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New Phaeoacremonium species isolated from sandalwood trees in Western Australia

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New Phaeoacremonium species isolated from sandalwood trees in Western Australia

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dc.contributor.author Gramaje Pérez, David es_ES
dc.contributor.author León Santana, Maela es_ES
dc.contributor.author Pérez Sierra, Ana María es_ES
dc.contributor.author Burgess, Treena es_ES
dc.contributor.author Armengol Fortí, Josep es_ES
dc.date.accessioned 2017-03-14T11:35:50Z
dc.date.available 2017-03-14T11:35:50Z
dc.date.issued 2014-05-12
dc.identifier.issn 2210-6340
dc.identifier.uri http://hdl.handle.net/10251/78762
dc.description.abstract Thirty-eight Phaeoacremonium isolates collected from pruning wounds of tropical sandalwood in Western Australia were studied with morphological and cultural characteristics as well as phylogenetic analyses of combined DNA sequences of the actin and beta-tubulin genes. Three known Phaeoacremonium species were found, namely P. alvesii, P. parasiticum, and P. venezuelense. Phaeoacremonium venezuelense represents a new record for Australia. Two new species are described: P. luteum sp. nov. can be identified by the ability to produce yellow pigment on MEA, PDA, and OA, the predominance of subcylindrical to subulate type II phialides, and the mycelium showing prominent exudate droplets observed as warts; and P. santali sp. nov. which can be separated from other species producing pink colonies on MEA by the predominance of type I and II phialides, the distinct brownish olive colonies in OA, and slow growth. es_ES
dc.description.sponsorship We acknowledge Pablo Castillo (IAS-CSIC) for sharing the equipment to perform microscopic observations. Isolations were made under project PRJ-004677 "Heartwood Rot Identification and Impact in Sandalwood (Santalum album)" funded by the Rural Industries Research and Development Corporation of Australia. We thank Len Norris and Diane White for assistance with collection and isolation. en_EN
dc.language Inglés es_ES
dc.publisher INT MYCOLOGICAL ASSOC es_ES
dc.relation.ispartof IMA fungus (Print) es_ES
dc.rights Reconocimiento - No comercial - Sin obra derivada (by-nc-nd) es_ES
dc.subject Actin es_ES
dc.subject Beta-tubulin es_ES
dc.subject DNA phylogeny es_ES
dc.subject Santalum es_ES
dc.subject Systematics es_ES
dc.subject Togninia es_ES
dc.subject.classification PRODUCCION VEGETAL es_ES
dc.title New Phaeoacremonium species isolated from sandalwood trees in Western Australia es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.5598/imafungus.2014.05.01.08
dc.relation.projectID info:eu-repo/grantAgreement/RIRDC//PRJ-004677/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto Agroforestal Mediterráneo - Institut Agroforestal Mediterrani es_ES
dc.contributor.affiliation Universitat Politècnica de València. Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural - Escola Tècnica Superior d'Enginyeria Agronòmica i del Medi Natural es_ES
dc.description.bibliographicCitation Gramaje Pérez, D.; León Santana, M.; Pérez Sierra, AM.; Burgess, T.; Armengol Fortí, J. (2014). New Phaeoacremonium species isolated from sandalwood trees in Western Australia. IMA fungus (Print). 5(1):67-77. https://doi.org/10.5598/imafungus.2014.05.01.08 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion http://dx.doi.org/10.5598/imafungus.2014.05.01.12 es_ES
dc.description.upvformatpinicio 67 es_ES
dc.description.upvformatpfin 77 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 5 es_ES
dc.description.issue 1 es_ES
dc.relation.senia 280471 es_ES
dc.identifier.eissn 2210-6359
dc.identifier.pmcid PMC4107898 en_EN
dc.contributor.funder Rural Industries Research and Development Corporation es_ES
dc.description.references Agustí-Brisach C, Gramaje D, García-Jiménez J, Armengol J (2013) Detection of black-foot and Petri disease pathogens in natural soils of grapevine nurseries and vineyards using bait plants. Plant and Soil 364: 5–13. es_ES
dc.description.references Arzanlou M, Groenewald JZ, Gams W, Braun U, Shin HD, Crous PW (2007) Phylogenetic and morphotaxonomic revision of Ramichloridium and allied genera. Studies in Mycology 58: 57–93. es_ES
dc.description.references Arzanlou M, Narmani A, Khodaei S, Moshari S (2014) Pome and stone fruit trees as possible reservoir hosts for Phaeoacremonium spp., the causal agents of grapevine esca disease in Iran. Archives of Phytopathology and Plant Protection 47: 717–727. es_ES
dc.description.references Baloyi MA, Halleen F, Mostert L, Eskalen A (2013) First report of Togninia minima perithecia on esca- and Petri-diseased grapevines in South Africa. Plant Disease 97: 1247. es_ES
dc.description.references Barbour L, Norris L, Burgess TI (2010) Heartwood rot identification and impact in sandalwood (Santalum album). Barton, ACT: Rural Industries Research and Development Corporation. es_ES
dc.description.references Barry K (2002) Heartrots in Plantation Hardwoods in Indonesia and Australia. [Technical Report no. 51.] Canberra, ACT: Australian Center for International Agricultural Research. es_ES
dc.description.references Berraf-Tebbal A, Bouznad Z, Santos JM, Coelho MA, Péros JP, Phillips AJL (2011) Phaeoacremonium species associated with Eutypa dieback and esca of grapevines in Algeria. Phytopathologia Mediterranea 50: S86–S97. es_ES
dc.description.references Carbone I, Kohn LM (1999) A method for designing primer sets for speciation studies in filamentous ascomycetes. Mycologia 91: 553–556 es_ES
dc.description.references Cloete M, Fourie PH, Damm U, Crous PW, Mostert L (2011) Fungi associated with die-back symptoms of apple and pear trees, a possible inoculum source of grapevine trunk disease pathogens. Phytopathologia Mediterranea 50: S176–S190. es_ES
dc.description.references Crous PW, Gams W (2000) Phaeomoniella chlamydospora gen. et comb. nov, a causal organism of Petri grapevine decline and esca. Phytopathologia Mediterranea 39: 112–188. es_ES
dc.description.references Crous PW, Gams W, Stalpers JA, Robert V, Stegehuis G (2004) MycoBank: an online initiative to launch mycology into the 21st century. Studies in Mycology 50: 19–22. es_ES
dc.description.references Crous PW, Gams W, Wingfield MJ, Van Wyk PS (1996) Phaeoacremonium gen. nov. associated with wilt and decline diseases of woody hosts and human infections. Mycologia 88: 786–796. es_ES
dc.description.references Crous PW, Verkley GJM, Groenewald JZ, Samson RA (eds) (2009) Fungal Biodiversity. [CBS Laboratory Manual Series no. 1.] Utrecht: CBS-KNAW Fungal Biodiversity Centre. es_ES
dc.description.references Damm U, Mostert L, Crous PW, Fourie PH (2008) Novel Phaeoacremonium species associated with necrotic wood of Prunus trees. Persoonia 20: 87–102. es_ES
dc.description.references de Albornoz MB (1974) Cephalosporium serrae, agente etiológico de micetomas. Mycopathologia et Mycologia Applicata: 54: 485–498. es_ES
dc.description.references Di Marco S, Calzarano F, Osti F, Mazzullo A (2004) Pathogenicity of fungi associated with a decay of kiwifruit. Australasian Plant Pathology 33: 337–342. es_ES
dc.description.references Dupont J, Laloui W, Magnin S, Larignon P, Roquebert MF (2000) Phaeoacremonium viticola, a new species associated with esca disease of grapevine in France. Mycologia 92: 499–504. es_ES
dc.description.references Dupont J, Magnin S, Césari C, Gatica M (2002) ITS and β-tubulin markers help delineate Phaeoacremonium species, and the occurrence of P. parasiticum in grapevine disease in Argentina. Mycological Research 106: 1143–1150. es_ES
dc.description.references Eskalen A, Rooney-Latham S, Gubler WD (2005) Occurrence of Togninia fraxinopennsylvanica on esca-diseased grapevines (Vitis vinifera) and declining ash trees (Fraxinus latifolia) in California. Plant Disease 89: 528. es_ES
dc.description.references Essakhi S, Mugnai L, Crous PW, Groenewald JZ, Surico G (2008) Molecular and phenotypic characterization of novel Phaeoacremonium species associated with Petri disease and esca of grapevine. Persoonia 21: 119–134. es_ES
dc.description.references Gramaje D, Agustí-Brisach C, Pérez-Sierra A, Moralejo E, Olmo D, Mostert L, Damm U, Armengol J (2012) Fungal trunk pathogens associated with wood decay of almond trees on Mallorca (Spain). Persoonia 28: 1–13. es_ES
dc.description.references Gramaje D, Armengol J, Mohammadi H, Banihashemi Z, Mostert L (2009) Novel Phaeoacremonium species associated with Petri disease and esca of grapevines in Iran and Spain. Mycologia 101: 920–929. es_ES
dc.description.references Graham AB, Johnston PR, Weir BS (2009) Three new Phaeoacremonium species on grapevines in New Zealand. Australasian Plant Pathology 38: 505–513. es_ES
dc.description.references Groenewald M, Kang J-C, Crous PW, Gams W (2001) ITS and beta-tubulin phylogeny of Phaeoacremonium and Phaeomoniella species. Mycological Research 105: 651–657. es_ES
dc.description.references Guarro J, Silvestre AM Jr, Verkley G, Cano J, Gompertz OF, Gené J, Ogawa MM, Tomimori-Yamashita J, Teixeira SP, de Almeida FA (2006) Limitations of DNA sequencing for diagnosis of a mixed infection by two fungi, Phaeoacremonium venezuelense and a Plectophomella sp., in a transplant recipient. Journal of Clinical Microbiology 44: 4279–4282. es_ES
dc.description.references Halliwell RS (1966) Association of Cephalosporium with a decline of oak in Texas. Plant Disease Reporter 50: 75–78. es_ES
dc.description.references Harrison CJ, Langdale JA (2006) A step by step guide to phylogeny reconstruction. Plant Journal 45: 561–572. es_ES
dc.description.references Harbaugh DT, Baldwin BG (2007) Phylogeny and biogeography of the sandalwoods (Santalum, Santalaceae): repeated dispersals throughout the Pacific. American Journal of Botany 94: 1028–1040. es_ES
dc.description.references Hausner G, Eyjólfsdóttir G, Reid J (1992) Two additional species of the genus Togninia. Canadian Journal of Botany 70: 724–734. es_ES
dc.description.references Hawksworth DL, Gibson IAS, Gams W (1976) Phialophora parasitica associated with disease conditions in various trees. Transactions of British Mycological Society 66: 427–431. es_ES
dc.description.references Hennion B, Baudry A, Lecompte P, Durpaire MP, Mouyon M, Tailleur JL, Larignon P (2001) Dépérissement du kiwi par maladie du bois. Infos-Ctifl 176: 25–27. es_ES
dc.description.references Hillis DM, Bull JJ (1993) An empirical test of bootstrapping as a method for assessing confidence in phylogenetic analysis. Systematic Biology 42: 182–192. es_ES
dc.description.references Katoh K, Standley DM (2013) MAFFT multiple sequence alignment software version 7: improvements in performance and usability (outlines version 7). Molecular Biology and Evolution 30: 772–780. es_ES
dc.description.references Lynch SC, Zambino PJ, Mayorquin JS, Wang DH, Eskalen A (2013) Identification of new fungal pathogens of coast live oak in California. Plant Disease 97: 1025–1036. es_ES
dc.description.references Mohammadi H (2014) Phaeoacremonium spp. and Botryosph-aeriaceae spp. associated with date palm (Phoenix dactylifera L.) decline in Iran. Journal of Phytopathology DOI: 10.1111/jph.12229 es_ES
dc.description.references Mostert L, Groenewald JZ, Summerbell RC, Gams W, Crous PW (2006) Taxonomy and pathology of Togninia (Diaporthales) and its Phaeoacremonium anamorphs. Studies in Mycology 54: 1–115. es_ES
dc.description.references Mostert L, Groenewald JZ, Summerbell RC, Robert V, Sutton DA, Padhye AA, Crous PW (2005) Species of Phaeoacremonium associated with human infections and environmental reservoirs in infected woody plants. Journal of Clinical Microbiology 43: 1752–1767. es_ES
dc.description.references Mostofi K, Blanchet D, Marnet D, Abboud P, Jeanbourquin D, Charles JI, Belzunc C (2012) Cervical spondylitis due to Phaeoacremonium venezuelense in an immunocompetent patient. A first case report. Journal de Mycologie Médicale 22: 197–200. es_ES
dc.description.references Moyo P, Allsopp E, Roets F, Mostert L, Halleen F (2014) Arthropods vector grapevine trunk disease pathogens. Phytopathology doi: https://doi.org/www.dx.doi.org/10.1094/PHYTO-11-13-0303-R es_ES
dc.description.references Nigro F, Boscia D, Antelmi I, Ippolito A (2013) Fungal species associated with a severe decline of olive in southern Italy. Journal of Plant Pathology 95: 668. es_ES
dc.description.references O’Donnell K, Cigelnik E (1997) Two divergent intragenomic rDNA ITS2 types within a monophyletic lineage of the fungus Fusarium are nonorthologous. Molecular Phylogenetics and Evolution 7: 103–116. es_ES
dc.description.references Olmo D, Gramaje D, Agustí-Brisach C, Leon M, Armengol J (2014) First report of Phaeoacremonium venezuelense associated with decay of apricot trees in Spain. Plant Disease DOI:https://doi.org/www.dx.doi.org/10.1094/PDIS-12-13-1198-PDN es_ES
dc.description.references Pascoe I, Cottral E (2000) Developments in grapevine trunk diseases research in Australia. Phytopathologia Mediterranea 39: 68–75. es_ES
dc.description.references Prodi A, Sandalo S, Tonti S, Nipoti P, Pisi A (2008) Phialophora-like fungi associated with kiwifruit elephantiasis. Journal of Plant Pathology 90: 487–494. es_ES
dc.description.references Rayner RW (1970) A Mycological Colour Chart. Kew: Commonwealth Mycological. es_ES
dc.description.references Réblová M, Mostert L (2007) Romellia is congeneric with Togninia, and description of Conidiotheca gen. nov. for one species of this genus with polysporous asci. Mycological Research 111: 299–307. es_ES
dc.description.references Richter H, Gindro K, Pezet R, Viret O (2007) Localization and quantification of fungi in esca diseased grapevine trunks. Phytopathologia Mediterranea 46: 105–106. es_ES
dc.description.references Rooney S, Eskalen A, Gubler WD (2001) Recovery of Phaeomoniella chlamydospora and Phaeoacremonium inflatipes from soil and grapevine tissues. Phytopathologia Mediterranea 40: S351–356. es_ES
dc.description.references Rooney-Latham S, Eskalen A, Gubler WD (2005) Teleomorph formation of Phaeoacremonium aleophilum, cause of esca and grapevine decline in California. Plant Disease 89: 177–184. es_ES
dc.description.references Rumbos I (1986) Phialophora parasitica, causal agent of cherry dieback. Journal of Phytopathology 117: 283–287. es_ES
dc.description.references Sánchez-Márquez S, Bills GF, Zabalgogeazcoa I (2007) The endophytic mycobiota of the grass Dactylis glomerata. Fungal Diversity 27: 171–195. es_ES
dc.description.references Swofford DL (2000) PAUP* 4.0: Phylogenetic analysis using parsimony (*and other methods). Sunderland, MA: Sinauer Associates. es_ES
dc.description.references Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: Molecular Evolutionary Genetics Analysis using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Molecular Biology and Evolution 28: 2731–2739. es_ES
dc.description.references Úrbez-Torres JR, Haag P, Bowen P, O’Gorman DT (2014) Grapevine trunk diseases in British Columbia: incidence and characterization of the fungal pathogens associated with esca and Petri diseases of grapevine. Plant Disease 98: 469–482. es_ES
dc.description.references Úrbez-Torres JR, Peduto F, Vossen PM, Krueger WH, Gubler WD (2013) Olive twig and branch dieback: etiology, incidence, and distribution in California. Plant Disease 97: 231–244. es_ES


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