L Zhao, J Z Groenewald, M Hernández-Restrepo, H-J Schroers, P W Crous
{"title":"Revising Clonostachys and allied genera in Bionectriaceae.","authors":"L Zhao, J Z Groenewald, M Hernández-Restrepo, H-J Schroers, P W Crous","doi":"10.3114/sim.2023.105.03","DOIUrl":null,"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 independently and that the frequently stroma-linked <i>Clonostachys</i> morphs evolved together with the occupation of woody host niches and mycoparasitism. <b>Taxonomic novelties:</b> <b>New species:</b> <i>Clonostachys aurantiaca</i> L. Zhao & Crous, <i>Clonostachys australiana</i> L. Zhao & Crous, <i>Clonostachys bambusae</i> L. Zhao & Crous, <i>Clonostachys</i> <i>buxicola</i> L. Zhao & Crous, <i>Clonostachys cylindrica</i> L. Zhao & Crous, <i>Clonostachys ellipsoidea</i> L. Zhao & Crous, <i>Clonostachys flava</i> L. Zhao, Crous & Schroers, <i>Clonostachys fujianensis</i> L. Zhao & Crous, <i>Clonostachys fusca</i> L. Zhao, Crous & Schroers, <i>Clonostachys garysamuelsii</i> L. Zhao & Crous, <i>Clonostachys hongkongensis</i> L. Zhao & Crous, <i>Clonostachys longiphialidica</i> L. Zhao, Crous & Schroers, <i>Clonostachys obovatispora</i>, L. Zhao & Crous, <i>Clonostachys palmae</i> L. Zhao, Crous & Schroers, <i>Clonostachys parasporodochialis</i> L. Zhao & Crous, <i>Clonostachys penicillata</i> L. Zhao, Crous & Schroers, <i>Clonostachys reniformis</i> L. Zhao & Crous, <i>Clonostachys vacuolata</i> L. Zhao, Crous & Schroers, <i>Clonostachys venezuelae</i> L. Zhao, Crous & Schroers, <i>Mycocitrus synnematus</i> L. Zhao & Crous, <i>Nectriopsis didymii</i> L. Zhao & Crous, <i>Sesquicillium intermediophialidicum</i> L. Zhao & Crous, <i>Sesquicillium neerlandicum</i> L. Zhao & Crous, <i>Sesquicillium symmetricum</i> L. Zhao & Crous. <b>New combinations:</b> <i>Mycocitrus coccicola</i> (J.A. Stev.) L. Zhao & Crous, <i>Mycocitrus coxeniae</i> (Y.P. Tan <i>et al</i>.) L. Zhao & Crous, <i>Sesquicillium essexcoheniae</i> (Y.P. Tan <i>et al</i>.) L. Zhao & Crous, <i>Sesquicillium lasiacidis</i> (Samuels) L. Zhao, Crous & Schroers, <i>Sesquicillium phyllophilum</i> (Schroers) L. Zhao, Crous & Schroers, <i>Sesquicillium rossmaniae</i> (Schroers) L. Zhao, Crous & Schroers, <i>Sesquicillium saulense</i> (Lechat & J. Fourn.) L. Zhao & Crous, <i>Sesquicillium sesquicillii</i> (Samuels) L. Zhao, Crous & Schroers, <i>Sesquicillium spinulosisporum</i> (Lechat & J. Fourn.) L. Zhao & Crous, <i>Sesquicillium tornatum</i> (Höhn.) Schroers. <b>New synonyms:</b> <i>Clonostachys aranearum</i> W.H. Chen <i>et al</i>., <i>Clonostachys chuyangsinensis</i> H. Yu & Y. Wang, <i>Clonostachys eriocamporesiana</i> R.H. Perera & K.D. Hyde, <i>Clonostachys granuligera</i> (Starbäck) Forin & Vizzini, <i>Clonostachys indica</i> Prasher & R. Chauhan, <i>Clonostachys spinulosa</i> R.H. Perera <i>et al</i>., <i>Clonostachys squamuligera</i> (Sacc.) Forin & Vizzini, <i>Clonostachys wenpingii</i> (J. Luo & W.Y. Zhuang) Z.Q. Zeng & W.Y. Zhuang. <b>Epitypes (basionyms):</b> <i>Fusidium buxi</i> J.C. Schmidt ex Link, <i>Verticillium candelabrum</i> Bonord. <b>Citation:</b> Zhao L, Groenewald JZ, Hernández-Restrepo M, Schroers H-J, Crous PW (2023). Revising <i>Clonostachys</i> and allied genera in <i>Bionectriaceae</i>. <i>Studies in Mycology</i> <b>105</b>: 205-266. doi: 10.3114/sim.2023.105.03.</p>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":null,"pages":null},"PeriodicalIF":14.1000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11182609/pdf/","citationCount":"0","resultStr":"{\"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\":null,\"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 independently and that the frequently stroma-linked <i>Clonostachys</i> morphs evolved together with the occupation of woody host niches and mycoparasitism. <b>Taxonomic novelties:</b> <b>New species:</b> <i>Clonostachys aurantiaca</i> L. Zhao & Crous, <i>Clonostachys australiana</i> L. Zhao & Crous, <i>Clonostachys bambusae</i> L. Zhao & Crous, <i>Clonostachys</i> <i>buxicola</i> L. Zhao & Crous, <i>Clonostachys cylindrica</i> L. Zhao & Crous, <i>Clonostachys ellipsoidea</i> L. Zhao & Crous, <i>Clonostachys flava</i> L. Zhao, Crous & Schroers, <i>Clonostachys fujianensis</i> L. Zhao & Crous, <i>Clonostachys fusca</i> L. Zhao, Crous & Schroers, <i>Clonostachys garysamuelsii</i> L. Zhao & Crous, <i>Clonostachys hongkongensis</i> L. Zhao & Crous, <i>Clonostachys longiphialidica</i> L. Zhao, Crous & Schroers, <i>Clonostachys obovatispora</i>, L. Zhao & Crous, <i>Clonostachys palmae</i> L. Zhao, Crous & Schroers, <i>Clonostachys parasporodochialis</i> L. Zhao & Crous, <i>Clonostachys penicillata</i> L. Zhao, Crous & Schroers, <i>Clonostachys reniformis</i> L. Zhao & Crous, <i>Clonostachys vacuolata</i> L. Zhao, Crous & Schroers, <i>Clonostachys venezuelae</i> L. Zhao, Crous & Schroers, <i>Mycocitrus synnematus</i> L. Zhao & Crous, <i>Nectriopsis didymii</i> L. Zhao & Crous, <i>Sesquicillium intermediophialidicum</i> L. Zhao & Crous, <i>Sesquicillium neerlandicum</i> L. Zhao & Crous, <i>Sesquicillium symmetricum</i> L. Zhao & Crous. <b>New combinations:</b> <i>Mycocitrus coccicola</i> (J.A. Stev.) L. Zhao & Crous, <i>Mycocitrus coxeniae</i> (Y.P. Tan <i>et al</i>.) L. Zhao & Crous, <i>Sesquicillium essexcoheniae</i> (Y.P. Tan <i>et al</i>.) L. Zhao & Crous, <i>Sesquicillium lasiacidis</i> (Samuels) L. Zhao, Crous & Schroers, <i>Sesquicillium phyllophilum</i> (Schroers) L. Zhao, Crous & Schroers, <i>Sesquicillium rossmaniae</i> (Schroers) L. Zhao, Crous & Schroers, <i>Sesquicillium saulense</i> (Lechat & J. Fourn.) L. Zhao & Crous, <i>Sesquicillium sesquicillii</i> (Samuels) L. Zhao, Crous & Schroers, <i>Sesquicillium spinulosisporum</i> (Lechat & J. Fourn.) L. Zhao & Crous, <i>Sesquicillium tornatum</i> (Höhn.) Schroers. <b>New synonyms:</b> <i>Clonostachys aranearum</i> W.H. Chen <i>et al</i>., <i>Clonostachys chuyangsinensis</i> H. Yu & Y. Wang, <i>Clonostachys eriocamporesiana</i> R.H. Perera & K.D. Hyde, <i>Clonostachys granuligera</i> (Starbäck) Forin & Vizzini, <i>Clonostachys indica</i> Prasher & R. Chauhan, <i>Clonostachys spinulosa</i> R.H. Perera <i>et al</i>., <i>Clonostachys squamuligera</i> (Sacc.) Forin & Vizzini, <i>Clonostachys wenpingii</i> (J. Luo & W.Y. Zhuang) Z.Q. Zeng & W.Y. Zhuang. <b>Epitypes (basionyms):</b> <i>Fusidium buxi</i> J.C. Schmidt ex Link, <i>Verticillium candelabrum</i> Bonord. <b>Citation:</b> Zhao L, Groenewald JZ, Hernández-Restrepo M, Schroers H-J, Crous PW (2023). 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引用次数: 0
摘要
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.
Revising Clonostachys and allied genera in Bionectriaceae.
Clonostachys (Bionectriaceae, Hypocreales) species are common soil-borne fungi, endophytes, epiphytes, and saprotrophs. Sexual morphs of Clonostachys spp. were placed in the genus Bionectria, which was further segregated into the six subgenera Astromata, Bionectria, Epiphloea, Myronectria, Uniparietina, and Zebrinella. However, with the end of dual nomenclature, Clonostachys became the single depository for sexual and asexual morph-typified species. Species of Clonostachys 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 Clonostachys 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 (RPB2), translation elongation factor 1-alpha (TEF1) and β-tubulin (TUB2). Based on these results, the subgenera Astromata, Bionectria, Myronectria and Zebrinella are supported within Clonostachys. Furthermore, the genus Sesquicillium is resurrected to accommodate the former subgenera Epiphloea and Uniparietina. The close relationship of Clonostachys and Sesquicillium is strongly supported as both are inferred phylogenetically as sister-genera. New taxa include 24 new species and 10 new combinations. Recognition of Sesquicillium distinguishes species typically forming a reduced perithecial stroma superficially on plant tissue from species in Clonostachys 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 Clonostachys and Sesquicillium 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 independently and that the frequently stroma-linked Clonostachys morphs evolved together with the occupation of woody host niches and mycoparasitism. Taxonomic novelties:New species:Clonostachys aurantiaca L. Zhao & Crous, Clonostachys australiana L. Zhao & Crous, Clonostachys bambusae L. Zhao & Crous, Clonostachysbuxicola L. Zhao & Crous, Clonostachys cylindrica L. Zhao & Crous, Clonostachys ellipsoidea L. Zhao & Crous, Clonostachys flava L. Zhao, Crous & Schroers, Clonostachys fujianensis L. Zhao & Crous, Clonostachys fusca L. Zhao, Crous & Schroers, Clonostachys garysamuelsii L. Zhao & Crous, Clonostachys hongkongensis L. Zhao & Crous, Clonostachys longiphialidica L. Zhao, Crous & Schroers, Clonostachys obovatispora, L. Zhao & Crous, Clonostachys palmae L. Zhao, Crous & Schroers, Clonostachys parasporodochialis L. Zhao & Crous, Clonostachys penicillata L. Zhao, Crous & Schroers, Clonostachys reniformis L. Zhao & Crous, Clonostachys vacuolata L. Zhao, Crous & Schroers, Clonostachys venezuelae L. Zhao, Crous & Schroers, Mycocitrus synnematus L. Zhao & Crous, Nectriopsis didymii L. Zhao & Crous, Sesquicillium intermediophialidicum L. Zhao & Crous, Sesquicillium neerlandicum L. Zhao & Crous, Sesquicillium symmetricum L. Zhao & Crous. New combinations:Mycocitrus coccicola (J.A. Stev.) L. Zhao & Crous, Mycocitrus coxeniae (Y.P. Tan et al.) L. Zhao & Crous, Sesquicillium essexcoheniae (Y.P. Tan et al.) L. Zhao & Crous, Sesquicillium lasiacidis (Samuels) L. Zhao, Crous & Schroers, Sesquicillium phyllophilum (Schroers) L. Zhao, Crous & Schroers, Sesquicillium rossmaniae (Schroers) L. Zhao, Crous & Schroers, Sesquicillium saulense (Lechat & J. Fourn.) L. Zhao & Crous, Sesquicillium sesquicillii (Samuels) L. Zhao, Crous & Schroers, Sesquicillium spinulosisporum (Lechat & J. Fourn.) L. Zhao & Crous, Sesquicillium tornatum (Höhn.) Schroers. New synonyms:Clonostachys aranearum W.H. Chen et al., Clonostachys chuyangsinensis H. Yu & Y. Wang, Clonostachys eriocamporesiana R.H. Perera & K.D. Hyde, Clonostachys granuligera (Starbäck) Forin & Vizzini, Clonostachys indica Prasher & R. Chauhan, Clonostachys spinulosa R.H. Perera et al., Clonostachys squamuligera (Sacc.) Forin & Vizzini, Clonostachys wenpingii (J. Luo & W.Y. Zhuang) Z.Q. Zeng & W.Y. Zhuang. Epitypes (basionyms):Fusidium buxi J.C. Schmidt ex Link, Verticillium candelabrum Bonord. Citation: Zhao L, Groenewald JZ, Hernández-Restrepo M, Schroers H-J, Crous PW (2023). Revising Clonostachys and allied genera in Bionectriaceae. Studies in Mycology105: 205-266. doi: 10.3114/sim.2023.105.03.
期刊介绍:
The international journal Studies in Mycology focuses on advancing the understanding of filamentous fungi, yeasts, and various aspects of mycology. It publishes comprehensive systematic monographs as well as topical issues covering a wide range of subjects including biotechnology, ecology, molecular biology, pathology, and systematics. This Open-Access journal offers unrestricted access to its content.
Each issue of Studies in Mycology consists of around 5 to 6 papers, either in the form of monographs or special focused topics. Unlike traditional length restrictions, the journal encourages submissions of manuscripts with a minimum of 50 A4 pages in print. This ensures a thorough exploration and presentation of the research findings, maximizing the depth of the published work.