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Generic Names in Magnaporthales Ning Zhang, Jing Luo, Amy Y
Generic names in Magnaporthales Ning Zhang, Jing Luo, Amy Y. Rossman, Takayuki Aoki, Izumi Chuma, Pedro W. Crous, Ralph Dean, Ronald P. de Vries, Nicole Donofrio, Kevin D. Hyde, et al. To cite this version: Ning Zhang, Jing Luo, Amy Y. Rossman, Takayuki Aoki, Izumi Chuma, et al.. Generic names in Magnaporthales. IMA Fungus, 2016, 7 (1), pp.155-159. 10.5598/imafungus.2016.07.01.09. hal- 01608608 HAL Id: hal-01608608 https://hal.archives-ouvertes.fr/hal-01608608 Submitted on 28 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - ShareAlike| 4.0 International License IMA FUNGUS · 7(1): 155–159 (2016) doi:10.5598/imafungus.2016.07.01.09 ARTICLE Generic names in Magnaporthales Ning Zhang1, Jing Luo1, Amy Y. Rossman2, Takayuki Aoki3, Izumi Chuma4, Pedro W. Crous5, Ralph Dean6, Ronald P. de Vries5,7, Nicole Donofrio8, Kevin D. Hyde9, Marc-Henri Lebrun10, Nicholas J. Talbot11, Didier Tharreau12, Yukio Tosa4, Barbara Valent13, Zonghua Wang14, and Jin-Rong Xu15 1Department of Plant Biology and Pathology, Rutgers University, New Brunswick, NJ 08901, USA; corresponding author e-mail: zhang@aesop. -
Resolving the Polyphyletic Nature of Pyricularia (Pyriculariaceae)
available online at www.studiesinmycology.org STUDIES IN MYCOLOGY ▪:1–36. Resolving the polyphyletic nature of Pyricularia (Pyriculariaceae) S. Klaubauf1,2, D. Tharreau3, E. Fournier4, J.Z. Groenewald1, P.W. Crous1,5,6*, R.P. de Vries1,2, and M.-H. Lebrun7* 1CBS-KNAW Fungal Biodiversity Centre, 3584 CT Utrecht, The Netherlands; 2Fungal Molecular Physiology, Utrecht University, Utrecht, The Netherlands; 3UMR BGPI, CIRAD, Campus International de Baillarguet, F-34398 Montpellier, France; 4UMR BGPI, INRA, Campus International de Baillarguet, F-34398 Montpellier, France; 5Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria 0002, South Africa; 6Wageningen University and Research Centre (WUR), Laboratory of Phytopathology, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands; 7UR1290 INRA BIOGER-CPP, Campus AgroParisTech, F-78850 Thiverval-Grignon, France *Correspondence: P.W. Crous, [email protected]; M.-H. Lebrun, [email protected] Abstract: Species of Pyricularia (magnaporthe-like sexual morphs) are responsible for major diseases on grasses. Pyricularia oryzae (sexual morph Magnaporthe oryzae) is responsible for the major disease of rice called rice blast disease, and foliar diseases of wheat and millet, while Pyricularia grisea (sexual morph Magnaporthe grisea) is responsible for foliar diseases of Digitaria. Magnaporthe salvinii, M. poae and M. rhizophila produce asexual spores that differ from those of Pyricularia sensu stricto that has pyriform, 2-septate conidia produced on conidiophores with sympodial proliferation. Magnaporthe salvinii was recently allocated to Nakataea, while M. poae and M. rhizophila were placed in Magnaporthiopsis. To clarify the taxonomic relationships among species that are magnaporthe- or pyricularia-like in morphology, we analysed phylogenetic relationships among isolates representing a wide range of host plants by using partial DNA sequences of multiple genes such as LSU, ITS, RPB1, actin and calmodulin. -
Myconet Volume 14 Part One. Outine of Ascomycota – 2009 Part Two
(topsheet) Myconet Volume 14 Part One. Outine of Ascomycota – 2009 Part Two. Notes on ascomycete systematics. Nos. 4751 – 5113. Fieldiana, Botany H. Thorsten Lumbsch Dept. of Botany Field Museum 1400 S. Lake Shore Dr. Chicago, IL 60605 (312) 665-7881 fax: 312-665-7158 e-mail: [email protected] Sabine M. Huhndorf Dept. of Botany Field Museum 1400 S. Lake Shore Dr. Chicago, IL 60605 (312) 665-7855 fax: 312-665-7158 e-mail: [email protected] 1 (cover page) FIELDIANA Botany NEW SERIES NO 00 Myconet Volume 14 Part One. Outine of Ascomycota – 2009 Part Two. Notes on ascomycete systematics. Nos. 4751 – 5113 H. Thorsten Lumbsch Sabine M. Huhndorf [Date] Publication 0000 PUBLISHED BY THE FIELD MUSEUM OF NATURAL HISTORY 2 Table of Contents Abstract Part One. Outline of Ascomycota - 2009 Introduction Literature Cited Index to Ascomycota Subphylum Taphrinomycotina Class Neolectomycetes Class Pneumocystidomycetes Class Schizosaccharomycetes Class Taphrinomycetes Subphylum Saccharomycotina Class Saccharomycetes Subphylum Pezizomycotina Class Arthoniomycetes Class Dothideomycetes Subclass Dothideomycetidae Subclass Pleosporomycetidae Dothideomycetes incertae sedis: orders, families, genera Class Eurotiomycetes Subclass Chaetothyriomycetidae Subclass Eurotiomycetidae Subclass Mycocaliciomycetidae Class Geoglossomycetes Class Laboulbeniomycetes Class Lecanoromycetes Subclass Acarosporomycetidae Subclass Lecanoromycetidae Subclass Ostropomycetidae 3 Lecanoromycetes incertae sedis: orders, genera Class Leotiomycetes Leotiomycetes incertae sedis: families, genera Class Lichinomycetes Class Orbiliomycetes Class Pezizomycetes Class Sordariomycetes Subclass Hypocreomycetidae Subclass Sordariomycetidae Subclass Xylariomycetidae Sordariomycetes incertae sedis: orders, families, genera Pezizomycotina incertae sedis: orders, families Part Two. Notes on ascomycete systematics. Nos. 4751 – 5113 Introduction Literature Cited 4 Abstract Part One presents the current classification that includes all accepted genera and higher taxa above the generic level in the phylum Ascomycota. -
Discovered and Re- Evaluation of Pleurophragmium
Fungal Diversity Teleomorph of Rhodoveronaea (Sordariomycetidae) discovered and re- evaluation of Pleurophragmium 1* Martina Réblová 1Department of Plant Taxonomy, Institute of Botany, Academy of Sciences, CZ-252 43 Průhonice, Czech Republic Réblová, M. (2009). Teleomorph of Rhodoveronaea (Sordariomycetidae) discovered and re-evolution of Pleurophragmium. Fungal Diversity 36: 129-139. An undescribed teleomorph was discovered for Rhodoveronaea (Sordariomycetidae), a previously known anamorph genus with the single species R. varioseptata characterized by pigmented, septate conidia and holoblastic-denticulate conidiogenesis. The teleomorph is a lignicolous perithecial ascomycete with nonstromatic, dark perithecia, consisting of a globose immersed venter and stout conical emerging neck; cylindrical long-stipitate asci, nonamyloid apical annulus and fusiform, septate, hyaline ascospores. The fertile conidiophores of R. varioseptata were associated with the perithecia on the natural substratum and they were also obtained in vitro. Because no teleomorph was designated in the protologue of Rhodoveronaea, the new Article 59.7 of the International Code of Botanical Nomenclature is applied in this case and Rhodoveronaea is expanded to holomorphic application by teleomorphic epitypification of the type species R. varioseptata. The name R. varioseptata is fully adopted for the discovered teleomorph. On the basis of detailed morphology, cultivation studies and phylogenetic analyses of ncLSU rDNA sequences, Rhodoveronaea is segregated from the morphologically similar genera Lentomitella and Ceratosphaeria; its relationship with Ceratosphaeria fragilis and C. rhenana is discussed. The relationship of Rhodoveronaea with the morphologically similar Dactylaria parvispora is investigated using morphological features and molecular sequence data. Phylogenetic findings based on ncLSU rDNA sequence data indicate that Dactylaria is polyphyletic. The genus Pleurophragmium is excluded from the synonymy of Dactylaria and is re-evaluated for P. -
Genome Wide Analysis of the Transition to Pathogenic Lifestyles in Magnaporthales Fungi Received: 25 January 2018 Ning Zhang1,2, Guohong Cai3, Dana C
www.nature.com/scientificreports OPEN Genome wide analysis of the transition to pathogenic lifestyles in Magnaporthales fungi Received: 25 January 2018 Ning Zhang1,2, Guohong Cai3, Dana C. Price4, Jo Anne Crouch 5, Pierre Gladieux6, Bradley Accepted: 29 March 2018 Hillman1, Chang Hyun Khang7, Marc-Henri LeBrun8, Yong-Hwan Lee9, Jing Luo1, Huan Qiu10, Published: xx xx xxxx Daniel Veltri11, Jennifer H. Wisecaver12, Jie Zhu7 & Debashish Bhattacharya2 The rice blast fungus Pyricularia oryzae (syn. Magnaporthe oryzae, Magnaporthe grisea), a member of the order Magnaporthales in the class Sordariomycetes, is an important plant pathogen and a model species for studying pathogen infection and plant-fungal interaction. In this study, we generated genome sequence data from fve additional Magnaporthales fungi including non-pathogenic species, and performed comparative genome analysis of a total of 13 fungal species in the class Sordariomycetes to understand the evolutionary history of the Magnaporthales and of fungal pathogenesis. Our results suggest that the Magnaporthales diverged ca. 31 millon years ago from other Sordariomycetes, with the phytopathogenic blast clade diverging ca. 21 million years ago. Little evidence of inter-phylum horizontal gene transfer (HGT) was detected in Magnaporthales. In contrast, many genes underwent positive selection in this order and the majority of these sequences are clade-specifc. The blast clade genomes contain more secretome and avirulence efector genes, which likely play key roles in the interaction between Pyricularia species and their plant hosts. Finally, analysis of transposable elements (TE) showed difering proportions of TE classes among Magnaporthales genomes, suggesting that species-specifc patterns may hold clues to the history of host/environmental adaptation in these fungi. -
A Worldwide List of Endophytic Fungi with Notes on Ecology and Diversity
Mycosphere 10(1): 798–1079 (2019) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/10/1/19 A worldwide list of endophytic fungi with notes on ecology and diversity Rashmi M, Kushveer JS and Sarma VV* Fungal Biotechnology Lab, Department of Biotechnology, School of Life Sciences, Pondicherry University, Kalapet, Pondicherry 605014, Puducherry, India Rashmi M, Kushveer JS, Sarma VV 2019 – A worldwide list of endophytic fungi with notes on ecology and diversity. Mycosphere 10(1), 798–1079, Doi 10.5943/mycosphere/10/1/19 Abstract Endophytic fungi are symptomless internal inhabits of plant tissues. They are implicated in the production of antibiotic and other compounds of therapeutic importance. Ecologically they provide several benefits to plants, including protection from plant pathogens. There have been numerous studies on the biodiversity and ecology of endophytic fungi. Some taxa dominate and occur frequently when compared to others due to adaptations or capabilities to produce different primary and secondary metabolites. It is therefore of interest to examine different fungal species and major taxonomic groups to which these fungi belong for bioactive compound production. In the present paper a list of endophytes based on the available literature is reported. More than 800 genera have been reported worldwide. Dominant genera are Alternaria, Aspergillus, Colletotrichum, Fusarium, Penicillium, and Phoma. Most endophyte studies have been on angiosperms followed by gymnosperms. Among the different substrates, leaf endophytes have been studied and analyzed in more detail when compared to other parts. Most investigations are from Asian countries such as China, India, European countries such as Germany, Spain and the UK in addition to major contributions from Brazil and the USA. -
Notes for Genera Update – Ascomycota: 6616-6821 Article
Mycosphere 9(1): 115–140 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/1/2 Copyright © Guizhou Academy of Agricultural Sciences Notes for genera update – Ascomycota: 6616-6821 Wijayawardene NN1,2, Hyde KD2, Divakar PK3, Rajeshkumar KC4, Weerahewa D5, Delgado G6, Wang Y7, Fu L1* 1Shandong Institute of Pomologe, Taian, Shandong Province, 271000, China 2Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3Departamento de Biologı ´a Vegetal II, Facultad de Farmacia, Universidad Complutense de Madrid, 28040 Madrid, Spain 4National Fungal Culture Collection of India (NFCCI), Biodiversity and Palaeobiology (Fungi) Group, Agharkar Research Institute, Pune, Maharashtra 411 004, India 5Department of Botany, The Open University of Sri Lanka, Nawala, Nugegoda, Sri Lanka 610900 Brittmoore Park Drive Suite G Houston, TX 77041 7Department of Plant Pathology, Agriculture College, Guizhou University, Guiyang 550025, People’s Republic of China Wijayawardene NN, Hyde KD, Divakar PK, Rajeshkumar KC, Weerahewa D, Delgado G, Wang Y, Fu L 2018 – Notes for genera update – Ascomycota: 6616-6821. Mycosphere 9(1), 115–140, Doi 10.5943/mycosphere/9/1/2 Abstract Taxonomic knowledge of the Ascomycota, is rapidly changing because of use of molecular data, thus continuous updates of existing taxonomic data with new data is essential. In the current paper, we compile existing data of several genera missing from the recently published “Notes for genera-Ascomycota”. This includes 206 entries. Key words – Asexual genera – Data bases – Sexual genera – Taxonomy Introduction Maintaining updated databases and checklists of genera of fungi is an important and essential task, as it is the base of all taxonomic studies. -
A New Order of Aquatic and Terrestrial Fungi for Achroceratosphaeria and Pisorisporium Gen
Persoonia 34, 2015: 40–49 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158515X685544 Pisorisporiales, a new order of aquatic and terrestrial fungi for Achroceratosphaeria and Pisorisporium gen. nov. in the Sordariomycetes M. Réblová1, J. Fournier 2, V. Štěpánek3 Key words Abstract Four morphologically similar specimens of an unidentified perithecial ascomycete were collected on decaying wood submerged in fresh water. Phylogenetic analysis of DNA sequences from protein-coding and Achroceratosphaeria ribosomal nuclear loci supports the placement of the unidentified fungus together with Achroceratosphaeria in a freshwater strongly supported monophyletic clade. The four collections are described as two new species of the new genus Hypocreomycetidae Pisorisporium characterised by non-stromatic, black, immersed to superficial perithecial ascomata, persistent para- Koralionastetales physes, unitunicate, persistent asci with an amyloid apical annulus and hyaline, fusiform, cymbiform to cylindrical, Lulworthiales transversely multiseptate ascospores with conspicuous guttules. The asexual morph is unknown and no conidia multigene analysis were formed in vitro or on the natural substratum. The clade containing Achroceratosphaeria and Pisorisporium is systematics introduced as the new order Pisorisporiales, family Pisorisporiaceae in the class Sordariomycetes. It represents a new lineage of aquatic fungi. A sister relationship for Pisorisporiales with the Lulworthiales and Koralionastetales is weakly supported -
The Abundance and Diversity of Fungi in a Hypersaline Microbial Mat from Guerrero Negro, Baja California, México
Journal of Fungi Article The Abundance and Diversity of Fungi in a Hypersaline Microbial Mat from Guerrero Negro, Baja California, México Paula Maza-Márquez 1,*, Michael D. Lee 1,2 and Brad M. Bebout 1 1 Exobiology Branch, NASA Ames Research Center, Moffett Field, CA 94035, USA; [email protected] (M.D.L.); [email protected] (B.M.B.) 2 Blue Marble Space Institute of Science, Seattle, WA 98104, USA * Correspondence: [email protected] Abstract: The abundance and diversity of fungi were evaluated in a hypersaline microbial mat from Guerrero Negro, México, using a combination of quantitative polymerase chain reaction (qPCR) amplification of domain-specific primers, and metagenomic sequencing. Seven different layers were analyzed in the mat (Layers 1–7) at single millimeter resolution (from the surface to 7 mm in depth). The number of copies of the 18S rRNA gene of fungi ranged between 106 and 107 copies per g mat, being two logarithmic units lower than of the 16S rRNA gene of bacteria. The abundance of 18S rRNA genes of fungi varied significantly among the layers with layers 2–5 mm from surface contained the highest numbers of copies. Fifty-six fungal taxa were identified by metagenomic sequencing, classified into three different phyla: Ascomycota, Basidiomycota and Microsporidia. The prevalent genera of fungi were Thermothelomyces, Pyricularia, Fusarium, Colletotrichum, Aspergillus, Botrytis, Candida and Neurospora. Genera of fungi identified in the mat were closely related to genera known to have saprotrophic and parasitic lifestyles, as well as genera related to human and plant pathogens and fungi able to perform denitrification. -
© 2019 Austin Lee Grimshaw All Rights Reserved
© 2019 AUSTIN LEE GRIMSHAW ALL RIGHTS RESERVED EVALUATION AND BREEDING OF FINE FESCUES FOR LOW MAINTENANCE APPLICATIONS by AUSTIN LEE GRIMSHAW A dissertation submitted to the School of Graduate Studies Rutgers, The State University of New Jersey In partial fulfillment of the requirements For the degree of Doctor of Philosophy Graduate Program in Plant Biology Written under the direction of Stacy A. Bonos And approved by New Brunswick, New Jersey May, 2019 ABSTRACT OF THE DISSERTATION EVALUATION AND BREEDING OF FINE FESCUES FOR LOW MAINTENANCE APPLICATIONS by AUSTIN LEE GRIMSHAW Dissertation Director: Stacy A. Bonos Fine fescues (Festuca spp.) are being bred for low-maintenance turfgrass applications. One of the major limitations to the widespread use of fine fescue is summer patch susceptibility and traffic tolerance. Magnaporthiopsis poae (Landschoot & Jackson), is the long known causal organism of summer patch, however recent research has found a new species, Magnaporthiopsis meyeri-festucae (Luo & Zhang) from the diseased roots of fine fescue turfgrasses exhibiting summer patch symptoms. Breeding for improved tolerance to summer patch is critical but in order to do so a better understanding of the pathogen(s) is necessary. During 2017 and 2018, isolates of M. meyeri-festucae were compared to isolates of M. poae through plant-fungal interaction in growth chamber experiments and in vitro fungicide sensitivity assays with penthiopyrad, azoxystrobin, and metconazole. In the plant-fungal interaction experiments, M. poae was shown to exhibit higher levels of virulence than M. meyeri-festucae; however, certain isolates of the two species were ranked equal. In the fungicide sensitivity assays, an isolate of M. -
Systematics & Biodiversity
Systematics & Biodiversity (IV) 13:30 - 15:15 Wednesday, 14th August, 2019 Think 4 Room 13:30 - 13:45 WED 26 The mycoflora of Mexico Ricardo Garcia-Sandoval1, Martha A. Reséndis-López2, Gala A. Viurcos-Martínez2,3, Mariana Del Olmo-Ruiz1, Diana R. Hernández-Robles2 1Facultad de Ciencias, UNAM, Mexico City, Mexico. 2CONABIO, Mexico City, Mexico. 3Instituto de Biologia, UNAM, Mexico City, Mexico Abstract Mexico may have up to 200,000 species of fungi. However in the national catalog of fungi, assembled ca. ten years ago by the Comisión Nacional Para el Conocimiento y Uso de la Biodiversidad (CONABIO), a Mexican government agency, only 2,300 species were recorded. A preliminary check-list for North American nonlichenized fungi, assembled with specimens data from fungaria located in Canada, United States and Mexico, reported up to 5,000 species in Mexico. This list had a number of caveats regarding orthographic errors, unsolved synonyms, and in its current version, it does not provide information regarding distribution or details on classification. In order to provide a comprehensive catalog of fungi from Mexico, we assembled a database of 8,882 records of 6,359 taxa, including 6,010 species and 349 taxa below species rank. Specimens records were retrieved from the database of the National System of Biodiversity Information (SNIB in spanish), hosted and maintained by CONABIO, and from peer-reviewed publications, and other relevant bibliographic sources. The results indicate that Basidiomycota accounts for 57.8% of the species, and Ascomycota represents 38.2%. In contrast, 53.6% of the 297 families known from Mexico belong to Ascomycota, and 38.7% to Basidiomycota. -
Newly Recognised Lineages of Perithecial Ascomycetes: the New Orders Conioscyphales and Pleurotheciales
Persoonia 37, 2016: 57–81 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158516X689819 Newly recognised lineages of perithecial ascomycetes: the new orders Conioscyphales and Pleurotheciales M. Réblová1, K.A. Seifert 2, J. Fournier 3, V. Štěpánek4 Key words Abstract Phylogenetic analyses of DNA sequences from nuclear ribosomal and protein-coding loci support the placement of several perithecial ascomycetes and dematiaceous hyphomycetes from freshwater and terrestrial freshwater fungi environments in two monophyletic clades closely related to the Savoryellales. One clade formed by five species of holoblastic conidiogenesis Conioscypha and a second clade containing several genera of uncertain taxonomic status centred on Pleurothe- Hypocreomycetidae cium, represent two distinct taxonomic groups at the ordinal systematic rank. They are proposed as new orders, multigene analysis the Conioscyphales and Pleurotheciales. Several taxonomic novelties are introduced in the Pleurotheciales, i.e. Phaeoisaria two new genera (Adelosphaeria and Melanotrigonum), three novel species (A. catenata, M. ovale, Phaeoisaria systematics fasciculata) and a new combination (Pleurotheciella uniseptata). A new combination is proposed for Savoryella limnetica in Ascotaiwania s.str. based on molecular data and culture characters. A strongly supported lineage containing a new genus Plagiascoma, species of Bactrodesmiastrum and Ascotaiwania persoonii, was identified as a sister to the Conioscyphales/Pleurotheciales/Savoryellales clade in our multilocus phylogeny. Together, they are nested in a monophyly in the Hypocreomycetidae, significantly supported by Bayesian inference and Maximum Likelihood analyses. Members of this clade share a few morphological characters, such as the absence of stromatic tissue or clypeus, similar anatomies of the 2-layered ascomatal walls, thin-walled unitunicate asci with a distinct, non-amyloid apical annulus, symmetrical, transversely septate ascospores and holoblastic conidiogenesis.