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Cryptococcus neoformans is an encapsulated yeast that can live in both plants and animals. Its teleomorph is Filobasidiella neoformans, a filamentous fungus belonging to the class Tremellomycetes. It is often found in pigeon excrement.
Cryptococcus neoformans is composed of two varieties (v.): C. neoformans v. neoformans and v. grubii. A third variety, C. neoformans v. gattii, is now considered a distinct species, Cryptococcus gattii. C. neoformans v. grubii and v. neoformans have a worldwide distribution and are often found in soil that has been contaminated by bird excrement. The genome sequence of C. neoformans v. neoformans was published in 2005. Recent studies suggest that colonies of Cryptococcus neoformans and related fungi growing on the ruins of the melted down reactor of the Chernobyl Nuclear Power Plant may be able to use the energy of radiation (primary beta radiation) for "radiotrophic" growth.
Cryptococcus neoformans grows as a yeast (unicellular) and replicates by budding. C. neoformans makes hyphae during mating, and eventually creates basidiospores at the end of the hyphae before producing spores. Under host-relevant conditions, including low glucose, serum, 5% carbon dioxide, and low iron, among others, the cells produce a characteristic polysaccharide capsule. When grown as a yeast, C. neoformans has a prominent capsule composed mostly of polysaccharides. Under the microscope, the India ink stain is used for easy visualization of the capsule in cerebral spinal fluid. The particles of ink pigment do not enter the capsule that surrounds the spherical yeast cell, resulting in a zone of clearance or "halo" around the cells. This allows for quick and easy identification of C. neoformans. Unusual morphological forms are rarely seen. For identification in tissue, Mucicarmine stain provides specific staining of polysaccharide cell wall in Cryptococcus neoformans. Cryptococcal antigen from cerebrospinal fluid is thought to be the best test for diagnosis of cryptococcal meningitis in terms of sensitivity, though it might be unreliable in HIV-positive patients.
Infection with C. neoformans is termed cryptococcosis. Most infections with C. neoformans consist of a lung infection. However, fungal meningitis and encephalitis, especially as a secondary infection for AIDS patients, are often caused by C. neoformans making it a particularly dangerous fungus. Infections with this fungus are rare in those with fully functioning immune systems. For this reason, C. neoformans is sometimes referred to as an opportunistic fungus. It is a facultative intracellular pathogen.
In human infection, C. neoformans is spread by inhalation of aerosolized spores (basidiospores) and can disseminate to the central nervous system where it can cause meningoencephalitis. In the lungs, C. neoformans are phagocytosed by alveolar macrophages Macrophages produce oxidative and nitrosative agents, creating a hostile environment, to kill invading pathogens. However, some C. neoformans can survive intracellularly in macrophages. Intracellular survival appears to be the basis for latency, disseminated disease, and resistance to eradication by antifungal agents. One mechanism by which C. neoformans survives the hostile intracellular environment of the macrophage involves up-regulation of expression of genes involved in responses to oxidative stress.
Traversal of the blood–brain barrier by C. neoformans plays a key role in meningitis pathogenesis.  However, precise mechanisms by which C. neoformans passes blood-brain barrier are still unknown; one recent study in rats suggested an important role of secreted serine proteases. 
Meiosis (sexual reproduction), another possible survival factor for intracellular C. neoformans
The vast majority of environmental and clinical isolates of C. neoformans are mating type a. Filaments of mating type an ordinarily have haploid nuclei, but these can undergo a process of diploidization (perhaps by endoduplication or stimulated nuclear fusion) to form diploid cells termed blastospores. The diploid nuclei of blastospores are able to undergo meiosis, including recombination, to form haploid basidiospores that can then be dispersed. This process is referred to as monokaryotic fruiting. Required for this process is a gene designated dmc1, a conserved homologue of genes recA in bacteria, and rad51 in eukaryotes (see articles recA and rad51). Dmc1 mediates homologous chromosome pairing during meiosis and repair of double-strand breaks in DNA. (Also see article Meiosis.) Lin et al. suggested that one benefit of meiosis in C. neoformans could be to promote DNA repair in the DNA-damaging environment caused by the oxidative and nitrosative agents produced in macrophages. Thus, C. neoformans can undergo a meiotic process, monokaryotic fruiting, that may promote recombinational repair in the oxidative, DNA-damaging environment of the host macrophage, and this may contribute to its virulence.
Cryptococcosis that does not affect the central nervous system can be treated with fluconazole alone.
Cryptococcal meningitis should be treated for two weeks with intrathecal Amphotericin B 0.7–1.0 mg/kg/day and oral flucytosine 100 mg/kg/day (or intravenous flucytosine 75 mg/kg/day if the patient is unable to swallow). This should then be followed by oral fluconazole 400–800 mg daily for ten weeks and then 200 mg daily for at least one year and until the patient's CD4 count is above 200 cells/mcL. Flucytosine is a generic, off-patent medicine. However, there has been a market failure with a two-week cost of flucytosine therapy being approximately $10,000. As a result, flucytosine is currently universally unavailable in low- and middle-income countries. In 1970, flucytosine was available in Africa.
Intravenous Ambisome 4 (mg/kg)/day may be used but is not superior: Its main use is in patients that do not tolerate Amphotericin B. The dose of 200 mg/kg/day for flucytosine is not more effective, is associated with more side-effects and should not be used.
In Africa, oral fluconazole at a rate of 200 mg daily is often used. However, this does not result in cure because it merely suppresses the fungus and does not kill it; viable fungus can continue to be grown from CSF of patients not having taken fluconazole for many months. An increased dose of 400 mg daily does not improve outcomes, but prospective studies from Uganda and Malawi reported that higher doses of 1200 mg per day have more fungicidal activity. The outcomes with fluconazole monotherapy have 30% worse survival than amphotericin-based therapies, in a recent systematic review.
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|Wikimedia Commons has media related to Cryptococcus neoformans.|
- A good overview of Cryptococcus neoformans biology from the Science Creative Quarterly
- Cryptococcus neoformans biology, general information, life cycle image at MetaPathogen
- The outcome of Cryptococcus neoformans intracellular pathogenesis in human monocytes