Difference between revisions of "Cryptococcosis"
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m (Text replace - "Lips - Anatomy & Physiology" to "Lips") |
m (Text replace - "[[Cardiorespiratory System - Anatomy & Physiology|" to "[[Cardiorespiratory System Overview - Anatomy & Physiology|") |
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*May be a primary pathogen or opportunistic | *May be a primary pathogen or opportunistic | ||
− | *Targets the [[Cardiorespiratory System - Anatomy & Physiology|respiratory system]] | + | *Targets the [[Cardiorespiratory System Overview - Anatomy & Physiology|respiratory system]] |
**Including the [[Paranasal sinuses - Anatomy & Physiology|paranasal sinuses]] | **Including the [[Paranasal sinuses - Anatomy & Physiology|paranasal sinuses]] | ||
**Also can be systemic, cutaneous, visceral, skeletal or ocular | **Also can be systemic, cutaneous, visceral, skeletal or ocular |
Revision as of 15:35, 9 September 2010
- Over 19 species
- C. neoformans only major pathogen
- Worldwide
- Occurs in high concentrations in pigeon droppings (high creatinine concentration)
- The pigeon is not infected
- C. neoformis colonise the droppings after they have been excreted
- Also found in fruit, milk and soil
- Exogenous, inhaled infection which is generally sporadic (non-contageous)
- Can also be absorbed via skin penetration and ingestion
- May be a primary pathogen or opportunistic
- Targets the respiratory system
- Including the paranasal sinuses
- Also can be systemic, cutaneous, visceral, skeletal or ocular
- Causes sporadic mastitis in cattle
- Can spread within the herd
- Affects the CNS of dogs and cats
- Causes cryptococcal meningitis in humans
- Also affects dolphins, foxes, ferrets, monkeys, birds, cheetahs and guinea-pigs
- Large yeast with capsule seen using India ink stain
- Stains with PAS (Periodic acis Schiff)
- Gram positive
- Grows on blood agar and Sabouraud's Dextrose agar forming white, granular colonies which become slimy, mucoid and turn creamy/brown within a week
- Species identified by carbohydrate assimilation tests
- Antigen and antibody should be tested for as antibody formed by the body is soon overwhelmed and neutralised by abundent polysaccharide antigen from the capsule in active, systemic infections
- Latex agglutination for antigen, complement fixation, ELISA and IFAT can be used