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a-h: Bipolaris luttrellii (holotype of dried culture of Cochliobolus luttrellii, j-n), Bipolaris maydis (neotype of Bipolaris maydis, a-h) a. Ascomata on host substrate. b. Section of the ascomata. c. Close up of 

a-h: Bipolaris luttrellii (holotype of dried culture of Cochliobolus luttrellii, j-n), Bipolaris maydis (neotype of Bipolaris maydis, a-h) a. Ascomata on host substrate. b. Section of the ascomata. c. Close up of 

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The family Pleosporaceae includes numerous saprobic, opportunistic human, and plant pathogenic taxa. The classification of genera and species Pleosporaceae has been a major challenge due to the lack of a clear understanding of the importance of the morphological characters used to distinguish taxa as well as the lack of reference strains. Recent tr...

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... species: Gibbago trianthemae E.G. Simmons, Mycotaxon 27: 108 (1986), Fig. 16 Facesoffungi number: FoF ...
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... with broadly rounded ends, hyaline to light brown when immature, becoming brown to chestnut brown when mature, muriform with 5-6 transverse septa, and single longitudinal septa in one or all cells, constricted at the septa, smooth-walled, relatively thick-walled, with a 5-9 μm thick mucilaginous sheath. Asexual morph of Drechslera teres (Fig. 26); Conidiophores 150-200×7-11 μm, solitary or in groups of 2-3, straight or flexuous, sometimes genicu- late, often swollen at the base, pale to mid brown or olivaceous brown. Conidia 70-160×16-23 μm, straight, cylindrical, rounded at the ends, subhyaline to straw-coloured, smooth, 1-10 (4-6), pseudoseptate, frequently with constriction. ...
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... (DAOM 222769), which is the type species for this genus. In the present study the genus Pyrenophora clusters in the suborder Pleosporineae of the fam- ily Pleosporaceae with a relatively high bootstrap support surrounded by a large, distinct, apical ring. h-j. Immature and mature ascospores. Scale bars: c=100 μm, d-e=50 μm, f-g=40 μm, h-j= 10 μm (Fig. 1, 60 %). Further phylogenetic analysis shows that sexual Pyrenophora morphs cluster with asexual Drechslera morphs, i.e. Pyrenophora dictyoides (DAOM 75616) clusters with Drechslera dictyoides (DAOM 63666). The putative strain of Pyrenophora phaeocomes (DAOM 222769), which is the type species of the genus, clusters with other Pyrenophora ...
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... ssp. rotundata (Asteraceae) and it is monotypic. In the same study Shivas and Morin (in Morin et al. 2010) ob- served Hendersonia osteospermi Wakef. on the same host and identified it as the asexual morph of A. osteospermi both in culture and by DNA sequence analysis. Based on ITS sequence analysis, Morin et al. (2010) placed Austropleospora Fig. 26 Morphology of Drechslera teres (Redrawn from Ellis 1971 , Fig 299.). Scale ...

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... genus is characterized by ascomata with circular lidlike openings and applanate reddish-brown to dark reddish-brown, muriform ascospores, with single longitudinal septa (Ariyawansa et al. 2015, Wijayawardene et al. 2017. Presently, the genus consists of 40 registered names in Index Fungorum (https://www.indexfungorum.org; ...
... The genus Exserohilum K.J. Leonard & Suggs belongs to the familyPleosporaceae of the Pleosporales in Dothideomycetes (Ascomycota) (Zhang et al. 2012, Ariyawansa et al. 2015, Hernández-Restrepo et al. 2018, Marin-Felix et al. 2019, and was introduced by Leonard & Suggs (1974), with E. turcicum (Pass.) K.J. Leonard & Suggs as the type species. ...
... Therefore, molecular data are essential for the accurate identification of species within this genus. Sequences of the large subunit ribosomal RNA gene (LSU), the internal transcribed spacer (ITS-rDNA) region, actin (act), β-tubulin (tub2), calmodulin (cam), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), histone H3 (his), translation elongation factor-1 alpha (TEF1) and RNA polymerase II second largest subunit (RPB2) have been used for delimitation of Exserohilum species (Berbee et al. 1999, Olivier et al. 2000, Zhang & Berbee 2001, Rossman et al. 2002, Kodsueb et al. 2006, Zhang et al. 2008, 2012, Amaradasa et al. 2014, Ariyawansa et al. 2015, Hernández-Restrepo et al. 2018, Marin-Felix et al. 2019. Recently the taxonomy and phylogeny of Exserohilum have been revised and based on molecular data 11 phylogenetic species have been accepted in this genus (Hernández-Restrepo et al. 2018, Marin-Felix et al. 2019. ...
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... Therefore, reclassifications of Pleosporaceae taxa have been frequently proposed (Kodsueb et al. 2006b). With increasing samplings and availability of molecular data, a more robust and natural taxonomy of Pleosporaceae taxa was delineated (Kodsueb et al. 2006b;Ariyawansa et al. 2015b;Hongsanan et al. 2020a). Twenty-three genera are currently accepted in the family ). ...
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Freshwater fungi comprises a highly diverse group of organisms occurring in freshwater habitats throughout the world. During a survey of freshwater fungi on submerged wood in streams and lakes, a wide range of sexual and asexual species were collected mainly from karst regions in China and Thailand. Phylogenetic inferences using partial gene regions of LSU, ITS, SSU, TEF1α, and RPB2 sequences revealed that most of these fungi belonged to Dothideomycetes and Sordariomycetes and a few were related to Eurotiomycetes. Based on the morphology and multi-gene phylogeny, we introduce four new genera, viz. Aquabispora, Neocirrenalia, Ocellisimilis and Uvarisporella, and 47 new species, viz. Acrodictys chishuiensis, A. effusa, A. pyriformis, Actinocladium aquaticum, Annulatascus tratensis, Aquabispora setosa, Aqualignicola setosa, Aquimassariosphaeria vermiformis, Ceratosphaeria flava, Chaetosphaeria polygonalis, Conlarium muriforme, Digitodesmium chishuiense, Ellisembia aquirostrata, Fuscosporella atrobrunnea, Halobyssothecium aquifusiforme, H. caohaiense, Hongkongmyces aquisetosus, Kirschsteiniothelia dushanensis, Monilochaetes alsophilae, Mycoenterolobium macrosporum, Myrmecridium splendidum, Neohelicascus griseoflavus, Neohelicomyces denticulatus, Neohelicosporium fluviatile, Neokalmusia aquibrunnea, Neomassariosphaeria aquimucosa, Neomyrmecridium naviculare, Neospadicoides biseptata, Ocellisimilis clavata, Ophioceras thailandense, Paragaeumannomyces aquaticus, Phialoturbella aquilunata, Pleurohelicosporium hyalinum, Pseudodactylaria denticulata, P. longidenticulata, P. uniseptata, Pseudohalonectria aurantiaca, Rhamphoriopsis aquimicrospora, Setoseptoria bambusae, Shrungabeeja fluviatilis, Sporidesmium tratense, S. versicolor, Sporoschisma atroviride, Stanjehughesia aquatica, Thysanorea amniculi, Uvarisporella aquatica and Xylolentia aseptata, with an illustrated account, discussion of their taxonomic placement and comparison with morphological similar taxa. Seven new combinations are introduced, viz. Aquabispora grandispora (≡ Boerlagiomyces grandisporus), A. websteri (≡ Boerlagiomyces websteri), Ceratosphaeria suthepensis (≡ Pseudohalonectria suthepensis), Gamsomyces aquaticus (≡ Pseudobactrodesmium aquaticum), G. malabaricus (≡ Gangliostilbe malabarica), Neocirrenalia nigrospora (≡ Cirrenalia nigrospora), and Rhamphoriopsis glauca (≡ Chloridium glaucum). Ten new geographical records are reported in China and Thailand and nine species are first reported from freshwater habitats. Reference specimens are provided for Diplocladiella scalaroides and Neocirrenalia nigrospora (≡ Cirrenalia nigrospora). Systematic placement of the previously introduced genera Actinocladium, Aqualignicola, and Diplocladiella is first elucidated based on the reference specimens and new collections. Species recollected from China and Thailand are also described and illustrated. The overall trees of freshwater Dothideomycetes and Sordariomycetes collected in this study are provided respectively and genera or family/order trees are constructed for selected taxa.
... The genus Curvularia, which belongs to the Pleosporaceae family, is characterized by widespread phytopathogenic species, additionally, opportunistic pathogens on animals and humans [48]. Obviously, Curvularia species are important phytopathogens reported worldwide as endophytes or pathogens [49][50][51]. Species of the Curvularia genus consist of major destructive plant pathogens isolated from soil and living or dead parts of plants [34,[38][39][40]. A study by Manamgoda et al. [48] reassessed the phylogenetic relationships of species of the genus Curvularia using Multilocus DNA sequence analysis with three loci, ITS, GPDH (glyceraldehyde-3-phosphate dehydrogenase), and TEF (Translation Elongation Factor). ...
... Additionally, a pathogenicity study revealed that C. purpureum showed moderate virulence against almond twigs and colonized the xylem of inoculated twigs. In an experiment conducted by Spiers et al. [51], C. purpureum was pathogenic to three genera (Salix, Populus, Malus), but was not able to colonize the cambium of apple cultivars in the same study. This outcome is not consistent with the results reported in another study which demonstrates that C. purpureum was isolated sporadically from infected almond trees in California [13]. ...
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Canker symptoms were observed on almond trees in the Fez-Meknes region, Morocco. Isolations were conducted from the infected branch and trunk showing internal and external brown lesions. Four representative fungal isolates were screened, and their identities were confirmed by cultural traits and sequence analysis of DNA using two genes, the ITS region (internal transcribed spacer) and calmodulin (cmdA). The identified fungi were Curvularia hawaiiensis, Fusarium ambrosium, Lasiodiplodia theobromae, and Chondrestereum purpureum. The pathogenicity test on almond twigs revealed that these species were pathogenic to their host with different degrees of virulence, with Lasiodiplodia theobromae as the most virulent causing the longest necrotic lesion (285.17 mm) and the death of twigs. Physiological traits analysis of the above-mentioned fungi showed that the optimum mycelium growth response at different temperatures varies from 10 to 35 °C, while the pH ranges between 3.0 and 8.0. This study confirms the presence of canker pathogens on almond trees, which will contribute valuable information to improve the understanding of the contemporary status of almond trees, thus helping the improvement of the management of almond orchards. To our knowledge, all these fungi represent new records in Morocco and some of them are confirmed on the almond trees for the first time in the world.
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... Pyrenophora is a genus of approximately 190 currently recognized species in the Dothidiomycete family Pleosporaceae [1]. Both the family Pleosporaceae and the genus Pyrenophora are well supported as monophyletic groups based on molecular phylogenetic Toxins 2022, 14, 588 2 of 20 analysis, and the Drechslera anamorphs traditionally associated with Pyrenophora species are also supported as genetically similar to their teleomorphs and conspecific with them [2][3][4]. Most Pyrenophora species are foliar pathogens of grasses, but some are also known as endophytes, as foliar pathogens of dicots, and in at least one case, as a seed pathogen. ...
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... Members of the Pleosporaceae are widely distributed across the environment and have a wide range of lifestyles, i.e., saprophytic, endo-/epiphytic, and parasitic on various hosts in terrestrial and aquatic environments [8]. Among them, species of Alternaria, Bipolaris, Curvularia, or Stemphylium are important pathogenic fungi to plants of various crops, resulting in yield and economic losses [8][9][10]. ...
... Members of the Pleosporaceae are widely distributed across the environment and have a wide range of lifestyles, i.e., saprophytic, endo-/epiphytic, and parasitic on various hosts in terrestrial and aquatic environments [8]. Among them, species of Alternaria, Bipolaris, Curvularia, or Stemphylium are important pathogenic fungi to plants of various crops, resulting in yield and economic losses [8][9][10]. However, they also include human and animal pathogens that cause infections with different clinical manifestations [11]. ...
... The aim of the present study was, therefore, to resolve the taxonomy of the above-mentioned isolates based on morphological features and multi-locus phylogenetic analysis inferred with sequences of the nuclear markers mostly represented in the different members of the Pleosporaceae. These are the LSU and ITS regions of the rDNA, and partial fragments of the RNA polymerase II largest subunit (rpb2), the translation elongation factor 1-α (tef1), and the glyceraldehyde-3-phosphate dehydrogenase (gapdh) genes [8,18,19]. Additionally, in order to elucidate the putative global geographic distribution of those isolates and to study their diversity hidden among environmental sequences, their ITS barcodes (i.e., full-length of ITS1 and ITS2 sequences) were blasted against the GlobalFungi database [20]. This is a recently created database, which currently includes accumulated data on fungal distribution and ecology generated from more than three hundred metagenomic studies published in the last decade (GlobalFungi database, accessed on 18 May 2022). ...
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Although the Pleosporaceae is one of the species-richest families in the Pleosporales, research into less-explored substrates can contribute to widening the knowledge of its diversity. In our ongoing survey on culturable Ascomycota from freshwater sediments in Spain, several pleosporacean specimens of taxonomic interest were isolated. Phylogenetic analyses based on five gene markers (ITS, LSU, gapdh, rbp2, and tef1) revealed that these fungi represent so far undescribed lineages, which are proposed as two novel genera in the family, i.e., Neostemphylium typified by Neostemphylium polymorphum sp. nov., and Scleromyces to accommodate Scleromyces submersus sp. nov. Neostemphylium is characterized by the production of phaeodictyospores from apically swollen and darkened conidiogenous cells, the presence of a synanamorph that consists of cylindrical and brown phragmoconidia growing terminally or laterally on hyphae, and by the ability to produce secondary conidia by a microconidiation cycle. Scleromyces is placed phylogenetically distant to any genera in the family and only produces sclerotium-like structures in vitro. The geographic distribution and ecology of N. polymorphum and Sc. submersus were inferred from metabarcoding data using the GlobalFungi database. The results suggest that N. polymorphum is a globally distributed fungus represented by environmental sequences originating primarily from soil samples collected in Australia, Europe, and the USA, whereas Sc. submersus is a less common species that has only been found associated with one environmental sequence from an Australian soil sample. The phylogenetic analyses of the environmental ITS1 and ITS2 sequences revealed at least four dark taxa that might be related to Neostemphylium and Scleromyces. The phylogeny presented here allows us to resolve the taxonomy of the genus Asteromyces as a member of the Pleosporaceae.
... Members of the Pleosporaceae are widely distributed across the environment and have a wide range of lifestyles, i.e., saprophytic, endo-/epiphytic, and parasitic on various hosts in terrestrial and aquatic environments [8]. Among them, species of Alternaria, Bipolaris, Curvularia, or Stemphylium are important pathogenic fungi to plants of various crops, resulting in yield and economic losses [8][9][10]. ...
... Members of the Pleosporaceae are widely distributed across the environment and have a wide range of lifestyles, i.e., saprophytic, endo-/epiphytic, and parasitic on various hosts in terrestrial and aquatic environments [8]. Among them, species of Alternaria, Bipolaris, Curvularia, or Stemphylium are important pathogenic fungi to plants of various crops, resulting in yield and economic losses [8][9][10]. However, they also include human and animal pathogens that cause infections with different clinical manifestations [11]. ...
... The aim of the present study was, therefore, to resolve the taxonomy of the above-mentioned isolates based on morphological features and multi-locus phylogenetic analysis inferred with sequences of the nuclear markers mostly represented in the different members of the Pleosporaceae. These are the LSU and ITS regions of the rDNA, and partial fragments of the RNA polymerase II largest subunit (rpb2), the translation elongation factor 1-α (tef 1), and the glyceraldehyde-3-phosphate dehydrogenase (gapdh) genes [8,18,19]. Additionally, in order to elucidate the putative global geographic distribution of those isolates and to study their diversity hidden among environmental sequences, their ITS barcodes (i.e., full-length of ITS1 and ITS2 sequences) were blasted against the GlobalFungi database [20]. This is a recently created database, which currently includes accumulated data on fungal distribution and ecology generated from more than three hundred metagenomic studies published in the last decade (GlobalFungi database, accessed on 18 May 2022). ...