Английская Википедия:Capronia mansonii
Шаблон:Short description Шаблон:Speciesbox
Capronia mansonii is a mesophilic black yeast that is a part of the Herpotrichiellaceae.[1] The species is uncommon in nature but is saprotrophic in nature and been discovered on decaying plant matter, particularly wood.[1] This fungus is naturally found in the Netherlands and has successfully been cultured in lab.[2] It is a teleomorph of the ascomycota division and possesses brown spores.[3]
History and taxonomy
Capronia mansonii is a type of black yeast that was first discovered from an isolated strain in 1968.[1][2] The fungus was originally described from a strain in vitro found in Norway by Marie Beatrice Schol-Schwarz on an aspen tree, and it has not yet been described in situ.[2][4] This fungus was the first species in Herpotrichiellaceae discovered to create ascomata in an isolated culture.[3] It is one of the only five species out of thirty Capronia species that has successfully produced ascomata in vitro.[4] The basionym for this species is Dictyotrichiella mansonii.[5] Its anamorph is thought to be Exophiala mansonii but uncertainty and discourse remains.[2][6] The original anamorph was first thought to be Rhinocladiella atrovirens and then Exophiala castellanii [7][6] An analysis of rRNA gene sequences concluded that C. mansonii is the same biological species as E. castellanii.[6] Capronia mansonii is often misidentified as its sister species Capronia munkii but can be differentiated by its larger and thicker cell walls and more frequent ascospores that transversely septate.[2] It is also differentiated from its anamorph because it lacks conidia, slimy colonies, and aerial hyphae.[8]
Growth and morphology
This fungus is a teleomorph or sexual form that is formed in vitro. This species has yet to be described in situ.[4] The fungus is thought to be closely related to Exophiala dermatitidis, and is often hypothesized in literature to be the teleomorph of E. dermatitidis.[2] The fungus is a part of the ascomycota phylum, also commonly defined as sac fungi. This phylum is often defined by its possession of asci, a microscope sexual structure that produces non-motile spores called ascospores. The asci of C. mansonii produce 8 ascospores upon germination.[2] These ascospores begin with a glassy transparent appearance and then progress to a more grey-yellow, olive, and finally brown colour.[2][5] These ascospores have 4–5 transverse thick-walled septa and 1 incomplete longitudinal septum.[5] The spores have been described in literature as not tight at the septa.[2] Juvenile asci have thicker, longer, and more lightly coloured ascus walls whereas as fully matured asci form thinner dark brown walls that are filled with ascospores.[2] The ascomatal wall itself can range from a brown-yellow to a light brown colour which is commonly seen in other black yeasts.[2]
Physiology and reproduction
This mesophilic fungus has been successfully cultured by Untereiner at room temperature ranging from 20–25 °C.[4][9] C. mansonii has also been observed in a yeast budding form.[1] This fungus has a homothallic breeding system indicating that it does not need a partner to sexually reproduce.[4] The ascospores of this fungus have been described to germinate within 12 hours on Oatmeal Agar.[4][3] They appear slimy and resemble yeast within 48 hours, reaching full maturity at 16 weeks.[4] The ascomata that have been grown in lab have been shown to fully mature and develop septae but are unable to produce asci and ascospores.[4] Artificial daylight is thought to be the limiting factor that prevents the production of asci.[9] Further replications of the above experiments revealed that the structure formed may actually be a pseudothecium, an ascocarp that resembles a ascocarp but whose asci do not organize into a hymenium.[9] The pseudothecia grew in abundance and also failed to produce ascospores.[9]
Habitat and ecology
Members of the Capronia family are described as saprotrophic meaning they get their nutrients from decaying matter.[9] Strains of this fungus have been found on various plant hosts, particularly on their leaves.[4] They are regularly found on other decaying ascomycota and basidiomycota in the Netherlands, particularly on the wood of Populus tremula.[5][10] The holotype was discovered on the stems of a Lupinus polyphyllus by Schol-Schwarz in 1968.[5][10] This fungus has occasionally been found on fresh sausages consisting of pork, beef, or mixed meats.[1] They remain unstable on meat and are unable to persist for more than three days in the presence of other lactic acid bacteria.[1]
References
- ↑ 1,0 1,1 1,2 1,3 1,4 1,5 Ошибка цитирования Неверный тег
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; для сносокcocolin2004
не указан текст - ↑ 2,00 2,01 2,02 2,03 2,04 2,05 2,06 2,07 2,08 2,09 2,10 Ошибка цитирования Неверный тег
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; для сносокuntereiner1997
не указан текст - ↑ 3,0 3,1 3,2 Ошибка цитирования Неверный тег
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; для сносокscholschwarz1968
не указан текст - ↑ 4,0 4,1 4,2 4,3 4,4 4,5 4,6 4,7 4,8 Ошибка цитирования Неверный тег
<ref>
; для сносокuntereiner1995
не указан текст - ↑ 5,0 5,1 5,2 5,3 5,4 Ошибка цитирования Неверный тег
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; для сносокmuller1987
не указан текст - ↑ 6,0 6,1 6,2 Ошибка цитирования Неверный тег
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; для сносокhaas1995
не указан текст - ↑ Ошибка цитирования Неверный тег
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; для сносокellis1971
не указан текст - ↑ Ошибка цитирования Неверный тег
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; для сносокhoog1977
не указан текст - ↑ 9,0 9,1 9,2 9,3 9,4 Ошибка цитирования Неверный тег
<ref>
; для сносокuntereiner1994
не указан текст - ↑ 10,0 10,1 Ошибка цитирования Неверный тег
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; для сносокuntereiner1999
не указан текст