Pub Date : 2026-01-01Epub Date: 2025-11-05DOI: 10.1080/00275514.2025.2564582
Gustavo Hernán Ramírez, María Virginia Bianchinotti, Freda Elizabeth Anderson
Native to South America, moth plant (Araujia hortorum, Apocynaceae) is an invasive vine that threatens natural ecosystems and agriculture in many parts of the world. Biological control studies involving fungal pathogens have primarily focused on the rust Puccinia araujiae, but other aggressive pathogens exist that may show potential as complementary agents. In its native range in Argentina, plants were quite frequently observed with severe leaf and fruit damage caused by a fungal disease. The pathogen associated with this disease was isolated and identified as Septoria araujiae based on morphological analyses. Multilocus analyses allowed the first phylogenetic placement of this species within the genus. Koch's postulates were fulfilled through inoculation experiments, confirming S. araujiae as the causal agent. The pathogen exhibited a hemibiotrophic life cycle, with an extended asymptomatic phase followed by a necrotrophic stage that led to severe defoliation. Host specificity experiments revealed a narrow host range, with susceptibility largely confined to species within the subtribe Oxypetalinae. These findings contribute new insights into the diversity, ecology, and host interactions of Septoria species and highlight the potential of S. araujiae as a biological control agent for A. hortorum.
{"title":"<i>Septoria araujiae</i>: Phylogeny, pathogenicity, and host specificity of a fungal pathogen with potential as a biocontrol agent for moth plant.","authors":"Gustavo Hernán Ramírez, María Virginia Bianchinotti, Freda Elizabeth Anderson","doi":"10.1080/00275514.2025.2564582","DOIUrl":"10.1080/00275514.2025.2564582","url":null,"abstract":"<p><p>Native to South America, moth plant (<i>Araujia hortorum</i>, Apocynaceae) is an invasive vine that threatens natural ecosystems and agriculture in many parts of the world. Biological control studies involving fungal pathogens have primarily focused on the rust <i>Puccinia araujiae</i>, but other aggressive pathogens exist that may show potential as complementary agents. In its native range in Argentina, plants were quite frequently observed with severe leaf and fruit damage caused by a fungal disease. The pathogen associated with this disease was isolated and identified as <i>Septoria araujiae</i> based on morphological analyses. Multilocus analyses allowed the first phylogenetic placement of this species within the genus. Koch's postulates were fulfilled through inoculation experiments, confirming <i>S. araujiae</i> as the causal agent. The pathogen exhibited a hemibiotrophic life cycle, with an extended asymptomatic phase followed by a necrotrophic stage that led to severe defoliation. Host specificity experiments revealed a narrow host range, with susceptibility largely confined to species within the subtribe Oxypetalinae. These findings contribute new insights into the diversity, ecology, and host interactions of <i>Septoria</i> species and highlight the potential of <i>S. araujiae</i> as a biological control agent for <i>A. hortorum</i>.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"102-115"},"PeriodicalIF":2.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145452105","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2026-01-21DOI: 10.1080/00275514.2025.2588831
Timothy J Baroni, Todd W Osmundson
A rarely collected rose-pink-colored Hericium americanum has now been documented with in situ images obtained by 11 different field naturalists in the northeastern United States and eastern Canada since 2018. These mushroom enthusiasts responded to a request for images and specimens of a rarely documented rose-pink-colored tooth fungus discussed in the comments section of a description of Hericium americanum and H. coralloides in Mushrooms of the Northeastern United States and Eastern Canada. Five of those finds were collected, preserved by drying, and sent to the authors for analysis. This strikingly colored tooth fungus is confirmed as a variant of H. americanum using morphological and molecular data (nuc rDNA ITS1-5.8S-ITS2 and partial nuc 28S rDNA D1-D6 regions) and proposed here as a new variety.
{"title":"<i>Hericium americanum</i> var. <i>roseum</i>-a new North American taxon.","authors":"Timothy J Baroni, Todd W Osmundson","doi":"10.1080/00275514.2025.2588831","DOIUrl":"10.1080/00275514.2025.2588831","url":null,"abstract":"<p><p>A rarely collected rose-pink-colored <i>Hericium americanum</i> has now been documented with in situ images obtained by 11 different field naturalists in the northeastern United States and eastern Canada since 2018. These mushroom enthusiasts responded to a request for images and specimens of a rarely documented rose-pink-colored tooth fungus discussed in the comments section of a description of <i>Hericium americanum</i> and <i>H. coralloides</i> in <i>Mushrooms of the Northeastern United States and Eastern Canada</i>. Five of those finds were collected, preserved by drying, and sent to the authors for analysis. This strikingly colored tooth fungus is confirmed as a variant of <i>H. americanum</i> using morphological and molecular data (nuc rDNA ITS1-5.8S-ITS2 and partial nuc 28S rDNA D1-D6 regions) and proposed here as a new variety.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"233-241"},"PeriodicalIF":2.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146018930","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-10-30DOI: 10.1080/00275514.2025.2568320
Karen K Nakasone, Beatriz Oritz-Santana
The new species Stereophlebia arizonica from southern Arizona is described and illustrated. Although similar to S. pendula, a widely distributed taxon in North America, molecular phylogenetic analyses and morphological evidence show that they are distinct, sister species. Phylogenetic analyses place Stereophlebia in a clade with Gelatinofungus within the Phanerochaetaceae (Polyporales). Critical morphological features of Gelatinofungus not reported earlier are presented, and G. betulinus is determined to be a later synonym of S. pendula.
{"title":"<i>Stereophlebia</i> in North America.","authors":"Karen K Nakasone, Beatriz Oritz-Santana","doi":"10.1080/00275514.2025.2568320","DOIUrl":"10.1080/00275514.2025.2568320","url":null,"abstract":"<p><p>The new species <i>Stereophlebia arizonica</i> from southern Arizona is described and illustrated. Although similar to <i>S. pendula</i>, a widely distributed taxon in North America, molecular phylogenetic analyses and morphological evidence show that they are distinct, sister species. Phylogenetic analyses place <i>Stereophlebia</i> in a clade with <i>Gelatinofungus</i> within the Phanerochaetaceae (Polyporales). Critical morphological features of <i>Gelatinofungus</i> not reported earlier are presented, and <i>G. betulinus</i> is determined to be a later synonym of <i>S. pendula</i>.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"205-213"},"PeriodicalIF":2.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145409442","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-12-15DOI: 10.1080/00275514.2025.2577604
Núria Pou-Solà, Kensuke Seto, Alan Denis Fernández-Valero, Jordina Gordi, Esther Garcés, Albert Reñé, Maiko Kagami
This study describes a novel parasitic fungus that infects the benthic and epiphytic dinoflagellate Ostreopsis cf. ovata during a coastal microalgal bloom in the Mediterranean Sea. Microscopic observations revealed a distinctive, irregularly shaped zoosporangium during the mature stages and spherical, posteriorly uniflagellate zoospores. This supports its affiliation within the phylum Chytridiomycota. Concatenated phylogenetic analysis based on 18S, 5.8S, and 28S ribosomal DNA placed the fungus within the order Lobulomycetales, thus establishing it as a distinct lineage separate from previously described species. Additional phylogenetic analyses including environmental DNA sequences revealed a close phylogenetic relationship with previously reported freshwater sequences. This suggests a possible ecological link between marine and freshwater habitats. Cross-infection experiments confirmed the ability of the fungus to infect healthy cells of both dinoflagellate and diatom species, rendering it the first known chytrid with a broad phytoplankton host range. Additionally, it is the first member of this order known to parasitize dinoflagellate species and only the second known to parasitize marine algae. Infection prevalence was higher in dinoflagellates than in diatoms. Furthermore, under laboratory conditions, the chytrid also developed zoosporangia on pollen grains, using them as an alternative nutrient source. Based on these findings, this study describes a new genus and species of zoosporic fungus, Algophthora mediterranea, within the order Lobulomycetales.
{"title":"<i>Algophthora mediterranea</i>, gen. et sp. nov.: Novel dinoflagellate- and diatom-infecting generalist marine chytrid from the Mediterranean Sea.","authors":"Núria Pou-Solà, Kensuke Seto, Alan Denis Fernández-Valero, Jordina Gordi, Esther Garcés, Albert Reñé, Maiko Kagami","doi":"10.1080/00275514.2025.2577604","DOIUrl":"10.1080/00275514.2025.2577604","url":null,"abstract":"<p><p>This study describes a novel parasitic fungus that infects the benthic and epiphytic dinoflagellate <i>Ostreopsis</i> cf. <i>ovata</i> during a coastal microalgal bloom in the Mediterranean Sea. Microscopic observations revealed a distinctive, irregularly shaped zoosporangium during the mature stages and spherical, posteriorly uniflagellate zoospores. This supports its affiliation within the phylum Chytridiomycota. Concatenated phylogenetic analysis based on 18S, 5.8S, and 28S ribosomal DNA placed the fungus within the order Lobulomycetales, thus establishing it as a distinct lineage separate from previously described species. Additional phylogenetic analyses including environmental DNA sequences revealed a close phylogenetic relationship with previously reported freshwater sequences. This suggests a possible ecological link between marine and freshwater habitats. Cross-infection experiments confirmed the ability of the fungus to infect healthy cells of both dinoflagellate and diatom species, rendering it the first known chytrid with a broad phytoplankton host range. Additionally, it is the first member of this order known to parasitize dinoflagellate species and only the second known to parasitize marine algae. Infection prevalence was higher in dinoflagellates than in diatoms. Furthermore, under laboratory conditions, the chytrid also developed zoosporangia on pollen grains, using them as an alternative nutrient source. Based on these findings, this study describes a new genus and species of zoosporic fungus, <i>Algophthora mediterranea</i>, within the order Lobulomycetales.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"10-20"},"PeriodicalIF":2.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145763310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-01-01Epub Date: 2025-11-03DOI: 10.1080/00275514.2025.2562792
Marcos V Caiafa, Mason A Rowe, Rosanne Healy, Benjamin Lemmond, Eduardo Nouhra, Donald H Pfister, Pablo Sandoval-Leiva, Giuliana Furci, Matthew E Smith
Truffles are enclosed, hypogeous fruiting bodies that have evolved hundreds of times across different fungal groups. Truffles are particularly diverse within Pezizales, a large and diverse order of Ascomycota where truffle forms have evolved multiple times. The majority of truffle species are ectomycorrhizal symbionts of trees and rely on animals for dispersal. Because of their hypogeous nature, truffles remain understudied and many new taxa remain to be discovered. Due to their obligate symbiosis with host plants and their dependence on animal dispersal, ectomycorrhizal truffle species often show distinct host associations, are restricted to certain forest types, and have notable biogeographic distribution patterns. Here, we present morphological and phylogenetic evidence in support of two new truffle species associated with Nothofagaceae trees in southern South America, Geomorium nahuelbutense (Geomoriaceae) and Paragalactinia nothofagacearum (Pezizaceae). The closest described relatives of these species form aboveground, apothecial ascomata, suggesting that these taxa are derived from independent evolutionary events leading to the truffle morphology. Paragalactinia nothofagacearum is widespread in northern Patagonia and has been documented as an ectomycorrhizal associate of Lophozonia alpina (= Nothofagus nervosa) seedlings. In contrast, Geomorium nahuelbutense has only been found in a well-preserved coastal forest in Chile toward the northern extent of the range of Nothofagaceae in South America. This is a conservation priority area that has been heavily impacted by fires, deforestation, and other human activities. This species is known only from two modern collections from Parque Nacional Nahuelbuta and one preserved specimen collected by Roland Thaxter near Concepción, Chile, in 1906.
{"title":"Unearthing two new ectomycorrhizal Pezizales truffle species from Nothofagaceae forests in southern South America.","authors":"Marcos V Caiafa, Mason A Rowe, Rosanne Healy, Benjamin Lemmond, Eduardo Nouhra, Donald H Pfister, Pablo Sandoval-Leiva, Giuliana Furci, Matthew E Smith","doi":"10.1080/00275514.2025.2562792","DOIUrl":"10.1080/00275514.2025.2562792","url":null,"abstract":"<p><p>Truffles are enclosed, hypogeous fruiting bodies that have evolved hundreds of times across different fungal groups. Truffles are particularly diverse within Pezizales, a large and diverse order of Ascomycota where truffle forms have evolved multiple times. The majority of truffle species are ectomycorrhizal symbionts of trees and rely on animals for dispersal. Because of their hypogeous nature, truffles remain understudied and many new taxa remain to be discovered. Due to their obligate symbiosis with host plants and their dependence on animal dispersal, ectomycorrhizal truffle species often show distinct host associations, are restricted to certain forest types, and have notable biogeographic distribution patterns. Here, we present morphological and phylogenetic evidence in support of two new truffle species associated with Nothofagaceae trees in southern South America, <i>Geomorium nahuelbutense</i> (Geomoriaceae) and <i>Paragalactinia nothofagacearum</i> (Pezizaceae). The closest described relatives of these species form aboveground, apothecial ascomata, suggesting that these taxa are derived from independent evolutionary events leading to the truffle morphology. <i>Paragalactinia nothofagacearum</i> is widespread in northern Patagonia and has been documented as an ectomycorrhizal associate of <i>Lophozonia alpina</i> (= <i>Nothofagus nervosa</i>) seedlings. In contrast, <i>Geomorium nahuelbutense</i> has only been found in a well-preserved coastal forest in Chile toward the northern extent of the range of Nothofagaceae in South America. This is a conservation priority area that has been heavily impacted by fires, deforestation, and other human activities. This species is known only from two modern collections from Parque Nacional Nahuelbuta and one preserved specimen collected by Roland Thaxter near Concepción, Chile, in 1906.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"190-204"},"PeriodicalIF":2.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145438467","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-09DOI: 10.1080/00275514.2025.2577610
Eero Kiviniemi, Matti Wahlsten, Jouni Jokela, Taina Lundell
Filamentous fungi produce secondary metabolites with multiple biochemical activities. For wood-decaying fungi of Basidiomycota, some of these compounds may act as redox-active mediators involved in biodegradation of lignocelluloses and biopolymers. Our aim was to identify natural aromatic compounds produced by white rot fungi of the genus Phlebia (Meruliaceae, Polyporales, Agaricomycetes), which comprises efficient decomposers of wood, wastes, and xenobiotics. Naturally produced aryl compounds were obtained by cultivating the fungi on a defined low-nitrogen liquid medium with glucose as carbon source. Culture supernatants were extracted and analyzed with UPLC-MS (ultra-performance liquid chromatography-mass spectrometry) and NMR (nuclear magnetic resonance). Enzyme assays, cultivation with 15N isotope-labeled nitrogen supplement, and aryl compound-feeding experiments were performed to assess biosynthesis mechanisms. Together with the well-known secondary metabolite veratryl alcohol and its enzymatic oxidation product veratraldehyde, we identified two nitroaryl derivatives, 6-nitroveratryl alcohol and 4-nitroveratrole, accumulating in culture supernatants of Phlebia spp. Cultivation of P. radiata isolate 2776 with NH4NO3 caused higher product yield of the nitroaryl compounds than 15NH4Cl supplementation, suggesting a role of nitrate ions in formation of nitroaryl products. With 15N-labeled supplementation, however, incorporation of nitrogen also from ammonium ions was observed. Although lignin peroxidase (LiP) enzyme activities correlated with appearance of nitroaryl compounds, their formation from veratryl alcohol by LiP was not accomplished in vitro in reaction mixtures with extracellular supernatants. In compound-feeding experiments, additional glycosylated derivative of 6-nitroveratryl alcohol was detected in P. radiata cultures, and nitroguaiacol was formed from nitroveratrole. These results indicate multiple pathways including both intra- and extracellular metabolism in biosynthesis and bioconversion of monoaromatic aryl compounds and their derivatives in fungi of Phlebia.
{"title":"Production of nitroaryl secondary metabolites by wood-decaying fungi of <i>Phlebia</i> spp.","authors":"Eero Kiviniemi, Matti Wahlsten, Jouni Jokela, Taina Lundell","doi":"10.1080/00275514.2025.2577610","DOIUrl":"https://doi.org/10.1080/00275514.2025.2577610","url":null,"abstract":"<p><p>Filamentous fungi produce secondary metabolites with multiple biochemical activities. For wood-decaying fungi of Basidiomycota, some of these compounds may act as redox-active mediators involved in biodegradation of lignocelluloses and biopolymers. Our aim was to identify natural aromatic compounds produced by white rot fungi of the genus <i>Phlebia</i> (Meruliaceae, Polyporales, Agaricomycetes), which comprises efficient decomposers of wood, wastes, and xenobiotics. Naturally produced aryl compounds were obtained by cultivating the fungi on a defined low-nitrogen liquid medium with glucose as carbon source. Culture supernatants were extracted and analyzed with UPLC-MS (ultra-performance liquid chromatography-mass spectrometry) and NMR (nuclear magnetic resonance). Enzyme assays, cultivation with <sup>15</sup>N isotope-labeled nitrogen supplement, and aryl compound-feeding experiments were performed to assess biosynthesis mechanisms. Together with the well-known secondary metabolite veratryl alcohol and its enzymatic oxidation product veratraldehyde, we identified two nitroaryl derivatives, 6-nitroveratryl alcohol and 4-nitroveratrole, accumulating in culture supernatants of <i>Phlebia</i> spp. Cultivation of <i>P. radiata</i> isolate 2776 with NH<sub>4</sub>NO<sub>3</sub> caused higher product yield of the nitroaryl compounds than <sup>15</sup>NH<sub>4</sub>Cl supplementation, suggesting a role of nitrate ions in formation of nitroaryl products. With <sup>15</sup>N-labeled supplementation, however, incorporation of nitrogen also from ammonium ions was observed. Although lignin peroxidase (LiP) enzyme activities correlated with appearance of nitroaryl compounds, their formation from veratryl alcohol by LiP was not accomplished in vitro in reaction mixtures with extracellular supernatants. In compound-feeding experiments, additional glycosylated derivative of 6-nitroveratryl alcohol was detected in <i>P. radiata</i> cultures, and nitroguaiacol was formed from nitroveratrole. These results indicate multiple pathways including both intra- and extracellular metabolism in biosynthesis and bioconversion of monoaromatic aryl compounds and their derivatives in fungi of <i>Phlebia</i>.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"1-17"},"PeriodicalIF":2.6,"publicationDate":"2025-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145714998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ectomycorrhizal (ECM) fungi are widely recognized for their ability to enhance plant survival and growth under saline conditions. Although extensive research has focused on the development of salt-tolerant ECM fungal strains, the cytological and morphological responses of ECM fungi to salt stress remain unclear. Moreover, the cellular mechanisms underlying fungal adaptation to high-salinity conditions remain poorly understood. This study investigated salinity tolerance and cellular adaptations of three R. roseolus strains subjected to increasing artificial seawater concentrations. The mycelia were grown on modified Melin-Norkrans (MMN) medium containing 0%, 50%, or 100% artificial seawater then observed under a phase-contrast light microscope. The hybrid strain TUFC102052 exhibited the highest tolerance to 50% artificial seawater, whereas significant growth inhibition was observed in both the wild-type strain TUFC10010 and the salt-sensitive strain TUFC102053 at higher salinity levels. Cellular alterations including subterminal cell size reduction and vacuole fragmentation were observed, indicating potential adaptive strategies for survival under saline conditions. These findings provide new insights into the morphological adaptations of the ECM fungus R. roseolus to salt stress.
{"title":"Cytological and morphological responses of the ectomycorrhizal fungus <i>Rhizopogon roseolus</i> to saline conditions.","authors":"Septyani Amini, Rena Rifki Safitri, Tadanori Aimi, Norihiro Shimomura","doi":"10.1080/00275514.2025.2572274","DOIUrl":"https://doi.org/10.1080/00275514.2025.2572274","url":null,"abstract":"<p><p>Ectomycorrhizal (ECM) fungi are widely recognized for their ability to enhance plant survival and growth under saline conditions. Although extensive research has focused on the development of salt-tolerant ECM fungal strains, the cytological and morphological responses of ECM fungi to salt stress remain unclear. Moreover, the cellular mechanisms underlying fungal adaptation to high-salinity conditions remain poorly understood. This study investigated salinity tolerance and cellular adaptations of three <i>R. roseolus</i> strains subjected to increasing artificial seawater concentrations. The mycelia were grown on modified Melin-Norkrans (MMN) medium containing 0%, 50%, or 100% artificial seawater then observed under a phase-contrast light microscope. The hybrid strain TUFC102052 exhibited the highest tolerance to 50% artificial seawater, whereas significant growth inhibition was observed in both the wild-type strain TUFC10010 and the salt-sensitive strain TUFC102053 at higher salinity levels. Cellular alterations including subterminal cell size reduction and vacuole fragmentation were observed, indicating potential adaptive strategies for survival under saline conditions. These findings provide new insights into the morphological adaptations of the ECM fungus <i>R. roseolus</i> to salt stress.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"1-10"},"PeriodicalIF":2.6,"publicationDate":"2025-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145596828","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-10-10DOI: 10.1080/00275514.2025.2549866
Kathryn Nash, Julia Vinzelj, Carrie J Pratt, Mostafa S Elshahed, Noha H Youssef
Anaerobic gut fungi (AGF; Neocallimastigomycota) are a clade of basal, zoospore-producing fungi within the subkingdom Chytridiomyceta and known inhabitants of the alimentary tract of animal hosts. To date, 22 genera and 38 species have been described, most originating from herbivorous mammals. Here, we report on the isolation and characterization of a novel species of Neocallimastigomycota from an avian host. Multiple AGF strains were isolated from ostrich feces obtained from a local farm in Oklahoma (USA). All strains formed small, irregular-shaped white colonies with darker centers, displayed a filamentous rhizoidal structure with monocentric thallus developmental patterns, and produced mostly monoflagellated zoospores. The type strain produced terminal sporangia that were predominantly globose, often exhibiting cup-shaped and occasionally elongated sporangiophores. Sporangiophores characteristically exhibited constrictions at irregular intervals, giving them a beads-on-a-string-like appearance. Phylogenetic analysis using the partial nuc 28S rDNA D1-D2 regions (D1-D2 28S), ribosomal internal transcribed spacer 1 (ITS1), and RNA polymerase II large subunit (RPB1) grouped all isolates as a separate species within the genus Piromyces. Transcriptomic analysis indicated an average amino acid identity (AAI) of 80.34% (± 3.27%) between the type species and members of the genus Piromyces and 62.93-76.05% between the type species and all other AGF taxa outside Piromyces. Based on the morphology, phylogenetic analysis, and AAI values, we propose accommodating these strains as a novel species of Piromyces, for which the name Piromyces struthionis is proposed. The type strain for this species is Ost1.
{"title":"<i>Piromyces struthionis</i>, sp. nov., a new anaerobic gut fungus from the feces of ostriches.","authors":"Kathryn Nash, Julia Vinzelj, Carrie J Pratt, Mostafa S Elshahed, Noha H Youssef","doi":"10.1080/00275514.2025.2549866","DOIUrl":"10.1080/00275514.2025.2549866","url":null,"abstract":"<p><p>Anaerobic gut fungi (AGF; <i>Neocallimastigomycota</i>) are a clade of basal, zoospore-producing fungi within the subkingdom Chytridiomyceta and known inhabitants of the alimentary tract of animal hosts. To date, 22 genera and 38 species have been described, most originating from herbivorous mammals. Here, we report on the isolation and characterization of a novel species of <i>Neocallimastigomycota</i> from an avian host. Multiple AGF strains were isolated from ostrich feces obtained from a local farm in Oklahoma (USA). All strains formed small, irregular-shaped white colonies with darker centers, displayed a filamentous rhizoidal structure with monocentric thallus developmental patterns, and produced mostly monoflagellated zoospores. The type strain produced terminal sporangia that were predominantly globose, often exhibiting cup-shaped and occasionally elongated sporangiophores. Sporangiophores characteristically exhibited constrictions at irregular intervals, giving them a beads-on-a-string-like appearance. Phylogenetic analysis using the partial nuc 28S rDNA D1-D2 regions (D1-D2 28S), ribosomal internal transcribed spacer 1 (ITS1), and RNA polymerase II large subunit (RPB1) grouped all isolates as a separate species within the genus <i>Piromyces</i>. Transcriptomic analysis indicated an average amino acid identity (AAI) of 80.34% (± 3.27%) between the type species and members of the genus <i>Piromyces</i> and 62.93-76.05% between the type species and all other AGF taxa outside <i>Piromyces</i>. Based on the morphology, phylogenetic analysis, and AAI values, we propose accommodating these strains as a novel species of <i>Piromyces</i>, for which the name <i>Piromyces struthionis</i> is proposed. The type strain for this species is Ost1.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"1044-1056"},"PeriodicalIF":2.6,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145275349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-01Epub Date: 2025-10-07DOI: 10.1080/00275514.2025.2548745
Hannah M Petronek, Shannon C Lynch, Brian Lovett, Angie M Martin, Danielle K H Martin, Matt T Kasson
The family Nectriaceae includes numerous phytopathogenic fungal genera that cause canker diseases on both angiosperm and conifer hosts worldwide. Among these, Neonectria species are globally important canker pathogens of numerous plant hosts, but their roles in contributing to forest decline and mortality outside their involvement in beech bark disease and apple canker are largely understudied. In the U.S.A. N. magnoliae causes perennial cankers on two native hosts in central Appalachia: Liriodendron tulipifera (tulip poplar) and Magnolia fraseri (Fraser magnolia) and has been recently confirmed from non-native M. stellata (star magnolia) in West Virginia, U.S.A. Both native hosts occur in the central Appalachian Mountains, but M. fraseri occurs mostly at higher elevations, from 600 to 1700 m. Neonectria magnoliae was first described in 1943 (as Nectria magnoliae), yet its impact across the forested landscape remains unclear. To clarify host-specific differences across the contemporary range of N. magnoliae, we used multilocus phylogenetics, comparative pathogenicity/virulence assays, and morphological analyses to determine whether N. magnoliae represents two cryptic species that specialize on L. tulipifera and Magnolia spp. or whether N. magnoliae has host-specific pathotypes. Our studies revealed two morphologically distinct formae speciales within N. magnoliae: (i) N. magnoliae f. sp. liriodendri-strains originating from L. tulipifera with increased virulence on L. tulipifera and lacking macroconidia production and (ii) N. magnoliae f. sp. magnoliae-strains originating from M. fraseri with increased virulence on M. fraseri and producing macroconidia readily in culture. Overall, the incidence of these two pathotypes indicates that neither pathotype poses serious risks to either plant host but can add to cumulative stresses that both tree species are experiencing in the face of shifting global weather patterns.
坏疽科包括许多植物病原真菌属,在世界范围内引起被子植物和针叶树宿主的溃疡病。其中,Neonectria是全球范围内许多植物宿主的重要溃疡病病原体,但除了参与山毛榉树皮病和苹果溃疡病外,它们在森林衰退和死亡中的作用在很大程度上尚未得到充分研究。在美国,N. magnoliae在阿巴拉契亚中部的两种本地寄主:Liriodendron tulipifera(郁金香杨树)和Magnolia fraseri(弗雷泽木兰)上引起多年生溃疡病,最近在美国西弗吉尼亚州的非本地寄主m. stellata(星木兰)上得到证实。两种本地寄主都出现在阿巴拉契亚山脉中部,但m. fraseri主要发生在海拔600至1700米的较高海拔地区。新木兰花(neectria magnoliae)于1943年首次被描述,但其对森林景观的影响尚不清楚。为了澄清不同种类木兰的宿主特异性差异,我们使用了多位点系统发育、比较致病性/毒力测定和形态学分析来确定木兰是否代表两种专门针对郁金香和木兰的隐种,或者木兰是否具有宿主特异性致病型。我们的研究揭示了两种形态上截然不同的木兰属菌株:(1)木兰属菌株(N. magnoliae f. sp. liriodendi)——源自于白桦尺蠖,对白桦尺蠖毒力增强,但缺乏大分生孢子;(2)木兰属菌株(N. magnoliae f. sp. magnolia)——源自于白桦尺蠖,对白桦尺蠖毒力增强,但在培养中容易产生大分生孢子。总的来说,这两种病型的发病率表明,两种病型都不会对植物宿主造成严重风险,但会增加两种树种在面对不断变化的全球天气模式时所经历的累积压力。
{"title":"Two morphologically distinct formae speciales in <i>Neonectria magnoliae</i> differ in their virulence on Magnolia family hosts <i>Liriodendron tulipifera</i> and <i>Magnolia fraseri</i>.","authors":"Hannah M Petronek, Shannon C Lynch, Brian Lovett, Angie M Martin, Danielle K H Martin, Matt T Kasson","doi":"10.1080/00275514.2025.2548745","DOIUrl":"10.1080/00275514.2025.2548745","url":null,"abstract":"<p><p>The family Nectriaceae includes numerous phytopathogenic fungal genera that cause canker diseases on both angiosperm and conifer hosts worldwide. Among these, <i>Neonectria</i> species are globally important canker pathogens of numerous plant hosts, but their roles in contributing to forest decline and mortality outside their involvement in beech bark disease and apple canker are largely understudied. In the U.S.A. <i>N. magnoliae</i> causes perennial cankers on two native hosts in central Appalachia: <i>Liriodendron tulipifera</i> (tulip poplar) and <i>Magnolia fraseri</i> (Fraser magnolia) and has been recently confirmed from non-native <i>M. stellata</i> (star magnolia) in West Virginia, U.S.A. Both native hosts occur in the central Appalachian Mountains, but <i>M. fraseri</i> occurs mostly at higher elevations, from 600 to 1700 m. <i>Neonectria magnoliae</i> was first described in 1943 (as <i>Nectria magnoliae</i>), yet its impact across the forested landscape remains unclear. To clarify host-specific differences across the contemporary range of <i>N. magnoliae</i>, we used multilocus phylogenetics, comparative pathogenicity/virulence assays, and morphological analyses to determine whether <i>N. magnoliae</i> represents two cryptic species that specialize on <i>L. tulipifera</i> and <i>Magnolia</i> spp. or whether <i>N. magnoliae</i> has host-specific pathotypes. Our studies revealed two morphologically distinct formae speciales within <i>N. magnoliae</i>: (i) <i>N. magnoliae</i> f. sp. <i>liriodendri</i>-strains originating from <i>L. tulipifera</i> with increased virulence on <i>L. tulipifera</i> and lacking macroconidia production and (ii) <i>N. magnoliae</i> f. sp. <i>magnoliae</i>-strains originating from <i>M. fraseri</i> with increased virulence on <i>M. fraseri</i> and producing macroconidia readily in culture. Overall, the incidence of these two pathotypes indicates that neither pathotype poses serious risks to either plant host but can add to cumulative stresses that both tree species are experiencing in the face of shifting global weather patterns.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"1088-1103"},"PeriodicalIF":2.6,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145244723","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}