Geotrichum candidum is a fungus which is a member of the human microbiome, notably associated with skin, sputum and feces where it occurs in 25-30% of specimens. It is common in soil and has been isolated from soil collected around the world, in all continents.
G. candidum is the causative agent of the human disease geotrichosis, the plant disease sour rot which infects citrus fruits, tomatoes, carrots, and other vegetables. It can affect havested fruit of durians such as Durio graveolens
G. candidum is used widely in the production of certain dairy products including rind cheeses such as Camembert, Saint-Nectaire, Reblochon and others. The fungus can also be also found in a Nordic yogurt-like product known as viili where it is responsible for the product's velvety texture.
The genus Geotrichum was described by Johann Heinrich Friedrich Link in 1809 to accommodate the species G. candidum found on decaying leaves. Since then, over 130 taxa have been described in the genus, and hundreds of synonyms have been generated. For example, G. candidum was misclassified as the Oidium lactis in much early literature. Species of Geotrichum resemble the genera Trichosporon and Protendomycopsis; however, Geotrichum is of ascomycetous affiliation whereas the latter are members of the Basidiomycota. Species of Geotrichum are occasionally mistaken for fast growing members of the genus Dipodascus, which are characterized by irregularly branched, 10-14 μm wide hyphae and the production of single-spored asci. However, unlike Geotrichum, members of the genus Dipodascus lack dichotomous branching of the peripheral hyphae and their growth rates are generally less than 3 mm per day.
Galactomyces candidus, formerly thought to be a distinct taxon, was found to be the sexual state of G. candidum using sequence-based methods Geotrichum candidum in the broad sense comprises 3 clades, corresponding to the species G. candidum, G. clavatum and G. fici, all of which are thought to have pathogenic potential. Species of Geotrichum can be differentiated by sequence analysis of the nuclear ribosomal large subunit (18S ribosomal RNA) or the internal transcribed spacer region of the nuclear ribosomal RNA gene.
G. candidum colonies are thin, spreading, soft, creamy and white in the anamorph state. The fungus G. candidum is characterized by hyphae that appear creeping, mostly submerged and septatee. The hyphae colour appears to be hyaline or lightly pigmented. When the hyphae becomes airborne it changes shape from arthroconidia to cylindrical or barrel-shaped or ellipsoidal. Chlamydospores are subglobose, solitary, borne on undifferentiated hyphae. Blastoconidia sometimes develop on hyphae laterally. Conidia appear arthrosporous, terminal or intercalary, aerial on an agar surface. The conidia size ranges from 4.8–12.5 μm x 2.4–2.5 μm.
G. candidum is thought to be homothallic but most isolates are self-sterile. Sexual reproduction was first observed in strains isolated from soils in Puerto Rico. The fungus produces globose asci that contain a single, thick walled, uninucleated, globose to oval ascospore measuring 6–7 μm by 7–10 μm. The ascospores have a smooth inner wall and a furrowed outer wall. The septa are perforated by microspores, arranged in a ring structure. The colonies appear to be growing faster in the sexual stage than the asexual stage. Colonies grow at a rate of 5–7 mm daily at 24 °C (75 °F).
. candidum is fast growing colony that can grow 5–6 cm diameter at 5 days on Sabouraud-glucose agar, wort agar and synthetic media. Microscopically, the growth is characterized by the production of dichotomously branched hyphae that resemble tuning forks along the colony margin. The condia chains become aerial, erect or decumbent and measures 6–12(–20) x 3–6(–9) μm. The fungus can grow on a variety of citrus fruits and cause rotting. It tends to cause rotting in fruits that are stored at 0–5 °C (32–41 °F). The conidia are colourless and have a slimy texture. G. candidum is also found occasionally in the human gut, feces, sputum and on skin. The fungus grows in soil, water, sewage, various plant substrates, baker’s dough, husks of fermentation, bread, milk and milk products The optimal temperature for growth is 25 °C (77 °F) with a pH range of 5.0–5.5. The temperature range changes depending on the surface that the fungus grows on. For example, in plants the optimum temperature ranges from 25–27 °C (77–81 °F). In animals the optimum temperature ranges from 30–31 °C (86–88 °F). The maximum temperature for growth is 35–38 °C (95–100 °F). Fungal growth can be supported by D-glucose, D-mannose, D-xylose, L-sorbose, D-fructose, D-galactose, sucrose, D-mannitol, SorbitolD-sorbital, ethanol and glycerol. Sporulation often requires balance of carbon and nitrogen.
G. candidum is extremely common in soil and has been isolated from substrates in Canada, United States, Britain, Germany, Austria, India, South Africa, Japan, Brazil and Peru. It is also found as a causal agent in sour rot in citrus fruits— a soft rot associated with the emission of a fruity odour. The fungus is also known as a post-harvest spoilage agent of muskmelon, squash and cucumber. It plays a role in tomato fruit rot when it is stored at 0–5 °C (32–41 °F).
G. candidum can be used commercially to inoculate wash-rinds and bloomy rind cheeses. Cultures can be added to milk, brine or sprayed onto cheese surface. The optimum pH range for growth on cheese ranges from 4.4 to 6.7. The fungus colonizes nearly the entire surface of the cheese during the early stages of ripening. It is found on soft cheeses like Camembert cheese and semi-hard cheese Saint-Nectaire and Reblochon. For the Camembert cheese the fungi grows on the outside of the cheese forming a rind. The fungus is responsible for the uniform, white, velvety coat on Saint-Marcellin cheese. Lipases and proteases from G. candidum release fatty acids and peptides that provide the cheese with distinctive flavors. G. candidum reduces the bitterness in Camembert cheese through the activity of the aminopeptidases that hydrolyze low molecular weight hydrophobic peptides. Aminopeptidases also contributes an aroma in traditional Norman Camembert. The fungus also neutralizes the curd by catabolizing lactic acid produced by bacteria. G. candidum prepares the cheese for colonization of other acid sensitive bacteria such as Brevibacterium. The fungus inhibits growth of the bacteria Listeria monocytogenes. Commercial strains of G. candidum are available for cheese ripening.
- Domsch, K.H., W. Gams, and T.H. Anderson (1980) Compendium of Soil Fungi Volume 1, Academic Press, London, UK
- Domsch, K.H.; W. Gams, W.; Andersen, T.H. (1980). Compendium of soil fungi (2nd ed.). London, UK: Academic Press. ISBN 9780122204029.
- "Geotrichum spp". Doctor Fungus. Archived from the original on 1 November 2010. Retrieved 27 October 2014.
- Thornton, C.R.; Slaughter, C.D.; Davis, R.M. (2010). "Detection of the Sour-Rot Pathogen Geotrichum candidum in Tomatoes Fruit and Juice by Using a Highly Specific Monoclonal Antibody-Based ELISA". International Journal of Food Microbiology. 143 (3): 166–172. doi:10.1016/j.ijfoodmicro.2010.08.012.
- Sivapalan, A.; Metussin, Rosidah; Harndan, Fuziah; Zain, Rokiah Mohd (December 1998). "Fungi associated with postharvest fruit rots of Durio graveolens and D. kutejensis in Brunei Darussalam" (PDF). Australasian Plant Pathology. Netherlands: Springer. 27 (4): 274–277. doi:10.1071/AP98033. ISSN 1448-6032. OCLC 204773204. Retrieved 21 November 2017.
- Etienne A, Datry A, Gaspar N, et al. (May 2008). "Successful Treatment of Disseminated Geotrichum capitatum Infection with a Combination of Caspofungin and Voriconazole in an Immunocompromised Patient". Mycoses. 51 (3): 270–2. doi:10.1111/j.1439-0507.2007.01484.x. PMID 18399909. Archived from the original on 2013-01-23.
- Bosch, Xavier (2001-06-27). "Fungus eats CD". Nature News. doi:10.1038/news010628-11 (inactive 2017-12-04).
- Anonymous. "Geotrichum". MycoBank.
- Boutrou, R; Gueguen, M (2005). "Interests in Geotrichum candidum for Cheese Technology". International Journal of Food Microbiology. 102 (1): 1–20. doi:10.1016/j.ijfoodmicro.2004.12.028. PMID 15924999.
- Alper, I; Michel, F; Labrie, S (2011). "Ribosomal DNA Polymorphisms in the Yeast Geotrichum candidum". Fungal Biology. 115 (12): 1259–1269. doi:10.1016/j.funbio.2011.09.002.
- Sybren de Hoog, G; Smith, M. T (2004). "Ribosomal Phylogeny and Species Delimitation in Geotrichum and its Teleomorphs". Studies in Mycology. 50: 489–515.
- Mycology Online, University of Adelaide, South Australia
- Onions, A.H.S.; Allsopp, D.; Eggins, H.O.W. (1981). Smith's Introduction to Industrial Mycology (7th ed.). London, UK: Arnold. ISBN 0-7131-2811-9.
- Watanabe, Tsuneo. (2010). Pictorial Atlas of Soil and seed Fungi (3rd ed.). Baca Raton, FL: CRC Press. ISBN 9781439804193.
- Barron, G.L. (1968). The Genera of Hyphomycetes from Soil. Baltimore, MD: Williams & Wilkins. ISBN 9780882750040.
- Kwon-Chung, K.J.; Bennett, J.E.; Bennett, John E. (1992). Medical mycology. Philadelphia: Lea & Febiger. ISBN 0812114639.
- Malloch, David (1981). Moulds: Their Isolation, Cultivation and Identification. Toronto, ON: University of Toronto Press. ISBN 978-0802024183.
- Samson, R.A.; Hoekstra, E.S.; Oorschot, C.A.N (1984). Introduction to Food-borne Fungi (2nd ed.). The Netherlands: Centraalbureau voor Schimmelcultures: Institute of the Royal Netherlands Academy of Arts and Sciences.
- Mdaini, N; Gargo, M; Hammami, M; Monser, L; Hamdi, M (2006). "Production of Natural Fruity Aroma by Geotrichum candidum". Applied Biochemistry and Biotechnology. 128 (3): 127–136. doi:10.1385/abab:128:3:227.
- Moore-Landecke, Elizabeth (1972). Fundamentals of the Fungi. Englewood Cliffs, N.J.: Prentice-Hall Incorporated. ISBN 0-13-339267-8.
- Marcellino, N; Beuvier, E; Grappin, R; Gueguen, M; Benson, D.R (2001). "Diversity of Geotrichum candidum Strains Isolated From Traditional Cheesemaking Fabrications in France". Applied and Environmental Microbiology. 67 (10): 4752–4759. doi:10.1128/aem.67.10.4752-4759.2001.