34 results on '"Jargeat P"'
Search Results
2. Untargeted metabolomics to evaluate antifungal mechanism: a study of Cophinforma mamane and Candida albicans interaction
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Asih Triastuti, Marieke Vansteelandt, Fatima Barakat, Carlos Amasifuen, Patricia Jargeat, and Mohamed Haddad
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Metabolomics ,Fungal co-culture ,Anti-fungal ,Virulence ,Botany ,QK1-989 - Abstract
Abstract Microbial interactions between filamentous fungi and yeast are still not fully understood. To evaluate a potential antifungal activity of a filamentous fungus while highlighting metabolomic changes, co-cultures between an endophytic strain of Cophinforma mamane (CM) and Candida albicans (CA) were performed. The liquid cultures were incubated under static conditions and metabolite alterations during the course were investigated by ultra-performance liquid chromatography–tandem mass spectrophotometry (UPLC–MS/MS). Results were analyzed using MS-DIAL, MS-FINDER, METLIN, Xcalibur, SciFinder, and MetaboAnalyst metabolomics platforms. The metabolites associated with catabolic processes, including the metabolism of branched-chain amino acids, carnitine, and phospholipids were upregulated both in the mono and co-cultures, indicating fungal adaptability to environmental stress. Several metabolites, including C20 sphinganine 1-phosphate, myo-inositol, farnesol, gamma-undecalactone, folinic acid, palmitoleic acid, and MG (12:/0:0/0:0) were not produced by CA during co-culture with CM, demonstrating the antifungal mechanism of CM. Our results highlight the crucial roles of metabolomics studies to provide essential information regarding the antifungal mechanism of C. mamane against C. albicans, especially when the lost/undetected metabolites are involved in fungal survival and pathogenicity. Graphical Abstract
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- 2023
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3. Lipo-chitooligosaccharides as regulatory signals of fungal growth and development
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Tomás Allen Rush, Virginie Puech-Pagès, Adeline Bascaules, Patricia Jargeat, Fabienne Maillet, Alexandra Haouy, Arthur QuyManh Maës, Cristobal Carrera Carriel, Devanshi Khokhani, Michelle Keller-Pearson, Joanna Tannous, Kevin R. Cope, Kevin Garcia, Junko Maeda, Chad Johnson, Bailey Kleven, Quanita J. Choudhury, Jessy Labbé, Candice Swift, Michelle A. O’Malley, Jin Woo Bok, Sylvain Cottaz, Sébastien Fort, Verena Poinsot, Michael R. Sussman, Corinne Lefort, Jeniel Nett, Nancy P. Keller, Guillaume Bécard, and Jean-Michel Ané
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Science - Abstract
Lipo-chitooligosaccharides (LCOs) are signaling molecules produced by certain bacteria and fungi that establish symbiotic relationships with plants. Here, the authors show that LCOs are produced also by many other, non-symbiotic fungi, and regulate fungal growth and development.
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- 2020
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4. Lipo-chitooligosaccharides as regulatory signals of fungal growth and development
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Rush, Tomás Allen, Puech-Pagès, Virginie, Bascaules, Adeline, Jargeat, Patricia, Maillet, Fabienne, Haouy, Alexandra, Maës, Arthur QuyManh, Carriel, Cristobal Carrera, Khokhani, Devanshi, Keller-Pearson, Michelle, Tannous, Joanna, Cope, Kevin R., Garcia, Kevin, Maeda, Junko, Johnson, Chad, Kleven, Bailey, Choudhury, Quanita J., Labbé, Jessy, Swift, Candice, O’Malley, Michelle A., Bok, Jin Woo, Cottaz, Sylvain, Fort, Sébastien, Poinsot, Verena, Sussman, Michael R., Lefort, Corinne, Nett, Jeniel, Keller, Nancy P., Bécard, Guillaume, and Ané, Jean-Michel
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- 2020
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5. Alder and the Golden Fleece: high diversity of Frankia and ectomycorrhizal fungi revealed from Alnus glutinosa subsp. barbata roots close to a Tertiary and glacial refugium
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Melanie Roy, Adrien C. Pozzi, Raphaëlle Gareil, Melissande Nagati, Sophie Manzi, Imen Nouioui, Nino Sharikadze, Patricia Jargeat, Hervé Gryta, Pierre-Arthur Moreau, Maria P. Fernandez, and Monique Gardes
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Frankia ,Ectomycorrhiza ,Colchis ,Alnus ,Alnicola ,Glacial refugia ,Medicine ,Biology (General) ,QH301-705.5 - Abstract
Background Recent climatic history has strongly impacted plant populations, but little is known about its effect on microbes. Alders, which host few and specific symbionts, have high genetic diversity in glacial refugia. Here, we tested the prediction that communities of root symbionts survived in refugia with their host populations. We expected to detect endemic symbionts and a higher species richness in refugia as compared to recolonized areas. Methods We sampled ectomycorrhizal (EM) root tips and the nitrogen-fixing actinomycete Frankia communities in eight sites colonized by Alnus glutinosa subsp. barbata close to the Caucasus in Georgia. Three sites were located in the Colchis, one major Eurasian climatic refugia for Arcto-Tertiary flora and alders, and five sites were located in the recolonized zone. Endemic symbionts and plant ITS variants were detected by comparing sequences to published data from Europe and another Tertiary refugium, the Hyrcanian forest. Species richness and community structure were compared between sites from refugia and recolonized areas for each symbionts. Results For both symbionts, most MOTUs present in Georgia had been found previously elsewhere in Europe. Three endemic Frankia strains were detected in the Colchis vs two in the recolonized zone, and the five endemic EM fungi were detected only in the recolonized zone. Frankia species richness was higher in the Colchis while the contrary was observed for EM fungi. Moreover, the genetic diversity of one alder specialist Alnicola xanthophylla was particularly high in the recolonized zone. The EM communities occurring in the Colchis and the Hyrcanian forests shared closely related endemic species. Discussion The Colchis did not have the highest alpha diversity and more endemic species, suggesting that our hypothesis based on alder biogeography may not apply to alder’s symbionts. Our study in the Caucasus brings new clues to understand symbioses biogeography and their survival in Tertiary and ice-age refugia, and reveals that isolated host populations could be of interest for symbiont diversity conservation.
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- 2017
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6. Do Host Plant and Associated Ant Species Affect Microbial Communities in Myrmecophytes?
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Mario X. Ruiz-González, Céline Leroy, Alain Dejean, Hervé Gryta, Patricia Jargeat, Angelo D. Armijos Carrión, and Jérôme Orivel
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microbial diversity ,domatia ,allomerus decemarticulatus ,allomerus octoarticulatus ,azteca sp. cf. depilis ,cordia nodosa ,hirtella physophora ,Science - Abstract
Ant-associated microorganisms can play crucial and often overlooked roles, and given the diversity of interactions that ants have developed, the study of the associated microbiomes is of interest. We focused here on specialist plant-ant species of the genus Allomerus that grow a fungus to build galleries on their host-plant stems. Allomerus-inhabited domatia, thus, might be a rich arena for microbes associated with the ants, the plant, and the fungus. We investigated the microbial communities present in domatia colonised by four arboreal ants: Allomerus decemarticulatus, A. octoarticulatus, A. octoarticulatus var. demerarae, and the non-fungus growing plant-ant Azteca sp. cf. depilis, inhabiting Hirtella physophora or Cordia nodosa in French Guiana. We hypothesized that the microbial community will differ among these species. We isolated microorganisms from five colonies of each species, sequenced the 16S rRNA or Internal TranscribedSpacer (ITS) regions, and described both the alpha and beta diversities. We identified 69 microbial taxa, which belong to five bacterial and two fungal phyla. The most diverse phyla were Proteobacteria and Actinobacteria. The microbial community of Azteca cf. depilis and Allomerus spp. differed in composition and richness. Geographical distance affected microbial communities and richness but plant species did not. Actinobacteria were only associated with Allomerus spp.
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- 2019
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7. Chemical modulation of the metabolism of an endophytic fungal strain of Cophinforma mamane using epigenetic modifiers and amino-acids
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Pacheco-Tapia, R., primary, Vásquez-Ocmín, P., additional, Duthen, S., additional, Ortíz, S., additional, Jargeat, P., additional, Amasifuen, C., additional, Haddad, M., additional, and Vansteelandt, M., additional
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- 2022
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8. Fungal Planet 953 – 18 December 2019
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Crous, P.W., Wingfield, M.J., Lombard, L., Roets, F., Swart, W.J., Alvarado, P., Carnegie, A.J., Moreno, G., Luangsaard, J., Thangavel, R., Alexandrova, A.V., Baseia, I.G., Bellanger, J.-M., Bessette, A.E., Bessette, A.R., De la Peña-Lastra, S., García, D., Gené, J., Pham, T.H.G., Heykoop, M., Malysheva, E., Malysheva, V., Martín, M.P., Morozova, O.V., Noisripoom, W., Overton, B.E., Rea, A.E., Sewall, B.J., Smith, M.E., Smyth, C.W., Tasanathai, K., Visagie, C.M., Adamčík, S., Alves, A., Andrade, J.P., Aninat, M.J., Araújo, R.V.B., Bordallo, J.J., Boufleur, T., Baroncelli, R., Barreto, R.W., Bolin, J., Cabero, J., Caboň, M., Cafà, G., Caffot, M.L.H., Cai, L., Carlavilla, J.R., Chávez, R., de Castro, R.R.L., Delgat, L., Deschuyteneer, D., Dios, M.M., Domínguez, L.S., Evans, H.C., Eyssartier, G., Ferreira, B.W., Figueiredo, C.N., Liu, F., Fournier, J., Galli-Terasawa, L.V., Gil-Durán, C., Glienke, C., Gonçalves, M.F.M., Gryta, H., Guarro, J., Himaman, W., Hywel-Jones, N., Iturrieta-González, I., Ivanushkina, N.E., Jargeat, P., Khalid, A.N., Khan, J., Kiran, M., Kiss, L., Kochkina, G.A., Kolařík, M., Kubátová, A., Lodge, D.J., Loizides, M., Luque, D., Manjón, J.L., Marbach, P.A.S., Massola, N.S., Mata, M., Miller, A.N., Mongkolsamrit, S., Moreau, P.-A., Morte, A., Mujic, A., Navarro-Ródenas, A., Németh, M.Z., Nóbrega, T.F., Nováková, A., Olariaga, I., Ozerskaya, S.M., Palma, M.A., Petters-Vandresen, D.A.L., Piontelli, E., Popov, E.S., Rodríguez, A., Requejo, Ó., Rodrigues, A.C.M., Rong, I.H., Roux, J., Seifert, K.A., Silva, B.D.B., Sklenář, F., Smith, J.A., Sousa, J.O., Souza, H.G., De Souza, J.T., Švec, K., Tanchaud, P., Tanney, J.B., Terasawa, F., Thanakitpipattana, D., Torres-Garcia, D., Vaca, I., Vaghefi, N., van Iperen, A.L., Vasilenko, O.V., Verbeken, A., Yilmaz, N., Zamora, J.C., Zapata, M., Jurjević, Ž., Groenewald, J.Z., Crous, Pedro W., van Iperen, Arien L., Groenewald, Johannes Z., Thangavel, Raja, Carnegie, Angus J., Wingfield, Michael J., Roux, Jolanda, Jurjević, Željko, Roets, Francois, Swart, Wijnand J., Smith, Jason A., Lombard, Lorenzo, Moreno, Gabriel, Carlavilla, Juan Ramón, Manjón, José Luis, Bellanger, Jean-Michel, Olariaga, Ibai, Giang, Pham Thi Ha, Alexandrova, Alina V., Morozova, Olga V., Rodrigues, Ana C.M., Baseia, Iuri G., Martín, María P., De la Peña-Lastra, Saúl, Alvarado, Pablo, Requejo, Óscar, Tanchaud, Patrice, Eyssartier, Guillaume, Jargeat, Patricia, Gryta, Hervé, Gil-Durán, Carlos, Chávez, Renato, Vaca, Inmaculada, Loizides, Michael, Moreau, Pierre-Arthur, Zapata, Mario, Palma, María Antonieta, Aninat, María José, Piontelli, Eduardo, Luangsa-ard, Jennifer, Tasanathai, Kanoksri, Noisripoom, Wasana, Hywel-Jones, Nigel, Mongkolsamrit, Suchada, Luangsa-ard, Janet Jennifer, Himaman, Winanda, Garcia, Daniel Torres, Guarro, Josep, Gené, Josepa, Petters-Vandresen, Desirrê Alexia Lourenço, Galli-Terasawa, Lygia Vitória, Terasawa, Francisco, Glienke, Chirlei, Araújo, Ruane V.B., Silva, Bianca D.B., Sousa, Julieth O., Zamora, Juan Carlos, Dios, Maria Martha, Caffot, María Luciana Hernández, Domínguez, Laura S., Kiss, Levente, Vaghefi, Niloofar, Németh, Márk Z., Miller, Andrew N., Fournier, Jacques, Nóbrega, Thaisa F., Ferreira, Bruno W., Barreto, Robert W., Evans, Harry C., Delgat, Lynn, Verbeken, Annemieke, Lodge, D. Jean, Thanakitpipattana, Donnaya, Visagie, Cobus M., Rong, Isabel H., Andrade, Jackeline Pereira, Marbach, Phellippe Arthur Santos, De Souza, Jorge Teodoro, Malysheva, Ekaterina, Malysheva, Vera, Deschuyteneer, Daniel, Heykoop, Michel, Mata, Milagro, Rea, Abigail E., Smyth, Christopher W., Overton, Barrie E., Sewall, Brent J., Smith, Matthew E., Mujic, Alija, Bolin, Jason, Bessette, Arleen, Bessette, Alan, Kiran, Munazza, Khalid, Abdul Nasir, Khan, Junaid, Adamčík, Slavomír, Caboň, Miroslav, Liu, Fang, Cai, Lei, Tanney, Joey B., Seifert, Keith A., Baroncelli, Riccardo, Cafà, Giovanni, de Castro, Renata Rebellato Linhares, Boufleur, Thais, Junior, Nelson Sidnei Massola, Yilmaz, Neriman, Nováková, Alena, Švec, Karel, Sklenář, František, Kolařík, Miroslav, Kubátová, Alena, Rodríguez, Antonio, Navarro-Ródenas, Alfonso, Morte, Asunción, Cabero, Julio, Luque, Diego, Gonçalves, Micael F.M., Alves, Artur, Bordallo, Juan Julián, Pham, Thi Ha Giang, Popov, Eugene S., Iturrieta-González, Isabel, García, Dania, Ivanushkina, Nataliya E., Kochkina, Galina A., Vasilenko, Oleg V., and Ozerskaya, Svetlana M.
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ITS nrDNA barcodes ,LSU ,Fungal Planet description sheets ,systematics ,new taxa ,Research Article - Abstract
Novel species of fungi described in this study include those from various countries as follows: Antarctica, Apenidiella antarctica from permafrost, Cladosporium fildesense from an unidentified marine sponge. Argentina, Geastrum wrightii on humus in mixed forest. Australia, Golovinomyces glandulariae on Glandularia aristigera, Neoanungitea eucalyptorum on leaves of Eucalyptus grandis, Teratosphaeria corymbiicola on leaves of Corymbia ficifolia, Xylaria eucalypti on leaves of Eucalyptus radiata. Brazil, Bovista psammophila on soil, Fusarium awaxy on rotten stalks of Zea mays, Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae (incl. Hermetothecium gen. nov.) on Mikania micrantha, Penicillium reconvexovelosoi in soil, Stagonosporopsis vannaccii from pod of Glycine max. British Virgin Isles, Lactifluus guanensis on soil. Canada, Sorocybe oblongispora on resin of Picea rubens. Chile, Colletotrichum roseum on leaves of Lapageria rosea. China, Setophoma caverna from carbonatite in Karst cave. Colombia, Lareunionomyces eucalypticola on leaves of Eucalyptus grandis. Costa Rica, Psathyrella pivae on wood. Cyprus, Clavulina iris on calcareous substrate. France, Chromosera ambigua and Clavulina iris var. occidentalis on soil. French West Indies, Helminthosphaeria hispidissima on dead wood. Guatemala, Talaromyces guatemalensis in soil. Malaysia, Neotracylla pini (incl. Tracyllales ord. nov. and Neotracylla gen. nov.) and Vermiculariopsiella pini on needles of Pinus tecunumanii. New Zealand, Neoconiothyrium viticola on stems of Vitis vinifera, Parafenestella pittospori on Pittosporum tenuifolium, Pilidium novae-zelandiae on Phoenix sp. Pakistan, Russula quercus-floribundae on forest floor. Portugal, Trichoderma aestuarinum from saline water. Russia, Pluteus liliputianus on fallen branch of deciduous tree, Pluteus spurius on decaying deciduous wood or soil. South Africa, Alloconiothyrium encephalarti, Phyllosticta encephalarticola and Neothyrostroma encephalarti (incl. Neothyrostroma gen. nov.) on leaves of Encephalartos sp., Chalara eucalypticola on leaf spots of Eucalyptus grandis × urophylla, Clypeosphaeria oleae on leaves of Olea capensis, Cylindrocladiella postalofficium on leaf litter of Sideroxylon inerme, Cylindromonium eugeniicola (incl. Cylindromonium gen. nov.) on leaf litter of Eugenia capensis, Cyphellophora goniomatis on leaves of Gonioma kamassi, Nothodactylaria nephrolepidis (incl. Nothodactylaria gen. nov. and Nothodactylariaceae fam. nov.) on leaves of Nephrolepis exaltata, Falcocladium eucalypti and Gyrothrix eucalypti on leaves of Eucalyptus sp., Gyrothrix oleae on leaves of Olea capensis subsp. macrocarpa, Harzia metrosideri on leaf litter of Metrosideros sp., Hippopotamyces phragmitis (incl. Hippopotamyces gen. nov.) on leaves of Phragmites australis, Lectera philenopterae on Philenoptera violacea, Leptosillia mayteni on leaves of Maytenus heterophylla, Lithohypha aloicola and Neoplatysporoides aloes on leaves of Aloe sp., Millesimomyces rhoicissi (incl. Millesimomyces gen. nov.) on leaves of Rhoicissus digitata, Neodevriesia strelitziicola on leaf litter of Strelitzia nicolai, Neokirramyces syzygii (incl. Neokirramyces gen. nov.) on leaf spots of Syzygium sp., Nothoramichloridium perseae (incl. Nothoramichloridium gen. nov. and Anungitiomycetaceae fam. nov.) on leaves of Persea americana, Paramycosphaerella watsoniae on leaf spots of Watsonia sp., Penicillium cuddlyae from dog food, Podocarpomyces knysnanus (incl. Podocarpomyces gen. nov.) on leaves of Podocarpus falcatus, Pseudocercospora heteropyxidicola on leaf spots of Heteropyxis natalensis, Pseudopenidiella podocarpi, Scolecobasidium podocarpi and Ceramothyrium podocarpicola on leaves of Podocarpus latifolius, Scolecobasidium blechni on leaves of Blechnum capense, Stomiopeltis syzygii on leaves of Syzygium chordatum, Strelitziomyces knysnanus (incl. Strelitziomyces gen. nov.) on leaves of Strelitzia alba, Talaromyces clemensii from rotting wood in goldmine, Verrucocladosporium visseri on Carpobrotus edulis. Spain, Boletopsis mediterraneensis on soil, Calycina cortegadensisi on a living twig of Castanea sativa, Emmonsiellopsis tuberculata in fluvial sediments, Mollisia cortegadensis on dead attached twig of Quercus robur, Psathyrella ovispora on soil, Pseudobeltrania lauri on leaf litter of Laurus azorica, Terfezia dunensis in soil, Tuber lucentum in soil, Venturia submersa on submerged plant debris. Thailand, Cordyceps jakajanicola on cicada nymph, Cordyceps kuiburiensis on spider, Distoseptispora caricis on leaves of Carex sp., Ophiocordyceps khonkaenensis on cicada nymph. USA, Cytosporella juncicola and Davidiellomyces juncicola on culms of Juncus effusus, Monochaetia massachusettsianum from air sample, Neohelicomyces melaleucae and Periconia neobrittanica on leaves of Melaleuca styphelioides × lanceolata, Pseudocamarosporium eucalypti on leaves of Eucalyptus sp., Pseudogymnoascus lindneri from sediment in a mine, Pseudogymnoascus turneri from sediment in a railroad tunnel, Pulchroboletus sclerotiorum on soil, Zygosporium pseudomasonii on leaf of Serenoa repens. Vietnam, Boletus candidissimus and Veloporphyrellus vulpinus on soil. Morphological and culture characteristics are supported by DNA barcodes.
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- 2019
9. Chemical modulation of the metabolism of an endophytic fungal strain of Cophinforma mamane using epigenetic modifiers and amino-acids
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Pacheco-Tapia, R., Vásquez-Ocmín, P., Duthen, S., Ortíz, S., Jargeat, P., Amasifuen, C., Haddad, M., and Vansteelandt, M.
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Cophinforma mamane ,Infectious Diseases ,Epigenetic modifiers ,Ascomycota ,Endophytic fungi ,Genetics ,Azacitidine ,Metabolomics ,Diketopiperazines ,Amino Acids ,Ecology, Evolution, Behavior and Systematics ,Epigenesis, Genetic - Abstract
Endophytic fungi are capable of producing a great diversity of bioactive metabolites. However, the presence of silent and lowly expressed genes represents a main challenge for the discovery of novel secondary metabolites with different potential uses. Epigenetic modifiers have shown to perturb the production of fungal metabolites through the induction of silent biosynthetic pathways leading to an enhanced chemical diversity. Moreover, the addition of bioprecursors to the culture medium has been described as a useful strategy to induce specific biosynthetic pathways. The aim of this study was to assess the effects of different chemical modulators on the metabolic profiles of an endophytic fungal strain of Cophinforma mamane (Botryosphaeriaceae), known to produce 3 thiodiketopiperazine (TDKP) alkaloids (botryosulfuranols A-C), previously isolated and characterized by our team. Four epigenetic modifiers, 5-azacytidine (AZA), sodium butyrate (SB), nicotinamide (NIC), homoserine lactone (HSL) as well as 2 amino acids, L-phenylalanine and L-tryptophan, as bioprecursors of TDKPs, were used. The metabolic profiles were analysed by UHPLC-HRMS/MS under an untargeted metabolomics approach. Our results show that the addition of the two amino acids in C. mamane culture and the treatment with AZA significantly reduced the production of the TDKPs botryosulfuranols A, B and C. Interestingly, the treatment with HSL significantly induced the production of different classes of diketopiperazines (DKPs). The treatment with AZA resulted as the most effective epigenetic modifier for the alteration of the secondary metabolite profile of C. mamane by promoting the expression of cryptic genes.
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- 2021
10. Fungal Planet description sheets: 951–1041
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Li-Zhen Cai, M. Heykoop, Rong Ih, Fengjiang Liu, D. Thanakitpipattana, Gonçalves Mfm, Lorenzo Lombard, Luque D, Carlavilla, Hywel-Jones N, J. Jennifer Luangsa-ard, Malysheva, Nóbrega Tf, Lygia Vitoria Galli-Terasawa, Rea Ae, Švec K, Iuri Goulart Baseia, Bolin J, Tanchaud P, Carlos Gil-Durán, Josep Guarro, E. Piontelli, O. V. Vasilenko, E. F. Malysheva, Jean-Michel Bellanger, Gabriel Moreno, Juan Carlos Zamora, Alena Nováková, Suchada Mongkolsamrit, Araújo Rvb, Juan-Julián Bordallo, Dania García, Miroslav Caboň, Inmaculada Vaca, Christopher W. Smyth, František Sklenář, Keith A. Seifert, Riccardo Baroncelli, Johannes Z. Groenewald, Pablo Alvarado, Giovanni Cafà, C.N. Figueiredo, B. E. Overton, Márk Z. Németh, Ibai Olariaga, Željko Jurjević, de Castro Rrl, Pierre-Arthur Moreau, Neriman Yilmaz, Petters-Vandresen Dal, Levente Kiss, Artur Alves, E. S. Popov, Pedro W. Crous, Alija B. Mujic, José Luis Manjón, Marbach Pas, Jason A. Smith, Renato Chávez, De la Peña-Lastra S, Julieth O. Sousa, Rodrigues Acm, Munazza Kiran, W. Noisripoom, O.V. Morozova, Cobus M. Visagie, Annemieke Verbeken, Himaman W, Deschuyteneer D, Robert W. Barreto, M.A. Palma, De Souza Jt, A. Rodríguez, Lodge Dj, N. E. Ivanushkina, M. Zapata, D. Torres-Garcia, Thaís Regina Boufleur, Requejo Ó, Caffot Mlh, Andrew N. Miller, Michael J. Wingfield, Brent J. Sewall, J.P. Andrade, Eyssartier G, Joey B. Tanney, R. Thangavel, Pham Thg, I. Iturrieta-González, Jolanda Roux, A. V. Alexandrova, Niloofar Vaghefi, Chirlei Glienke, Francois Roets, Khan J, Souza Hg, Abdul Nasir Khalid, Asunción Morte, Harry C. Evans, Svetlana Ozerskaya, Aninat Mj, K. Tasanathai, Matthew E. Smith, Alfonso Navarro-Ródenas, María P. Martín, Slavomír Adamčík, Mata M, B.W. Ferreira, Wijnand J. Swart, Domínguez Ls, Gryta H, A.R. Bessette, Lynn Delgat, Josepa Gené, Julio Cabero, van Iperen Al, Michael Loizides, G. A. Kochkina, Jargeat P, Jacques Fournier, Dios Mm, Angus J. Carnegie, Alena Kubátová, Silva Bdb, A.E. Bessette, Terasawa F, Miroslav Kolařík, Nelson Sidnei Massola, Naturalis Biodiversity Center (The Netherlands), Centre d’Ecologie Fonctionnelle et Evolutive (CEFE), Université Paul-Valéry - Montpellier 3 (UPVM)-École Pratique des Hautes Études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD [France-Sud])-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)-Institut Agro - Montpellier SupAgro, Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), Muséum national d'Histoire naturelle (MNHN), Evolution et Diversité Biologique (EDB), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Impact de l'environnement chimique sur la santé humaine - ULR 4483 (IMPECS), Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Westerdijk Fungal Biodiversity Institute - Evolutionary Phytopathology, Westerdijk Fungal Biodiversity Institute, Westerdijk Fungal Biodiversity Institute - Collection, CHU Lille, Institut Pasteur de Lille, Université de Lille, Centre d’Ecologie Fonctionnelle et Evolutive [CEFE], IMPact de l'Environnement Chimique sur la Santé humaine (IMPECS) - EA 4483, Muséum national d'Histoire naturelle [MNHN], Evolution et Diversité Biologique [EDB], Crous P.W., Wingfield M.J., Lombard L., Roets F., Swart W.J., Alvarado P., Carnegie A.J., Moreno G., Luangsa-Ard J., Thangavel R., Alexandrova A.V., Baseia I.G., Bellanger J.-M., Bessette A.E., Bessette A.R., De la Pena-Lastra S., Garcia D., Gene J., Pham T.H.G., Heykoop M., Malysheva E., Malysheva V., Martin M.P., Morozova O.V., Noisripoom W., Overton B.E., Rea A.E., Sewall B.J., Smith M.E., Smyth C.W., Tasanathai K., Visagie C.M., Adamcik S., Alves A., Andrade J.P., Aninat M.J., Araujo R.V.B., Bordallo J.J., Boufleur T., Baroncelli R., Barreto R.W., Bolin J., Cabero J., Cabon M., Cafa G., Caffot M.L.H., Cai L., Carlavilla J.R., Chavez R., de Castro R.R.L., Delgat L., Deschuyteneer D., Dios M.M., Dominguez L.S., Evans H.C., Eyssartier G., Ferreira B.W., Figueiredo C.N., Liu F., Fournier J., Galli-Terasawa L.V., Gil-Duran C., Glienke C., Goncalves M.F.M., Gryta H., Guarro J., Himaman W., Hywel-Jones N., Iturrieta-Gonzalez I., Ivanushkina N.E., Jargeat P., Khalid A.N., Khan J., Kiran M., Kiss L., Kochkina G.A., Kolarik M., Kubatova A., Lodge D.J., Loizides M., Luque D., Manjon J.L., Marbach P.A.S., Massola N.S., Mata M., Miller A.N., Mongkolsamrit S., Moreau P.-A., Morte A., Mujic A., Navarro-Rodenas A., Nemeth M.Z., Nobrega T.F., Novakova A., Olariaga I., Ozerskaya S.M., Palma M.A., Petters-Vandresen D.A.L., Piontelli E., Popov E.S., Rodriguez A., Requejo O., Rodrigues A.C.M., Rong I.H., Roux J., Seifert K.A., Silva B.D.B., Sklenar F., Smith J.A., Sousa J.O., Souza H.G., De Souza J.T., Svec K., Tanchaud P., Tanney J.B., Terasawa F., Thanakitpipattana D., Torres-Garcia D., Vaca I., Vaghefi N., van Iperen A.L., Vasilenko O.V., Verbeken A., Yilmaz N., Zamora J.C., Zapata M., Jurjevic Z., and Groenewald J.Z.
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ITS nrDNA barcodes ,new taxa ,systematics ,LSU ,Phyllosticta ,BASIDIOMYCOTA ,Evolution ,[SDV]Life Sciences [q-bio] ,1ST REPORT ,CLASSIFICATION ,030308 mycology & parasitology ,03 medical and health sciences ,GENUS ,Behavior and Systematics ,Systematics ,Botany ,ITS nrDNA barcode ,Ecology, Evolution, Behavior and Systematics ,Olea capensis ,Eugenia capensis ,0303 health sciences ,Ecology ,biology ,Pittosporum tenuifolium ,Biology and Life Sciences ,CLADOSPORIUM ,FUNGOS ,BAYESIAN PHYLOGENETIC INFERENCE ,TAXONOMY ,15. Life on land ,Plant litter ,biology.organism_classification ,Eucalyptus ,Corymbia ficifolia ,GUMMY STEM BLIGHT ,SP-NOV ,Geastrum - Abstract
Las nuevas especies de hongos descritas en este estudio incluyen las de varios países de la siguiente manera: Antártida, Apenidiella antarctica de permafrost, Cladosporium fildesense de una esponja marina no identificada. Argentina, Geastrum wrightii sobre humus en bosque mixto. Australia, Golovinomyces glandulariae en Glandularia aristigera, Neoanungitea eucalyptorum en hojas de Eucalyptus grandis, Teratosphaeria corymbiicola en hojas de Corymbia ficifolia, Xylaria eucalypti en hojas de Eucalyptus radiata. Brasil, Bovista psammophila en suelo, Fusarium awaxy en tallos podridos de Zea mays, Geastrum lanuginosum en suelo cubierto de hojarasca, Hermetothecium mikaniae-micranthae (incl. Hermetothecium gen. Nov.) En Mikania micrantha, Penicillium reconvexovelosoi en suelo, Stagonoscciiops de podnacciiopsis de glicina máx. Islas Vírgenes Británicas, Lactifluus guanensis en suelo., Novel species of fungi described in this study include those from various countries as follows: Antarctica , Apenidiella antarctica from permafrost, Cladosporium fildesense from an unidentified marine sponge. Argentina , Geastrum wrightii on humus in mixed forest. Australia , Golovinomyces glandulariae on Glandularia aristigera, Neoanungitea eucalyptorum on leaves of Eucalyptus grandis, Teratosphaeria corymbiicola on leaves of Corymbia ficifolia, Xylaria eucalypti on leaves of Eucalyptus radiata. Brazil , Bovista psammophila on soil, Fusarium awaxy on rotten stalks of Zea mays, Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae (incl. Hermetothecium gen. nov.)on Mikania micrantha, Penicillium reconvexovelosoi in soil, Stagonosporopsis vannaccii from pod of Glycine max. British Virgin Isles, Lactifluus guanensis on soil. Canada , Sorocybe oblongispora on resin of Picea rubens. Chile , Colletotrichum roseum on leaves of Lapageria rosea. China, Setophoma caverna from carbonatite in Karst cave. Colombia , Lareunionomyces eucalypticola on leaves of Eucalyptus grandis. Costa Rica , Psathyrella pivae on wood. Cyprus, Clavulina iris on calcareous substrate. France, Chromosera ambigua and Clavulina iris var. occidentalis on soil. French West Indies, Helminthosphaeria hispidissima on dead wood. Guatemala , Talaromyces guatemalensis in soil. Malaysia, Neotracylla pini (incl. Tracyllales ord. nov. and Neotra- cylla gen. nov.)and Vermiculariopsiella pini on needles of Pinus tecunumanii. New Zealand , Neoconiothyrium viticola on stems of Vitis vinifera, Parafenestella pittospori on Pittosporum tenuifolium, Pilidium novae-zelandiae on Phoenix sp. Pakistan , Russula quercus-floribundae on forest floor. Portugal, Trichoderma aestuarinum from saline water. Russia, Pluteus liliputianus on fallen branch of deciduous tree, Pluteus spurius on decaying deciduous wood or soil. South Africa, Alloconiothyrium encephalarti, Phyllosticta encephalarticola and Neothyrostroma encephalarti (incl. Neothyrostroma gen. nov.)on leaves of Encephalartos sp., Chalara eucalypticola on leaf spots of Eucalyptus grandis × urophylla, Clypeosphaeria oleae on leaves of Olea capensis, Cylindrocladiella postalofficium on leaf litter of Sideroxylon inerme, Cylindromonium eugeniicola (incl. Cylindromonium gen. nov.)on leaf litter of Eugenia capensis, Cyphellophora goniomatis on leaves of Gonioma kamassi, Nothodactylaria nephrolepidis (incl. Nothodactylaria gen. nov. and Nothodactylariaceae fam. nov.)on leaves of Nephrolepis exaltata , Falcocladium eucalypti and Gyrothrix eucalypti on leaves of Eucalyptus sp., Gyrothrix oleae on leaves of Olea capensis subsp. macrocarpa, Harzia metrosideri on leaf litter of Metrosideros sp., Hippopotamyces phragmitis (incl. Hippopota-myces gen. nov.)on leaves of Phragmites australis, Lectera philenopterae on Philenoptera violacea , Leptosillia mayteni on leaves of Maytenus heterophylla , Lithohypha aloicola and Neoplatysporoides aloes on leaves of Aloe sp., Millesimomyces rhoicissi (incl. Millesimomyces gen. nov.) on leaves of Rhoicissus digitata, Neodevriesia strelitziicola on leaf litter of Strelitzia nicolai, Neokirramyces syzygii (incl. Neokirramyces gen. nov.)on leaf spots of Syzygium sp., Nothoramichloridium perseae (incl. Nothoramichloridium gen.nov.and Anungitiomycetaceae fam. nov.)on leaves of Persea americana, Paramycosphaerella watsoniae on leaf spots of Watsonia sp., Penicillium cuddlyae from dog food, Podocarpomyces knysnanus (incl. Podocarpomyces, gen.nov.)on leaves of Podocarpus falcatus, Pseudocercospora heteropyxidicola on leaf spots of Heteropyxis natalensis, Pseudopenidiella podocarpi, Scolecobasidium podocarpi and Ceramothyrium podocarpicola on leaves of Podocarpus latifolius, Scolecobasidium blechni on leaves of Blechnum capense, Stomiopeltis syzygii on leaves of Syzygium chordatum, Strelitziomyces knysnanus (incl. Strelitziomyces gen.nov.)on leaves of Strelitzia alba, Talaromyces clemensii from rotting wood in goldmine, Verrucocladosporium visseri on Carpobrotus edulis. Spain, Boletopsis mediterraneensis on soil, Calycina cortegadensisi on a living twig of Castanea sativa, Emmonsiellopsis tuberculata in fluvial sediments, Mollisia cor-tegadensis on dead attached twig of Quercus robur, Psathyrella ovispora on soil, Pseudobeltrania lauri on leaf litter of Laurus azorica, Terfezia dunensis in soil, Tuber lucentum in soil, Venturia submersa on submerged plant debris. Thailand,/b>, Cordyceps jakajanicola on cicada nymph, Cordyceps kuiburiensis on spider, Distoseptispora caricis on leaves of Carex sp., Ophiocordyceps khonkaenensis on cicada nymph. USA, Cytosporella juncicola and Davidiello- myces juncicola on culms of Juncus effusus, Monochaetia massachusettsianum from air sample, Neohelicomyces melaleucae and Periconia neobrittanica on leaves of Melaleuca styphelioides ?? lanceolata, Pseudocamarosporium eucalypti on leaves of Eucalyptus sp., Pseudogymnoascus lindneri from sediment in a mine, Pseudogymnoascus turneri from sediment in a railroad tunnel, Pulchroboletus sclerotiorum on soil, Zygosporium pseudomasonii on leaf of Serenoa repens. Vietnam, Boletus candidissimus and Veloporphyrellus vulpinus on soil.Morphological and culture characteristics are supported by DNA barcodes.
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- 2019
11. Dynamics of chemical diversity during co-cultures : an integrative time-scale metabolomics study of fungal endophytes Cophinforma mamane and Fusarium solani
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Triastuti, A., Haddad, Mohamed, Barakat, F., Mejia, K., Rabouille, G., Fabre, N., Amasifuen, C., Jargeat, P., and Vansteelandt, M.
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Cophinforma mamane ,time-scale analysis ,co-cultures ,metabolomics ,Fusarium solani - Abstract
A rapid and efficient metabolomic study of Cophinforma mamane and Fusarium solani co-cultivation in time-series based analysis was developed to study metabolome variations during their fungal interactions. The fungal metabolomes were studied through the integration of four metabolomic tools: MS-DIAL, a chromatographic deconvolution of liquid-chromatography-mass spectrometry (LC/MS); MS-FINDER, a structure-elucidation program with a wide range metabolome database; GNPS, an effective method to organize MS/MS fragmentation spectra, and MetaboAnalyst, a comprehensive web application for metabolomic data analysis and interpretation. Co-cultures of C. mamane and F. solani induced different patterns of metabolite production over 10 days of incubation and induced production of five de novo compounds not occurring in monocultures. These results emphasize that co-culture in time-frame analysis is an interesting method to unravel hidden metabolome in the investigation of fungal chemodiversity.
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- 2020
12. Fungal Planet description sheets: 951–1041
- Author
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Crous, P.W., primary, Wingfield, M.J., additional, Lombard, L., additional, Roets, F., additional, Swart, W.J., additional, Alvarado, P., additional, Carnegie, A.J., additional, Moreno, G., additional, Luangsa-Ard, J., additional, Thangavel, R., additional, Alexandrova, A.V., additional, Baseia, I.G., additional, Bellanger, J.-M., additional, Bessette, A.E., additional, Bessette, A.R., additional, Delapeña-Lastra, S., additional, García, D., additional, Gené, J., additional, Pham, T.H.G., additional, Heykoop, M., additional, Malysheva, E., additional, Malysheva, V., additional, Martín, M.P., additional, Morozova, O.V., additional, Noisripoom, W., additional, Overton, B.E., additional, Rea, A.E., additional, Sewall, B.J., additional, Smith, M.E., additional, Smyth, C.W., additional, Tasanathai, K., additional, Visagie, C.M., additional, Adamík, S., additional, Alves, A., additional, Andrade, J.P., additional, Aninat, M.J., additional, Araújo, R.V.B., additional, Bordallo, J.J., additional, Boufleur, T., additional, Baroncelli, R., additional, Barreto, R.W., additional, Bolin, J., additional, Cabero, J., additional, Cabo, M., additional, Cafà, G., additional, Caffot, M.L.H., additional, Cai, L., additional, Carlavilla, J.R., additional, Chávez, R., additional, Decastro, R.R.L., additional, Delgat, L., additional, Deschuyteneer, D., additional, Dios, M.M., additional, Domínguez, L.S., additional, Evans, H.C., additional, Eyssartier, G., additional, Ferreira, B.W., additional, Figueiredo, C.N., additional, Liu, F., additional, Fournier, J., additional, Galli-Terasawa, L.V., additional, Gil-Durán, C., additional, Glienke, C., additional, Gonçalves, M.F.M., additional, Gryta, H., additional, Guarro, J., additional, Himaman, W., additional, Hywel-Jones, N., additional, Iturrieta-González, I., additional, Ivanushkina, N.E., additional, Jargeat, P., additional, Khalid, A.N., additional, Khan, J., additional, Kiran, M., additional, Kiss, L., additional, Kochkina, G.A., additional, Kolaík, M., additional, Kubátová, A., additional, Lodge, D.J., additional, Loizides, M., additional, Luque, D., additional, Manjón, J.L., additional, Marbach, P.A.S., additional, Massolajr, N.S., additional, Mata, M., additional, Miller, A.N., additional, Mongkolsamrit, S., additional, Moreau, P.-A., additional, Morte, A., additional, Mujic, A., additional, Navarro-Ródenas, A., additional, Németh, M.Z., additional, Nóbrega, T.F., additional, Nováková, A., additional, Olariaga, I., additional, Ozerskaya, S.M., additional, Palma, M.A., additional, Petters-Vandresen, D.A.L., additional, Piontelli, E., additional, Popov, E.S., additional, Rodríguez, A., additional, Requejo, Ó, additional, Rodrigues, A.C.M., additional, Rong, I.H., additional, Roux, J., additional, Seifert, K.A., additional, Silva, B.D.B., additional, Sklená, F., additional, Smith, J.A., additional, Sousa, J.O., additional, Souza, H.G., additional, Desouza, J.T., additional, Vec, K., additional, Tanchaud, P., additional, Tanney, J.B., additional, Terasawa, F., additional, Thanakitpipattana, D., additional, Torres-Garcia, D., additional, Vaca, I., additional, Vaghefi, N., additional, Vaniperen, A.L., additional, Vasilenko, O.V., additional, Verbeken, A., additional, Yilmaz, N., additional, Zamora, J.C., additional, Zapata, M., additional, Jurjević, Ž, additional, and Groenewald, J.Z., additional
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- 2019
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13. How histone deacetylase inhibitors alter the secondary metabolites of Botryosphaeria mamane, an endophytic fungus isolated fromllana Bixa orellana
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Triastuti, A., Vansteelandt, M., Barakat, F., Trinel, M., Jargeat, P., Fabre, N., Guerra, C. A. A., Mejia, K., Valentin, A., and Haddad, Mohamed
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epigenetic modifier ,Botryosphaeria mamane ,Bixa orellana ,suberoylanilide hydroxamic acid (SAHA) ,sodium valproate - Abstract
Fungi are talented organisms able to produce several natural products with a wide range of structural and pharmacological activities. The conventional fungal cultivation used in laboratories is too poor to mimic the natural habitats of fungi, and this can partially explain why most of the genes responsible for the production of metabolites are transcriptionally silenced. The use of Histone Deacetylase inhibitors (HDACis) to perturb fungal secondary biosynthetic machinery has proven to be an effective approach for discovering new fungal natural products. The present study relates the effects of suberoylanilide hydroxamic acid (SAHA) and sodium valproate (VS) on the metabolome of Botryosphaeria mamane, an endophytic fungus isolated from Bixa orellana L. UHPLC/HR-MS analysis, integrated with four metabolomics tools: MS-DIAL, MS-FINDER, MetaboAnalyst and GNPS molecular networking, was established. This study highlighted that SAHA and VS changed metabolites in B. mamane, causing upregulation and downregulation of metabolites production. In addition, twelve compounds were detected in the extracts as metabolites structurally correlated to SAHA, indicating its important reactivity in the medium or its metabolism by the fungus. An addition of SAHA induced the production of eight metabolites while VS induced only two metabolites undetected in the control strain. This result illustrates the importance of adding HDACis to a fungal culture in order to induce metabolite production.
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- 2019
14. Fungal Planet description sheets : 951-1041
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Crous, P. W., Wingfield, M. J., Lombard, L., Roets, F., Swart, W. J., Alvarado, P., Carnegie, A. J., Moreno, G., Luangsa-ard, J., Thangavel, R., Alexandrova, A. V., Baseia, I. G., Bellanger, J. -M, Bessette, A. E., Bessette, A. R., De la Pena-Lastra, S., Garcia, D., Gene, J., Pham, T. H. G., Heykoop, M., Malysheva, E., Malysheva, V., Martin, M. P., Morozova, O. V., Noisripoom, W., Overton, B. E., Rea, A. E., Sewall, B. J., Smith, M. E., Smyth, C. W., Tasanathai, K., Visagie, C. M., Adamcik, S., Alves, A., Andrade, J. P., Aninat, M. J., Araujo, R. V. B., Bordallo, J. J., Boufleur, T., Baroncelli, R., Barreto, R. W., Bolin, J., Cabero, J., Cabon, M., Cafa, G., Caffot, M. L. H., Cai, L., Carlavilla, J. R., Chavez, R., de Castro, R. R. L., Delgat, L., Deschuyteneer, D., Dios, M. M., Dominguez, L. S., Evans, H. C., Eyssartier, G., Ferreira, B. W., Figueiredo, C. N., Liu, F., Fournier, J., Galli-Terasawa, L. V., Gil-Duran, C., Glienke, C., Goncalves, M. F. M., Gryta, H., Guarro, J., Himaman, W., Hywel-Jones, N., Iturrieta-Gonzalez, I., Ivanushkina, N. E., Jargeat, P., Khalid, A. N., Khan, J., Kiran, M., Kiss, L., Kochkina, G. A., Kolarik, M., Kubatova, A., Lodge, D. J., Loizides, M., Luque, D., Manjon, J. L., Marbach, P. A. S., Massola, N. S., Jr., Mata, M., Miller, A. N., Mongkolsamrit, S., Moreau, P. -A, Morte, A., Mujic, A., Navarro-Rodenas, A., Nemeth, M. Z., Nobrega, T. F., Novakova, A., Olariaga, I., Ozerskaya, S. M., Palma, M. A., Petters-Vandresen, D. A. L., Piontelli, E., Popov, E. S., Rodriguez, A., Requejo, O., Rodrigues, A. C. M., Rong, I. H., Roux, J., Seifert, K. A., Silva, B. D. B., Sklenar, F., Smith, J. A., Sousa, J. O., Souza, H. G., De Souza, J. T., Svec, K., Tanchaud, P., Tanney, J. B., Terasawa, F., Thanakitpipattana, D., Torres-Garcia, D., Vaca, I., Vaghefi, N., van Iperen, A. L., Vasilenko, O. V., Verbeken, A., Yilmaz, N., Zamora, Juan Carlos, Zapata, M., Jurjevic, Z., Groenewald, J. Z., Crous, P. W., Wingfield, M. J., Lombard, L., Roets, F., Swart, W. J., Alvarado, P., Carnegie, A. J., Moreno, G., Luangsa-ard, J., Thangavel, R., Alexandrova, A. V., Baseia, I. G., Bellanger, J. -M, Bessette, A. E., Bessette, A. R., De la Pena-Lastra, S., Garcia, D., Gene, J., Pham, T. H. G., Heykoop, M., Malysheva, E., Malysheva, V., Martin, M. P., Morozova, O. V., Noisripoom, W., Overton, B. E., Rea, A. E., Sewall, B. J., Smith, M. E., Smyth, C. W., Tasanathai, K., Visagie, C. M., Adamcik, S., Alves, A., Andrade, J. P., Aninat, M. J., Araujo, R. V. B., Bordallo, J. J., Boufleur, T., Baroncelli, R., Barreto, R. W., Bolin, J., Cabero, J., Cabon, M., Cafa, G., Caffot, M. L. H., Cai, L., Carlavilla, J. R., Chavez, R., de Castro, R. R. L., Delgat, L., Deschuyteneer, D., Dios, M. M., Dominguez, L. S., Evans, H. C., Eyssartier, G., Ferreira, B. W., Figueiredo, C. N., Liu, F., Fournier, J., Galli-Terasawa, L. V., Gil-Duran, C., Glienke, C., Goncalves, M. F. M., Gryta, H., Guarro, J., Himaman, W., Hywel-Jones, N., Iturrieta-Gonzalez, I., Ivanushkina, N. E., Jargeat, P., Khalid, A. N., Khan, J., Kiran, M., Kiss, L., Kochkina, G. A., Kolarik, M., Kubatova, A., Lodge, D. J., Loizides, M., Luque, D., Manjon, J. L., Marbach, P. A. S., Massola, N. S., Jr., Mata, M., Miller, A. N., Mongkolsamrit, S., Moreau, P. -A, Morte, A., Mujic, A., Navarro-Rodenas, A., Nemeth, M. Z., Nobrega, T. F., Novakova, A., Olariaga, I., Ozerskaya, S. M., Palma, M. A., Petters-Vandresen, D. A. L., Piontelli, E., Popov, E. S., Rodriguez, A., Requejo, O., Rodrigues, A. C. M., Rong, I. H., Roux, J., Seifert, K. A., Silva, B. D. B., Sklenar, F., Smith, J. A., Sousa, J. O., Souza, H. G., De Souza, J. T., Svec, K., Tanchaud, P., Tanney, J. B., Terasawa, F., Thanakitpipattana, D., Torres-Garcia, D., Vaca, I., Vaghefi, N., van Iperen, A. L., Vasilenko, O. V., Verbeken, A., Yilmaz, N., Zamora, Juan Carlos, Zapata, M., Jurjevic, Z., and Groenewald, J. Z.
- Abstract
Novel species of fungi described in this study include those from various countries as follows: Antarctica,Apenidiella antarctica from permafrost, Cladosporium fildesense from an unidentified marine sponge. Argentina,Geastrum wrightii on humus in mixed forest. Australia, Golovinomyces glandulariae on Glandularia aristigera,Neoanungitea eucalyptorum on leaves of Eucalyptus grandis, Teratosphaeria corymbiicola on leaves of Corymbiaficifolia, Xylaria eucalypti on leaves of Eucalyptus radiata. Brazil, Bovista psammophila on soil, Fusarium awaxy onrotten stalks of Zea mays, Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae(incl. Hermetothecium gen. nov.) on Mikania micrantha, Penicillium reconvexovelosoi in soil, Stagonosporopsis vannacciifrom pod of Glycine max. British Virgin Isles, Lactifluus guanensis on soil. Canada, Sorocybe oblongisporaon resin of Picea rubens. Chile, Colletotrichum roseum on leaves of Lapageria rosea. China, Setophoma cavernafrom carbonatite in Karst cave. Colombia, Lareunionomyces eucalypticola on leaves of Eucalyptus grandis. CostaRica, Psathyrella pivae on wood. Cyprus, Clavulina iris on calcareous substrate. France, Chromosera ambiguaand Clavulina iris var. occidentalis on soil. French West Indies, Helminthosphaeria hispidissima on dead wood.Guatemala, Talaromyces guatemalensis in soil. Malaysia, Neotracylla pini (incl. Tracyllales ord. nov. and Neotracyllagen. nov.) and Vermiculariopsiella pini on needles of Pinus tecunumanii. New Zealand, Neoconiothyriumviticola on stems of Vitis vinifera, Parafenestella pittospori on Pittosporum tenuifolium, Pilidium novae-zelandiaeon Phoenix sp. Pakistan, Russula quercus-floribundae on forest floor. Portugal, Trichoderma aestuarinum fromsaline water. Russia, Pluteus liliputianus on fallen branch of deciduous tree, Pluteus spurius on decaying deciduous wood or soil. South Africa, Alloconiothyrium encephalarti, Phyllosticta encephalarticola and Neothyrostromaencephalarti (
- Published
- 2019
- Full Text
- View/download PDF
15. Fungal Planet description sheets: 951-1041
- Author
-
Crous, P.W., Wingfield, M.J., Lombard, L., Roets, F., Swart, W.J., Alvarado, P., Carnegie, A.J., Moreno, G., Luangsa-ard, J., Thangavel, R., Alexandrova, A.V., Baseia, I.G., Bellanger, J.-M., Bessette, A.E., Bessette, A.R., De la Peña-Lastra, S., García, D., Gené, J., Pham, T.H.G., Heykoop, M., Malysheva, E., Malysheva, V., Martín, M.P., Morozova, O.V., Noisripoom, W., Overton, B.E., Rea, A.E., Sewall, B.J., Smith, M.E., Smyth, C.W., Tasanathai, K., Visagie, C.M., Adamčík, S., Alves, A., Andrade, J.P., Aninat, M.J., Araujo, R.V.B., Bordallo, J.J., Bonfleur, T., Baroncelli, R., Barreto, R.W., Bolin, J., Cabero, J., M. Caboň, M., Cafà, G., Caffot, M.L.H., Cai, L., Carlavilla, J.R., Chávez, R., de Castro, R.R.L., Delgat, L., Deschuyteneer, D., Dios, M.M., Domínguez, L.S., Evans, H.C., Eyssartier, G., Ferreira, B.W., Figueiredo, C.N., Liu, F., Fournier, J., Galli-Terasawa, L.V., Gil-Durán, C., Glienke, C., Gonçalves, M.F.M., Gryta, H., Guarro, J., Himaman, W., Hywel-Jones, N., Iturrieta-González, I., Ivanushkina, N.E., Jargeat, P., Khalid, A.N., Khan, J., Kiran, M., Kiss, L., Kochkina, G.A., Kolařík, M., Kubátová, A., Lodge, D.J., Loizides, M., Luque, D., Manjón, J.L., Marbach, P.A.S., Massola Jr, N.S., Mata, M., Miller, A.N., Mongkolsamrit, S., Moreau, P.-A., Morte, A., Mujic, A., Navarro-Ródenas, A., Németh, M.Z., Nóbrega, T.F., Nováková, A., Olariaga, I., Ozerskaya, S.M., Palma, M.A., Petters-Vandresen, D.A.L., Piontelli, E., Popov, E.S., Rodríguez, A., Requejo, Ó., Rodrigues, A.C.M., Rong, I.H., Roux, J., Seifert, K.A., Silva, B.D.B., Sklenář, F., Smith, J.A., Sousa, J.O., Souza, H.G., De Souza, J.T., Švec, K., Tanchaud, P., Tanney, J.B., Terasawa, F., Thanakitpipattana, D., Torres-Garcia, D., Vaca, I., Vaghefi, N., van Iperen, A.L., Vasilenko, O.V., Verbeken, A., Yilmaz, N., Zamora, J.C., Zapata, M., Jurjević, Ž., Groenewald, J.Z., Crous, P.W., Wingfield, M.J., Lombard, L., Roets, F., Swart, W.J., Alvarado, P., Carnegie, A.J., Moreno, G., Luangsa-ard, J., Thangavel, R., Alexandrova, A.V., Baseia, I.G., Bellanger, J.-M., Bessette, A.E., Bessette, A.R., De la Peña-Lastra, S., García, D., Gené, J., Pham, T.H.G., Heykoop, M., Malysheva, E., Malysheva, V., Martín, M.P., Morozova, O.V., Noisripoom, W., Overton, B.E., Rea, A.E., Sewall, B.J., Smith, M.E., Smyth, C.W., Tasanathai, K., Visagie, C.M., Adamčík, S., Alves, A., Andrade, J.P., Aninat, M.J., Araujo, R.V.B., Bordallo, J.J., Bonfleur, T., Baroncelli, R., Barreto, R.W., Bolin, J., Cabero, J., M. Caboň, M., Cafà, G., Caffot, M.L.H., Cai, L., Carlavilla, J.R., Chávez, R., de Castro, R.R.L., Delgat, L., Deschuyteneer, D., Dios, M.M., Domínguez, L.S., Evans, H.C., Eyssartier, G., Ferreira, B.W., Figueiredo, C.N., Liu, F., Fournier, J., Galli-Terasawa, L.V., Gil-Durán, C., Glienke, C., Gonçalves, M.F.M., Gryta, H., Guarro, J., Himaman, W., Hywel-Jones, N., Iturrieta-González, I., Ivanushkina, N.E., Jargeat, P., Khalid, A.N., Khan, J., Kiran, M., Kiss, L., Kochkina, G.A., Kolařík, M., Kubátová, A., Lodge, D.J., Loizides, M., Luque, D., Manjón, J.L., Marbach, P.A.S., Massola Jr, N.S., Mata, M., Miller, A.N., Mongkolsamrit, S., Moreau, P.-A., Morte, A., Mujic, A., Navarro-Ródenas, A., Németh, M.Z., Nóbrega, T.F., Nováková, A., Olariaga, I., Ozerskaya, S.M., Palma, M.A., Petters-Vandresen, D.A.L., Piontelli, E., Popov, E.S., Rodríguez, A., Requejo, Ó., Rodrigues, A.C.M., Rong, I.H., Roux, J., Seifert, K.A., Silva, B.D.B., Sklenář, F., Smith, J.A., Sousa, J.O., Souza, H.G., De Souza, J.T., Švec, K., Tanchaud, P., Tanney, J.B., Terasawa, F., Thanakitpipattana, D., Torres-Garcia, D., Vaca, I., Vaghefi, N., van Iperen, A.L., Vasilenko, O.V., Verbeken, A., Yilmaz, N., Zamora, J.C., Zapata, M., Jurjević, Ž., and Groenewald, J.Z.
- Abstract
Novel species of fungi described in this study include those from various countries as follows: Antarctica, Apenidiella antarctica from permafrost, Cladosporium fildesense from an unidentified marine sponge. Argentina, Geastrum wrightii on humus in mixed forest. Australia, Golovinomyces glandulariae on Glandularia aristigera, Neoanungitea eucalyptorum on leaves of Eucalyptus grandis, Teratosphaeria corymbiicola on leaves of Corymbia ficifolia, Xylaria eucalypti on leaves of Eucalyptus radiata. Brazil, Bovista psammophila on soil, Fusarium awaxy on rotten stalks of Zea mays, Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae (incl. Hermetothecium gen. nov.) on Mikania micrantha, Penicillium reconvexovelosoi in soil, Stagonosporopsis vannaccii from pod of Glycine max. British Virgin Isles, Lactifluus guanensis on soil. Canada, Sorocybe oblongispora on resin of Picea rubens. Chile, Colletotrichum roseum on leaves of Lapageria rosea. China, Setophoma caverna from carbonatite in Karst cave. Colombia, Lareunionomyces eucalypticola on leaves of Eucalyptus grandis. Costa Rica, Psathyrella pivae on wood. Cyprus, Clavulina iris on calcareous substrate. France, Chromosera ambigua and Clavulina iris var. occidentalis on soil. French West Indies, Helminthosphaeria hispidissima on dead wood. Guatemala, Talaromyces guatemalensis in soil. Malaysia, Neotracylla pini (incl. Tracyllales ord. nov. and Neotracylla gen. nov.) and Vermiculariopsiella pini on needles of Pinus tecunumanii. New Zealand, Neoconiothyrium viticola on stems of Vitis vinifera
- Published
- 2019
16. Fungal Planet description sheets: 951-1041
- Author
-
Crous, PW, Wingfield, MJ, Lombard, L, Roets, F, Swart, WJ, Alvarado, P, Carnegie, AJ, Moreno, G, Luangsa-ard, J, Thangavel, R, Alexandrova, AV, Baseia, IG, Bellanger, J-M, Bessette, AE, Bessette, AR, De la Pena-Lastra, S, Garcia, D, Gene, J, Pham, THG, Heykoop, M, Malysheva, E, Malysheva, V, Martin, MP, Morozova, OV, Noisripoom, W, Overton, BE, Rea, AE, Sewall, BJ, Smith, ME, Smyth, CW, Tasanathai, K, Visagie, CM, Adamcik, S, Alves, A, Andrade, JP, Aninat, MJ, Araujo, RVB, Bordallo, JJ, Boufleur, T, Baroncelli, R, Barreto, RW, Bolin, J, Cabero, J, Cabon, M, Cafa, G, Caffot, MLH, Cai, L, Carlavilla, JR, Chavez, R, de Castro, RRL, Delgat, L, Deschuyteneer, D, Dios, MM, Dominguez, LS, Evans, HC, Eyssartier, G, Ferreira, BW, Figueiredo, CN, Liu, F, Fournier, J, Galli-Terasawa, LV, Gil-Duran, C, Glienke, C, Goncalves, MFM, Gryta, H, Guarro, J, Himaman, W, Hywel-Jones, N, Iturrieta-Gonzalez, I, Ivanushkina, NE, Jargeat, P, Khalid, AN, Khan, J, Kiran, M, Kiss, L, Kochkina, GA, Kolarik, M, Kubatova, A, Lodge, DJ, Loizides, M, Luque, D, Manjon, JL, Marbach, PAS, Massola, NS, Mata, M, Miller, AN, Mongkolsamrit, S, Moreau, P-A, Morte, A, Mujic, A, Navarro-Rodenas, A, Nemeth, MZ, Nobrega, TF, Novakova, A, Olariaga, I, Ozerskaya, SM, Palma, MA, Petters-Vandresen, DAL, Piontelli, E, Popov, ES, Rodriguez, A, Requejo, O, Rodrigues, ACM, Rong, IH, Roux, J, Seifert, KA, Silva, BDB, Sklenar, F, Smith, JA, Sousa, JO, Souza, HG, De Souza, JT, Svec, K, Tanchaud, P, Tanney, JB, Terasawa, F, Thanakitpipattana, D, Torres-Garcia, D, Vaca, I, Vaghefi, N, van Iperen, AL, Vasilenko, OV, Verbeken, A, Yilmaz, N, Zamora, JC, Zapata, M, Jurjevic, Z, Groenewald, JZ, Crous, PW, Wingfield, MJ, Lombard, L, Roets, F, Swart, WJ, Alvarado, P, Carnegie, AJ, Moreno, G, Luangsa-ard, J, Thangavel, R, Alexandrova, AV, Baseia, IG, Bellanger, J-M, Bessette, AE, Bessette, AR, De la Pena-Lastra, S, Garcia, D, Gene, J, Pham, THG, Heykoop, M, Malysheva, E, Malysheva, V, Martin, MP, Morozova, OV, Noisripoom, W, Overton, BE, Rea, AE, Sewall, BJ, Smith, ME, Smyth, CW, Tasanathai, K, Visagie, CM, Adamcik, S, Alves, A, Andrade, JP, Aninat, MJ, Araujo, RVB, Bordallo, JJ, Boufleur, T, Baroncelli, R, Barreto, RW, Bolin, J, Cabero, J, Cabon, M, Cafa, G, Caffot, MLH, Cai, L, Carlavilla, JR, Chavez, R, de Castro, RRL, Delgat, L, Deschuyteneer, D, Dios, MM, Dominguez, LS, Evans, HC, Eyssartier, G, Ferreira, BW, Figueiredo, CN, Liu, F, Fournier, J, Galli-Terasawa, LV, Gil-Duran, C, Glienke, C, Goncalves, MFM, Gryta, H, Guarro, J, Himaman, W, Hywel-Jones, N, Iturrieta-Gonzalez, I, Ivanushkina, NE, Jargeat, P, Khalid, AN, Khan, J, Kiran, M, Kiss, L, Kochkina, GA, Kolarik, M, Kubatova, A, Lodge, DJ, Loizides, M, Luque, D, Manjon, JL, Marbach, PAS, Massola, NS, Mata, M, Miller, AN, Mongkolsamrit, S, Moreau, P-A, Morte, A, Mujic, A, Navarro-Rodenas, A, Nemeth, MZ, Nobrega, TF, Novakova, A, Olariaga, I, Ozerskaya, SM, Palma, MA, Petters-Vandresen, DAL, Piontelli, E, Popov, ES, Rodriguez, A, Requejo, O, Rodrigues, ACM, Rong, IH, Roux, J, Seifert, KA, Silva, BDB, Sklenar, F, Smith, JA, Sousa, JO, Souza, HG, De Souza, JT, Svec, K, Tanchaud, P, Tanney, JB, Terasawa, F, Thanakitpipattana, D, Torres-Garcia, D, Vaca, I, Vaghefi, N, van Iperen, AL, Vasilenko, OV, Verbeken, A, Yilmaz, N, Zamora, JC, Zapata, M, Jurjevic, Z, and Groenewald, JZ
- Abstract
Novel species of fungi described in this study include those from various countries as follows: Antarctica, Apenidiella antarctica from permafrost, Cladosporium fildesense from an unidentified marine sponge. Argentina, Geastrum wrightii on humus in mixed forest. Australia, Golovinomyces glandulariae on Glandularia aristigera, Neoanungitea eucalyptorum on leaves of Eucalyptus grandis, Teratosphaeria corymbiicola on leaves of Corymbia ficifolia, Xylaria eucalypti on leaves of Eucalyptus radiata. Brazil, Bovista psammophila on soil, Fusarium awaxy on rotten stalks of Zea mays, Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae (incl. Hermetothecium gen. nov.) on Mikania micrantha, Penicillium reconvexovelosoi in soil, Stagonosporopsis vannaccii from pod of Glycine max. British Virgin Isles, Lactifluus guanensis on soil. Canada, Sorocybe oblongispora on resin of Picea rubens. Chile, Colletotrichum roseum on leaves of Lapageria rosea. China, Setophoma caverna from carbonatite in Karst cave. Colombia, Lareunionomyces eucalypticola on leaves of Eucalyptus grandis. Costa Rica, Psathyrella pivae on wood. Cyprus, Clavulina iris on calcareous substrate. France, Chromosera ambigua and Clavulina iris var. occidentalis on soil. French West Indies, Helminthosphaeria hispidissima on dead wood. Guatemala, Talaromyces guatemalensis in soil. Malaysia, Neotracylla pini (incl. Tracyllales ord. nov. and Neotracylla gen. nov.) and Vermiculariopsiella pini on needles of Pinus tecunumanii. New Zealand, Neoconiothyrium viticola on stems of Vitis vinifera, Parafenestella pittospori on Pittosporum tenuifolium, Pilidium novae-zelandiae on Phoenix sp. Pakistan, Russula quercus-floribundae on forest floor. Portugal, Trichoderma aestuarinum from saline water. Russia, Pluteus liliputianus on fallen branch of deciduous tree, Pluteus spurius on decaying deciduous wood or soil. South Africa, Alloconiothyrium encephalarti, Phyllosticta encephalarticola and Neothyrostro
- Published
- 2019
17. Fungal Planet description sheets: 951-1041
- Author
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Universitat Rovira i Virgili, Crous, P. W.; Wingfield, M. J.; Lombard, L.; Roets, F.; Swart, W. J.; Alvarado, P.; Carnegie, A. J.; Moreno, G.; Luangsa-ard, J.; Thangavel, R.; Alexandrova, A. V.; Baseia, I. G.; Bellanger, J. -M.; Bessette, A. E.; Bessette, A. R.; De la Pena-Lastra, S.; Garcia, D.; Gene, J.; Pham, T. H. G.; Heykoop, M.; Malysheva, E.; Malysheva, V.; Martin, M. P.; Morozova, O. V.; Noisripoom, W.; Overton, B. E.; Rea, A. E.; Sewall, B. J.; Smith, M. E.; Smyth, C. W.; Tasanathai, K.; Visagie, C. M.; Adamcik, S.; Alves, A.; Andrade, J. P.; Aninat, M. J.; Araujo, R. V. B.; Bordallo, J. J.; Boufleur, T.; Baroncelli, R.; Barreto, R. W.; Bolin, J.; Cabero, J.; Cabon, M.; Cafa, G.; Caffot, M. L. H.; Cai, L.; Carlavilla, J. R.; Chavez, R.; de Castro, R. R. L.; Delgat, L.; Deschuyteneer, D.; Dios, M. M.; Dominguez, L. S.; Evans, H. C.; Eyssartier, G.; Ferreira, B. W.; Figueiredo, C. N.; Liu, F.; Fournier, J.; Galli-Terasawa, L. V.; Gil-Duran, C.; Glienke, C.; Goncalves, M. F. M.; Gryta, H.; Guarro, J.; Himaman, W.; Hywel-Jones, N.; Iturrieta-Gonzalez, I.; Ivanushkina, N. E.; Jargeat, P.; Khalid, A. N.; Khan, J.; Kiran, M.; Kiss, L.; Kochkina, G. A.; Kolarik, M.; Kubatova, A.; Lodge, D. J.; Loizides, M.; Luque, D.; Manjon, J. L.; Marbach, P. A. S.; Massola, N. S., Jr.; Mata, M.; Miller, A. N.; Mongkolsamrit, S.; Moreau, P. -A.; Morte, A.; Mujic, A.; Navarro-Rodenas, A.; Nemeth, M. Z.; Nobrega, T. F.; Novakova, A.; Olariaga, I.; Ozerskaya, S. M.; Palma, M. A.; Petters-Vandresen, D. A. L.; Piontelli, E.; Popov, E. S.; Rodriguez, A.; Requejo, O.; Rodrigues, A. C. M.; Rong, I. H.; Roux, J.; Seifert, K. A.; Silva, B. D. B.; Sklenar, F.; Smith, J. A.; Sousa, J. O.; Souza, H. G.; De Souza, J. T.; Svec, K.; Tanchaud, P.; Tanney, J. B.; Terasawa, F.; Thanakitpipattana, D.; Torres-Garcia, D.; Vaca, I.; Va, Universitat Rovira i Virgili, and Crous, P. W.; Wingfield, M. J.; Lombard, L.; Roets, F.; Swart, W. J.; Alvarado, P.; Carnegie, A. J.; Moreno, G.; Luangsa-ard, J.; Thangavel, R.; Alexandrova, A. V.; Baseia, I. G.; Bellanger, J. -M.; Bessette, A. E.; Bessette, A. R.; De la Pena-Lastra, S.; Garcia, D.; Gene, J.; Pham, T. H. G.; Heykoop, M.; Malysheva, E.; Malysheva, V.; Martin, M. P.; Morozova, O. V.; Noisripoom, W.; Overton, B. E.; Rea, A. E.; Sewall, B. J.; Smith, M. E.; Smyth, C. W.; Tasanathai, K.; Visagie, C. M.; Adamcik, S.; Alves, A.; Andrade, J. P.; Aninat, M. J.; Araujo, R. V. B.; Bordallo, J. J.; Boufleur, T.; Baroncelli, R.; Barreto, R. W.; Bolin, J.; Cabero, J.; Cabon, M.; Cafa, G.; Caffot, M. L. H.; Cai, L.; Carlavilla, J. R.; Chavez, R.; de Castro, R. R. L.; Delgat, L.; Deschuyteneer, D.; Dios, M. M.; Dominguez, L. S.; Evans, H. C.; Eyssartier, G.; Ferreira, B. W.; Figueiredo, C. N.; Liu, F.; Fournier, J.; Galli-Terasawa, L. V.; Gil-Duran, C.; Glienke, C.; Goncalves, M. F. M.; Gryta, H.; Guarro, J.; Himaman, W.; Hywel-Jones, N.; Iturrieta-Gonzalez, I.; Ivanushkina, N. E.; Jargeat, P.; Khalid, A. N.; Khan, J.; Kiran, M.; Kiss, L.; Kochkina, G. A.; Kolarik, M.; Kubatova, A.; Lodge, D. J.; Loizides, M.; Luque, D.; Manjon, J. L.; Marbach, P. A. S.; Massola, N. S., Jr.; Mata, M.; Miller, A. N.; Mongkolsamrit, S.; Moreau, P. -A.; Morte, A.; Mujic, A.; Navarro-Rodenas, A.; Nemeth, M. Z.; Nobrega, T. F.; Novakova, A.; Olariaga, I.; Ozerskaya, S. M.; Palma, M. A.; Petters-Vandresen, D. A. L.; Piontelli, E.; Popov, E. S.; Rodriguez, A.; Requejo, O.; Rodrigues, A. C. M.; Rong, I. H.; Roux, J.; Seifert, K. A.; Silva, B. D. B.; Sklenar, F.; Smith, J. A.; Sousa, J. O.; Souza, H. G.; De Souza, J. T.; Svec, K.; Tanchaud, P.; Tanney, J. B.; Terasawa, F.; Thanakitpipattana, D.; Torres-Garcia, D.; Vaca, I.; Va
- Abstract
Novel species of fungi described in this study include those from various countries as follows: Antarctica,Apenidiella antarctica from permafrost, Cladosporium fildesense from an unidentified marine sponge. Argentina,Geastrum wrightii on humus in mixed forest. Australia, Golovinomyces glandulariae on Glandularia aristigera,Neoanungitea eucalyptorum on leaves of Eucalyptus grandis, Teratosphaeria corymbiicola on leaves of Corymbiaficifolia, Xylaria eucalypti on leaves of Eucalyptus radiata. Brazil, Bovista psammophila on soil, Fusarium awaxy onrotten stalks of Zea mays, Geastrum lanuginosum on leaf litter covered soil, Hermetothecium mikaniae-micranthae(incl. Hermetothecium gen. nov.) on Mikania micrantha, Penicillium reconvexovelosoi in soil, Stagonosporopsis vannacciifrom pod of Glycine max. British Virgin Isles, Lactifluus guanensis on soil. Canada, Sorocybe oblongisporaon resin of Picea rubens. Chile, Colletotrichum roseum on leaves of Lapageria rosea. China, Setophoma cavernafrom carbonatite in Karst cave. Colombia, Lareunionomyces eucalypticola on leaves of Eucalyptus grandis. CostaRica, Psathyrella pivae on wood. Cyprus, Clavulina iris on calcareous substrate. France, Chromosera ambiguaand Clavulina iris var. occidentalis on soil. French West Indies, Helminthosphaeria hispidissima on dead wood.Guatemala, Talaromyces guatemalensis in soil. Malaysia, Neotracylla pini (incl. Tracyllales ord. nov. and Neotracyllagen. nov.) and Vermiculariopsiella pini on needles of Pinus tecunumanii. New Zealand, Neoconiothyriumviticola on stems of Vitis vinifera, Parafenestella pittospori on Pittosporum tenuifolium, Pilidium novae-zelandiaeon Phoenix sp. Pakistan, Russula quercus-floribundae on forest floor. Portugal, Trichoderma aestuarinum fromsaline water. Russia, Pluteus liliputi
- Published
- 2019
18. Antiproliferative and antibiofilm potentials of endolichenic fungi associated with the lichen Nephroma laevigatum
- Author
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Lagarde, A., primary, Millot, M., additional, Pinon, A., additional, Liagre, B., additional, Girardot, M., additional, Imbert, C., additional, Ouk, T.S., additional, Jargeat, P., additional, and Mambu, L., additional
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- 2019
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19. Cytotoxic activity of endolichenic fungi isolated from the lichen Nephroma laevigatum
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Lagarde, A, additional, Millot, M, additional, Jargeat, P, additional, Ouk, TS, additional, Sol, V, additional, and Mambu, L, additional
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- 2016
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20. Biodiversity of fungal community associated to lichens active against Candida biofilms
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Jargeat, P, additional, Girardot, M, additional, Rouger, C, additional, Aucher, W, additional, Millot, M, additional, Imbert, C, additional, and Mambu, L, additional
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- 2016
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21. Search for novel metabolites in fungal endophytes: study of Phomopsis sp. and Colletotrichum sp. co-cultivation and Botryosphaeria mamane epigenetic modification
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Triastuti, A, additional, Vansteelandt, M, additional, Barakat, F, additional, Jargeat, P, additional, Rieusset, L, additional, Fabre, N, additional, Amasifuen, C, additional, Valentin, A, additional, and Haddad, M, additional
- Published
- 2016
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22. Inside the medicinal plants: the fungal endophytes, a hidden community as a source of bioactive compounds
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Vansteelandt, Marieke, Jargeat, P, Haddad, Mohamed, Marti, Guillaume, Fabre, Nicolas, Pharmacochimie et Biologie pour le Développement (PHARMA-DEV), Institut de Recherche pour le Développement (IRD)-Institut de Chimie de Toulouse (ICT-FR 2599), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC), Institut de Recherche pour le Développement (IRD)-Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), and Université de Toulouse (UT)
- Subjects
[SDV]Life Sciences [q-bio] ,ComputingMilieux_MISCELLANEOUS - Abstract
International audience
- Published
- 2015
23. Untargeted metabolomics to evaluate antifungal mechanism: a study of Cophinforma mamaneand Candida albicansinteraction
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Triastuti, Asih, Vansteelandt, Marieke, Barakat, Fatima, Amasifuen, Carlos, Jargeat, Patricia, and Haddad, Mohamed
- Abstract
Graphical Abstract:
- Published
- 2023
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24. Metabotyping of Andean pseudocereals and characterization of emerging mycotoxins.
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Vásquez-Ocmín PG, Marti G, Gadea A, Cabanac G, Vásquez-Briones JA, Casavilca-Zambrano S, Ponts N, Jargeat P, Haddad M, and Bertani S
- Subjects
- Edible Grain chemistry, Crops, Agricultural chemistry, Alternaria, Food Contamination analysis, Mycotoxins analysis, Chenopodium quinoa chemistry
- Abstract
Pseudocereals are best known for three crops derived from the Andes: quinoa (Chenopodium quinoa), canihua (C. pallidicaule), and kiwicha (Amaranthus caudatus). Their grains are recognized for their nutritional benefits; however, there is a higher level of polyphenism. Meanwhile, the chemical food safety of pseudocereals remains poorly documented. Here, we applied untargeted and targeted metabolomics approaches by LC-MS to achieve both: i) a comprehensive chemical mapping of pseudocereal samples collected in the Andes; and ii) a quantification of their contents in emerging mycotoxins. An inventory of the fungal community was also realized to better know the fungi present in these grains. Metabotyping permitted to add new insights into the chemotaxonomy of pseudocereals, confirming the previously established phylotranscriptomic clades. Sixteen samples from Peru (out of 27) and one from France (out of one) were contaminated with Beauvericin, an emerging mycotoxin. Several mycotoxigenic fungi were detected, including Aspergillus sp., Penicillium sp., and Alternaria sp., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)
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- 2023
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25. Exploration of the Production of Three Thiodiketopiperazines by an Endophytic Fungal Strain of Cophinforma mamane.
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Pacheco-Tapia R, Ortíz S, Jargeat P, Amasifuen C, Vansteelandt M, and Haddad M
- Subjects
- Bixaceae microbiology, Fungi metabolism, Ascomycota chemistry, Endophytes metabolism, Piperazines chemistry
- Abstract
Endophytic fungi possess a versatile metabolism which is related to their ability to live in diverse ecological niches. While culturing under laboratory conditions, their metabolism is mainly influenced by the culture media, time of incubation and other physicochemical factors. In this study, we focused on the production of 3 thiodiketopiperazines (TDKPs) botryosulfuranols A-C produced by an endophytic strain of Cophinforma mamane isolated from the leaves of Bixa orellana L collected in the Peruvian Amazon. We studied the time-course production of botryosulfuranols A-C during 28 days and evaluated the variations in the production of secondary metabolites, including the TDKPs, produced by C. mamane in response to different culture media, light versus dark conditions and different incubation times. We observed a short time-frame production of botryosulfuranol C while its production was significantly affected by the light conditions and nutrients of the culture media. Botryosulfuranols A and B showed a similar production pattern and a similar response to culturing conditions. Molecular networking allowed us to detect three compounds related to TDKPs that will be the focus of future experiments., (© 2023 Wiley-VHCA AG, Zurich, Switzerland.)
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- 2023
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26. Microbial community associated with the crustose lichen Rhizocarpon geographicum L. (DC.) living on oceanic seashore: A large source of diversity revealed by using multiple isolation methods.
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Miral A, Jargeat P, Mambu L, Rouaud I, Tranchimand S, and Tomasi S
- Subjects
- Phylogeny, Symbiosis, Lichens microbiology, Ascomycota, Microbiota
- Abstract
Recently, the study of the interactions within a microcosm between hosts and their associated microbial communities drew an unprecedented interest arising from the holobiont concept. Lichens, a symbiotic association between a fungus and an alga, are redefined as complex ecosystems considering the tremendous array of associated microorganisms that satisfy this concept. The present study focuses on the diversity of the microbiota associated with the seashore located lichen Rhizocarpon geographicum, recovered by different culture-dependent methods. Samples harvested from two sites allowed the isolation and the molecular identification of 68 fungal isolates distributed in 43 phylogenetic groups, 15 bacterial isolates distributed in five taxonomic groups and three microalgae belonging to two species. Moreover, for 12 fungal isolates belonging to 10 different taxa, the genus was not described in GenBank. These fungal species have never been sequenced or described and therefore non-studied. All these findings highlight the novel and high diversity of the microflora associated with R. geographicum. While many species disappear every day, this work suggests that coastal and wild environments still contain an unrevealed variety to offer and that lichens constitute a great reservoir of new microbial taxa which can be recovered by multiplying the culture-dependent techniques., (© 2022 The Authors. Environmental Microbiology Reports published by Society for Applied Microbiology and John Wiley & Sons Ltd.)
- Published
- 2022
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27. Dynamics of Chemical Diversity during Co-Cultures: An Integrative Time-Scale Metabolomics Study of Fungal Endophytes Cophinforma mamane and Fusarium solani.
- Author
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Triastuti A, Haddad M, Barakat F, Mejia K, Rabouille G, Fabre N, Amasifuen C, Jargeat P, and Vansteelandt M
- Subjects
- Ascomycota chemistry, Ascomycota cytology, Chromatography, High Pressure Liquid, Coculture Techniques, Fusarium chemistry, Fusarium cytology, Metabolomics, Microbial Interactions, Tandem Mass Spectrometry, Ascomycota metabolism, Fusarium metabolism, Metabolome
- Abstract
A rapid and efficient metabolomic study of Cophinforma mamane and Fusarium solani co-cultivation in time-series based analysis was developed to study metabolome variations during their fungal interactions. The fungal metabolomes were studied through the integration of four metabolomic tools: MS-DIAL, a chromatographic deconvolution of liquid-chromatography-mass spectrometry (LC/MS); MS-FINDER, a structure-elucidation program with a wide range metabolome database; GNPS, an effective method to organize MS/MS fragmentation spectra, and MetaboAnalyst, a comprehensive web application for metabolomic data analysis and interpretation. Co-cultures of C. mamane and F. solani induced different patterns of metabolite production over 10 days of incubation and induced production of five de novo compounds not occurring in monocultures. These results emphasize that co-culture in time-frame analysis is an interesting method to unravel hidden metabolome in the investigation of fungal chemodiversity., (© 2020 Wiley-VHCA AG, Zurich, Switzerland.)
- Published
- 2021
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28. Do Host Plant and Associated Ant Species Affect Microbial Communities in Myrmecophytes?
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Ruiz-González MX, Leroy C, Dejean A, Gryta H, Jargeat P, Armijos Carrión AD, and Orivel J
- Abstract
Ant-associated microorganisms can play crucial and often overlooked roles, and given the diversity of interactions that ants have developed, the study of the associated microbiomes is of interest. We focused here on specialist plant-ant species of the genus Allomerus that grow a fungus to build galleries on their host-plant stems. Allomerus -inhabited domatia, thus, might be a rich arena for microbes associated with the ants, the plant, and the fungus. We investigated the microbial communities present in domatia colonised by four arboreal ants: Allomerus decemarticulatus , A. octoarticulatus , A. octoarticulatus var. demerarae , and the non-fungus growing plant-ant Azteca sp. cf. depilis , inhabiting Hirtella physophora or Cordia nodosa in French Guiana. We hypothesized that the microbial community will differ among these species. We isolated microorganisms from five colonies of each species, sequenced the 16S rRNA or Internal TranscribedSpacer (ITS) regions, and described both the alpha and beta diversities. We identified 69 microbial taxa, which belong to five bacterial and two fungal phyla. The most diverse phyla were Proteobacteria and Actinobacteria. The microbial community of Azteca cf. depilis and Allomerus spp. differed in composition and richness. Geographical distance affected microbial communities and richness but plant species did not. Actinobacteria were only associated with Allomerus spp.
- Published
- 2019
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29. The Ectomycorrhizal Fungus Laccaria bicolor Produces Lipochitooligosaccharides and Uses the Common Symbiosis Pathway to Colonize Populus Roots.
- Author
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Cope KR, Bascaules A, Irving TB, Venkateshwaran M, Maeda J, Garcia K, Rush TA, Ma C, Labbé J, Jawdy S, Steigerwald E, Setzke J, Fung E, Schnell KG, Wang Y, Schlief N, Bücking H, Strauss SH, Maillet F, Jargeat P, Bécard G, Puech-Pagès V, and Ané JM
- Subjects
- Calcium-Calmodulin-Dependent Protein Kinases genetics, Gene Expression Regulation, Plant, Lipopolysaccharides chemistry, Mycorrhizae growth & development, Mycorrhizae metabolism, Mycorrhizae physiology, Plant Roots chemistry, Plant Roots growth & development, Plant Roots metabolism, Plants, Genetically Modified, Populus genetics, Populus metabolism, Signal Transduction, Calcium metabolism, Calcium Channels metabolism, Calcium-Calmodulin-Dependent Protein Kinases metabolism, Laccaria metabolism, Lipopolysaccharides metabolism, Plant Roots microbiology, Symbiosis physiology
- Abstract
Mycorrhizal fungi form mutualistic associations with the roots of most land plants and provide them with mineral nutrients from the soil in exchange for fixed carbon derived from photosynthesis. The common symbiosis pathway (CSP) is a conserved molecular signaling pathway in all plants capable of associating with arbuscular mycorrhizal fungi. It is required not only for arbuscular mycorrhizal symbiosis but also for rhizobia-legume and actinorhizal symbioses. Given its role in such diverse symbiotic associations, we hypothesized that the CSP also plays a role in ectomycorrhizal associations. We showed that the ectomycorrhizal fungus Laccaria bicolor produces an array of lipochitooligosaccharides (LCOs) that can trigger both root hair branching in legumes and, most importantly, calcium spiking in the host plant Populus in a CASTOR/POLLUX -dependent manner. Nonsulfated LCOs enhanced lateral root development in Populus in a calcium/calmodulin-dependent protein kinase ( CCaMK )-dependent manner, and sulfated LCOs enhanced the colonization of Populus by L. bicolor Compared with the wild-type Populus , the colonization of CASTOR / POLLUX and CCaMK RNA interference lines by L. bicolor was reduced. Our work demonstrates that similar to other root symbioses, L. bicolor uses the CSP for the full establishment of its mutualistic association with Populus ., (© 2019 American Society of Plant Biologists. All rights reserved.)
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- 2019
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30. How Histone Deacetylase Inhibitors Alter the Secondary Metabolites of Botryosphaeria mamane, an Endophytic Fungus Isolated from Bixa orellana.
- Author
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Triastuti A, Vansteelandt M, Barakat F, Trinel M, Jargeat P, Fabre N, Amasifuen Guerra CA, Mejia K, Valentin A, and Haddad M
- Subjects
- Ascomycota isolation & purification, Dose-Response Relationship, Drug, Histone Deacetylase Inhibitors chemical synthesis, Histone Deacetylase Inhibitors chemistry, Humans, Molecular Structure, Structure-Activity Relationship, Ascomycota chemistry, Bixaceae microbiology, Histone Deacetylase Inhibitors pharmacology, Histone Deacetylases metabolism
- Abstract
Fungi are talented organisms able to produce several natural products with a wide range of structural and pharmacological activities. The conventional fungal cultivation used in laboratories is too poor to mimic the natural habitats of fungi, and this can partially explain why most of the genes responsible for the production of metabolites are transcriptionally silenced. The use of Histone Deacetylase inhibitors (HDACis) to perturb fungal secondary biosynthetic machinery has proven to be an effective approach for discovering new fungal natural products. The present study relates the effects of suberoylanilide hydroxamic acid (SAHA) and sodium valproate (VS) on the metabolome of Botryosphaeria mamane, an endophytic fungus isolated from Bixa orellana L. UHPLC/HR-MS analysis, integrated with four metabolomics tools: MS-DIAL, MS-FINDER, MetaboAnalyst and GNPS molecular networking, was established. This study highlighted that SAHA and VS changed metabolites in B. mamane, causing upregulation and downregulation of metabolites production. In addition, twelve compounds were detected in the extracts as metabolites structurally correlated to SAHA, indicating its important reactivity in the medium or its metabolism by the fungus. An addition of SAHA induced the production of eight metabolites while VS induced only two metabolites undetected in the control strain. This result illustrates the importance of adding HDACis to a fungal culture in order to induce metabolite production., (© 2019 Wiley-VHCA AG, Zurich, Switzerland.)
- Published
- 2019
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31. Thiodiketopiperazines with two spirocyclic centers extracted from Botryosphaeria mamane, an endophytic fungus isolated from Bixa orellana L.
- Author
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Barakat F, Vansteelandt M, Triastuti A, Jargeat P, Jacquemin D, Graton J, Mejia K, Cabanillas B, Vendier L, Stigliani JL, Haddad M, and Fabre N
- Subjects
- Antineoplastic Agents isolation & purification, Ascomycota physiology, Bixaceae microbiology, Caco-2 Cells, Cell Line, Circular Dichroism, Crystallography, X-Ray, Diketopiperazines isolation & purification, Drug Screening Assays, Antitumor, Endophytes chemistry, HT29 Cells, HeLa Cells, Hep G2 Cells, Humans, Magnetic Resonance Spectroscopy, Molecular Structure, Antineoplastic Agents chemistry, Antineoplastic Agents pharmacology, Ascomycota chemistry, Diketopiperazines chemistry, Diketopiperazines pharmacology
- Abstract
Three thiodiketopiperazines, botryosulfuranols A-C (1-3) were isolated from the endophytic fungus Botryosphaeria mamane. The three compounds present sulfur atoms on α- and β-positions of phenylalanine derived residues and unprecedented two spirocyclic centers at C-4 and C-2'. Their planar structures were determined by spectroscopic analysis and absolute configurations were achieved by X-ray diffraction analysis and ECD and NMR chemical shifts calculations. Botryosulfuranol A (1) was the most cytotoxic compound against four cancer cell lines (HT-29, HepG2, Caco-2, HeLa) and two healthy cell lines (IEC6, Vero) highlighting the importance of an electrophilic center for cell growth inhibition., (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Published
- 2019
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- View/download PDF
32. Fungal communities associated with Evernia prunastri, Ramalina fastigiata and Pleurosticta acetabulum: Three epiphytic lichens potentially active against Candida biofilms.
- Author
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Lagarde A, Jargeat P, Roy M, Girardot M, Imbert C, Millot M, and Mambu L
- Subjects
- Ascomycota classification, Ascomycota enzymology, Ascomycota genetics, Ascomycota isolation & purification, DNA Barcoding, Taxonomic, DNA, Fungal genetics, France, Parmeliaceae genetics, Peptide Synthases genetics, Peptide Synthases metabolism, Phylogeny, Polyketide Synthases genetics, Polyketide Synthases metabolism, Secondary Metabolism genetics, Symbiosis, Biofilms drug effects, Candida physiology, Lichens microbiology, Parmeliaceae classification, Parmeliaceae enzymology, Parmeliaceae isolation & purification
- Abstract
Fungal communities associated to three epiphytic lichens active against Candida, were investigated using culture-based methods We hypothetized that associated fungi would contribute to lichens activities. The ability of specific fungi to grow inside or outside lichens was investigated. To detect biogenesis pathways involved in the production of secondary metabolites, genes coding for nonribosomal peptide synthetase (NRPS) and polyketide synthase I (PKS I) were screened by PCR from fungal DNA extracts. Both endo and epilichenic communities were isolated from two fructicose (Evernia prunastri and Ramalina fastigiata) and one foliose (Pleurosticta acetabulum) lichens. A total of 86 endolichenic and 114 epilichenic isolates were obtained, corresponding to 18 and 24 phylogenetic groups respectively suggesting a wide diversity of fungi. The communities and the species richness were distinct between the three lichens which hosted potentially new fungal species. Additionally, the endo- and epilichenic communities differed in their composition: Sordariomycetes were particularly abundant among endolichenic fungi and Dothideomycetes among epilichenic fungi. Only a few fungi colonized both habitats, such as S. fimicola, Cladosporium sp1 and Botrytis cinerea. Interestingly, Nemania serpens (with several genotypes) was the most abundant endolichenic fungus (53% of isolates) and was shared by the three lichens. Finally, 12 out of 36 phylogenetic groups revealed the presence of genes coding for nonribosomal peptide synthetase (NRPs) and polyketide synthase I (PKS I). This study shows that common lichens are reservoirs of diverse fungal communities, which could potentially contribute to global activity of the lichen and, therefore, deserve to be isolated for further chemical studies., (Copyright © 2018 Elsevier GmbH. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
33. Alder and the Golden Fleece: high diversity of Frankia and ectomycorrhizal fungi revealed from Alnus glutinosa subsp. barbata roots close to a Tertiary and glacial refugium.
- Author
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Roy M, Pozzi AC, Gareil R, Nagati M, Manzi S, Nouioui I, Sharikadze N, Jargeat P, Gryta H, Moreau PA, Fernandez MP, and Gardes M
- Abstract
Background: Recent climatic history has strongly impacted plant populations, but little is known about its effect on microbes. Alders, which host few and specific symbionts, have high genetic diversity in glacial refugia. Here, we tested the prediction that communities of root symbionts survived in refugia with their host populations. We expected to detect endemic symbionts and a higher species richness in refugia as compared to recolonized areas., Methods: We sampled ectomycorrhizal (EM) root tips and the nitrogen-fixing actinomycete Frankia communities in eight sites colonized by Alnus glutinosa subsp . barbata close to the Caucasus in Georgia. Three sites were located in the Colchis, one major Eurasian climatic refugia for Arcto-Tertiary flora and alders, and five sites were located in the recolonized zone. Endemic symbionts and plant ITS variants were detected by comparing sequences to published data from Europe and another Tertiary refugium, the Hyrcanian forest. Species richness and community structure were compared between sites from refugia and recolonized areas for each symbionts., Results: For both symbionts, most MOTUs present in Georgia had been found previously elsewhere in Europe. Three endemic Frankia strains were detected in the Colchis vs two in the recolonized zone, and the five endemic EM fungi were detected only in the recolonized zone. Frankia species richness was higher in the Colchis while the contrary was observed for EM fungi. Moreover, the genetic diversity of one alder specialist Alnicola xanthophylla was particularly high in the recolonized zone. The EM communities occurring in the Colchis and the Hyrcanian forests shared closely related endemic species., Discussion: The Colchis did not have the highest alpha diversity and more endemic species, suggesting that our hypothesis based on alder biogeography may not apply to alder's symbionts. Our study in the Caucasus brings new clues to understand symbioses biogeography and their survival in Tertiary and ice-age refugia, and reveals that isolated host populations could be of interest for symbiont diversity conservation., Competing Interests: The authors declare there are no competing interests.
- Published
- 2017
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34. Paxillus rubicundulus (Boletales, Paxillaceae) and two new alder-specific ectomycorrhizal species, Paxillus olivellus and Paxillus adelphus, from Europe and North Africa.
- Author
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Jargeat P, Moreau PA, Gryta H, Chaumeton JP, and Gardes M
- Subjects
- Algeria, Basidiomycota genetics, Cluster Analysis, DNA, Fungal chemistry, DNA, Fungal genetics, DNA, Ribosomal Spacer chemistry, DNA, Ribosomal Spacer genetics, France, Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) genetics, Mycorrhizae cytology, Mycorrhizae genetics, Sequence Analysis, DNA, Alnus microbiology, Basidiomycota classification, Basidiomycota isolation & purification, Mycorrhizae classification, Mycorrhizae isolation & purification, Phylogeny
- Abstract
Paxillus rubicundulus P.D. Orton has been shown to be a complex of at least three ectomycorrhizal taxa strictly associated with alders (Alnus) in Europe, P. rubicundulus s. str., and two undescribed clades. To assess the taxonomic status of these three clades and their phylogenetic relationships, phylogenetic analyses of two independent gene regions (ITS and gpd), combined with macro- and micromorphological comparisons of genetically identified specimens, were carried out. A total of 85 sequences were successfully obtained from basidiomata and alder mycorrhizae collected in France and Algeria and combined with GenBank and UNITE sequences. The phylogenetic results and estimates of genetic diversity confirmed that the three clades are distinct species, often found in sympatry. As a result, P. rubicundulus s. str. was redefined based on the revision of type material, and Paxillus adelphus and Paxillus olivellus are introduced as new Linnaean names. The often used name Paxillus filamentosus is rejected since it could not be applied to any of the new species. The three species are distinguished micromorphologically by spore size and shape. They are widely distributed in Europe, North Africa and western Asia; P. rubicundulus is rare, and all species have a limited host range., (Copyright © 2016 The British Mycological Society. Published by Elsevier Ltd. All rights reserved.)
- Published
- 2016
- Full Text
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