Effects of hemin, CO₂, and pH on the branching of Candida albicans filamentous forms

Morphological transitions of wild-type and oxidative stress-tolerant Candida albicans strains were followed in the RPMI-FBS culture medium at pH values and CO2 levels characteristic for the anatomical niches inhabited by this opportunistic human pathogen fungus, including the oral cavity as well as the intestinal and vaginal lumens. Selected cultures were also supplemented with hemin modeling bleedings. Germination as well as elongation and branching of hyphae were monitored in the cultures using time-lapse video microscopy. Unexpectedly, branching time, which is defined as the time taken until the first branch of hypha emerges for the first time after germination, correlated well with alterations in the environmental conditions meanwhile no such correlations were found for germination time (time lasted until the appearance of the germination tube). Based on these observations, hypotheses were set up to estimate the significance of branching time in the pathogenesis of both superficial and systemic candidiases

Fungal Systematics and Evolution: FUSE 6

Fungal Systematics and Evolution (FUSE) is one of the journal series to address the “fusion” between morphological data and molecular phylogenetic data and to describe new fungal taxa and interesting observations. This paper is the 6th contribution in the FUSE series—presenting one new genus, twelve new species, twelve new country records, and three new combinations. The new genus is: Pseudozeugandromyces (Laboulbeniomycetes, Laboulbeniales). The new species are: Albatrellopsis flettioides from Pakistan, Aureoboletus garciae from Mexico, Entomophila canadense from Canada, E. frigidum from Sweden, E. porphyroleucum from Vietnam, Erythrophylloporus flammans from Vietnam, Marasmiellus boreoorientalis from Kamchatka Peninsula in the Russian Far East, Marasmiellus longistipes from Pakistan, Pseudozeugandromyces tachypori on Tachyporus pusillus (Coleoptera, Staphylinidae) from Belgium, Robillarda sohagensis from Egypt, Trechispora hondurensis from Honduras, and Tricholoma kenanii from Turkey. The new records are: Arthrorhynchus eucampsipodae on Eucampsipoda africanum (Diptera, Nycteribiidae) from Rwanda and South Africa, and on Nycteribia vexata (Diptera, Nycteribiidae) from Bulgaria; A. nycteribiae on Eucampsipoda africanum from South Africa, on Penicillidia conspicua (Diptera, Nycteribiidae) from Bulgaria (the first undoubtful country record), and on Penicillidia pachymela from Tanzania; Calvatia lilacina from Pakistan; Entoloma shangdongense from Pakistan; Erysiphe quercicola on Ziziphus jujuba (Rosales, Rhamnaceae) and E. urticae on Urtica dioica (Rosales, Urticaceae) from Pakistan; Fanniomyces ceratophorus on Fannia canicularis (Diptera, Faniidae) from the Netherlands; Marasmiellus biformis and M. subnuda from Pakistan; Morchella anatolica from Turkey; Ophiocordyceps ditmarii on Vespula vulgaris (Hymenoptera, Vespidae) from Austria; and Parvacoccum pini on Pinus cembra (Pinales, Pinaceae) from Austria. The new combinations are: Appendiculina gregaria, A. scaptomyzae, and Marasmiellus rodhallii. Analysis of an LSU dataset of Arthrorhynchus including isolates of A. eucampsipodae from Eucampsipoda africanum and Nycteribia spp. hosts, revealed that this taxon is a complex of multiple species segregated by host genus. Analysis of an SSU–LSU dataset of Laboulbeniomycetes sequences revealed support for the recognition of four monophyletic genera within Stigmatomyces sensu lato: Appendiculina, Fanniomyces, Gloeandromyces, and Stigmatomyces sensu stricto. Finally, phylogenetic analyses of Rhytismataceae based on ITS–LSU ribosomal DNA resulted in a close relationship of Parvacoccum pini with Coccomyces strobi

Die Schulkind-Lehrperson-Beziehung im institutionellen Kontext der Primarschule

Data for the 45 bat flies infected with Laboulbeniales fungi encountered during this study. Given are bat and bat fly species, sex of bat and bat fly (F = female, M = male), country (H = Hungary, RO = Romania) and locality, year of collection, and position of infection on the bat fly host. (DOC 86 kb

Additional file 2: Table S2. of Parasites of parasites of bats: Laboulbeniales (Fungi: Ascomycota) on bat flies (Diptera: Nycteribiidae) in central Europe

Collection data of all 1,494 bat fly specimens sampled in this study and screened for presence of Laboulbeniales. Infected bat flies are highlighted and documentation is provided about the identification of the fungus and the position(s) on which thalli were found. (XLS 395 kb

Fungal Systematics and Evolution: FUSE 6

With only 138,000 formally described fungal species (Kirk 2019) out of an estimated 2.2–3.8 million (Hawksworth & Lücking 2017) to 6 million (Taylor et al. 2014), between 97.7 and 93.7% of fungal species are left to be characterized. These may be discovered in poorly studied habitats and geographic areas (e.g., tropical rainforests), as molecular novelties, within cryptic taxa, in fungal collections (e.g., new species hidden under current names and in unidentified material), and during studies of plant and insect collections (Hawksworth & Lücking 2017, Wijayawardene et al. 2020). This large discrepancy between described and undescribed species needs to be addressed and recent work has shown that mycologists are nowhere near levelling off the curve in describing new species (Hyde et al. 2020b). Together with other series—Fungal Biodiversity Profiles (Rossi et al. 2020), Fungal Diversity Notes (Hyde et al. 2020a), Fungal Planet (Crous et al. 2020a), Mycosphere Notes (Pem et al. 2019), New and Interesting Fungi (Crous et al. 2020b)—the Fungal Systematics and Evolution series published by Sydowia contributes to a much-needed acceleration of discovery and description of fungal diversity. The present paper is the sixth contribution in the FUSE series published by Sydowia, after Crous et al. (2015), Hernández-Restrepo et al. (2016), KrisaiGreilhuber et al. (2017), Liu et al. (2018), and Song et al. (2019). Altogether, one family, six genera, 67 species, and 22 combinations have been introduced in the FUSE series.publishedVersio

Fungal Systematics and Evolution: FUSE 6

With only 138,000 formally described fungal species (Kirk 2019) out of an estimated 2.2–3.8 million (Hawksworth & Lücking 2017) to 6 million (Taylor et al. 2014), between 97.7 and 93.7% of fungal species are left to be characterized. These may be discovered in poorly studied habitats and geographic areas (e.g., tropical rainforests), as molecular novelties, within cryptic taxa, in fungal collections (e.g., new species hidden under current names and in unidentified material), and during studies of plant and insect collections (Hawksworth & Lücking 2017, Wijayawardene et al. 2020). This large discrepancy between described and undescribed species needs to be addressed and recent work has shown that mycologists are nowhere near levelling off the curve in describing new species (Hyde et al. 2020b). Together with other series—Fungal Biodiversity Profiles (Rossi et al. 2020), Fungal Diversity Notes (Hyde et al. 2020a), Fungal Planet (Crous et al. 2020a), Mycosphere Notes (Pem et al. 2019), New and Interesting Fungi (Crous et al. 2020b)—the Fungal Systematics and Evolution series published by Sydowia contributes to a much-needed acceleration of discovery and description of fungal diversity. The present paper is the sixth contribution in the FUSE series published by Sydowia, after Crous et al. (2015), Hernández-Restrepo et al. (2016), KrisaiGreilhuber et al. (2017), Liu et al. (2018), and Song et al. (2019). Altogether, one family, six genera, 67 species, and 22 combinations have been introduced in the FUSE series

Notes for genera – Ascomycota

Knowledge of the relationships and thus the classification of fungi, has developed rapidly with increasingly widespread use of molecular techniques, over the past 10--15 years, and continues to accelerate. Several genera have been found to be polyphyletic, and their generic concepts have subsequently been emended. New names have thus been introduced for species which are phylogenetically distinct from the type species of particular genera. The ending of the separate naming of morphs of the same species in 2011, has also caused changes in fungal generic names. In order to facilitate access to all important changes, it was desirable to compile these in a single document. The present article provides a list of generic names of Ascomycota (approximately 6500 accepted names published to the end of 2016), including those which are lichen-forming. Notes and summaries of the changes since the last edition of `Ainsworth Bisby's Dictionary of the Fungi' in 2008 are provided. The notes include the number of accepted species, classification, type species (with location of the type material), culture availability, life-styles, distribution, and selected publications that have appeared since 2008. This work is intended to provide the foundation for updating the ascomycete component of the ``Without prejudice list of generic names of Fungi'' published in 2013, which will be developed into a list of protected generic names. This will be subjected to the XIXth International Botanical Congress in Shenzhen in July 2017 agreeing to a modification in the rules relating to protected lists, and scrutiny by procedures determined by the Nomenclature Committee for Fungi (NCF). The previously invalidly published generic names Barriopsis, Collophora (as Collophorina), Cryomyces, Dematiopleospora, Heterospora (as Heterosporicola), Lithophila, Palmomyces (as Palmaria) and Saxomyces are validated, as are two previously invalid family names, Bartaliniaceae and Wiesneriomycetaceae. Four species of Lalaria, which were invalidly published are transferred to Taphrina and validated as new combinations. Catenomycopsis Tibell Constant. is reduced under Chaenothecopsis Vain., while Dichomera Cooke is reduced under Botryosphaeria Ces. De Not. (Art. 59)