On Phaeosphaeria Nodorum in Wheat
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Cryptogamie, Mycologie, 2015, 36 (2): 225-236 © 2015 Adac. Tous droits réservés Poaceascoma helicoides gen et sp. nov., a new genus with scolecospores in Lentitheciaceae Rungtiwa PHOOkAmSAk a,b,c,d, Dimuthu S. mANAmGOdA c,d, Wen-jing LI a,b,c,d, Dong-Qin DAI a,b,c,d, Chonticha SINGTRIPOP a,b,c,d & kevin d. HYdE a,b,c,d* akey Laboratory for Plant diversity and Biogeography of East Asia, kunming Institute of Botany, Chinese Academy of Sciences, kunming 650201, China bWorld Agroforestry Centre, East and Central Asia, kunming 650201, China cInstitute of Excellence in Fungal Research, mae Fah Luang University, Chiang Rai 57100, Thailand dSchool of Science, mae Fah Luang University, Chiang Rai 57100, Thailand Abstract – An ophiosphaerella-like species was collected from dead stems of a grass (Poaceae) in Northern Thailand. Combined analysis of LSU, SSU and RPB2 gene data, showed that the species clusters with Lentithecium arundinaceum, Setoseptoria phragmitis and Stagonospora macropycnidia in the family Lentitheciaceae and is close to katumotoa bambusicola and Ophiosphaerella sasicola. Therefore, a monotypic genus, Poaceascoma is introduced to accommodate the scolecosporous species Poaceascoma helicoides. The species has similar morphological characters to the genera Acanthophiobolus, Leptospora and Ophiosphaerella and these genera are compared. Lentitheciaceae / Leptospora / Ophiosphaerella / phylogeny InTRoDuCTIon Lentitheciaceae was introduced by Zhang et al. (2012) to accommodate massarina-like species in the suborder Massarineae. In the recent monograph of Dothideomycetes (Hyde et al., 2013), the family Lentitheciaceae comprised the genera Lentithecium, katumotoa, keissleriella and Tingoldiago and all species had fusiform to cylindrical, 1-3-septate ascospores and mostly occurred on grasses. -
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cryptogamie Mycologie 2019 ● 40 ● 7 Vittaliana mangrovei Devadatha, Nikita, A.Baghela & V.V.Sarma, gen. nov, sp. nov. (Phaeosphaeriaceae), from mangroves near Pondicherry (India), based on morphology and multigene phylogeny Bandarupalli DEVADATHA, Nikita MEHTA, Dhanushka N. WANASINGHE, Abhishek BAGHELA & V. Venkateswara SARMA art. 40 (7) — Published on 8 November 2019 www.cryptogamie.com/mycologie DIRECTEUR DE LA PUBLICATION : Bruno David, Président du Muséum national d’Histoire naturelle RÉDACTEUR EN CHEF / EDITOR-IN-CHIEF : Bart BuyCk ASSISTANT DE RÉDACTION / ASSISTANT EDITOR : Étienne CAyEuX ([email protected]) MISE EN PAGE / PAGE LAYOUT : Étienne CAyEuX RÉDACTEURS ASSOCIÉS / ASSOCIATE EDITORS Slavomír AdAmčík Institute of Botany, Plant Science and Biodiversity Centre, Slovak Academy of Sciences, Dúbravská cesta 9, Sk-84523, Bratislava, Slovakia André APTROOT ABL Herbarium, G.v.d. Veenstraat 107, NL-3762 Xk Soest, The Netherlands Cony decock Mycothèque de l’université catholique de Louvain, Earth and Life Institute, Microbiology, université catholique de Louvain, Croix du Sud 3, B-1348 Louvain-la- Neuve, Belgium André FRAITURE Botanic Garden Meise, Domein van Bouchout, B-1860 Meise, Belgium kevin HYDE School of Science, Mae Fah Luang university, 333 M.1 T.Tasud Muang District - Chiang Rai 57100, Thailand Valérie HOFSTETTER Station de recherche Agroscope Changins-Wädenswil, Dépt. Protection des plantes, Mycologie, CH-1260 Nyon 1, Switzerland Sinang HONGSANAN College of life science and oceanography, ShenZhen university, 1068, Nanhai Avenue, Nanshan, ShenZhen 518055, China egon HorAk Schlossfeld 17, A-6020 Innsbruck, Austria Jing LUO Department of Plant Biology & Pathology, Rutgers university New Brunswick, NJ 08901, uSA ruvishika S. JAYAWARDENA Center of Excellence in Fungal Research, Mae Fah Luang university, 333 M. -
Phylogeny and Morphology of Premilcurensis Gen
Phytotaxa 236 (1): 040–052 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.236.1.3 Phylogeny and morphology of Premilcurensis gen. nov. (Pleosporales) from stems of Senecio in Italy SAOWALUCK TIBPROMMA1,2,3,4,5, ITTHAYAKORN PROMPUTTHA6, RUNGTIWA PHOOKAMSAK1,2,3,4, SARANYAPHAT BOONMEE2, ERIO CAMPORESI7, JUN-BO YANG1,2, ALI H. BHAKALI8, ERIC H. C. MCKENZIE9 & KEVIN D. HYDE1,2,4,5,8 1Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, People’s Republic of China 2Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 4World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, P. R. China 5Mushroom Research Foundation, 128 M.3 Ban Pa Deng T. Pa Pae, A. Mae Taeng, Chiang Mai 50150, Thailand 6Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, 50200, Thailand 7A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy; A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy; Società per gli Studi Naturalistici della Romagna, C.P. 144, Bagnacavallo (RA), Italy 8Botany and Microbiology Department, College of Science, King Saud University, Riyadh, KSA 11442, Saudi Arabia 9Manaaki Whenua Landcare Research, Private Bag 92170, Auckland, New Zealand *Corresponding author: Dr. Itthayakorn Promputtha, Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, 50200, Thailand. -
Molecular Systematics of the Marine Dothideomycetes
available online at www.studiesinmycology.org StudieS in Mycology 64: 155–173. 2009. doi:10.3114/sim.2009.64.09 Molecular systematics of the marine Dothideomycetes S. Suetrong1, 2, C.L. Schoch3, J.W. Spatafora4, J. Kohlmeyer5, B. Volkmann-Kohlmeyer5, J. Sakayaroj2, S. Phongpaichit1, K. Tanaka6, K. Hirayama6 and E.B.G. Jones2* 1Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90112, Thailand; 2Bioresources Technology Unit, National Center for Genetic Engineering and Biotechnology (BIOTEC), 113 Thailand Science Park, Paholyothin Road, Khlong 1, Khlong Luang, Pathum Thani, 12120, Thailand; 3National Center for Biothechnology Information, National Library of Medicine, National Institutes of Health, 45 Center Drive, MSC 6510, Bethesda, Maryland 20892-6510, U.S.A.; 4Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, 97331, U.S.A.; 5Institute of Marine Sciences, University of North Carolina at Chapel Hill, Morehead City, North Carolina 28557, U.S.A.; 6Faculty of Agriculture & Life Sciences, Hirosaki University, Bunkyo-cho 3, Hirosaki, Aomori 036-8561, Japan *Correspondence: E.B. Gareth Jones, [email protected] Abstract: Phylogenetic analyses of four nuclear genes, namely the large and small subunits of the nuclear ribosomal RNA, transcription elongation factor 1-alpha and the second largest RNA polymerase II subunit, established that the ecological group of marine bitunicate ascomycetes has representatives in the orders Capnodiales, Hysteriales, Jahnulales, Mytilinidiales, Patellariales and Pleosporales. Most of the fungi sequenced were intertidal mangrove taxa and belong to members of 12 families in the Pleosporales: Aigialaceae, Didymellaceae, Leptosphaeriaceae, Lenthitheciaceae, Lophiostomataceae, Massarinaceae, Montagnulaceae, Morosphaeriaceae, Phaeosphaeriaceae, Pleosporaceae, Testudinaceae and Trematosphaeriaceae. Two new families are described: Aigialaceae and Morosphaeriaceae, and three new genera proposed: Halomassarina, Morosphaeria and Rimora. -
Etiology of Spring Dead Spot of Bermudagrass
ETIOLOGY OF SPRING DEAD SPOT OF BERMUDAGRASS By FRANCISCO FLORES Bachelor of Science in Biotechnology Engineering Escuela Politécnica del Ejército Quito, Ecuador 2008 Master of Science in Entomology and Plant Pathology Oklahoma State University Stillwater, Oklahoma 2010 Submitted to the Faculty of the Graduate College of the Oklahoma State University in partial fulfillment of the requirements for the Degree of DOCTOR OF PHILOSOPHY December, 2014 ETIOLOGY OF SPRING DEAD SPOT OF BERMUDAGRASS Thesis Approved: Dr. Nathan Walker Thesis Adviser Dr. Stephen Marek Dr. Jeffrey Anderson Dr. Thomas Mitchell ii ACKNOWLEDGEMENTS I would like to acknowledge all the people who made the successful completion of this project possible. Thanks to my major advisor, Dr. Nathan Walker, who guided me through every step of the process, was always open to answer any question, and offered valuable advice whenever it was needed. Thanks to all the members of my advisory committee, Dr. Stephen Marek, Dr. Jeff Anderson, and Dr. Thomas Mitchell, whose expertise provided relevant insight for solving the problems I found in the way. I also want to thank the department of Entomology and Plant Pathology at Oklahoma State University for being a welcoming family and for keeping things running smoothly. Special thanks to the members of the turfgrass pathology lab, Kelli Black and Andrea Payne, to Dr. Carla Garzón and members of her lab, to Dr. Stephen Marek and members of his lab, and to Dr. Jack Dillwith, who were always eager to help with their technical and intellectual capacities. Thanks to my friends and family, especially to my wife Patricia, who helped me regain my strength several times during this process. -
The Phylogeny of Plant and Animal Pathogens in the Ascomycota
Physiological and Molecular Plant Pathology (2001) 59, 165±187 doi:10.1006/pmpp.2001.0355, available online at http://www.idealibrary.com on MINI-REVIEW The phylogeny of plant and animal pathogens in the Ascomycota MARY L. BERBEE* Department of Botany, University of British Columbia, 6270 University Blvd, Vancouver, BC V6T 1Z4, Canada (Accepted for publication August 2001) What makes a fungus pathogenic? In this review, phylogenetic inference is used to speculate on the evolution of plant and animal pathogens in the fungal Phylum Ascomycota. A phylogeny is presented using 297 18S ribosomal DNA sequences from GenBank and it is shown that most known plant pathogens are concentrated in four classes in the Ascomycota. Animal pathogens are also concentrated, but in two ascomycete classes that contain few, if any, plant pathogens. Rather than appearing as a constant character of a class, the ability to cause disease in plants and animals was gained and lost repeatedly. The genes that code for some traits involved in pathogenicity or virulence have been cloned and characterized, and so the evolutionary relationships of a few of the genes for enzymes and toxins known to play roles in diseases were explored. In general, these genes are too narrowly distributed and too recent in origin to explain the broad patterns of origin of pathogens. Co-evolution could potentially be part of an explanation for phylogenetic patterns of pathogenesis. Robust phylogenies not only of the fungi, but also of host plants and animals are becoming available, allowing for critical analysis of the nature of co-evolutionary warfare. Host animals, particularly human hosts have had little obvious eect on fungal evolution and most cases of fungal disease in humans appear to represent an evolutionary dead end for the fungus. -
101 Dothideomycetes Genomes: a Test Case for Predicting Lifestyles and Emergence of Pathogens
available online at www.studiesinmycology.org STUDIES IN MYCOLOGY 96: 141–153 (2020). 101 Dothideomycetes genomes: A test case for predicting lifestyles and emergence of pathogens S. Haridas1, R. Albert1,2, M. Binder3, J. Bloem3, K. LaButti1, A. Salamov1, B. Andreopoulos1, S.E. Baker4, K. Barry1, G. Bills5, B.H. Bluhm6, C. Cannon7, R. Castanera1,8,20, D.E. Culley4, C. Daum1, D. Ezra9, J.B. Gonzalez10, B. Henrissat11,12,13, A. Kuo1, C. Liang14,21, A. Lipzen1, F. Lutzoni15, J. Magnuson4, S.J. Mondo1,16, M. Nolan1, R.A. Ohm1,17, J. Pangilinan1, H.-J. Park10, L. Ramírez8, M. Alfaro8, H. Sun1, A. Tritt1, Y. Yoshinaga1, L.-H. Zwiers3, B.G. Turgeon10, S.B. Goodwin18, J.W. Spatafora19, P.W. Crous3,17*, and I.V. Grigoriev1,2* 1US Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, USA; 2Department of Plant and Microbial Biology, University of California Berkeley, Berkeley, CA, USA; 3Westerdijk Fungal Biodiversity Institute, Utrecht, The Netherlands; 4Functional and Systems Biology Group, Environmental Molecular Sciences Division, Earth and Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA; 5University of Texas Health Science Center, Houston, TX, USA; 6University of Arkansas, Fayelletville, AR, USA; 7Texas Tech University, Lubbock, TX, USA; 8Institute for Multidisciplinary Research in Applied Biology (IMAB-UPNA), Universidad Pública de Navarra, Pamplona, Navarra, Spain; 9Agricultural Research Organization, Volcani Center, Rishon LeTsiyon, Israel; 10Section -
The Genus Pseudodidymosphaeria
Asian Journal of Mycology 1(1): 1–8 (2018) ISSN TBA www.asianjournalofmycology.org Article Doi 10.5943/ajom/1/1/1 Copyright © Mushroom Research Foundation The genus Pseudodidymosphaeria Thambugala KM1, Peršoh D2, Perera RH1 and Hyde KD1 1Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 2Geobotany, Ruhr-Universität Bochum, Universitätsstraße 150, 44780 Bochum, Germany Thambugala KM, Peršoh D, Perera RH, Hyde KD 2018 – The genus Pseudodidymosphaeria. Asian Journal of Mycology 1(1), 1–8, Doi 10.5943/ajom/1/1/1 Abstract The genus Pseudodidymosphaeria is revisited with an overview of its history, a generic description with amendments and notes and illustrations of the genus. Molecular data from two species of the genus are analyzed using single and combined ITS and LSU gene datasets and the workflow of phylogenetic analysis is provided in an appendix. The genus Pseudodidymosphaeria formed a well-supported clade in the family Massarinaceae. Key words – ARB – ITS – LSU – Massarinaceae – Poaceae Introduction The family Massarinaceae was established to accommodate four genera, Keissleriella, Massarina, Metasphaeria, Pseudotrichia, and Trichometasphaeria (Munk 1956). Barr (1987) treated Massarinaceae as a synonym of Lophiostomataceae. However, these two families are now recognized as separate lineages in Pleosporales, Dothideomycetes (Zhang et al. 2012, Hyde et al. 2013, Thambugala et al. 2015b, Wijayawardene et al. 2018). During the past 60 years many genera were included or removed from Massarinaceae depending on the various taxonomic treatments and accessibility of sequence data (Zhang et al. 2012, Hyde et al. 2013, Wijayawardene et al. 2014, 2017, Tanaka et al. 2015, Thambugala et al. -
Microplastics Accumulate Fungal Pathogens in Terrestrial Ecosystems
www.nature.com/scientificreports OPEN Microplastics accumulate fungal pathogens in terrestrial ecosystems Gerasimos Gkoutselis1,5, Stephan Rohrbach2,5, Janno Harjes1, Martin Obst3, Andreas Brachmann4, Marcus A. Horn2* & Gerhard Rambold1* Microplastic (MP) is a pervasive pollutant in nature that is colonised by diverse groups of microbes, including potentially pathogenic species. Fungi have been largely neglected in this context, despite their afnity for plastics and their impact as pathogens. To unravel the role of MP as a carrier of fungal pathogens in terrestrial ecosystems and the immediate human environment, epiplastic mycobiomes from municipal plastic waste from Kenya were deciphered using ITS metabarcoding as well as a comprehensive meta-analysis, and visualised via scanning electron as well as confocal laser scanning microscopy. Metagenomic and microscopic fndings provided complementary evidence that the terrestrial plastisphere is a suitable ecological niche for a variety of fungal organisms, including important animal and plant pathogens, which formed the plastisphere core mycobiome. We show that MPs serve as selective artifcial microhabitats that not only attract distinct fungal communities, but also accumulate certain opportunistic human pathogens, such as cryptococcal and Phoma-like species. Therefore, MP must be regarded a persistent reservoir and potential vector for fungal pathogens in soil environments. Given the increasing amount of plastic waste in terrestrial ecosystems worldwide, this interrelation may have severe consequences for the trans-kingdom and multi-organismal epidemiology of fungal infections on a global scale. Plastic waste, an inevitable and inadvertent marker of the Anthropocene, has become a ubiquitous pollutant in nature1. Plastics can therefore exert negative efects on biota in both, aquatic and terrestrial ecosystems. -
The Sexual State of Setophoma
Phytotaxa 176 (1): 260–269 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ Article PHYTOTAXA Copyright © 2014 Magnolia Press ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.176.1.25 The sexual state of Setophoma RUNGTIWA PHOOKAMSAK1,2,3,4,5, JIAN-KUI LIU3,4, DIMUTHU S. MANAMGODA3,4, EKACHAI CHUKEATIROTE3,4, PETER E. MORTIMER1,2, ERIC H.C. MCKENZIE6 & KEVIN D. HYDE1,2,3,4,5 1 World Agroforestry Centre, East and Central Asia, Kunming 650201, China 2 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China 3 Institute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 4School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand 5 International Fungal Research & Development Centre, Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, Yunnan, 650224, PR China 6 Landcare Research, Private Bag 92170, Auckland, New Zealand Abstract A sexual state of Setophoma, a coelomycete genus of Phaeosphaeriaceae, was found causing leaf spots of sugarcane (Saccharum officinarum). Pure cultures from single ascospores produced the asexual morph on rice straw and bamboo pieces on water agar. Multiple gene phylogenetic analysis using ITS, LSU and RPB2 showed that our strains belong to the family Phaeosphaeriaceae. The strains clustered with Setophoma sacchari with strong support (100% ML, 100% MP and 1.00 PP) and formed a well-supported clade with other Setophoma species. Therefore our strains are identified as S. sacchari. In this paper descriptions and photographs of the sexual and asexual morphs of S. -
Necrotrophic Pathogens of Wheat
This article was originally published in the Encyclopedia of Food Grains published by Elsevier, and the attached copy is provided by Elsevier for the author's benefit and for the benefit of the author’s institution, for non-commercial research and educational use including without limitation use in instruction at your institution, sending it to specific colleagues who you know, and providing a copy to your institution’s administrator. All other uses, reproduction and distribution, including without limitation commercial reprints, selling or licensing copies or access, or posting on open internet sites, your personal or institution’s website or repository, are prohibited. For exceptions, permission may be sought for such use through Elsevier's permissions site at: http://www.elsevier.com/locate/permissionusematerial Oliver R.P., Tan K.-C. and Moffat C.S. (2016) Necrotrophic Pathogens of Wheat. In: Wrigley, C., Corke, H., and Seetharaman, K., Faubion, J., (eds.) Encyclopedia of Food Grains, 2nd Edition, pp. 273-278. Oxford: Academic Press. © 2016 Elsevier Ltd. All rights reserved. Author's personal copy Necrotrophic Pathogens of Wheat RPOliver, K-C Tan, and CS Moffat, Curtin University, Bentley, WA, Australia ã 2016 Elsevier Ltd. All rights reserved. Topic Highlights give information of trends over decades (Brennan and Murray, 1988, 1998). Table 2 lists estimates of current wheat disease • Diseases of wheat. losses in Australia. It can be seen that across all regions, TS is • Genetic analysis of resistance to tan spot and Septoria the major disease, currently costing more than all rusts com- nodorum blotch (SNB) necrotrophic effectors. bined. SNB is restricted to Western Australia where it ranks as Tan spot effectors. -
Pseudodidymosphaeria Gen. Nov. in Massarinaceae
Phytotaxa 231 (3): 271–282 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.231.3.5 Pseudodidymosphaeria gen. nov. in Massarinaceae KASUN M. THAMBUGALA1, 2, 3, YU CHUNFANG4, ERIO CAMPORESI5, ALI H. BAHKALI6, ZUO-YI LIU1, * & KEVIN D. HYDE2, 3 1Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Xiaohe District, Guiyang City, Guizhou Province 550006, People’s Republic of China 2Institute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai. 57100, Thailand 4Institute of Basic Medical Sciences, Hubei University of Medicine, shiyan, Hubei Province, 442000, People’s Republic of China 5A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy; A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy 6Department of Botany and Microbiology, King Saudi University, Riyadh, Saudi Arabia *Corresponding author: email: [email protected] Abstract Didymosphaeria spartii was collected from dead branches of Spartium junceum in Italy. Multi-gene phylogenetic analyses of ITS, 18S and 28S nrDNA sequence data were carried out using maximum likelihood and Bayesian analysis. The resulting phylogenetic trees showed this to be a new genus in a well-supported clade in Massarinaceae. A new genus Pseudodidymo- sphaeria is therefore introduced to accommodate this species based on molecular phylogeny and morphology. A illustrated account is provided for the new genus with its asexual morph and the new taxon is compared with Massarina and Didymo- sphaeria.