Capillaureum caryovora gen. sp. nov. (Cryphonectriaceae) pathogenic to pequi (Caryocar brasiliense) in Brazil

Ferreira, M. A.; Oliveira, Mara Elisa Soares de; Silva, Gabrielle Avelar; Mathioni, Sandra M.; Máfia, Reginaldo Gonçalves

doi:10.1007/s11557-018-01461-3

Cited by 11 publications

(23 citation statements)

References 32 publications

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“…The datasets of the sequences of the LSU gene region, as well as a combination of the sequences of 5.8S rDNA and the exon regions of the tub ( tub2 and tub1 ) gene regions (including partial exon 4, exon 5, partial exon 6 and partial exon 7), were used successfully to clarify the genera of Cryphonectriaceae ( Gryzenhout et al 2009 , Chen et al 2011 , 2013a , b , 2016 , 2018 , Ali et al 2018 , Ferreira et al 2019 ). To determine the generic placement of the isolates collected from Myrtales in this study, LSU and 5.8S rRNA/exons of tub ( tub2 and tub1 ) gene sequences from ex-type strains of the described species/genera in Cryphonectriaceae were compared with sequences generated in the current study ( Table 2 ).…”

Section: Methodsmentioning

confidence: 99%

“…The Cryphonectriaceae accommodates fungi previously classified in the Cryphonectria - Endothia complex ( Castlebury et al 2002 , Gryzenhout et al 2006c ), which was established to include Cryphonectria , Endothia and three other genera, namely Amphilogia , Chrysoporthe , and Rostraureum ( Gryzenhout et al 2006c ). Currently, 25 genera have been identified and described in the Cryphonectriaceae ( Cheewangkoon et al 2009 , Gryzenhout et al 2009 , 2010 , Begoude et al 2010 , Vermeulen et al 2011 , 2013 , Crous et al 2012a , b , 2015 , Chen et al 2013a , b , 2016 , 2018 , Crane & Burgess 2013 , Beier et al 2015 , Ali et al 2018 , Ferreira et al 2019 ). With the exception of Chrysocrypta , Chrysofolia , and Foliocryphia , which were isolated from leaf spots of eucalypts ( Myrtaceae , Myrtales ) ( Cheewangkoon et al 2009 , Crous et al 2012a , b , 2015 , 2019 ) and healthy leaves of Barringtonia acutangula ( Lecythidaceae , Ericales ) ( Suwannarach et al 2016 ), the other genera were isolated from trees associated with blight, die-back or canker ( Gryzenhout et al 2009 , 2010 , Begoude et al 2010 , Vermeulen et al 2011 , 2013 , Chen et al 2013a , b , 2016 , 2018 , Crane & Burgess 2013 , Beier et al 2015 , Ali et al 2018 , Ferreira et al 2019 , Jiang et al 2019 ).…”

Section: Introductionmentioning

confidence: 99%

“…Host plants of the Cryphonectriaceae include more than 100 tree species in over 26 families of 16 orders, particularly in the families Fagaceae , Melastomataceae , and Myrtaceae ( Myrtales ) ( Cheewangkoon et al 2009 , Gryzenhout et al 2009 , 2010 , Begoude et al 2010 , Vermeulen et al 2011 , 2013 , Chen et al 2013a , b , 2016 , 2018 , Crane & Burgess 2013 , Beier et al 2015 , Ali et al 2018 , Ferreira et al 2019 ). In China, seven Cryphonectriaceae genera, Aurantiosacculus , Cryphonectria , Chrysoporthe , Celoporthe , Corticimorbus , Chrysomorbus and Endothia have been identified from diseased trees.…”

Section: Introductionmentioning

confidence: 99%

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Cryphonectriaceae on Myrtales in China: phylogeny, host range, and pathogenicity

Wang

Liu

et al. 2020

persoonia

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Plantation-grown Eucalyptus (Myrtaceae) and other trees residing in the Myrtales have been widely planted in southern China. These fungal pathogens include species of Cryphonectriaceae that are well-known to cause stem and branch canker disease on Myrtales trees. During recent disease surveys in southern China, sporocarps with typical characteristics of Cryphonectriaceae were observed on the surfaces of cankers on the stems and branches of Myrtales trees. In this study, a total of 164 Cryphonectriaceae isolates were identified based on comparisons of DNA sequences of the partial conserved nuclear large subunit (LSU) ribosomal DNA, internal transcribed spacer (ITS) regions including the 5.8S gene of the ribosomal DNA operon, two regions of the β-tubulin (tub2/tub1) gene, and the translation elongation factor 1-alpha (tef1) gene region, as well as their morphological characteristics. The results showed that eight species reside in four genera of Cryphonectriaceae occurring on the genera Eucalyptus, Melastoma (Melastomataceae), Psidium (Myrtaceae), Syzygium (Myrtaceae), and Terminalia (Combretaceae) in Myrtales. These fungal species include Chrysoporthe deuterocubensis, Celoporthe syzygii, Cel. eucalypti, Cel. guangdongensis, Cel. cerciana, a new genus and two new species, as well as one new species of Aurifilum. These new taxa are hereby described as Parvosmorbus gen. nov., Par. eucalypti sp. nov., Par. guangdongensis sp. nov., and Aurifilum terminali sp. nov. Pathogenicity tests showed that the eight species of Cryphonectriaceae are pathogenic to two Eucalyptus hybrid seedlings, Melastoma sanguineum branches, and Psidium guajava and Syzygium jambos seedlings. The overall data showed that Chr. deuterocubensis is the most aggressive, followed by Par. eucalypti. Significant differences in tolerance were observed between the two tested Eucalyptus hybrid genotypes, suggesting that disease-tolerant genotypes can be selected for disease management in the Eucalyptus industry.

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Section: Methodsmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

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Cryphonectriaceae on Myrtales in China: phylogeny, host range, and pathogenicity

Wang

Liu

et al. 2020

persoonia

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“…by Gryzenhout et al (2006). Twenty-six genera were subsequently added to the family based on morphological and phylogenetic support by different authors (Gryzenhout et al 2004(Gryzenhout et al , 2005bNakabonge et al 2006;Chen et al 2013aChen et al , 2016Jiang et al 2019b;Wijayawardene et al 2018a;Ferreira et al 2019). We introduce a novel genus Eriocamporesia as a monotypic genus to accommodate E. aurantia based on morphological characteristics and phylogenetic support.…”

Section: Cryphonectriaceae Gryzenh and Mj Wingfmentioning

confidence: 99%

Fungal diversity notes 1151–1276: taxonomic and phylogenetic contributions on genera and species of fungal taxa

et al. 2020

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Fungal diversity notes is one of the important journal series of fungal taxonomy that provide detailed descriptions and illustrations of new fungal taxa, as well as providing new information of fungal taxa worldwide. This article is the 11th contribution to the fungal diversity notes series, in which 126 taxa distributed in two phyla, six classes, 24 orders and 55 families are described and illustrated. Taxa in this study were mainly collected from Italy by Erio Camporesi and also collected from China, India and Thailand, as well as in some other European, North American and South American countries. Taxa described in the present study include two new families, 12 new genera, 82 new species, five new combinations and 25 new records on new hosts and new geographical distributions as well as sexual-asexual reports. The two new families are Eriomycetaceae (Dothideomycetes, family incertae sedis) and Fasciatisporaceae (Xylariales, Sordariomycetes). The twelve new genera comprise Bhagirathimyces (Phaeosphaeriaceae), Camporesiomyces (Tubeufiaceae), Eriocamporesia (Cryphonectriaceae), Eriomyces (Eriomycetaceae), Neomonodictys (Pleurotheciaceae), Paraloratospora (Phaeosphaeriaceae), Paramonodictys (Parabambusicolaceae), Pseudoconlarium (Diaporthomycetidae, genus incertae sedis), Pseudomurilentithecium (Lentitheciaceae), Setoapiospora (Muyocopronaceae), Srinivasanomyces (Vibrisseaceae) and Xenoanthostomella (Xylariales, genera incertae sedis). The 82 new species comprise Acremonium chiangraiense, Adustochaete nivea, Angustimassarina camporesii, Bhagirathimyces himalayensis, Brunneoclavispora camporesii, Camarosporidiella camporesii, Camporesiomyces mali, Camposporium appendiculatum, Camposporium multiseptatum, Camposporium septatum, Canalisporium aquaticium, Clonostachys eriocamporesiana, Clonostachys eriocamporesii, Colletotrichum hederiicola, Coniochaeta vineae, Conioscypha verrucosa, Cortinarius ainsworthii, Cortinarius aurae, Cortinarius britannicus, Cortinarius heatherae, Cortinarius scoticus, Cortinarius subsaniosus, Cytospora fusispora, Cytospora rosigena, Diaporthe camporesii, Diaporthe nigra, Diatrypella yunnanensis, Dictyosporium muriformis, Didymella camporesii, Diutina bernali, Diutina sipiczkii, Eriocamporesia aurantia, Eriomyces heveae, Ernakulamia tanakae, Falciformispora uttaraditensis, Fasciatispora cocoes, Foliophoma camporesii, Fuscostagonospora camporesii, Helvella subtinta, Kalmusia erioi, Keissleriella camporesiana, Keissleriella camporesii, Lanspora cylindrospora, Loratospora arezzoensis, Mariannaea atlantica, Melanographium phoenicis, Montagnula camporesii, Neodidymelliopsis camporesii, Neokalmusia kunmingensis, Neoleptosporella camporesiana, Neomonodictys muriformis, Neomyrmecridium guizhouense, Neosetophoma camporesii, Paraloratospora camporesii, Paramonodictys solitarius, Periconia palmicola, Plenodomus triseptatus, Pseudocamarosporium camporesii, Pseudocercospora maetaengensis, Pseudochaetosphaeronema kunmingense, Pseudoconlarium punctiforme, Pseudodactylaria camporesiana, Pseudomurilentithecium camporesii, Pseudotetraploa rajmachiensis, Pseudotruncatella camporesii, Rhexocercosporidium senecionis, Rhytidhysteron camporesii, Rhytidhysteron erioi, Septoriella camporesii, Setoapiospora thailandica, Srinivasanomyces kangrensis, Tetraploa dwibahubeeja, Tetraploa pseudoaristata, Tetraploa thrayabahubeeja, Torula camporesii, Tremateia camporesii, Tremateia lamiacearum, Uzbekistanica pruni, Verruconis mangrovei, Wilcoxina verruculosa, Xenoanthostomella chromolaenae and Xenodidymella camporesii. The five new combinations are Camporesiomyces patagoniensis, Camporesiomyces vaccinia, Camposporium lycopodiellae, Paraloratospora gahniae and Rhexocercosporidium microsporum. The 22 new records on host and geographical distribution comprise Arthrinium marii, Ascochyta medicaginicola, Ascochyta pisi, Astrocystis bambusicola, Camposporium pellucidum, Dendryphiella phitsanulokensis, Diaporthe foeniculina, Didymella macrostoma, Diplodia mutila, Diplodia seriata, Heterosphaeria patella, Hysterobrevium constrictum, Neodidymelliopsis ranunculi, Neovaginatispora fuckelii, Nothophoma quercina, Occultibambusa bambusae, Phaeosphaeria chinensis, Pseudopestalotiopsis theae, Pyxine berteriana, Tetraploa sasicola, Torula gaodangensis and Wojnowiciella dactylidis. In addition, the sexual morphs of Dissoconium eucalypti and Phaeosphaeriopsis pseudoagavacearum are reported from Laurus nobilis and Yucca gloriosa in Italy, respectively. The holomorph of Diaporthe cynaroidis is also reported for the first time.

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“…Fungi in the Cryphonectriaceae (Diaporthales) include at least twenty-three genera of bark-, wood-and leaf-infecting fungi (Gryzenhout et al 2009(Gryzenhout et al , 2010Begoude et al 2010;Vermeulen et al 2011Vermeulen et al , 2013Crous et al 2012;Chen et al 2013aChen et al , b, 2016Chen et al , 2018Crane and Burgess 2013;Beier et al 2015;Ali et al 2018;Ferreira et al 2019;Jiang et al 2020;Wang et al 2020). They occur on trees and shrubs in various parts of the world and include saprophytes, facultative parasites and important pathogens of woody plants (Gryzenhout et al 2009).…”

Section: Introductionmentioning

confidence: 99%

Figure 1 from: Roux J, Kamgan Nkuekam G, Marincowitz S, van der Merwe NA, Uchida J, Wingfield MJ, Chen SF (2020) Cryphonectriaceae associated with rust-infected Syzygium jambos in Hawaii. MycoKeys 76: 49-79. https://doi.org/10.3897/mycokeys.76.58406

Roux,

Kamgan Nkuekam,

Marincowitz

et al. 2020

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Capillaureum caryovora gen. sp. nov. (Cryphonectriaceae) pathogenic to pequi (Caryocar brasiliense) in Brazil

Cited by 11 publications

References 32 publications

Cryphonectriaceae on Myrtales in China: phylogeny, host range, and pathogenicity

Cryphonectriaceae on Myrtales in China: phylogeny, host range, and pathogenicity

Fungal diversity notes 1151–1276: taxonomic and phylogenetic contributions on genera and species of fungal taxa

Figure 1 from: Roux J, Kamgan Nkuekam G, Marincowitz S, van der Merwe NA, Uchida J, Wingfield MJ, Chen SF (2020) Cryphonectriaceae associated with rust-infected Syzygium jambos in Hawaii. MycoKeys 76: 49-79. https://doi.org/10.3897/mycokeys.76.58406

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