Neofabraea Brasiliensis Fungal Planet Description Sheets 309

Total Page:16

File Type:pdf, Size:1020Kb

Neofabraea Brasiliensis Fungal Planet Description Sheets 309 308 Persoonia – Volume 35, 2015 Neofabraea brasiliensis Fungal Planet description sheets 309 Fungal Planet 391 – 4 December 2015 Neofabraea brasiliensis Sanhueza & Bogo, sp. nov. Etymology. Name reflects the location where original isolates were col- ITS and β-tubulin II sequences — Sequence data for tub2 lected. and ITS retrieved from GenBank was reviewed for all avail- Classification — Dermateaceae, Helotiales, Leotiomycetes. able strains with more than 88 % homology for ITS and 82 % for tub2. Including the sequences generated in this study, this Conidiogenous cells straight or sinuous, 8–14 × 3–5 µm, more amounted to 343 available strains for the ITS region and 108 or less cylindrical, tapering to narrow apex; usually held on ir- strains for tub2. Strains with sequences available for both regularly branched conidiophores, sometimes arising directly regions were selected for phylogenetic analyses and only from hyphae, sometimes with acropleurogenous conidiogenous the sequences belonging to the Neofabraea genus concept loci. Macroconidia 12–22 × 2.5–3.7 µm, aseptate, oblong- were kept, including those Cryptosporiopsis species that were ellipsoidal, apex rounded to more or less pointed, base slightly recently introduced as new combinations for Neofabraea. The conical. Microconidia mostly 2.5–3.5 × 1–1.5 µm, ellipsoidal to two regions were then concatenated into a single dataset in oblong-ellipsoidal, base slightly conical then truncated; micro- the order of ITS–tub2. Pezicula cinnamomea and Pezicula conidia can be produced in conidial masses with a white, cot- corticola were included as the outgroup. There were 55 strains tony appearance. available to be included in the concatenated alignment including Culture characteristics — Colonies on MA, PDA and V8 are the outgroup; once the identical sequences were removed this 28, 31 and 32 mm diam, respectively, after 15 d at 22 °C. On left 34 unique sequences representing eight Cryptosporiopsis/ PDA the diameters are 12, 15, 12 and 12 mm after 3 wk at 4, Neofabraea species and the two Pezicula species. 5, 30 and 31 °C, respectively. Aerial mycelium more or less lacking, slimy in appearance, surface covered with copious conidial zone. Cultures on PDA and V8 observed from above are intense reddish purple to reddish orange. Typus. BRAZIL, Santa Catarina, Fraiburgo/SC, isolated from canker of Malus domestica cv. ‘Fuji’, 2003, Empresa Brasileira de Pesquisa Agro- pecuária (EMBRAPA - Brazilian Corporation of Agricultural Research) (holo- type metabolically inert CNPUV499, culture ex-type CNPUV499, both held in CNPUV (Centro Nacional de Pesquisa de Uva e Vinho, Bento Gonçalves, RS, Brazil); ITS sequence GenBank KR107002, LSU sequence GenBank 100/1 Neofabraea alba KR107002, tub2 sequence GenBank KR107011, MycoBank MB812129). 8 strains 85/0.99 Additional specimens examined. BRAZIL, Santa Catarina State, Fraiburgo 100/1 Neofabraea citricarpa Municipality, isolated from Malus domestica cv. ‘Fuji’, 2002, CNPUV503 (ITS 8 strains sequence GenBank KR107003, tub2 sequence GenBank KR107012); Rio -/o Grande do Sul State, Vacaria Municipality, isolated from Malus domestica 95/1 Neofabraea perennans cv. ‘Fuji’, 2002, CNPUV506 no longer viable in collection (ITS sequence 15 strains GenBank KR107001, tub2 sequence GenBank KR107010). -/o 97/ 1 Neofabraea malicorticis 90/ 7 strains Notes — This species was previously treated as Cryptospo- 0.98 95/0.99 Neofabraea kienholzii riopsis perennans in Bogo et al. (2008). However, upon investi- 57/o gation of morphological and DNA sequence data collected from 4 strains 93/ this strain it was recognised as phylogenetically distinct from 0.99 Neofabraea actinidae all described Neofabraea /Cryptosporiopsis species (Chen et 6 strains 100/1 99/1 al. 2015). Three isolates from Brazil were identified as N. bra- 100/1 Neofabraea brasiliensis siliensis, and upon analyses of available ITS sequences in Gen- 3 strains Bank two further strains from Ecuador were found to group with Neofabraea krawtzewii this taxon (GenBank accessions JN546212 and HQ007246). 2 strains Besides sequence differences, particularly for tub2, the most Pezicula cinnamomea evident difference between N. brasiliensis and its most closely Pezicula corticola related species, N. actinidae, is the rate of growth which is 0.04 significantly lower in N. brasiliensis. The mycelium growth index (average daily growth over the first 7 d) on PDA at the The phylogenetic tree with N. brasiliensis was constructed with temperatures 4, 5, 30 and 31 °C for N. brasiliensis is 0.50, maximum likelihood (ML) analysis of concatenated ITS–tub2 0.54, 0.88 and 0.65 mm/d and for N. actinidae is 1.67, 1.75, sequences under the GTR+I+G model using PhyML v. 3.0 and 1.57 and 1.38 mm/d. with Bayesian inference (BI) using MrBayes v. 3.2.1. Support values were generated as nonparametric ML bootstraps with 100 bootstrap replicates and as Bayesian probabilities. Boot- strap support values (BV) over 50 percent or posterior prob- abilities (PB) greater than 0.5 are shown on the tree as BV/PB, Colour illustrations. Apple orchard in Brazil where this new species was isolated, macroconidia, microconidia and conidiogenous cell, 21-d-old colony BVs that were below 50 % in the PhyML tree are noted as (–) on PDA, bull’s eye rot caused by N. brasiliensis on Fuji apple fruits, canker and clades that were absent in the MrBayes tree are noted as caused by N. brasiliensis on Fuji apple branch. Scale bar = 10 µm. (o) (TreeBASE S17434). Rosa M. V. Sanhueza, Proterra Research Center, Proterra Agriculture Company, 95200-000, Vacaria/RS, Brazil; e-mail: [email protected] Amauri Bogo, Crop Production Graduate Program, Santa Catarina State University, 88.520-000, Lages/SC, Brazil; e-mail: [email protected] C. André Lévesque, Tharcisse Barasubiye & Tara Rintoul, Agriculture and Agri-Food Canada, Ottawa, Ontario, Canada, K1A 0C6; e-mail: [email protected], [email protected] & [email protected] © 2015 Naturalis Biodiversity Center & Centraalbureau voor Schimmelcultures.
Recommended publications
  • Psychrophilic Fungi from the World's Roof
    Persoonia 34, 2015: 100–112 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158515X685878 Psychrophilic fungi from the world’s roof M. Wang1,2, X. Jiang3, W. Wu3, Y. Hao1, Y. Su1, L. Cai1, M. Xiang1, X. Liu1 Key words Abstract During a survey of cold-adapted fungi in alpine glaciers on the Qinghai-Tibet Plateau, 1 428 fungal isolates were obtained of which 150 species were preliminary identified. Phoma sclerotioides and Pseudogymnoascus pan- glaciers norum were the most dominant species. Psychrotolerant species in Helotiales (Leotiomycetes, Ascomycota) were Phoma sclerotioides studied in more detail as they represented the most commonly encountered group during this investigation. Two Pseudogymnoascus pannorum phylogenetic trees were constructed based on the partial large subunit nrDNA (LSU) to infer the taxonomic place- Psychrophila ments of these strains. Our strains nested in two well-supported major clades, which represented Tetracladium and psychrotolerant a previously unknown lineage. The unknown lineage is distant to any other currently known genera in Helotiales. Tetracladium Psychrophila gen. nov. was therefore established to accommodate these strains which are characterised by globose or subglobose conidia formed from phialides on short or reduced conidiophores. Our analysis also showed that an LSU-based phylogeny is insufficient in differentiating strains at species level. Additional analyses using combined sequences of ITS+TEF1+TUB regions were employed to further investigate the phylogenetic relationships of these strains. Together with the recognisable morphological distinctions, six new species (i.e. P. antarctica, P. lutea, P. oli- vacea, T. ellipsoideum, T. globosum and T. psychrophilum) were described. Our preliminary investigation indicates a high diversity of cold-adapted species in nature, and many of them may represent unknown species.
    [Show full text]
  • Preliminary Classification of Leotiomycetes
    Mycosphere 10(1): 310–489 (2019) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/10/1/7 Preliminary classification of Leotiomycetes Ekanayaka AH1,2, Hyde KD1,2, Gentekaki E2,3, McKenzie EHC4, Zhao Q1,*, Bulgakov TS5, Camporesi E6,7 1Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, 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 4Landcare Research Manaaki Whenua, Private Bag 92170, Auckland, New Zealand 5Russian Research Institute of Floriculture and Subtropical Crops, 2/28 Yana Fabritsiusa Street, Sochi 354002, Krasnodar region, Russia 6A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy. 7A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314 Brescia, Italy. Ekanayaka AH, Hyde KD, Gentekaki E, McKenzie EHC, Zhao Q, Bulgakov TS, Camporesi E 2019 – Preliminary classification of Leotiomycetes. Mycosphere 10(1), 310–489, Doi 10.5943/mycosphere/10/1/7 Abstract Leotiomycetes is regarded as the inoperculate class of discomycetes within the phylum Ascomycota. Taxa are mainly characterized by asci with a simple pore blueing in Melzer’s reagent, although some taxa have lost this character. The monophyly of this class has been verified in several recent molecular studies. However, circumscription of the orders, families and generic level delimitation are still unsettled. This paper provides a modified backbone tree for the class Leotiomycetes based on phylogenetic analysis of combined ITS, LSU, SSU, TEF, and RPB2 loci. In the phylogenetic analysis, Leotiomycetes separates into 19 clades, which can be recognized as orders and order-level clades.
    [Show full text]
  • Three New Species and a New Combination Of
    A peer-reviewed open-access journal MycoKeys 60: 1–15 (2019) News species of Triblidium 1 doi: 10.3897/mycokeys.60.46645 RESEARCH ARTICLE MycoKeys http://mycokeys.pensoft.net Launched to accelerate biodiversity research Three new species and a new combination of Triblidium Tu Lv1, Cheng-Lin Hou1, Peter R. Johnston2 1 College of Life Science, Capital Normal University, Xisanhuanbeilu 105, Haidian, Beijing 100048, China 2 Manaaki Whenua Landcare Research, Private Bag 92170, Auckland 1142, New Zealand Corresponding author: Cheng-Lin Hou ([email protected]) Academic editor: D.Haelewaters | Received 17 September 2019 | Accepted 18 October 2019 | Published 31 October 2019 Citation: Lv T, Hou C-L, Johnston PR (2019) Three new species and a new combination of Triblidium. MycoKeys 60: 1–15. https://doi.org/10.3897/mycokeys.60.46645 Abstract Triblidiaceae (Rhytismatales) currently consists of two genera: Triblidium and Huangshania. Triblidium is the type genus and is characterised by melanized apothecia that occur scattered or in small clusters on the substratum, cleistohymenial (opening in the mesohymenial phase), inamyloid thin-walled asci and hyaline muriform ascospores. Before this study, only the type species, Triblidium caliciiforme, had DNA sequences in the NCBI GenBank. In this study, six specimens of Triblidium were collected from China and France and new ITS, mtSSU, LSU and RPB2 sequences were generated. Our molecular phylogenetic analysis and morphological study demonstrated three new species of Triblidium, which are formally de- scribed here: T. hubeiense, T. rostriforme and T. yunnanense. Additionally, our results indicated that Huang- shania that was considered to be distinct from Triblidium because of its elongated, transversely-septate ascospores, is congeneric with Triblidium.
    [Show full text]
  • Efficacy of Excision, Cauterization, and Fungicides for Management of Apple Anthracnose Canker in Maritime Climate
    limited and contradictory (Borecki Efficacy of Excision, Cauterization, and and Czynczyk, 1985; Braun, 1997), Fungicides for Management of Apple and currently all cider apple cultivars are considered susceptible (British Anthracnose Canker in Maritime Climate Columbia Ministry of Agriculture, 2016; Pscheidt and Ocamb, 2017). 1 2 3 Neofabraea malicorticis can di- Whitney J. Garton , Mark Mazzola , Nairanjana Dasgupta , rectly infect intact bark tissue, with Travis R. Alexander1, and Carol A. Miles1,4 most infections occurring through the lenticels (Kienholz, 1939). Stem and trunk infections appear to occur ADDITIONAL INDEX WORDS. Bordeaux mixture, copper hydroxide, Malus ·domestica, primarily in the autumn but can take Neofabraea place throughout the winter and early SUMMARY. This study was designed to determine the efficacy of canker excision (CE) spring during mild, moist conditions followed by a subsequent application of cauterization (CAU) and/or fungicide (Davidson and Byther, 1992; Rahe, treatment to the excised area for the management of anthracnose canker (caused by 2010). Cankers develop during the Neofabraea malicorticis) on cider apple (Malus ·domestica) trees. Three experiments autumn and to a lesser extent in the were conducted from 2015 to 2017, with one experiment each year, in an winter. In the following spring, can- experimental cider apple orchard in western Washington where trees were naturally kers resume development, reaching N. malicorticis infested with . Treatments were applied once in December and data full size in the summer, and pycnidia were collected January through March. Treatments in the 2015 experiment were D D D D that form on the canker margin are CE CAU, CE CAU copper hydroxide, CE 0.5% sodium hypochlorite, the source of inoculum for new in- Bordeaux mixture (BM) only, and CE D copper hydroxide (control).
    [Show full text]
  • A Multigene Phylogeny Toward a New Phylogenetic Classification of Leotiomycetes Peter R
    Johnston et al. IMA Fungus (2019) 10:1 https://doi.org/10.1186/s43008-019-0002-x IMA Fungus RESEARCH Open Access A multigene phylogeny toward a new phylogenetic classification of Leotiomycetes Peter R. Johnston1* , Luis Quijada2, Christopher A. Smith1, Hans-Otto Baral3, Tsuyoshi Hosoya4, Christiane Baschien5, Kadri Pärtel6, Wen-Ying Zhuang7, Danny Haelewaters2,8, Duckchul Park1, Steffen Carl5, Francesc López-Giráldez9, Zheng Wang10 and Jeffrey P. Townsend10 Abstract Fungi in the class Leotiomycetes are ecologically diverse, including mycorrhizas, endophytes of roots and leaves, plant pathogens, aquatic and aero-aquatic hyphomycetes, mammalian pathogens, and saprobes. These fungi are commonly detected in cultures from diseased tissue and from environmental DNA extracts. The identification of specimens from such character-poor samples increasingly relies on DNA sequencing. However, the current classification of Leotiomycetes is still largely based on morphologically defined taxa, especially at higher taxonomic levels. Consequently, the formal Leotiomycetes classification is frequently poorly congruent with the relationships suggested by DNA sequencing studies. Previous class-wide phylogenies of Leotiomycetes have been based on ribosomal DNA markers, with most of the published multi-gene studies being focussed on particular genera or families. In this paper we collate data available from specimens representing both sexual and asexual morphs from across the genetic breadth of the class, with a focus on generic type species, to present a phylogeny based on up to 15 concatenated genes across 279 specimens. Included in the dataset are genes that were extracted from 72 of the genomes available for the class, including 10 new genomes released with this study. To test the statistical support for the deepest branches in the phylogeny, an additional phylogeny based on 3156 genes from 51 selected genomes is also presented.
    [Show full text]
  • 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.
    [Show full text]
  • Phylogeny of Pezicula, Dermea and Neofabraea Inferred from Partial Sequences of the Nuclear Ribosomal RNA Gene Cluster Author(S): Edwin C
    Mycological Society of America Phylogeny of Pezicula, Dermea and Neofabraea Inferred from Partial Sequences of the Nuclear Ribosomal RNA Gene Cluster Author(s): Edwin C. A. Abeln, Marian A. de Pagter, Gerard J. M. Verkley Reviewed work(s): Source: Mycologia, Vol. 92, No. 4 (Jul. - Aug., 2000), pp. 685-693 Published by: Mycological Society of America Stable URL: http://www.jstor.org/stable/3761426 . Accessed: 06/11/2011 14:32 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. Mycological Society of America is collaborating with JSTOR to digitize, preserve and extend access to Mycologia. http://www.jstor.org Mycologia, 92(4), 2000, pp. 685-693. © 2000 by The Mycological Society of America, Lawrence, KS 66044-8897 Phylogeny of Pezicula, Dermea and Neofabraea inferred from partial sequences of the nuclear ribosomal RNA gene cluster Edwin C. A. Abeln1 resulted in a rather artificial host-based classification. Marian A. de Pagter (Wollenweber 1939). Gerard J. M. Verkley Traditionally, material on conifers is identified as Centraalbureauvoor Schimmelcultures,PO. Box 273, Pe. livida and morphologically similar material on de- 3740 AG Baarn, The Netherlands ciduous trees as Pe. cinnamomea. Kowalski and Kehr (1992) reported the presence of Pe.
    [Show full text]
  • Mycosphere Notes 169–224 Article
    Mycosphere 9(2): 271–430 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/2/8 Copyright © Guizhou Academy of Agricultural Sciences Mycosphere notes 169–224 Hyde KD1,2, Chaiwan N2, Norphanphoun C2,6, Boonmee S2, Camporesi E3,4, Chethana KWT2,13, Dayarathne MC1,2, de Silva NI1,2,8, Dissanayake AJ2, Ekanayaka AH2, Hongsanan S2, Huang SK1,2,6, Jayasiri SC1,2, Jayawardena RS2, Jiang HB1,2, Karunarathna A1,2,12, Lin CG2, Liu JK7,16, Liu NG2,15,16, Lu YZ2,6, Luo ZL2,11, Maharachchimbura SSN14, Manawasinghe IS2,13, Pem D2, Perera RH2,16, Phukhamsakda C2, Samarakoon MC2,8, Senwanna C2,12, Shang QJ2, Tennakoon DS1,2,17, Thambugala KM2, Tibpromma, S2, Wanasinghe DN1,2, Xiao YP2,6, Yang J2,16, Zeng XY2,6, Zhang JF2,15, Zhang SN2,12,16, Bulgakov TS18, Bhat DJ20, Cheewangkoon R12, Goh TK17, Jones EBG21, Kang JC6, Jeewon R19, Liu ZY16, Lumyong S8,9, Kuo CH17, McKenzie EHC10, Wen TC6, Yan JY13, Zhao Q2 1 Key Laboratory for Plant Biodiversity and Biogeography of East Asia (KLPB), Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P.R. China 2 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 3 A.M.B. Gruppo Micologico Forlivese ‘‘Antonio Cicognani’’, Via Roma 18, Forlı`, Italy 4 A.M.B. Circolo Micologico ‘‘Giovanni Carini’’, C.P. 314, Brescia, Italy 5 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, P.R. China 6 Engineering and Research Center for Southwest Bio-Pharmaceutical Resources of national education Ministry of Education, Guizhou University, Guiyang, Guizhou Province 550025, P.R.
    [Show full text]
  • AR TICLE Lessons Learned from Moving to One
    IMA FUNGUS · VOLUME 5 · A%/BB$DE./%F/B/%%/ [ ARTICLE #G <HH=K<L#9#G<%/5//O#&O&H./P/BK<#S9A#GT & ! With the changes implemented in the International Code of Nomenclature for algae, fungi and plants, fungi "#$ &[#[ Clonostachys * Nomenclature *6*[ V [&* V= !U * &&[ K !*+ (AEE*E)#Clonostachys <APH./%FS#A.5H./%FSVA%8X./%F INTRODUCTION [ # With the changes implemented in the International Code #*& of Nomenclature for algae, fungi and plants (ICN; McNeill [6 et al. 2012), fungi may no longer have more than one Chalara [!" that “…for a taxon of non- fraxinea 7 et al .//8 9 lichen-forming Ascomycota and Basidiomycota… [all names] *&<* compete for priority” regardless of their particular morph & [ Hymenoscyphus #$%#&only albidus [ H. pseudoalbidus (Queloz & !" [ et al. ./%%# [ * '& * & * ' !" principle of priority does not contribute to the nomenclatural [Chalara stability of fungi, thus exceptions can and should be made to fraxinea .//8 H. pseudoalbidus 2011, must become '[ #[ species? in Hypocreales (Rossman et al. 2013) and Leotiomycetes + (Johnston et al. 2014), I have noticed a number of issues, * * !" species of Chalara is C. fusidioides + Hymenoscyphus is H. fructigenus= [!"[ of these type species, one sees that C. fusidioides and H. The Code Decoded: a user’s guide to fructigenus the International Code of Nomenclature for algae, fungi, and presented by Réblová et al. ./%% plants./%5&!" in one genus, then most Leotiomycetes [ Chalara and Hymenoscyphus ' [ sexual state and others for one or more asexual states, one 6>@et al. (2012) © 2014 International Mycological Association You are free to share - to copy, distribute and transmit the work, under the following conditions: Attribution: [ Non-commercial: No derivative works: For any reuse or distribution, you must make clear to others the license terms of this work, which can be found at http://creativecommons.org/licenses/by-nc-nd/3.0/legalcode.
    [Show full text]
  • Etiologia Da Podridão Olho De Boi Da Maçã No Brasil Bianca Samay
    UNIVERSIDADE DE BRASÍLIA INSTITUTO DE CIÊNCIAS BIOLÓGICAS DEPARTAMENTO DE FITOPATOLOLOGIA PROGRAMA DE PÓS-GRADUAÇÃO EM FITOPATOLOGIA ETIOLOGIA DA PODRIDÃO OLHO DE BOI DA MAÇÃ NO BRASIL BIANCA SAMAY ANGELINO BONFIM BRASÍLIA -DF 2017 BIANCA SAMAY ANGELINO BONFIM ETIOLOGIA DA PODRIDÃO OLHO DE BOI DA MAÇÃ NO BRASIL Dissertação apresentada à Universidade de Brasília como requisito parcial para obtenção do título de Mestre em Fitopatologia pelo Programa de Pós- graduação em Fitopatologia. Orientador Dr. Danilo Batista Pinho, Doutor em Fitopatologia BRASÍLIA - DISTRITO FEDERAL BRASIL 2017 FICHA CATALOGRÁFICA Bonfim, Bianca Samay Angelino. Etiologia da Podridão olho de boi da maçã no Brasil. / Bianca Samay Angelino Bonfim. Brasília, 2017. p. 48. Dissertação de mestrado. Programa de Pós-graduação em Fitopatologia, Universidade de Brasília, Brasília. 1. Maçã – Podridão olho de boi. I. Universidade de Brasília. PPG/FIT. II. Etiologia da Podridão olho de boi da maçã no Brasil. Aos meus pais João Batista e Neuraci, ao meu esposo Flávio, aos meus familiares e amigos, fontes de força e coragem... Dedico! AGRADECIMENTOS Minha maior gratidão nesse momento é a Deus, meu porto seguro... Agradeço aos meus pais, pela educação e ensinamentos, aos meus irmãos Dione e Lucas, por todo amor. Ao meu esposo Flávio, por estar presente em todas as horas, por toda compreensão e ajuda. Aos meus amigos, sem os quais não seria possível a realização desse trabalho, em especial a Thaís Ramos. Agradeço a todos que de alguma forma contribuíram para o término desse trabalho, em especial aos amigos: Bruno Souza, Cristiano da Silva Rodrigues, Camila Pereira de Almeida e Débora Cervieri Guterres.
    [Show full text]
  • Tree Disease Identification: Cankers, Wilts, and Stem Decays
    Tree Disease Identification Stem and Branch 1: Cankers & Phytophthora diseases Marianne Elliott Plant Pathologist WSU Puyallup Research and Extension Center Invasive plant diseases Fungi Oomycetes • Chestnut blight • Phytophthora cinnamomi root (Cryphonectria disease parasitica) on American chestnut • Port Orford cedar root disease (P. lateralis) • White pine blister rust • Sudden oak death and (Cronartium ribicola) on Ramorum blight (P. ramorum) Western white pine on tanoak, oak, larch, many more. • Dutch elm disease (Ophiostoma ulmi) on American elm These are capable of eliminating certain Chestnut blight caused by the fungus host species from an ecosystem Cryphonectria parasitica Stem and branch diseases 1 • Cankers • Wetwood • Phytophthora • Management of canker diseases Cankers • Localized necrosis of the bark and cambium on stems, branches or twigs caused by fungi, bacteria, or abiotic agents. • Often centered around a wound or branch stub Cankers on Pacific madrone stem Types of Cankers • Annual • Perennial or Target • Diffuse Perennial or “target” canker caused by Nectria spp. Annual canker caused by Fusarium spp. Diffuse canker caused by Endothia parasitica (chestnut blight) Typical life cycle of canker fungi http://nysipm.cornell.edu/factsheets/treefruit/diseases/pc/pc_cycle.gif Nectria canker Tree hosts: Hardwood - maple, apple, pear, plum, alder, oak Conifer- true firs, spruce, pine Shrubs: rhododendron, hydrangea, daphne Many others “Target” canker on alder Nectria canker • Asexual stage: Nectria cinnabarina, Neonectria galligena,
    [Show full text]
  • Evolution of Helotialean Fungi (Leotiomycetes, Pezizomycotina): a Nuclear Rdna Phylogeny
    Molecular Phylogenetics and Evolution 41 (2006) 295–312 www.elsevier.com/locate/ympev Evolution of helotialean fungi (Leotiomycetes, Pezizomycotina): A nuclear rDNA phylogeny Zheng Wang a,¤, Manfred Binder a, Conrad L. Schoch b, Peter R. Johnston c, Joseph W. Spatafora b, David S. Hibbett a a Department of Biology, Clark University, 950 Main Street, Worcester, MA 01610, USA b Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR 97331, USA c Herbarium PDD, Landcare Research, Private bag 92170, Auckland, New Zealand Received 5 December 2005; revised 21 April 2006; accepted 24 May 2006 Available online 3 June 2006 Abstract The highly divergent characters of morphology, ecology, and biology in the Helotiales make it one of the most problematic groups in traditional classiWcation and molecular phylogeny. Sequences of three rDNA regions, SSU, LSU, and 5.8S rDNA, were generated for 50 helotialean fungi, representing 11 out of 13 families in the current classiWcation. Data sets with diVerent compositions were assembled, and parsimony and Bayesian analyses were performed. The phylogenetic distribution of lifestyle and ecological factors was assessed. Plant endophytism is distributed across multiple clades in the Leotiomycetes. Our results suggest that (1) the inclusion of LSU rDNA and a wider taxon sampling greatly improves resolution of the Helotiales phylogeny, however, the usefulness of rDNA in resolving the deep relationships within the Leotiomycetes is limited; (2) a new class Geoglossomycetes, including Geoglossum, Trichoglossum, and Sarcoleo- tia, is the basal lineage of the Leotiomyceta; (3) the Leotiomycetes, including the Helotiales, Erysiphales, Cyttariales, Rhytismatales, and Myxotrichaceae, is monophyletic; and (4) nine clades can be recognized within the Helotiales.
    [Show full text]