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Brunneosphaerella jonkershoekensis (CBS H-20333). a, b. Leaf spots; c. globose ascomata visible on lesion surface; d. substomatal ascoma with central ostiole; e. vertical section through ascoma wall of textura angularis; f. germinating ascospore; g-i. asci; j. ascospores.-Scale bars = 10 µm.

Brunneosphaerella jonkershoekensis (CBS H-20333). a, b. Leaf spots; c. globose ascomata visible on lesion surface; d. substomatal ascoma with central ostiole; e. vertical section through ascoma wall of textura angularis; f. germinating ascospore; g-i. asci; j. ascospores.-Scale bars = 10 µm.

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... by P. telopea Maharachch., K.D. Hyde & Crous in Australia (Maharachchikumbura et al. 2014, Peng et al. 2022 (Ge et al. 2009, Feng et al. 2014. Neopestalotiopsis protearum (Crous & L. Swart) Maharachch., K.D. Hyde & Crous was identified as a pathogen causing widely distributed leaf spot and blight on several Protea and Leucospermum hosts in Australia, South Africa and Zimbabwe (Swart et al. 1999, Crous et al. 2011. Similarly, Pseudopestalotiopsis is mainly recognized as a leaf spot-causing foliar pathogenic genus on many hosts (Peng et al. 2022). ...
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Camellia sinensis (L.) Kuntze var. assamica (Miang tea) is widely distributed in northern Thailand due to its traditional and industrial attributes, including black tea and Miang production. In this study, two Pestalotioid taxa associated with C. sinensis leaf spots were collected in Mae Taeng district, Chiang Mai Province, Thailand. Species delineation was based on the evidence from morphological and multi-locus phylogenies using ITS, tub2 and tef1-α. Neopestalotiopsis saprophytica is herein reported as a new record on Camellia sinensis, while Pseudopestalotiopsis chinensis is recorded as a new geographical record from Thailand. The findings of this research have the potential to offer fresh insights into the two previously documented species within the existing fungal community associated with C. sinensis in Thailand. This, in turn, could enhance our comprehension of their interactions with the host plant in the times ahead.
... Currently, 32 DNA-identified Aureobasidium species are known (Table 1). These species include the best known Aureobasidium species, Aureobasidium pullulans, as well as the most recently identified species Aureobasidium insectorum, Aureobasidium planticola, Aureobasidium motuoense, and Aureobasidium intercalariosporum (Arnaud 1918;Arzanlou and Khodaei 2012;Ashish and Pratibha 2018;Barr 2001;Bills et al. 2012;Ciferri et al. 1957;Cooke 1962;Crous et al. 2021Crous et al. , 2011Hermanides-Nijhof 1977a, 1977b;Gostinčar et al. 2014;Inamdar et al. 2019;Jia et al. 2019;Jiang et al. 2021Jiang et al. , 2019Lee et al. 2021;Nasr et al. 2018;Onetto et al. 2020;Peterson et al. 2013;Ramaley 1992;Wang et al. 2022a;Wu et al. 2023). An additional 15 species have been identified based on morphology (Table 2) (Cooke 1962;Crisan and Hodisan 1964;Della Torre 1963;de Hoog and Hermanides-Nijhof 1977a;Pande and Ghate 1985;Richardson and Pitkäranta 2011). ...
... An additional 15 species have been identified based on morphology (Table 2) (Cooke 1962;Crisan and Hodisan 1964;Della Torre 1963;de Hoog and Hermanides-Nijhof 1977a;Pande and Ghate 1985;Richardson and Pitkäranta 2011). Various loci (i.e., the internal transcribed spacer (ITS) rDNA, intergenic spacer 1, translation elongation factor-1α, β-tubulin, large ribosomal subunit (LSU), and RNA polymerase II) have been used for the phylogeny of Aureobasidium (Crous et al. 2011;Gostinčar et al. 2014;Manitchotpisit et al. 2009;Peterson et al. 2013;Wang et al. 2022a;Zalar et al. 2008). Kabatiella and Aureobasidium are closely related based on morphology and DNA sequences, which makes them difficult to distinguish (Bills et al. 2012;Crous et al. 2011). ...
... Various loci (i.e., the internal transcribed spacer (ITS) rDNA, intergenic spacer 1, translation elongation factor-1α, β-tubulin, large ribosomal subunit (LSU), and RNA polymerase II) have been used for the phylogeny of Aureobasidium (Crous et al. 2011;Gostinčar et al. 2014;Manitchotpisit et al. 2009;Peterson et al. 2013;Wang et al. 2022a;Zalar et al. 2008). Kabatiella and Aureobasidium are closely related based on morphology and DNA sequences, which makes them difficult to distinguish (Bills et al. 2012;Crous et al. 2011). In fact, Kabatiella lini is now proposed to be part of the Aureobasidium clade (Thambugala et al. 2014). ...
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... Notes: Microsphaeropsis rafniae is phylogenetically close to M. proteae and M. fusca. However, it can be distinguished from those species by its smaller conidia (3-5 × 2-3 µm in vivo); M. fusca (5-10.5 × 3.5-6.5 μm in vitro) (Hou et al. 2020) and M. proteae (5-8 × 3.5-4 µm in vivo) (Swart et al. 1998, Crous et al. 2011. Microsphaeropsis fusca was originally isolated from twig lesions of Sarothamnus scoparius (Fabaceae) in the Netherlands, and M. proteae from leaves of Protea nitida (Proteaceae) in Hermanus, Western Cape Province, South Africa (Swart et al. 1998, Hou et al. 2020. ...
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... In recent years, with the high accessibility of sequencing services and a large amount of available molecular data, the number of novel Aureobasidium species is increasing. Thirteen new species have been proposed, namely, Aureobasidium acericola [10], A. aerium [11], A. castaneae [12], A. iranianum [13], A. leucospermi [14], A. mangrovei [15], A. microtermitis [16], A. mustum [17], A. pini [18], A. thailandense [19], A. tremulum [20], and A. uvarum and A. vineae [17]. ...
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Rosa (Rosaceae) is an important ornamental and medicinal plant genus worldwide, with several species being cultivated in China. Members of Sporocadaceae (pestalotioid fungi) are globally distributed and include endophytes, saprobes but also plant pathogens, infecting a broad range of host plants on which they can cause important plant diseases. Although several Sporocadaceae species were recorded to inhabit Rosa spp., the taxa occurring on Rosa remain largely unresolved. In this study, a total of 295 diseased samples were collected from branches, fruits, leaves and spines of eight Rosa species (R. chinensis, R. helenae, R. laevigata, R. multiflora, R. omeiensis, R. rugosa, R. spinosissima and R. xanthina) in Gansu, Henan, Hunan, Qinghai, Shaanxi Provinces and the Ningxia Autonomous Region of China. Subsequently 126 strains were obtained and identified based on comparisons of DNA sequence data. Based on these results 15 species residing in six genera of Sporocadaceae were delineated, including four known species (Pestalotiopsis chamaeropis, Pes. rhodomyrtus, Sporocadus sorbi and Spo. trimorphus) and 11 new species described here as Monochaetia rosarum, Neopestalotiopsis concentrica, N. subepidermalis, Pestalotiopsis tumida, Seimatosporium centrale, Seim. gracile, Seim. nonappendiculatum, Seim. parvum, Seiridium rosae, Sporocadus brevis, and Spo. spiniger. This study also represents the first report of Pes. chamaeropis, Pes. rhodomyrtus and Spo. sorbi on Rosa. The overall data revealed that Pestalotiopsis was the most prevalent genus, followed by Seimatosporium, while Pes. chamaeropis and Pes. rhodomyrtus were the two most prevalent species. Analysis of Sporocadaceae abundance on Rosa species and plant organs revealed that spines of R. chinensis had the highest species diversity. Citation: Peng C, Crous PW, Jiang N, et al. 2022. Diversity of Sporocadaceae (pestalotioid fungi) from Rosa in China. Persoonia 49: 201–260. https://doi.org/10.3767/persoonia.2022.49.07.
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Pestalotiod fungi are associated with a wide variety of plants worldwide and occur as endophytes, pathogens, and saprobes. The present study provides an updated phylogeny for genera Neopestalotiopsis, Pestalotiopsis, and Seiridium using fresh collections from woody oil plants (Camellia oleifera, Olea europaea, Paeonia suffruticosa, Sapium sebiferum, and Vernicia fordii) in Sichuan Province, China. We coupled morphology and combined sequence data analyses of ITS, tub2, and tef1-α for Neopestalotiopsis and Pestalotiopsis, with ITS, LSU, tub2, tef1-α, and rpb2 for Seiridium. Three novel species of Neopestalotiopsis (N. mianyangensis, N. paeonia-suffruticosa, N. terricola) and three of Seiridium (S. guangyuanum, S. vernicola, S. oleae), were found. Three other species, Pestalotiopsis kenyana, Seiridium ceratosporum, and S. rosarum were identified and reported as new records. All isolated species are fully described and illustrated. Additionally, the sexual morph of Pestalotiopsis kenyana is described for the first time. Pathogenicity tests revealed that Neopestalotiopsis mianyangensis, N. paeonia-suffruticosa, N. terricola, Pestalotiopsis kenyana, Seiridium guangyuanum, S. vernicola, and S. oleae are pathogenic on detached olive leaves.
... Initially, the internal transcribed spacers and intervening 5.8S nrDNA (ITS) and glyceraldehyde-3-phosphate dehydrogenase gene (GPDH) sequences well separated the three genera Pyrenophora, Bipolaris, and Curvularia (Berbee et al. 1999;Zhang and Berbee 2001); the same result was thereafter verified (Ariyawansa et al. 2014;Manamgoda et al. 2012). To date, many gene regions have been used to distinguish different Pyrenophora species, including ITS, the partial small subunit nrRNA gene (SSU), large subunit (28S) nrRNA gene (LSU), GPDH, chitin synthase gene (CHS), DNAdirected RNA polymerase II largest subunit gene (RPB1), DNAdirected RNA polymerase II second largest subunit gene (RPB2), and translation elongation factor 1-alpha gene (TEF) (Ariyawansa et al. 2014;Crous et al. 2011;Manamgoda et al. 2014;Schoch et al. 2012). DNA sequences of former isolates (e.g., CBS 258.80, ...
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Pyrenophora is not only as a genus of pathogens causing leaf damage but also as common seedborne fungi of Italian ryegrass (Lolium multiflorum Lam.). To elucidate the main seedborne Pyrenophora species, 36 seed samples of Italian ryegrass were collected; in total, 113 strains, representing 12.3% of all isolated strains (921), were identified as Pyrenophora species by the identity of ITS sequences in NCBI as well as the similarity of morphological characteristics, of which P. dictyoides (97) was the most frequent species. By pure culture technique, 24 representative pure isolates were eventually retained for further study. Based on DNA analysis of multiple loci (ITS, LSU, GPDH, CHS-1 and RPB1) and morphological characters, eight Pyrenophora species were finally identified, including P. avenicola, P. chaetomioides, P. dictyoides, P. lolii, P. nobleae, P. teres, P. triseptata and P. tritici-repentis; among them, P. avenicola, P. tritici-repentis and P. triseptata were newly reported on Italian ryegrass worldwide. Seed inoculation showed that P. dictyoides, P. lolii and P. teres remarkably decreased the final germination percentages (FGP) and germination indexes (GI) compared with control treatments (P ≤ 0.05); and plant inoculation showed that P. dictyoides, P. lolii and P. nobleae could cause typical brown spot in vivo with higher infection rate (P ≤ 0.05). In conclusion, pathogenicity tests showed that all Pyrenophora species could both inhibit seed germination and infect Italian ryegrass plant to different degrees; among them, P. dictyoides was the most important seedborne pathogen coupled with the isolation and infection rate, followed by P. lolii and P. nobleae. The data generated in this study are helpful for the accurate identification of Pyrenophora species, and the development of seedborne disease management strategies.
... 3.75 × 1.5 μm) and E. singularis (av. 3.5 × 1.5 μm) (Gryzenhout et al. 2009, Jiang et al. 2019b (Saccardo 1905, Graham & Luttrell 1961, Roux 1986, Inderbitzin et al. 2000, Abler 2003, Crous et al. 2011c, Hou et al. 2020a initially hyaline, becoming brown to dark brown, mostly with 3-4 transverse septa and 0-1 longitudinal septa (Phookamsak et al. 2013). (Graham & Luttrell 1961, Inderbitzin et al. 2000, Abler 2003, Phookamsak et al. 2013, Chen et al. 2015b, Tennakoon et al. 2019). ...
... References: Graham & Luttrell 1961, Roux 1986, Inderbitzin et al. 2000, Abler 2003, Crous et al. 2011c, Phookamsak et al. 2013, Tennakoon et al. 2019, Hou et al. 2020a (morphology and pathogenicity); de , Chen et al. 2015b. Notes: Leptosphaerulina miscanthi formed a sister clade to L. briosiana and L. trifolii in the phylogenetic analysis based on four loci ( Fig. 34; LSU, ITS, rpb2 and tub2), but differs from L. briosiana in producing slightly longer asci (72-173 × 23.5-58.5 μm vs 109-122 × 55-59 μm), and from L. trifolii in its narrower asci (72-173 × 23.5-58.5 μm vs 91-137 × 65-71 μm) and smaller ascospores (32-42.5 × 13.5-18 μm vs 38-62 × 17-26 μm) (Graham & Luttrell 1961 Disease symptoms: Yellow aecia are sometimes visible on cones or needles of coniferous trees and other aecial hosts, infected needles shrivel and die soon after sporulation; yellow to brownish uredinia in small orange-yellow pustules on one or both leaf surfaces on telial hosts, commonly with yellow spots on leaves, eventually become necrotic; the whole trees have a golden appearance in severe infection; heavily infected leaves turn brown, wither, and curl at the margin before falling. ...
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