity, and practical implications with regard to the effects of climate change and on the food, feed, and livestock elements of the agro-economy. In this study, we present the first large-scale, whole-genome comparison of 101 <em>Dothideomycetes</em> introducing 55 newly sequenced species. The availability of whole-genome data produced a high-confidence phylogeny leading to reclassification of 25 organisms, provided a clearer picture of the relationships among the various families, and indicated that pathogenicity evolved multiple times within this class. We also identified gene family expansions and contractions across the <em>Dothideomycetes</em> phylogeny linked to ecological niches providing insights into genome evolution and adaptation across this group. Using machine-learning methods we classified fungi into lifestyle classes with >95 % accuracy and identified a small number of gene families that positively correlated with these distinctions. This can become a valuable tool for genome-based prediction of species lifestyle, especially for rarely seen and poorly studied species.</p></div>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"96 ","pages":"Pages 141-153"},"PeriodicalIF":16.5,"publicationDate":"2020-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2020.01.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37766338","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 : 2020-03-01DOI: 10.1016/j.simyco.2020.04.001
S. Mongkolsamrit , A. Khonsanit , D. Thanakitpipattana , K. Tasanathai , W. Noisripoom , S. Lamlertthon , W. Himaman , J. Houbraken , R.A. Samson , J. Luangsa-ard
<div><p>Over the last two decades the molecular phylogeny and classification of <em>Metarhizium</em> has been widely studied. Despite these efforts to understand this enigmatic genus, the basal lineages in <em>Metarhizium</em> are still poorly resolved. In this study, a phylogenetic framework is reconstructed for the <em>Clavicipitaceae</em> focusing on <em>Metarhizium</em> through increased taxon-sampling using five genomic loci (SSU, LSU, <em>tef, rpb1, rpb</em>2) and the barcode marker ITS rDNA. Multi-gene phylogenetic analyses and morphological characterisation of green-spored entomopathogenic <em>Metarhizium</em> isolates from Thailand and soil isolates of <em>M. carneum</em> and <em>M. marquandii</em> reveal their ecological, genetic and species diversity. Nineteen new species are recognised in the <em>Metarhizium</em> clade with narrow host ranges: two new species are found in the <em>M. anisopliae</em> complex – <em>M. clavatum</em> on <em>Coleoptera</em> larvae and <em>M. sulphureum</em> on <em>Lepidoptera</em> larvae; four new species are found in the <em>M. flavoviride</em> complex – <em>M. biotecense</em> and <em>M. fusoideum</em> on brown plant hoppers (<em>Hemiptera</em>), <em>M. culicidarum</em> on mosquitoes, <em>M. nornnoi</em> on <em>Lepidoptera</em> larvae; three new species <em>M. megapomponiae, M. cicadae, M. niveum</em> occur on cicadas; five new species <em>M. candelabrum, M. cercopidarum, M. ellipsoideum, M. huainamdangense M. ovoidosporum</em> occur on planthoppers, leafhoppers and froghoppers (<em>Hemiptera</em>); one new species <em>M. eburneum</em> on <em>Lepidoptera</em> pupae; and four new species <em>M. phuwiangense, M. purpureum, M. purpureonigrum, M. flavum</em> on <em>Coleoptera</em><em>.</em> Of these 19 new species, seven produce a sexual morph (<em>M. clavatum, M. eburneum, M. flavum, M. phuwiangense, M. purpureonigrum, M. purpureum,</em> and <em>M. sulphureum</em>) and asexual morphs are found in the remaining new species and also in <em>M. sulphureum, M. purpureonigrum</em> and <em>M. purpureum. Metarhizium blattodeae, M. koreanum</em> and <em>M. viridulum</em> are new records for Thailand. An alternative neotype for <em>Metarhizium anisopliae</em> is proposed based on multi-gene and 5′<em>tef</em> analyses showing that CBS 130.71 from Ukraine is more suitable, being from a much closer geographical location to Metchnikoff’s <em>Metarhizium anisopliae.</em> This isolate is distinct from the neotype of <em>Metarhizium anisopliae</em> var. <em>anisopliae</em> proposed by M. Tulloch from Ethiopia (ARSEF 7487). Six new genera are established for monophyletic clades subtending the core <em>Metarhizium</em> clade, including <em>Keithomyces, Marquandomyces, Papiliomyces, Purpureomyces, Sungia,</em> and <em>Yosiokobayasia. Metarhizium carneum, M. aciculare,</em> and <em>M. neogunnii</em> are combined in <em>Keithomyces</em> and one new combination for <em>M. marquandii</em> in <em>Marquandomyces</em> is proposed. <em
{"title":"Revisiting Metarhizium and the description of new species from Thailand","authors":"S. Mongkolsamrit , A. Khonsanit , D. Thanakitpipattana , K. Tasanathai , W. Noisripoom , S. Lamlertthon , W. Himaman , J. Houbraken , R.A. Samson , J. Luangsa-ard","doi":"10.1016/j.simyco.2020.04.001","DOIUrl":"10.1016/j.simyco.2020.04.001","url":null,"abstract":"<div><p>Over the last two decades the molecular phylogeny and classification of <em>Metarhizium</em> has been widely studied. Despite these efforts to understand this enigmatic genus, the basal lineages in <em>Metarhizium</em> are still poorly resolved. In this study, a phylogenetic framework is reconstructed for the <em>Clavicipitaceae</em> focusing on <em>Metarhizium</em> through increased taxon-sampling using five genomic loci (SSU, LSU, <em>tef, rpb1, rpb</em>2) and the barcode marker ITS rDNA. Multi-gene phylogenetic analyses and morphological characterisation of green-spored entomopathogenic <em>Metarhizium</em> isolates from Thailand and soil isolates of <em>M. carneum</em> and <em>M. marquandii</em> reveal their ecological, genetic and species diversity. Nineteen new species are recognised in the <em>Metarhizium</em> clade with narrow host ranges: two new species are found in the <em>M. anisopliae</em> complex – <em>M. clavatum</em> on <em>Coleoptera</em> larvae and <em>M. sulphureum</em> on <em>Lepidoptera</em> larvae; four new species are found in the <em>M. flavoviride</em> complex – <em>M. biotecense</em> and <em>M. fusoideum</em> on brown plant hoppers (<em>Hemiptera</em>), <em>M. culicidarum</em> on mosquitoes, <em>M. nornnoi</em> on <em>Lepidoptera</em> larvae; three new species <em>M. megapomponiae, M. cicadae, M. niveum</em> occur on cicadas; five new species <em>M. candelabrum, M. cercopidarum, M. ellipsoideum, M. huainamdangense M. ovoidosporum</em> occur on planthoppers, leafhoppers and froghoppers (<em>Hemiptera</em>); one new species <em>M. eburneum</em> on <em>Lepidoptera</em> pupae; and four new species <em>M. phuwiangense, M. purpureum, M. purpureonigrum, M. flavum</em> on <em>Coleoptera</em><em>.</em> Of these 19 new species, seven produce a sexual morph (<em>M. clavatum, M. eburneum, M. flavum, M. phuwiangense, M. purpureonigrum, M. purpureum,</em> and <em>M. sulphureum</em>) and asexual morphs are found in the remaining new species and also in <em>M. sulphureum, M. purpureonigrum</em> and <em>M. purpureum. Metarhizium blattodeae, M. koreanum</em> and <em>M. viridulum</em> are new records for Thailand. An alternative neotype for <em>Metarhizium anisopliae</em> is proposed based on multi-gene and 5′<em>tef</em> analyses showing that CBS 130.71 from Ukraine is more suitable, being from a much closer geographical location to Metchnikoff’s <em>Metarhizium anisopliae.</em> This isolate is distinct from the neotype of <em>Metarhizium anisopliae</em> var. <em>anisopliae</em> proposed by M. Tulloch from Ethiopia (ARSEF 7487). Six new genera are established for monophyletic clades subtending the core <em>Metarhizium</em> clade, including <em>Keithomyces, Marquandomyces, Papiliomyces, Purpureomyces, Sungia,</em> and <em>Yosiokobayasia. Metarhizium carneum, M. aciculare,</em> and <em>M. neogunnii</em> are combined in <em>Keithomyces</em> and one new combination for <em>M. marquandii</em> in <em>Marquandomyces</em> is proposed. <em","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"95 ","pages":"Pages 171-251"},"PeriodicalIF":16.5,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2020.04.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38318130","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}
The Capnodiales, which includes fungi known as the sooty moulds, represents the second largest order in Dothideomycetes, encompassing morphologically and ecologically diverse fungi with different lifestyles and modes of nutrition. They include saprobes, plant and human pathogens, mycoparasites, rock-inhabiting fungi (RIF), lichenised, epi-, ecto- and endophytes. The aim of this study was to elucidate the lifestyles and evolutionary patterns of the Capnodiales as well as to reconsider their phylogeny by including numerous new collections of sooty moulds, and using four nuclear loci, LSU, ITS, TEF-1α and RPB2. Based on the phylogenetic results, combined with morphology and ecology, Capnodiales s. lat. is shown to be polyphyletic, representing seven different orders. The sooty moulds are restricted to Capnodiales s. str., while Mycosphaerellales is resurrected, and five new orders including Cladosporiales, Comminutisporales, Neophaeothecales, Phaeothecales and Racodiales are introduced. Four families, three genera, 21 species and five combinations are introduced as new. Furthermore, ancestral reconstruction analysis revealed that the saprobic lifestyle is a primitive state in Capnodiales s. lat., and that several transitions have occurred to evolve lichenised, plant and human parasitic, ectophytic (sooty blotch and flyspeck) and more recently epiphytic (sooty mould) lifestyles.
Capnodiales,其中包括被称为烟霉的真菌,代表了dothideomytes的第二大目,包括形态和生态上多样化的真菌,具有不同的生活方式和营养模式。它们包括腐殖菌、植物和人类病原体、分枝寄生虫、岩石真菌(RIF)、地衣菌、外生菌、外生菌和内生菌。本研究利用LSU、ITS、TEF-1α和RPB2 4个核位点,对大量新收集的烟霉菌进行研究,旨在阐明烟霉菌科的生活方式和进化模式,并重新思考其系统发育。根据系统发育的结果,结合形态学和生态学,对其进行了研究。被证明是多系的,代表七个不同的目。烟灰霉菌仅限于Capnodiales s.str .,而Mycosphaerellales被复活,并引入了Cladosporiales、Comminutisporales、nephaeocalales、phaeocalales和Racodiales 5个新目。新引进4科3属21种5个组合。此外,祖先重建分析还表明,Capnodiales s. lat的野蛮生活方式是一种原始状态。并且已经发生了几次转变,进化出地衣、植物和人类寄生、外生(煤烟斑和飞斑)和最近的附生(煤烟霉)生活方式。
{"title":"Evolution of lifestyles in Capnodiales","authors":"J. Abdollahzadeh , J.Z. Groenewald , M.P.A. Coetzee , M.J. Wingfield , P.W. Crous","doi":"10.1016/j.simyco.2020.02.004","DOIUrl":"10.1016/j.simyco.2020.02.004","url":null,"abstract":"<div><p>The <em>Capnodiales</em>, which includes fungi known as the sooty moulds, represents the second largest order in <em>Dothideomycetes</em>, encompassing morphologically and ecologically diverse fungi with different lifestyles and modes of nutrition. They include saprobes, plant and human pathogens, mycoparasites, rock-inhabiting fungi (RIF), lichenised, epi-, ecto- and endophytes. The aim of this study was to elucidate the lifestyles and evolutionary patterns of the <em>Capnodiales</em> as well as to reconsider their phylogeny by including numerous new collections of sooty moulds, and using four nuclear loci, LSU, ITS, <em>TEF-1α</em> and <em>RPB2</em>. Based on the phylogenetic results, combined with morphology and ecology, <em>Capnodiales s. lat.</em> is shown to be polyphyletic, representing seven different orders. The sooty moulds are restricted to <em>Capnodiales s. str.</em>, while <em>Mycosphaerellales</em> is resurrected, and five new orders including <em>Cladosporiales</em>, <em>Comminutisporales</em>, <em>Neophaeothecales</em>, <em>Phaeothecales</em> and <em>Racodiales</em> are introduced. Four families, three genera, 21 species and five combinations are introduced as new. Furthermore, ancestral reconstruction analysis revealed that the saprobic lifestyle is a primitive state in <em>Capnodiales s. lat</em>., and that several transitions have occurred to evolve lichenised, plant and human parasitic, ectophytic (sooty blotch and flyspeck) and more recently epiphytic (sooty mould) lifestyles.</p></div>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"95 ","pages":"Pages 381-414"},"PeriodicalIF":16.5,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2020.02.004","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38318638","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 : 2020-03-01DOI: 10.1016/j.simyco.2020.02.005
J.B. Tanney , K.A. Seifert
Mollisia is a taxonomically neglected discomycete genus (Helotiales, Leotiomycetes) of commonly encountered saprotrophs on decaying plant tissues throughout temperate regions. The combination of indistinct morphological characters, more than 700 names in the literature, and lack of reference DNA sequences presents a major challenge when working with Mollisia. Unidentified endophytes, including strains that produced antifungal or antiinsectan secondary metabolites, were isolated from conifer needles in New Brunswick and placed with uncertainty in Phialocephala and Mollisia, necessitating a more comprehensive treatment of these genera. In this study, morphology and multigene phylogenetic analyses were used to explore the taxonomy of Mollisiaceae, including Mollisia, Phialocephala, and related genera, using new field collections, herbarium specimens, and accessioned cultures and sequences. The phylogeny of Mollisiaceae was reconstructed and compared using the nuc internal transcribed spacer rDNA (ITS) barcode and partial sequences of the 28S nuc rDNA (LSU) gene, largest subunit of RNA polymerase II (RPB1), DNA topoisomerase I (TOP1), and the hypothetical protein Lipin/Ned1/Smp2 (LNS2). The results show that endophytism is common throughout the Mollisiaceae lineage in a diverse range of hosts but is infrequently attributed to Mollisia because of a paucity of reference sequences. Generic boundaries within Mollisiaceae are poorly resolved and based on phylogenetic evidence the family included species placed in Acephala, Acidomelania, Barrenia, Bispora, Cheirospora, Cystodendron, Fuscosclera, Hysteronaevia, Loramyces, Mollisia, Neopyrenopeziza, Obtectodiscus, Ombrophila, Patellariopsis, Phialocephala, Pulvinata, Tapesia (=Mollisia), and Trimmatostroma. Taxonomic novelties included the description of five novel Mollisia species and five novel Phialocephala species and the synonymy of Fuscosclera with Phialocephala, Acidomelania with Mollisia, and Loramycetaceae with Mollisiaceae.
{"title":"Mollisiaceae: An overlooked lineage of diverse endophytes","authors":"J.B. Tanney , K.A. Seifert","doi":"10.1016/j.simyco.2020.02.005","DOIUrl":"10.1016/j.simyco.2020.02.005","url":null,"abstract":"<div><p><em>Mollisia</em> is a taxonomically neglected discomycete genus (<em>Helotiales, Leotiomycetes</em>) of commonly encountered saprotrophs on decaying plant tissues throughout temperate regions. The combination of indistinct morphological characters, more than 700 names in the literature, and lack of reference DNA sequences presents a major challenge when working with <em>Mollisia</em>. Unidentified endophytes, including strains that produced antifungal or antiinsectan secondary metabolites, were isolated from conifer needles in New Brunswick and placed with uncertainty in <em>Phialocephala</em> and <em>Mollisia</em>, necessitating a more comprehensive treatment of these genera. In this study, morphology and multigene phylogenetic analyses were used to explore the taxonomy of <em>Mollisiaceae</em>, including <em>Mollisia</em>, <em>Phialocephala</em>, and related genera, using new field collections, herbarium specimens, and accessioned cultures and sequences. The phylogeny of <em>Mollisiaceae</em> was reconstructed and compared using the nuc internal transcribed spacer rDNA (ITS) barcode and partial sequences of the 28S nuc rDNA (LSU) gene, largest subunit of RNA polymerase II (<em>RPB1</em>), DNA topoisomerase I (<em>TOP1</em>), and the hypothetical protein Lipin/Ned1/Smp2 (<em>LNS2</em>). The results show that endophytism is common throughout the <em>Mollisiaceae</em> lineage in a diverse range of hosts but is infrequently attributed to <em>Mollisia</em> because of a paucity of reference sequences. Generic boundaries within <em>Mollisiaceae</em> are poorly resolved and based on phylogenetic evidence the family included species placed in <em>Acephala</em>, <em>Acidomelania</em>, <em>Barrenia</em>, <em>Bispora</em>, <em>Cheirospora</em>, <em>Cystodendron</em>, <em>Fuscosclera</em>, <em>Hysteronaevia, Loramyces, Mollisia, Neopyrenopeziza</em>, <em>Obtectodiscus, Ombrophila, Patellariopsis</em>, <em>Phialocephala</em>, <em>Pulvinata</em>, <em>Tapesia</em> (=<em>Mollisia</em>), and <em>Trimmatostroma.</em> Taxonomic novelties included the description of five novel <em>Mollisia</em> species and five novel <em>Phialocephala</em> species and the synonymy of <em>Fuscosclera</em> with <em>Phialocephala</em>, <em>Acidomelania</em> with <em>Mollisia</em>, and <em>Loramycetaceae</em> with <em>Mollisiaceae</em>.</p></div>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"95 ","pages":"Pages 293-380"},"PeriodicalIF":16.5,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2020.02.005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38318132","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 : 2020-03-01DOI: 10.1016/j.simyco.2020.02.002
Martina Réblová , Margarita Hernández-Restrepo , Jacques Fournier , Jana Nekvindová
The newly discovered systematic placement of Bactrodesmium abruptum, the lectotype species of the genus, prompted a re-evaluation of the traditionally broadly conceived genus Bactrodesmium. Fresh material, axenic cultures and new DNA sequence data of five gene regions of six species, i.e. B. abruptum, B. diversum, B. leptopus, B. obovatum, B. pallidum and B. spilomeum, were studied. Bactrodesmium is a strongly resolved lineage in the Savoryellales (Sordariomycetes), supported by Bayesian and Maximum Likelihood methods. The genus Bactrodesmium is emended and delimited to hyphomycetes characterised by sporodochial conidiomata, mononematous often fasciculate conidiophores, holoblastic conidiogenesis and acrogenous, solitary, dry, pigmented, transversely or rarely longitudinally septate conidia. The conidia are seceding rhexolytically, exhibiting multiple secession patterns. An identification key to 35 species accepted in Bactrodesmium is given, providing the most important diagnostic characters. Novel DNA sequence data of B. longisporum and B. stilboideum confirmed their placement in the Sclerococcales (Eurotiomycetes). For other Bactrodesmium, molecular data are available for B. cubense and B. gabretae, which position them in the Dothideomycetes and Leotiomycetes, respectively. All four species are excluded from Bactrodesmium and segregated into new genera, Aphanodesmium, Gamsomyces and Kaseifertia. Classification of 20 other species and varieties not recognised in the genus is discussed. Based on new collections of Dematiosporium aquaticum, the type species of Dematiosporium, the genus is emended to accommodate monodictys-like freshwater lignicolous fungi of the Savoryellales characterised by effuse colonies, holoblastic conidiogenous cells and dictyosporous, pigmented conidia with a pore in each cell. Study of additional new collections, cultures and DNA sequence data revealed several unknown species, which are proposed as taxonomic novelties in the Savoryellales and closely related Pleurotheciales. Ascotaiwania latericolla, Helicoascotaiwania lacustris and Pleurotheciella erumpens are described from terrestrial, lentic and lotic habitats from New Zealand and France, respectively. New combinations are proposed for Helicoascotaiwania farinosa and Neoascotaiwania fusiformis. Relationships and systematics of the Savoryellales are discussed in the light of recent phylogenies and morphological patterns newly linked with the order through cultural studies.
新发现的bactrodesium abruptum的系统位置,是该属的典型种,促使人们对传统上广泛认为的Bactrodesmium属进行重新评估。本文对6个物种(abruptum、diversum、leptopus、obovatum、pallidum和spilomeum)的5个基因区进行了新鲜材料、无菌培养和新的DNA序列分析。Bactrodesmium是savooryellales (sordariomytes)中一个很强的分离谱系,得到了贝叶斯和最大似然方法的支持。小芽孢杆菌属被修正并划分为菌丝菌,其特征是孢子孢子孢子体、单生的通常束状的分生孢子、全胚分生孢子和顶生的、单生的、干燥的、有色素的、横向或很少纵向分开的分生孢子。分生孢子裂解性分裂,呈现多种分裂模式。给出了小蠊属35种的鉴定键,提供了最重要的诊断特征。长孢芽孢杆菌(b.l unisporum)和stilboideum的新DNA序列数据证实它们属于硬球菌(eurotiomytes)。对于其他bactrodesium, B. cubense和B. gabretae的分子数据可用,它们分别属于dothideomycates和leotiomycates。这4个种均被从Bactrodesmium中排除,并分离为Aphanodesmium、Gamsomyces和Kaseifertia新属。讨论了本属中未发现的其他20种和变种的分类。基于新收集的海苔孢,海苔孢的模式种,该属被修正,以适应单调的淡水木质真菌的Savoryellales,其特征是液体菌落,完整的分生细胞和双孢子,色素分生孢子在每个细胞中有一个孔。对新的标本、培养和DNA序列数据的研究发现了一些未知的物种,这些物种被认为是Savoryellales和近亲Pleurotheciales的分类新种。分别在新西兰和法国的陆地生境、陆地生境和陆地生境中描述了红叶松果虫(ascotaia latericolla)、湖栖松果虫(helicoascotaia湖栖松果虫(helicoascotaia湖栖松果虫(Pleurotheciella erumpens)。提出了粉尾螺螺虫和新尾螺螺虫的新组合。根据最近的系统发育和通过文化研究与该目新联系的形态模式,讨论了该目的关系和系统分类学。
{"title":"New insights into the systematics of Bactrodesmium and its allies and introducing new genera, species and morphological patterns in the Pleurotheciales and Savoryellales (Sordariomycetes)","authors":"Martina Réblová , Margarita Hernández-Restrepo , Jacques Fournier , Jana Nekvindová","doi":"10.1016/j.simyco.2020.02.002","DOIUrl":"10.1016/j.simyco.2020.02.002","url":null,"abstract":"<div><p>The newly discovered systematic placement of <em>Bactrodesmium abruptum</em>, the lectotype species of the genus, prompted a re-evaluation of the traditionally broadly conceived genus <em>Bactrodesmium</em>. Fresh material, axenic cultures and new DNA sequence data of five gene regions of six species, i.e. <em>B. abruptum</em>, <em>B. diversum, B. leptopus</em>, <em>B. obovatum</em>, <em>B. pallidum</em> and <em>B. spilomeum</em>, were studied. <em>Bactrodesmium</em> is a strongly resolved lineage in the <em>Savoryellales</em> (<em>Sordariomycetes</em>), supported by Bayesian and Maximum Likelihood methods. The genus <em>Bactrodesmium</em> is emended and delimited to hyphomycetes characterised by sporodochial conidiomata, mononematous often fasciculate conidiophores, holoblastic conidiogenesis and acrogenous, solitary, dry, pigmented, transversely or rarely longitudinally septate conidia. The conidia are seceding rhexolytically, exhibiting multiple secession patterns. An identification key to 35 species accepted in <em>Bactrodesmium</em> is given, providing the most important diagnostic characters. Novel DNA sequence data of <em>B. longisporum</em> and <em>B. stilboideum</em> confirmed their placement in the <em>Sclerococcales</em> (<em>Eurotiomycetes</em>). For other <em>Bactrodesmium</em>, molecular data are available for <em>B. cubense</em> and <em>B. gabretae</em>, which position them in the <em>Dothideomycetes</em> and <em>Leotiomycetes</em>, respectively. All four species are excluded from <em>Bactrodesmium</em> and segregated into new genera, <em>Aphanodesmium</em>, <em>Gamsomyces</em> and <em>Kaseifertia</em>. Classification of 20 other species and varieties not recognised in the genus is discussed. Based on new collections of <em>Dematiosporium aquaticum</em>, the type species of <em>Dematiosporium</em>, the genus is emended to accommodate monodictys-like freshwater lignicolous fungi of the <em>Savoryellales</em> characterised by effuse colonies, holoblastic conidiogenous cells and dictyosporous, pigmented conidia with a pore in each cell. Study of additional new collections, cultures and DNA sequence data revealed several unknown species, which are proposed as taxonomic novelties in the <em>Savoryellales</em> and closely related <em>Pleurotheciales</em>. <em>Ascotaiwania latericolla</em>, <em>Helicoascotaiwania lacustris</em> and <em>Pleurotheciella erumpens</em> are described from terrestrial, lentic and lotic habitats from New Zealand and France, respectively. New combinations are proposed for <em>Helicoascotaiwania farinosa</em> and <em>Neoascotaiwania fusiformis</em>. Relationships and systematics of the <em>Savoryellales</em> are discussed in the light of recent phylogenies and morphological patterns newly linked with the order through cultural studies.</p></div>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"95 ","pages":"Pages 415-466"},"PeriodicalIF":16.5,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2020.02.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38318639","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 : 2020-03-01DOI: 10.1016/j.simyco.2020.05.002
J. Houbraken , S. Kocsubé , C.M. Visagie , N. Yilmaz , X.-C. Wang , M. Meijer , B. Kraak , V. Hubka , K. Bensch , R.A. Samson , J.C. Frisvad
<div><p>The <em>Eurotiales</em> is a relatively large order of <em>Ascomycetes</em> with members frequently having positive and negative impact on human activities. Species within this order gain attention from various research fields such as food, indoor and medical mycology and biotechnology. In this article we give an overview of families and genera present in the <em>Eurotiales</em> and introduce an updated subgeneric, sectional and series classification for <em>Aspergillus</em> and <em>Penicillium</em>. Finally, a comprehensive list of accepted species in the <em>Eurotiales</em> is given. The classification of the <em>Eurotiales</em> at family and genus level is traditionally based on phenotypic characters, and this classification has since been challenged using sequence-based approaches. Here, we re-evaluated the relationships between families and genera of the <em>Eurotiales</em> using a nine-gene sequence dataset. Based on this analysis, the new family <em>Penicillaginaceae</em> is introduced and four known families are accepted: <em>Aspergillaceae</em>, <em>Elaphomycetaceae</em>, <em>Thermoascaceae</em> and <em>Trichocomaceae</em>. The <em>Eurotiales</em> includes 28 genera: 15 genera are accommodated in the <em>Aspergillaceae</em> (<em>Aspergillago</em>, <em>Aspergillus</em>, <em>Evansstolkia</em>, <em>Hamigera</em>, <em>Leiothecium</em>, <em>Monascus</em>, <em>Penicilliopsis</em>, <em>Penicillium</em>, <em>Phialomyces</em>, <em>Pseudohamigera</em>, <em>Pseudopenicillium</em>, <em>Sclerocleista</em>, <em>Warcupiella</em>, <em>Xerochrysium</em> and <em>Xeromyces</em>), eight in the <em>Trichocomaceae</em> (<em>Acidotalaromyces</em>, <em>Ascospirella</em>, <em>Dendrosphaera</em>, <em>Rasamsonia</em>, <em>Sagenomella</em>, <em>Talaromyces</em>, <em>Thermomyces</em>, <em>Trichocoma</em>), two in the <em>Thermoascaceae</em> (<em>Paecilomyces</em>, <em>Thermoascus</em>) and one in the <em>Penicillaginaceae</em> (<em>Penicillago</em>). The classification of the <em>Elaphomycetaceae</em> was not part of this study, but according to literature two genera are present in this family (<em>Elaphomyces</em> and <em>Pseudotulostoma</em>). The use of an infrageneric classification system has a long tradition in <em>Aspergillus</em> and <em>Penicillium</em>. Most recent taxonomic studies focused on the sectional level, resulting in a well-established sectional classification in these genera. In contrast, a series classification in <em>Aspergillus</em> and <em>Penicillium</em> is often outdated or lacking, but is still relevant, <em>e.g.</em>, the allocation of a species to a series can be highly predictive in what functional characters the species might have and might be useful when using a phenotype-based identification. The majority of the series in <em>Aspergillus</em> and <em>Penicillium</em> are invalidly described and here we introduce a new series classification. Using a phylogenetic approach, often supported by phenotypic, physiologic and/or ext
{"title":"Classification of Aspergillus, Penicillium, Talaromyces and related genera (Eurotiales): An overview of families, genera, subgenera, sections, series and species","authors":"J. Houbraken , S. Kocsubé , C.M. Visagie , N. Yilmaz , X.-C. Wang , M. Meijer , B. Kraak , V. Hubka , K. Bensch , R.A. Samson , J.C. Frisvad","doi":"10.1016/j.simyco.2020.05.002","DOIUrl":"10.1016/j.simyco.2020.05.002","url":null,"abstract":"<div><p>The <em>Eurotiales</em> is a relatively large order of <em>Ascomycetes</em> with members frequently having positive and negative impact on human activities. Species within this order gain attention from various research fields such as food, indoor and medical mycology and biotechnology. In this article we give an overview of families and genera present in the <em>Eurotiales</em> and introduce an updated subgeneric, sectional and series classification for <em>Aspergillus</em> and <em>Penicillium</em>. Finally, a comprehensive list of accepted species in the <em>Eurotiales</em> is given. The classification of the <em>Eurotiales</em> at family and genus level is traditionally based on phenotypic characters, and this classification has since been challenged using sequence-based approaches. Here, we re-evaluated the relationships between families and genera of the <em>Eurotiales</em> using a nine-gene sequence dataset. Based on this analysis, the new family <em>Penicillaginaceae</em> is introduced and four known families are accepted: <em>Aspergillaceae</em>, <em>Elaphomycetaceae</em>, <em>Thermoascaceae</em> and <em>Trichocomaceae</em>. The <em>Eurotiales</em> includes 28 genera: 15 genera are accommodated in the <em>Aspergillaceae</em> (<em>Aspergillago</em>, <em>Aspergillus</em>, <em>Evansstolkia</em>, <em>Hamigera</em>, <em>Leiothecium</em>, <em>Monascus</em>, <em>Penicilliopsis</em>, <em>Penicillium</em>, <em>Phialomyces</em>, <em>Pseudohamigera</em>, <em>Pseudopenicillium</em>, <em>Sclerocleista</em>, <em>Warcupiella</em>, <em>Xerochrysium</em> and <em>Xeromyces</em>), eight in the <em>Trichocomaceae</em> (<em>Acidotalaromyces</em>, <em>Ascospirella</em>, <em>Dendrosphaera</em>, <em>Rasamsonia</em>, <em>Sagenomella</em>, <em>Talaromyces</em>, <em>Thermomyces</em>, <em>Trichocoma</em>), two in the <em>Thermoascaceae</em> (<em>Paecilomyces</em>, <em>Thermoascus</em>) and one in the <em>Penicillaginaceae</em> (<em>Penicillago</em>). The classification of the <em>Elaphomycetaceae</em> was not part of this study, but according to literature two genera are present in this family (<em>Elaphomyces</em> and <em>Pseudotulostoma</em>). The use of an infrageneric classification system has a long tradition in <em>Aspergillus</em> and <em>Penicillium</em>. Most recent taxonomic studies focused on the sectional level, resulting in a well-established sectional classification in these genera. In contrast, a series classification in <em>Aspergillus</em> and <em>Penicillium</em> is often outdated or lacking, but is still relevant, <em>e.g.</em>, the allocation of a species to a series can be highly predictive in what functional characters the species might have and might be useful when using a phenotype-based identification. The majority of the series in <em>Aspergillus</em> and <em>Penicillium</em> are invalidly described and here we introduce a new series classification. Using a phylogenetic approach, often supported by phenotypic, physiologic and/or ext","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"95 ","pages":"Pages 5-169"},"PeriodicalIF":16.5,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2020.05.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38318641","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 : 2020-03-01DOI: 10.1016/j.simyco.2020.02.003
C.M. Visagie , J. Houbraken
The taxonomy and nomenclature of the genus Aspergillus and its associated sexual (teleomorphic) genera have been greatly stabilised over the last decade. This was in large thanks to the accepted species list published in 2014 and associated metadata such as DNA reference sequences released at the time. It had a great impact on the community and it has never been easier to identify, publish and describe the missing Aspergillus diversity. To further stabilise its taxonomy, it is crucial to not only discover and publish new species but also to capture infraspecies variation in the form of DNA sequences. This data will help to better characterise and distinguish existing species and make future identifications more robust. South Africa has diverse fungal communities but remains largely unexplored in terms of Aspergillus with very few sequences available for local strains. In this paper, we re-identify Aspergillus previously accessioned in the PPRI and MRC culture collections using modern taxonomic approaches. In the process, we re-identify strains to 63 species, describe seven new species and release a large number of new DNA reference sequences.
{"title":"Updating the taxonomy of Aspergillus in South Africa","authors":"C.M. Visagie , J. Houbraken","doi":"10.1016/j.simyco.2020.02.003","DOIUrl":"10.1016/j.simyco.2020.02.003","url":null,"abstract":"<div><p>The taxonomy and nomenclature of the genus <em>Aspergillus</em> and its associated sexual (teleomorphic) genera have been greatly stabilised over the last decade. This was in large thanks to the accepted species list published in 2014 and associated metadata such as DNA reference sequences released at the time. It had a great impact on the community and it has never been easier to identify, publish and describe the missing <em>Aspergillus</em> diversity. To further stabilise its taxonomy, it is crucial to not only discover and publish new species but also to capture infraspecies variation in the form of DNA sequences. This data will help to better characterise and distinguish existing species and make future identifications more robust. South Africa has diverse fungal communities but remains largely unexplored in terms of <em>Aspergillus</em> with very few sequences available for local strains. In this paper, we re-identify <em>Aspergillus</em> previously accessioned in the PPRI and MRC culture collections using modern taxonomic approaches. In the process, we re-identify strains to 63 species, describe seven new species and release a large number of new DNA reference sequences.</p></div>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"95 ","pages":"Pages 253-292"},"PeriodicalIF":16.5,"publicationDate":"2020-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2020.02.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38318131","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 : 2019-09-01DOI: 10.1016/j.simyco.2019.08.001
P.W. Crous , M.J. Wingfield , R. Cheewangkoon , A.J. Carnegie , T.I. Burgess , B.A. Summerell , J. Edwards , P.W.J. Taylor , J.Z. Groenewald
<div><p>Species of eucalypts are commonly cultivated for solid wood and pulp products. The expansion of commercially managed eucalypt plantations has chiefly been driven by their rapid growth and suitability for propagation across a very wide variety of sites and climatic conditions. Infection of foliar fungal pathogens of eucalypts is resulting in increasingly negative impacts on commercial forest industries globally. To assist in evaluating this threat, the present study provides a global perspective on foliar pathogens of eucalypts. We treat 110 different genera including species associated with foliar disease symptoms of these hosts. The vast majority of these fungi have been grown in axenic culture, and subjected to DNA sequence analysis, resolving their phylogeny. During the course of this study several new genera and species were encountered, and these are described. New genera include: <em>Lembosiniella</em> (<em>L. eucalyptorum</em> on <em>E. dunnii,</em> Australia), <em>Neosonderhenia</em> (<em>N. eucalypti</em> on <em>E. costata,</em> Australia), <em>Neothyriopsis</em> (<em>N. sphaerospora</em> on <em>E. camaldulensis</em>, South Africa), <em>Neotrichosphaeria</em> (<em>N. eucalypticola</em> on <em>E. deglupta</em>, Australia), <em>Nothotrimmatostroma</em> (<em>N. bifarium</em> on <em>E. dalrympleana</em>, Australia), <em>Nowamyces</em> (incl. <em>Nowamycetaceae fam. nov</em>., <em>N. globulus</em> on <em>E. globulus</em>, Australia), and <em>Walkaminomyces</em> (<em>W. medusae</em> on <em>E. alba</em>, Australia). New species include (all from Australia): <em>Disculoides fraxinoides</em> on <em>E. fraxinoides, Elsinoe piperitae on E. piperita, Fusculina regnans</em> on <em>E. regnans, Marthamyces johnstonii</em> on <em>E. dunnii</em>, <em>Neofusicoccum corticosae</em> on <em>E. corticosa</em>, <em>Neotrimmatostroma dalrympleanae</em> on <em>E. dalrympleana, Nowamyces piperitae</em> on <em>E. piperita</em>, <em>Phaeothyriolum dunnii</em> on <em>E. dunnii</em>, <em>Pseudophloeospora eucalyptigena</em> on <em>E. obliqua</em>, <em>Pseudophloeospora jollyi</em> on <em>Eucalyptus</em> sp., <em>Quambalaria tasmaniae</em> on <em>Eucalyptus</em> sp., <em>Q. rugosae</em> on <em>E. rugosa</em>, <em>Sonderhenia radiata</em> on <em>E. radiata</em>, <em>Teratosphaeria pseudonubilosa</em> on <em>E. globulus</em> and <em>Thyrinula dunnii</em> on <em>E. dunnii</em>. A new name is also proposed for <em>Heteroconium eucalypti</em> as <em>Thyrinula uruguayensis</em> on <em>E. dunnii</em>, Uruguay. Although many of these genera and species are commonly associated with disease problems, several appear to be opportunists developing on stressed or dying tissues. For the majority of these fungi, pathogenicity remains to be determined. This represents an important goal for forest pathologists and biologists in the future. Consequently, this study will promote renewed interest in foliar pathogens of eucalypts, leading to investigations that will provide an impr
桉树的种类通常用于种植实木和纸浆产品。商业管理桉树种植园的扩张主要是由于它们的快速生长和适合在各种各样的地点和气候条件下繁殖。桉树叶面真菌病原菌感染对全球商业林业的负面影响越来越大。为了帮助评估这种威胁,本研究提供了桉树叶面病原体的全球视角。我们处理110个不同的属,包括与这些寄主的叶面疾病症状相关的物种。这些真菌绝大多数都是在无菌培养中培养的,并进行了DNA序列分析,确定了它们的系统发育。在研究过程中,我们发现了一些新的属和种,并对它们进行了描述。新属包括:Lembosiniella (L. eucalyptus on E. dunnii, Australia)、Neosonderhenia (N. eucalyptus on E. costata, Australia)、Neothyriopsis (N. sphaerospora on E. camaldulensis, South Africa)、Neotrichosphaeria (N. eucalyptus on E. deglupta, Australia)、Nothotrimmatostroma (N. bifarium on E. dalrympleana, Australia)、Nowamyces(包括Nowamycetaceae fam)。11月,N. globulus在E. globulus上,澳大利亚)和Walkaminomyces (W. medusae在E. alba上,澳大利亚)。新种包括(全部来自澳大利亚):黄曲霉上的黄曲霉属、油梨上的油梨属、油梨上的褐霉属、敦氏褐霉属、敦氏褐霉属、敦氏褐霉属、敦氏褐霉属、油梨上的褐霉属、敦氏褐霉属、尤加利上的桉树假孢子虫、尤加利上的乔利假孢子虫、尤加利上的塔斯马属、尤加利上的褐霉属、尤加利上的褐霉属辐射棘球绦虫寄生在辐射棘球绦虫上,假棘球绦虫寄生在球棘球绦虫上,邓恩棘球绦虫寄生在邓恩棘球绦虫上。在乌拉圭的E. dunnii上,还提出了一个新名称为Thyrinula uruguayensis。虽然这些属和种中的许多通常与疾病问题有关,但有些似乎是在压力或死亡组织上发展的机会主义者。对于这些真菌中的大多数,致病性仍有待确定。这是未来森林病理学家和生物学家的一个重要目标。因此,这项研究将促进人们对桉树叶面病原体的重新兴趣,从而导致对这些真菌生物学的更好理解的调查。
{"title":"Foliar pathogens of eucalypts","authors":"P.W. Crous , M.J. Wingfield , R. Cheewangkoon , A.J. Carnegie , T.I. Burgess , B.A. Summerell , J. Edwards , P.W.J. Taylor , J.Z. Groenewald","doi":"10.1016/j.simyco.2019.08.001","DOIUrl":"10.1016/j.simyco.2019.08.001","url":null,"abstract":"<div><p>Species of eucalypts are commonly cultivated for solid wood and pulp products. The expansion of commercially managed eucalypt plantations has chiefly been driven by their rapid growth and suitability for propagation across a very wide variety of sites and climatic conditions. Infection of foliar fungal pathogens of eucalypts is resulting in increasingly negative impacts on commercial forest industries globally. To assist in evaluating this threat, the present study provides a global perspective on foliar pathogens of eucalypts. We treat 110 different genera including species associated with foliar disease symptoms of these hosts. The vast majority of these fungi have been grown in axenic culture, and subjected to DNA sequence analysis, resolving their phylogeny. During the course of this study several new genera and species were encountered, and these are described. New genera include: <em>Lembosiniella</em> (<em>L. eucalyptorum</em> on <em>E. dunnii,</em> Australia), <em>Neosonderhenia</em> (<em>N. eucalypti</em> on <em>E. costata,</em> Australia), <em>Neothyriopsis</em> (<em>N. sphaerospora</em> on <em>E. camaldulensis</em>, South Africa), <em>Neotrichosphaeria</em> (<em>N. eucalypticola</em> on <em>E. deglupta</em>, Australia), <em>Nothotrimmatostroma</em> (<em>N. bifarium</em> on <em>E. dalrympleana</em>, Australia), <em>Nowamyces</em> (incl. <em>Nowamycetaceae fam. nov</em>., <em>N. globulus</em> on <em>E. globulus</em>, Australia), and <em>Walkaminomyces</em> (<em>W. medusae</em> on <em>E. alba</em>, Australia). New species include (all from Australia): <em>Disculoides fraxinoides</em> on <em>E. fraxinoides, Elsinoe piperitae on E. piperita, Fusculina regnans</em> on <em>E. regnans, Marthamyces johnstonii</em> on <em>E. dunnii</em>, <em>Neofusicoccum corticosae</em> on <em>E. corticosa</em>, <em>Neotrimmatostroma dalrympleanae</em> on <em>E. dalrympleana, Nowamyces piperitae</em> on <em>E. piperita</em>, <em>Phaeothyriolum dunnii</em> on <em>E. dunnii</em>, <em>Pseudophloeospora eucalyptigena</em> on <em>E. obliqua</em>, <em>Pseudophloeospora jollyi</em> on <em>Eucalyptus</em> sp., <em>Quambalaria tasmaniae</em> on <em>Eucalyptus</em> sp., <em>Q. rugosae</em> on <em>E. rugosa</em>, <em>Sonderhenia radiata</em> on <em>E. radiata</em>, <em>Teratosphaeria pseudonubilosa</em> on <em>E. globulus</em> and <em>Thyrinula dunnii</em> on <em>E. dunnii</em>. A new name is also proposed for <em>Heteroconium eucalypti</em> as <em>Thyrinula uruguayensis</em> on <em>E. dunnii</em>, Uruguay. Although many of these genera and species are commonly associated with disease problems, several appear to be opportunists developing on stressed or dying tissues. For the majority of these fungi, pathogenicity remains to be determined. This represents an important goal for forest pathologists and biologists in the future. Consequently, this study will promote renewed interest in foliar pathogens of eucalypts, leading to investigations that will provide an impr","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"94 ","pages":"Pages 125-298"},"PeriodicalIF":16.5,"publicationDate":"2019-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2019.08.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41213510","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 : 2019-09-01DOI: 10.1016/j.simyco.2019.05.001
Y. Marin-Felix , M. Hernández-Restrepo , I. Iturrieta-González , D. García , J. Gené , J.Z. Groenewald , L. Cai , Q. Chen , W. Quaedvlieg , R.K. Schumacher , P.W.J. Taylor , C. Ambers , G. Bonthond , J. Edwards , S.A. Krueger-Hadfield , J.J. Luangsa-ard , L. Morton , A. Moslemi , M. Sandoval-Denis , Y.P. Tan , P.W. Crous
This paper represents the third contribution in the Genera of Phytopathogenic Fungi (GOPHY) series. The series provides morphological descriptions, information about the pathology, distribution, hosts and disease symptoms for the treated genera, as well as primary and secondary DNA barcodes for the currently accepted species included in these. This third paper in the GOPHY series treats 21 genera of phytopathogenic fungi and their relatives including: Allophoma, Alternaria, Brunneosphaerella, Elsinoe, Exserohilum, Neosetophoma, Neostagonospora, Nothophoma, Parastagonospora, Phaeosphaeriopsis, Pleiocarpon, Pyrenophora, Ramichloridium, Seifertia, Seiridium, Septoriella, Setophoma, Stagonosporopsis, Stemphylium, Tubakia and Zasmidium. This study includes three new genera, 42 new species, 23 new combinations, four new names, and three typifications of older names.
{"title":"Genera of phytopathogenic fungi: GOPHY 3","authors":"Y. Marin-Felix , M. Hernández-Restrepo , I. Iturrieta-González , D. García , J. Gené , J.Z. Groenewald , L. Cai , Q. Chen , W. Quaedvlieg , R.K. Schumacher , P.W.J. Taylor , C. Ambers , G. Bonthond , J. Edwards , S.A. Krueger-Hadfield , J.J. Luangsa-ard , L. Morton , A. Moslemi , M. Sandoval-Denis , Y.P. Tan , P.W. Crous","doi":"10.1016/j.simyco.2019.05.001","DOIUrl":"10.1016/j.simyco.2019.05.001","url":null,"abstract":"<div><p>This paper represents the third contribution in the Genera of Phytopathogenic Fungi (GOPHY) series. The series provides morphological descriptions, information about the pathology, distribution, hosts and disease symptoms for the treated genera, as well as primary and secondary DNA barcodes for the currently accepted species included in these. This third paper in the GOPHY series treats 21 genera of phytopathogenic fungi and their relatives including: <em>Allophoma</em>, <em>Alternaria</em>, <em>Brunneosphaerella</em>, <em>Elsinoe</em>, <em>Exserohilum</em>, <em>Neosetophoma</em>, <em>Neostagonospora</em>, <em>Nothophoma</em>, <em>Parastagonospora</em>, <em>Phaeosphaeriopsis</em>, <em>Pleiocarpon</em>, <em>Pyrenophora</em>, <em>Ramichloridium</em>, <em>Seifertia</em>, <em>Seiridium</em>, <em>Septoriella</em>, <em>Setophoma</em>, <em>Stagonosporopsis</em>, <em>Stemphylium</em>, <em>Tubakia</em> and <em>Zasmidium</em>. This study includes three new genera, 42 new species, 23 new combinations, four new names, and three typifications of older names.</p></div>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"94 ","pages":"Pages 1-124"},"PeriodicalIF":16.5,"publicationDate":"2019-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2019.05.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41213511","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 : 2019-06-01DOI: 10.1016/j.simyco.2018.06.001
J.C. Frisvad , V. Hubka , C.N. Ezekiel , S.-B. Hong , A. Nováková , A.J. Chen , M. Arzanlou , T.O. Larsen , F. Sklenář , W. Mahakarnchanakul , R.A. Samson , J. Houbraken
<div><p>Aflatoxins and ochratoxins are among the most important mycotoxins of all and producers of both types of mycotoxins are present in <em>Aspergillus</em> section <em>Flavi</em>, albeit never in the same species. Some of the most efficient producers of aflatoxins and ochratoxins have not been described yet. Using a polyphasic approach combining phenotype, physiology, sequence and extrolite data, we describe here eight new species in section <em>Flavi</em>. Phylogenetically, section <em>Flavi</em> is split in eight clades and the section currently contains 33 species. Two species only produce aflatoxin B<sub>1</sub> and B<sub>2</sub> (<em>A. pseudotamarii</em> and <em>A. togoensis</em>), and 14 species are able to produce aflatoxin B<sub>1</sub>, B<sub>2</sub>, G<sub>1</sub> and G<sub>2</sub>: three newly described species <em>A. aflatoxiformans, A. austwickii</em> and <em>A. cerealis</em> in addition to <em>A. arachidicola</em>, <em>A. minisclerotigenes</em>, <em>A. mottae, A. luteovirescens</em> (formerly <em>A. bombycis</em>)<em>, A. nomius, A. novoparasiticus, A. parasiticus, A. pseudocaelatus, A. pseudonomius, A. sergii</em> and <em>A. transmontanensis</em>. It is generally accepted that <em>A. flavus</em> is unable to produce type G aflatoxins, but here we report on Korean strains that also produce aflatoxin G<sub>1</sub> and G<sub>2</sub>. One strain of <em>A. bertholletius</em> can produce the immediate aflatoxin precursor 3-O-methylsterigmatocystin, and one strain of <em>Aspergillus sojae</em> and two strains of <em>Aspergillus alliaceus</em> produced versicolorins. Strains of the domesticated forms of <em>A. flavus</em> and <em>A. parasiticus</em>, <em>A. oryzae</em> and <em>A. sojae</em>, respectively, lost their ability to produce aflatoxins, and from the remaining phylogenetically closely related species (belonging to the <em>A. flavus</em>-, <em>A. tamarii</em>-, <em>A. bertholletius</em>- and <em>A. nomius</em>-clades), only <em>A. caelatus</em>, <em>A. subflavus</em> and <em>A. tamarii</em> are unable to produce aflatoxins. With exception of <em>A. togoensis</em> in the <em>A. coremiiformis</em>-clade, all species in the phylogenetically more distant clades (<em>A. alliaceus</em>-, <em>A. coremiiformis</em>-, <em>A. leporis</em>- and <em>A. avenaceus</em>-clade) are unable to produce aflatoxins. Three out of the four species in the <em>A. alliaceus</em>-clade can produce the mycotoxin ochratoxin A: <em>A. alliaceus s</em>. <em>str</em>. and two new species described here as <em>A. neoalliaceus</em> and <em>A. vandermerwei</em>. Eight species produced the mycotoxin tenuazonic acid: <em>A. bertholletius</em>, <em>A. caelatus, A. luteovirescens</em>, <em>A. nomius, A. pseudocaelatus</em>, <em>A. pseudonomius, A. pseudotamarii</em> and <em>A. tamarii</em> while the related mycotoxin cyclopiazonic acid was produced by 13 species: <em>A. aflatoxiformans, A. austwickii, A. bertholletius, A. cerealis, A. flavus, A. minisclerotigenes,
{"title":"Taxonomy of Aspergillus section Flavi and their production of aflatoxins, ochratoxins and other mycotoxins","authors":"J.C. Frisvad , V. Hubka , C.N. Ezekiel , S.-B. Hong , A. Nováková , A.J. Chen , M. Arzanlou , T.O. Larsen , F. Sklenář , W. Mahakarnchanakul , R.A. Samson , J. Houbraken","doi":"10.1016/j.simyco.2018.06.001","DOIUrl":"10.1016/j.simyco.2018.06.001","url":null,"abstract":"<div><p>Aflatoxins and ochratoxins are among the most important mycotoxins of all and producers of both types of mycotoxins are present in <em>Aspergillus</em> section <em>Flavi</em>, albeit never in the same species. Some of the most efficient producers of aflatoxins and ochratoxins have not been described yet. Using a polyphasic approach combining phenotype, physiology, sequence and extrolite data, we describe here eight new species in section <em>Flavi</em>. Phylogenetically, section <em>Flavi</em> is split in eight clades and the section currently contains 33 species. Two species only produce aflatoxin B<sub>1</sub> and B<sub>2</sub> (<em>A. pseudotamarii</em> and <em>A. togoensis</em>), and 14 species are able to produce aflatoxin B<sub>1</sub>, B<sub>2</sub>, G<sub>1</sub> and G<sub>2</sub>: three newly described species <em>A. aflatoxiformans, A. austwickii</em> and <em>A. cerealis</em> in addition to <em>A. arachidicola</em>, <em>A. minisclerotigenes</em>, <em>A. mottae, A. luteovirescens</em> (formerly <em>A. bombycis</em>)<em>, A. nomius, A. novoparasiticus, A. parasiticus, A. pseudocaelatus, A. pseudonomius, A. sergii</em> and <em>A. transmontanensis</em>. It is generally accepted that <em>A. flavus</em> is unable to produce type G aflatoxins, but here we report on Korean strains that also produce aflatoxin G<sub>1</sub> and G<sub>2</sub>. One strain of <em>A. bertholletius</em> can produce the immediate aflatoxin precursor 3-O-methylsterigmatocystin, and one strain of <em>Aspergillus sojae</em> and two strains of <em>Aspergillus alliaceus</em> produced versicolorins. Strains of the domesticated forms of <em>A. flavus</em> and <em>A. parasiticus</em>, <em>A. oryzae</em> and <em>A. sojae</em>, respectively, lost their ability to produce aflatoxins, and from the remaining phylogenetically closely related species (belonging to the <em>A. flavus</em>-, <em>A. tamarii</em>-, <em>A. bertholletius</em>- and <em>A. nomius</em>-clades), only <em>A. caelatus</em>, <em>A. subflavus</em> and <em>A. tamarii</em> are unable to produce aflatoxins. With exception of <em>A. togoensis</em> in the <em>A. coremiiformis</em>-clade, all species in the phylogenetically more distant clades (<em>A. alliaceus</em>-, <em>A. coremiiformis</em>-, <em>A. leporis</em>- and <em>A. avenaceus</em>-clade) are unable to produce aflatoxins. Three out of the four species in the <em>A. alliaceus</em>-clade can produce the mycotoxin ochratoxin A: <em>A. alliaceus s</em>. <em>str</em>. and two new species described here as <em>A. neoalliaceus</em> and <em>A. vandermerwei</em>. Eight species produced the mycotoxin tenuazonic acid: <em>A. bertholletius</em>, <em>A. caelatus, A. luteovirescens</em>, <em>A. nomius, A. pseudocaelatus</em>, <em>A. pseudonomius, A. pseudotamarii</em> and <em>A. tamarii</em> while the related mycotoxin cyclopiazonic acid was produced by 13 species: <em>A. aflatoxiformans, A. austwickii, A. bertholletius, A. cerealis, A. flavus, A. minisclerotigenes, ","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"93 ","pages":"Pages 1-63"},"PeriodicalIF":16.5,"publicationDate":"2019-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.simyco.2018.06.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36398323","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}