Colletotrichum Truncatum (Schwein.) Andrus & W.D
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Colletotrichum – Names in Current Use
Online advance Fungal Diversity Colletotrichum – names in current use Hyde, K.D.1,7*, Cai, L.2, Cannon, P.F.3, Crouch, J.A.4, Crous, P.W.5, Damm, U. 5, Goodwin, P.H.6, Chen, H.7, Johnston, P.R.8, Jones, E.B.G.9, Liu, Z.Y.10, McKenzie, E.H.C.8, Moriwaki, J.11, Noireung, P.1, Pennycook, S.R.8, Pfenning, L.H.12, Prihastuti, H.1, Sato, T.13, Shivas, R.G.14, Tan, Y.P.14, Taylor, P.W.J.15, Weir, B.S.8, Yang, Y.L.10,16 and Zhang, J.Z.17 1,School of Science, Mae Fah Luang University, Chaing Rai, Thailand 2Research & Development Centre, Novozymes, Beijing 100085, PR China 3CABI, Bakeham Lane, Egham, Surrey TW20 9TY, UK and Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3AB, UK 4Cereal Disease Laboratory, U.S. Department of Agriculture, Agricultural Research Service, 1551 Lindig Street, St. Paul, MN 55108, USA 5CBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands 6School of Environmental Sciences, University of Guelph, Guelph, Ontario, N1G 2W1, Canada 7International Fungal Research & Development Centre, The Research Institute of Resource Insects, Chinese Academy of Forestry, Bailongsi, Kunming 650224, PR China 8Landcare Research, Private Bag 92170, Auckland 1142, New Zealand 9BIOTEC Bioresources Technology Unit, National Center for Genetic Engineering and Biotechnology, NSTDA, 113 Thailand Science Park, Paholyothin Road, Khlong 1, Khlong Luang, Pathum Thani, 12120, Thailand 10Guizhou Academy of Agricultural Sciences, Guiyang, Guizhou 550006 PR China 11Hokuriku Research Center, National Agricultural Research Center, -
Colletotrichum: a Catalogue of Confusion
Online advance Fungal Diversity Colletotrichum: a catalogue of confusion Hyde, K.D.1,2*, Cai, L.3, McKenzie, E.H.C.4, Yang, Y.L.5,6, Zhang, J.Z.7 and Prihastuti, H.2,8 1International Fungal Research & Development Centre, The Research Institute of Resource Insects, Chinese Academy of Forestry, Bailongsi, Kunming 650224, PR China 2School of Science, Mae Fah Luang University, Thasud, Chiang Rai 57100, Thailand 3Novozymes China, No. 14, Xinxi Road, Shangdi, HaiDian, Beijing, 100085, PR China 4Landcare Research, Private Bag 92170, Auckland, New Zealand 5Guizhou Academy of Agricultural Sciences, Guiyang, Guizhou 550006 PR China 6Department of Biology and Geography, Liupanshui Normal College. Shuicheng, Guizhou 553006, P.R. China 7Institute of Biotechnology, College of Agriculture & Biotechnology, Zhejiang University, Kaixuan Rd 258, Hangzhou 310029, PR China 8Department of Biotechnology, Faculty of Agriculture, Brawijaya University, Malang 65145, Indonesia Hyde, K.D., Cai, L., McKenzie, E.H.C., Yang, Y.L., Zhang, J.Z. and Prihastuti, H. (2009). Colletotrichum: a catalogue of confusion. Fungal Diversity 39: 1-17. Identification of Colletotrichum species has long been difficult due to limited morphological characters. Single gene phylogenetic analyses have also not proved to be very successful in delineating species. This may be partly due to the high level of erroneous names in GenBank. In this paper we review the problems associated with taxonomy of Colletotrichum and difficulties in identifying taxa to species. We advocate epitypification and use of multi-locus phylogeny to delimit species and gain a better understanding of the genus. We review the lifestyles of Colletotrichum species, which may occur as epiphytes, endophytes, saprobes and pathogens. -
Protecting the Australian Capsicum Industry from Incursions of Colletotrichum Pathogens
Protecting the Australian Capsicum industry from incursions of Colletotrichum pathogens Dilani Danushika De Silva ORCID identifier 0000-0003-4294-6665 Submitted in total fulfilment of the requirements of the degree of Doctor of Philosophy Faculty of Veterinary and Agricultural Sciences The University of Melbourne January 2019 1 2 Declaration I declare that this thesis comprises only my original work towards the degree of Doctor of Philosophy. Due acknowledgement has been made in the text to all other material used. This thesis does not exceed 100,000 words and complies with the stipulations set out for the degree of Doctor of Philosophy by the University of Melbourne. Dilani De Silva January 2019 i Acknowledgements I am truly grateful to my supervisor Professor Paul Taylor for his immense support during my PhD, his knowledge, patience and enthusiasm was key for my success. Your passion and knowledge on plant pathology has always inspired me to do more. I appreciate your time and the effort you put in to help me with my research as well as taking the time to understand and help me cope during the most difficult times of my life. This achievement would not have been possible without your guidance and encouragement. I am blessed to have a supervisor like you and I could not have imagined having a better advisor for my PhD study. I sincerely thank Dr. Peter Ades whose great advice, your vast knowledge in statistical analysis, insightful comments and encouragement is what incented me to widen my research to various perspectives. I extend my gratitude to my external supervisor Professor Pedro Crous for his invaluable contribution in taxonomy and phylogenetic studies of my research. -
Anthracnose Fungi with Curved Conidia, Colletotrichum Spp
JARQ 49 (4), 351 - 362 (2015) http://www.jircas.affrc.go.jp Anthracnose Fungi with Curved Conidia, Colletotrichum spp. belonging to Ribosomal Groups 9-13, and Their Host Ranges in Japan Toyozo SATO1*, Jouji MORIWAKI2 and Shigeru KANEKO1 1 Genetic Resources Center, National Institute of Agrobiological Sciences (Tsukuba, Ibaraki 305-8602, Japan) 2 Horticulture Research Division, NARO Kyushu Okinawa Agricultural Research Center, National Agriculture and Food Research Organization (Kurume, Fukuoka 839-8503, Japan) Abstract Ninety fungal strains with falcate conidia belonging to Colletotrichum spp. classified into the ribosomal groups 9-13 (the RG 9-13 spp.) and preserved at the NIAS Genebank, Japan were re-identified based on molecular phylogenetic analysis of the internal transcribed spacer (ITS) region of the rRNA gene, sequences of the glyceraldehyde 3-phosphate dehydrogenase, chitin synthase 1, histone3, and actin genes, and partial sequences of β-tubulin-2 (TUB2) genes, or by BLASTN searches with TUB2 gene sequences. Seventy strains were reclassified into nine recently revised species, C. chlorophyti, C. circinans, C. dematium sensu stricto, C. lineola, C. liriopes, C. spaethianum, C. tofieldiae, C. trichel- lum and C. truncatum, whereas 20 strains were grouped into four unidentified species. RG 9, 10 and 12 corresponded to the C. spaethianum, C. dematium and C. truncatum species complex, respectively, while RG 11 and 13 agreed with C. chlorophyti and C. trichellum, respectively. Phylograms derived from a six-locus analysis and from TUB2 single-locus analysis were very similar to one another with the exception of the association between C. dematium s. str. and C. lineola. Thus, TUB2 partial gene sequences are proposed as an effective genetic marker to differentiate species of RG 9-13 in Japan except for C. -
Notes on Currently Accepted Species of Colletotrichum
Mycosphere 7(8) 1192-1260(2016) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/si/2c/9 Copyright © Guizhou Academy of Agricultural Sciences Notes on currently accepted species of Colletotrichum Jayawardena RS1,2, Hyde KD2,3, Damm U4, Cai L5, Liu M1, Li XH1, Zhang W1, Zhao WS6 and Yan JY1,* 1 Institute of Plant and Environment Protection, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, People’s Republic of China 2 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 3 Key Laboratory for Plant Biodiversity and Biogeography of East Asia (KLPB), Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, China 4 Senckenberg Museum of Natural History Görlitz, PF 300 154, 02806 Görlitz, Germany 5State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China 6Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China. Jayawardena RS, Hyde KD, Damm U, Cai L, Liu M, Li XH, Zhang W, Zhao WS, Yan JY 2016 – Notes on currently accepted species of Colletotrichum. Mycosphere 7(8) 1192–1260, Doi 10.5943/mycosphere/si/2c/9 Abstract Colletotrichum is an economically important plant pathogenic genus worldwide, but can also have endophytic or saprobic lifestyles. The genus has undergone numerous revisions in the past decades with the addition, typification and synonymy of many species. In this study, we provide an account of the 190 currently accepted species, one doubtful species and one excluded species that have molecular data. Species are listed alphabetically and annotated with their habit, host and geographic distribution, phylogenetic position, their sexual morphs and uses (if there are any known). -
The Colletotrichum Destructivum Species Complex – Hemibiotrophic Pathogens of Forage and field Crops
available online at www.studiesinmycology.org STUDIES IN MYCOLOGY 79: 49–84. The Colletotrichum destructivum species complex – hemibiotrophic pathogens of forage and field crops U. Damm1*, R.J. O'Connell2, J.Z. Groenewald1, and P.W. Crous1,3,4 1CBS-KNAW Fungal Biodiversity Centre, Uppsalalaan 8, 3584 CT Utrecht, The Netherlands; 2UMR1290 BIOGER-CPP, INRA-AgroParisTech, 78850 Thiverval-Grignon, France; 3Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria 0002, South Africa; 4Wageningen University and Research Centre (WUR), Laboratory of Phytopathology, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands *Correspondence: U. Damm, [email protected], Present address: Senckenberg Museum of Natural History Görlitz, PF 300 154, 02806 Görlitz, Germany. Abstract: Colletotrichum destructivum is an important plant pathogen, mainly of forage and grain legumes including clover, alfalfa, cowpea and lentil, but has also been reported as an anthracnose pathogen of many other plants worldwide. Several Colletotrichum isolates, previously reported as closely related to C. destructivum, are known to establish hemibiotrophic infections in different hosts. The inconsistent application of names to those isolates based on outdated species concepts has caused much taxonomic confusion, particularly in the plant pathology literature. A multilocus DNA sequence analysis (ITS, GAPDH, CHS-1, HIS3, ACT, TUB2) of 83 isolates of C. destructivum and related species revealed 16 clades that are recognised as separate species in the C. destructivum complex, which includes C. destructivum, C. fuscum, C. higginsianum, C. lini and C. tabacum. Each of these species is lecto-, epi- or neotypified in this study. Additionally, eight species, namely C. americae- borealis, C. antirrhinicola, C. bryoniicola, C. -
AFLP Characterization in Pathogenic and Coprophilous Fungi
MYCOTAXON Volume 110, pp. 81–87 October–December 2009 AFLP characterization in pathogenic and coprophilous fungi Isabel E. Cinto1*, Alexandra M. Gottlieb2, Marcela Gally3, Maria E. Ranalli1 & Araceli M. Ramos1 *[email protected] 1 Lab 9, Departamento Biodiversidad y Biología Experimental Facultad de Cs. Exactas y Naturales, Universidad de Buenos Aires Int. Güiraldes 2620 - C1428EHA - Buenos Aires - Argentina 2 LACyE, Departamento Ecología Genética y Evolución Facultad de Cs. Exactas y Naturales, Universidad de Buenos Aires Int. Güiraldes 2620 - C1428EHA - Buenos Aires - Argentina 3 Cátedra de Fitopatología, Facultad de Agronomía, Universidad de Buenos Aires Av. San Martín 4453 - C1417DSE - Buenos Aires - Argentina Abstract — The objective of this study was to ascertain the usefulness of the AFLP technique in assessing genetic diversity among 47 strains belonging to three Ascomycota genera and as a tool for solving taxonomic problems in related morphological species. Four MseI +1 primers were assayed in combination with two EcoRI +2 and four EcoRI +3 primers. In the present study both +2 and +3 EcoRI primers were informative, but EcoRI +2 produced profiles with high complexity. The addition of the extra selective nucleotide reduced the complexity of the banding patterns generating easily readable patterns to evaluate genetic diversity within and among species. Of the three ascomycetous genera assessed in this study, Colletotrichum (Glomerellaceae) presented the highest proportion of polymorphic AFLP loci, followed in order by Iodophanus (Pezizaceae) and Saccobolus (Ascobolaceae). Key words — ascomycetes, genetic characterization, molecular markers, taxonomy Introduction Morphological and biochemical characterization of microscopic fungi have usually led to uncertainties in identification when dealing with closely related species or nearly clonal fungal isolates (van Brummelen 1967, Kimbrough et al. -
Colletotrichum: Biological Control, Bio- Catalyst, Secondary Metabolites and Toxins
Mycosphere 7(8) 1164-1176(2016) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/si/2c/7 Copyright © Guizhou Academy of Agricultural Sciences Mycosphere Essay 16: Colletotrichum: Biological control, bio- catalyst, secondary metabolites and toxins Jayawardena RS1,2, Li XH1, Liu M1, Zhang W1 and Yan JY1* 1 Institute of Plant and Environment Protection, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, People’s Republic of China 2 Center of Excellence in Fungal Research and School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand Jayawardena RS, Li XH, Liu M, Zhang W, Yan JY 2016 – Mycosphere Essay 16: Colletotrichum: Biological control, bio-catalyst, secondary metabolites and toxins. Mycosphere 7(8) 1164–1176, Doi 10.5943/mycosphere/si/2c/7 Abstract The genus Colletotrichum has received considerable attention in the past decade because of its role as an important plant pathogen. The importance of Colletotrichum with regard to industrial application has however, received little attention from scientists over many years. The aim of the present paper is to explore the importance of Colletotrichum species as bio-control agents and as a bio-catalyst as well as secondary metabolites and toxin producers. Often the names assigned to the above four industrial applications have lacked an accurate taxonomic basis and this needs consideration. The current paper provides detailed background of the above topics. Key words – biotransformation – colletotrichin – mycoherbicide – mycoparasites – pathogenisis – phytopathogen Introduction Colletotrichum was introduced by Corda (1831), and is a coelomycete belonging to the family Glomerellaceae (Maharachchikumbura et al. 2015, 2016). Species of this genus are widely known as pathogens of economical crops worldwide (Cannon et al. -
Colletotrichum Graminicola
Apr 19Pathogen of the month – April 2019 SH V (1914) a b c d e Fig. 1. (a) Colletotrichum graminicola asexual falcate conidia stained with calcofluor white; (b) acervuli with setae; (c) cross section of an acervulus (black arrow); (d) lobed, melanized appressoria, and (e) intracellular hyphae in a mesophyll cell. Note two distinct types of hyphae: vesicles (V; also known as biotrophic hyphae) and necrotrophic secondary hyphae (SH). Figs (b-e) were observed on maize leaf sheaths. Figs (b- e) were cleared in chloral hydrate and (d-e) stained with lactophenol blue. Wilson Wilson Common Name: Maize anthracnose fungus Disease: Maize Anthracnose; Anthracnose leaf blight (ALB); anthracnose stalk rot (ASR) Classification: K: Fungi P: Ascomycota C: Sordariomycetes O:Glomerellales F: Glomerellaceae The hemibiotrophic fungal pathogen, Colletotrichum graminicola (Teleomorph – Glomerella graminicola D.J. Politis G.W (1975)) causes anthracnose in maize (corn) and is a major problem as some varieties of engineered maize seem more susceptible to infection resulting in increasing economic concerns in the US. With a 57.4-Mb genome .) .) distributed among 13 chromosomes, it belongs to the graminicola species complex with other 14 closely related species. Such graminicolous Colletotrichum species infect other cereals and grasses such as C. sublineolum in sorghum, C. falcatum in sugarcane and C. cereale in wheat and turfgrass. Of the 44 Colletotrichum species that exist in Australia, graminicolous Colletotrichum isolates still need to be verified in the Australian collection. Ces Biology and Ecology: of pith tissue in the corn stalk around the stalk internodes. ( The fungus forms fluffly aerial mycelium and produces two Maize roots can be infected by the fungus leading to differently shaped hyaline conidia: (a) falcate (24-30 x 4-5 asymptomatic systemic colonization of the plants. -
Name = Colletotrichum Truncatum and Its Synonyms
19/9/2019 All data for a single taxon * **Tell us why you value the fungal databases*** Fungus-Host - 932 records were found using the criteria: name = Colletotrichum truncatum and its synonyms Colletotrichum truncatum (Schwein.) Andrus & W.D. Moore 1935 (Ascomycetes, Phyllachorales) ≡ Vermicularia truncata Schwein. 1832 ≡Colletotrichum dematium f. truncatum (Schwein.) Arx 1957 Note: As 'truncata'. = Vermicularia capsici Syd. 1913 ≡ Colletotrichum capsici (Syd.) E.J. Butler & Bisby 1931 ≡ Steirochaete capsici (Syd.) Sacc. 1921 = Colletotrichum curvatum Briant & E.B. Martyn 1929 = Colletotrichum indicum Dastur 1934 ≡ Vermicularia indica (Dastur) Vassiljevsky 1950 Notes: Roberts and Snow (1990) considered C. capcisi and C. indicum conspecific based on morphological and pathological studies. Distribution: Cosmopolitan. Substrate: Leaves, stems, flowers, fruit. Disease Note: Anthracnose, blight, dieback, leaf, fruit, and stem rots. Host: Multiple genera in multiple families; major pathogen of Jatropha curcas (Euphorbiaceae). Supporting Literature: Aktaruzzaman, M., Afroz, T., Lee, Y.-G., and Kim, B.-S. 2018. Post-harvest anthracnose of papaya caused by Colletotrichum truncatum in Korea. Eur. J. Pl. Pathol. 150(1): 259-265. Bahri, B.A., Saadani, M., Mechichi, G., and Rouissi, W. 2019. Genetic diversity of Colletotrichum gloeosporioides species complex associated with Citrus wither-tip of twigs in Tunisia using microsatellite markers. J. Phytopathol. 167(6): 351-362. Bi, Y., Guo, W., Zhang, G.J., Liu, S.C., and Chen, Y. 2017. First report of Colletotrichum truncatum causing anthracnose of strawberry in China. Pl. Dis. 101(5): 832. Cavalcante, G.R.S., Barguil, B.M., Vieira, W.A.S., Lima, W.G., Michereff, S.J., Doyle, V.P., and Camara, M.P.S. -
Agricultural Microbiology E Acarologia, Av
DOI: http://dx.doi.org/10.1590/1678-992X-2018-0269 ISSN 1678-992X Research Article Colletotrichum nymphaeae var. entomophilum var. nov. a natural enemy of the citrus scale insect, Praelongorthezia praelonga (Hemiptera: Ortheziidae) Anja Amtoft Wynns1 , Annette Bruun Jensen1* , Jørgen Eilenberg1 , Italo Delalibera Júnior2 1University of Copenhagen – Dept. of Plant and ABSTRACT: The citrus scale insect Praelongorthezia praelonga (Douglas), a major pest of citrus Environmental Sciences, Thorvaldsensvej 40, 1871 – and other economically important crops, has only two commonly documented natural enemies: Frederiksberg C – Denmark. an entomopathogenic strain of the fungus Colletotrichum nymphaeae (Pass.) Aa and several 2Universidade de São Paulo/ESALQ – Depto. de Entomologia parasitoids. The entomopathogenic strain of C. nymphaeae, formerly recognized under the syn- Agricultural Microbiology e Acarologia, Av. Pádua Dias, 11 – 13418-900 – Piracicaba, onym C. gloeosporioides f. sp. ortheziidae, is under development for commercial application as SP – Brasil. a biological control agent in citrus in Brazil-the top exporter of citrus globally. The synonomy of *Corresponding author <[email protected]> C. gloeosporioides f. sp. ortheziidae with C. nymphaeae remains based on limited DNA sequence data and without morphological study. To qualify for future approval as a biological control agent Edited by: Richard V. Glatz by federal agencies in Brazil and the European Union, the circumscription of a microorganism must be explicit and without ambiguities. Herein, through morphological study and phylogenetic Received August 20, 2018 analysis of five DNA regions we clarify the circumscription and affinity of entomopathogenic C. Accepted April 30, 2019 nymphaeae and describe it as a new variety. Keywords: Biological control, Colletotrichum (Sordariomycetes: Glomerellaceae), entomopathogen Introduction In Brazil, C. -
Fungal Planet Description Sheets: 400–468
Persoonia 36, 2016: 316– 458 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158516X692185 Fungal Planet description sheets: 400–468 P.W. Crous1,2, M.J. Wingfield3, D.M. Richardson4, J.J. Le Roux4, D. Strasberg5, J. Edwards6, F. Roets7, V. Hubka8, P.W.J. Taylor9, M. Heykoop10, M.P. Martín11, G. Moreno10, D.A. Sutton12, N.P. Wiederhold12, C.W. Barnes13, J.R. Carlavilla10, J. Gené14, A. Giraldo1,2, V. Guarnaccia1, J. Guarro14, M. Hernández-Restrepo1,2, M. Kolařík15, J.L. Manjón10, I.G. Pascoe6, E.S. Popov16, M. Sandoval-Denis14, J.H.C. Woudenberg1, K. Acharya17, A.V. Alexandrova18, P. Alvarado19, R.N. Barbosa20, I.G. Baseia21, R.A. Blanchette22, T. Boekhout3, T.I. Burgess23, J.F. Cano-Lira14, A. Čmoková8, R.A. Dimitrov24, M.Yu. Dyakov18, M. Dueñas11, A.K. Dutta17, F. Esteve- Raventós10, A.G. Fedosova16, J. Fournier25, P. Gamboa26, D.E. Gouliamova27, T. Grebenc28, M. Groenewald1, B. Hanse29, G.E.St.J. Hardy23, B.W. Held22, Ž. Jurjević30, T. Kaewgrajang31, K.P.D. Latha32, L. Lombard1, J.J. Luangsa-ard33, P. Lysková34, N. Mallátová35, P. Manimohan32, A.N. Miller36, M. Mirabolfathy37, O.V. Morozova16, M. Obodai38, N.T. Oliveira20, M.E. Ordóñez39, E.C. Otto22, S. Paloi17, S.W. Peterson40, C. Phosri41, J. Roux3, W.A. Salazar 39, A. Sánchez10, G.A. Sarria42, H.-D. Shin43, B.D.B. Silva21, G.A. Silva20, M.Th. Smith1, C.M. Souza-Motta44, A.M. Stchigel14, M.M. Stoilova-Disheva27, M.A. Sulzbacher 45, M.T. Telleria11, C. Toapanta46, J.M. Traba47, N.