Filobasidiella Kwon-Chung (1975)
Tsuchiyaea Y. Yamada, H. Kawas., Itoh, I. Banno & Nakase (1988)
Cryptococcus is a genus of fungi in the familyCryptococcaceae that includes both yeasts and filamentous species. The filamentous, sexual forms or teleomorphs were formerly classified in the genus Filobasidiella, while Cryptococcus was reserved for the yeasts. Most yeast species formerly referred to Cryptococcus have now been placed in different genera. The name Cryptococcus comes from the Greek for "hidden sphere" (literally "hidden berry"). Some Cryptococcus species cause a disease called cryptococcosis.
Taxonomy
The genus was described by French mycologist Jean Paul Vuillemin in 1901, when he failed to find ascospores characteristic of the genus Saccharomyces in the yeast previously known as Saccharomyces neoformans.[1] Over 300 additional names were subsequently added to the genus, almost all of which were later removed following molecular research based on cladistic analysis of DNA sequences. As a result, some ten species are currently recognized in Cryptococcus.[2]
The teleomorph was first described in 1975 by K.J. Kwon-Chung, who obtained cultures of the type species, Filobasidiella neoformans, by crossing strains of the yeast Cryptococcus neoformans. She was able to observe basidia similar to those of the genus Filobasidium, hence the name Filobasidiella for the new genus.[3] Following changes to the International Code of Nomenclature for algae, fungi, and plants, the practice of giving different names to teleomorph and anamorph forms of the same fungus was discontinued, meaning that Filobasidiella became a synonym of the earlier name Cryptococcus.
General characteristics
The cells of species that produce yeasts are covered in a thin layer of glycoprotein capsular material that has a gelatin-like consistency, and that among other functions, serves to help extract nutrients from the soil. The C. neoformanscapsule consists of several polysaccharides, of which the major one is the immunomodulatory polysaccharide called glucuronoxylomannan (GXM).[4] GXM is made up of the monosaccharidesglucuronic acid, xylose and mannose and can also contain O-acetyl groups. The capsule functions as the major virulence factor in cryptococcal infection and disease.[5]
Some Cryptococcus species have a huge diversity at the infraspecific level with different molecular types based on their genetic differences, mainly due to their geographical distribution, molecular characteristics, and ecological niches.[6]
Cryptococcus species are not known to produce distinct, visible fruitbodies. All teleomorph forms appear to be parasites of other fungi. In teleomorphs the hyphae are colourless, are clamped or unclamped, and bear haustorial cells with filaments that attach to the hyphae of host fungi.[7][8] The basidia are club-shaped and highly elongated. Spores arise in succession from four loci at the apex (which is sometimes partly septate). These spores are passively released and may remain on the basidium in chains, unless disturbed.[3] In the type species, the spores germinate to form yeast cells, but yeast states are not known for all species.
Habitat, distribution and species
Field stain showing Cryptococcus species in lung tissue
Cryptococcus neoformans is cosmopolitan and is the most prominent medically important species. It is best known for causing a severe form of meningitis and meningoencephalitis in people with HIV/AIDS. It may also infect organ-transplant recipients and people receiving certain cancer treatments.[9] In its yeast state C. neoformans is found in the droppings of wild birds, often pigeons; when dust of the droppings is stirred up, it can infect humans or pets that inhale the dust. Infected humans and animals do not transmit their infection to others.[9] The taxonomy of C. neoformans has been reviewed: it has now been divided into two species: Cryptococcus neoformanssensu stricto and Cryptococcus deneoformans.[10][2]
Cryptococcus gattii (formerly C. neoformans var. gattii) is endemic to tropical parts of the continent of Africa and Australia. It is capable of causing disease in non-immunocompromised people. In its yeast state it has been isolated from eucalyptus trees in Australia. The taxonomy of C. gattii has been reviewed; it has now been divided into five species: C. gattiisensu stricto, C. bacillisporus, 'C. deuterogattii, C. tetragattii, and C. decagattii.[10][2]
Cryptococcus depauperatus is parasitic on Lecanicillium lecanii, an entomopathogenic fungus, and is known from Sri Lanka, England, the Netherlands, the Czech Republic, and Canada.[8][11] It is not known to produce a yeast state.[12] This species grows as long, branching filaments and is self-fertile, i.e. it is homothallic.[13] It can reproduce sexually with itself throughout its life cycle.[13]
Cryptococcus luteus is parasitic on Granulobasidium vellereum, a corticioid fungus, and is known from England and Italy.[14] It too is not known to produce a yeast state.[15]
Cryptococcus amylolentus was originally isolated as a yeast from beetle tunnels in South African trees. It forms a basidia-bearing teleomorph in culture.[16]
^ abKwon-Chung KJ. (1975). "A new genus, Filobasidiella, the perfect state of Cryptococcus neoformans". Mycologia. 67 (6): 1197–1200. doi:10.2307/3758842. JSTOR3758842. PMID765816.
