From Wikipedia, the free encyclopedia

Exophiala phaeomuriformis
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Fungi
Division: Ascomycota
Class: Eurotiomycetes
Order: Chaetothyriales
Family: Herpotrichiellaceae
Genus: Exophiala
Species:
E. phaeomuriformis
Binomial name
Exophiala phaeomuriformis
Matos (2003)
Synonyms
  • Sarcinomyces phaeomuriformis T. Matsumoto (1986)

Exophiala phaeomuriformis is thermophilic fungus belonging to the genus Exophiala and the family Herpotrichiellaceae. [1] [2] it is a member of the group of fungi known as black yeasts, and is typically found in hot and humid locations, such as saunas, bathrooms, and dishwashers. [3] This species can cause skin infections [4] and is typically classified as a Biosafety Risk Group 2 agent. [5]

History

Exophiala phaeomuriformis is a member of the genus Exophiala, described in 1952 based on E. jeanselmei. [1] Thirty species of Exophiala are currently recognized [6] amongst which Exophiala (Wangiella) dermatitidis is the most common. [7] When studying samples of E. dermatitidis, Tadahiko Matsumoto and colleagues observed strains with a granular colonial form and distinctive microscopic morphology. [8] Based on the resemblance of these strains to the genus Sarcinomyces, they proposed the new name, S. phaeomuriformis. [8] This taxon was transferred to the genus Exophiala by Tiago Matos and co-workers in 2003 because of its yeast-like morphology (rather than the meristematic form characteristic to members of the genus Sarcinomyces), and its closer DNA homology to the genus Exophiala. [9]

Exophiala phaeomuriformis is a dematiceous (darkly pigmented) fungus and member of the group of fungi known as the black yeasts. [10] [11] Black yeasts are an unrelated category of fungi that share yeast-like morphology and possess darkly melanized cell walls. [5] Although their DNA sequences are distinctive, E. phaeomuriformis and E. dermatitidis are so closely related that the two cannot be reliably differentiated morphologically or physiologically. [5] [12] Antigenic cross-reactivity suggests that E. phaeomuriformis may have originated as multicellular variant of E. dematitidis. [10]

Growth and morphology

Like many other black yeasts, Exophiala phaeomuriformis is known only by its asexual form and no sexual form has been found. [4] [5] [8] It is a thermophilic fungus preferring temperatures between 37–42 °C (99–108 °F) [2] but growing at any temperature between 15–42 °C (59–108 °F). [3] Exophilala phaeomuriformis is more sensitive than other black yeasts to salt, incapable of growth at concentrations of sodium chloride exceeding 17%. [3] Like other members of the genus Exophiala, it is able to tolerate a wide range of pH (2.5–12.5). [3]

Colonies of E. phaeomuriformis are hyaline, mycoid, and smooth when young [9] but become black, dry, crumbly, raised, and mulberry-like in texture with age. [4] [8] Some strains fail to undergo this morphological switch and remain yeast-like in age. [5] [8] By contrast, many strains of E. dermatitidis become mycelial with age. [8] Hyphal growth has not been observed in E. phaeomuriformis. [8] Instead, colonies develop from loosely packed, single, and rounded budding yeast cells that are either scattered or aggregated in groups. [5] [8] Vegetative cells can either by unicellular or muriform (septate in all planes) or become divided by transverse septa only. [4] [8] Yeast cells are thick-walled and spherical or near-spherical in shape. [4] [5] Budding cells can have broad bases, occur in chains, and be multilateral, budding in different directions. [9]

Physiology

Like other member of the genus Exophiala, E. phaeomuriformis is saprotrophic, obtaining its energy exclusively from non-living organic materials. [6] When inoculated on a suitable growth medium under optimal conditions, the growth of E. phaeomuriformis is initiated in roughly 3 days; [3] however, when subject to competition, the cells may remain in a stationary state for many weeks prior to the development of visible growth. [3] Similar to E. dematitidis, E. phaeomuriformis is unable to assimilate nitrate, nitrite and melibiose; however it differs in it that some strains are unable to metabolize D-gluconate, D-glucuronate, D-galacturonate and glucono-δ-lactone. [10]

Habitat and ecology

Exophiala phaeomuriformis has a proclivity for environments rich in mono- and polyaromatic compounds, such as hydrocarbons, where it uses these compounds as sources of energy. [3] The species is plurivorous, occurring on a wide range of materials from contaminated soils and toluene rich environments to wild berries and animal feces. [3] It is also found in environments containing the preservative creosote, such as railroad ties where it is an important agent of biodeterioration. [3] [13] In indoor environments, E. phaeomuriformis occurs in warm and moist environments such as toilets, saunas, or dishwashers. [2] This species is found world-wide. [14]

Human disease

Exophiala phaeomuriformis is a rare causative agent of phaeohyphomycosis [15] in cutaneous, subcutaneous and deep tissues, [4] and is responsible for 6.4% of infections caused by black yeasts. [7] Infection usually occurs following skin abrasion or penetrating injuries. [11] Exophiala phaeomuriformis can also cause corneal infection following eye exposure to contaminated water. [1] People with cystic fibrosis (CF) are considered abnormally susceptible to Exophiala infections, including E. phaeomuriformis. [14] [16] It has been suggested that differences in the microbiota profiles of CF patients may be responsible for this predisposition. [17] Treatment of E. phaeomuriformis involves a combination of surgical debridement and antifungal therapy. [15] A range of antifungal agents including caspofungin, voriconazole, itraconazole, posaconazole, and amphotericin B are active against this species. [16] [18] Due to its pathogenic potential, E. phaeomuriformis is regarded as a Biosafety Risk Group 2 agent in the laboratory. [5]

References

  1. ^ a b c Aggarwal, Shruti; Yamaguchi, Takefumi; Dana, Reza; Hamrah, Pedram (October 2015). "Exophiala phaeomuriformis Fungal Keratitis". Eye & Contact Lens: Science & Clinical Practice. 43 (2): e4–e6. doi: 10.1097/ICL.0000000000000193. PMID  26513718.
  2. ^ a b c Ozhak-Baysan, B.; O unc, D.; Do en, A.; Ilkit, M.; de Hoog, G. S. (6 April 2015). "MALDI-TOF MS-based identification of black yeasts of the genus Exophiala". Medical Mycology. 53 (4): 347–352. doi: 10.1093/mmy/myu093. PMID  25851261.
  3. ^ a b c d e f g h i Döğen, Aylin; Kaplan, Engin; Ilkit, Macit; de Hoog, G. Sybren (3 November 2012). "Massive Contamination of Exophiala dermatitidis and E. phaeomuriformis in Railway Stations in Subtropical Turkey". Mycopathologia. 175 (5–6): 381–386. doi: 10.1007/s11046-012-9594-z. PMID  23124309. S2CID  16726797.
  4. ^ a b c d e f Howard, Dexter H., ed. (2003). Pathogenic fungi in humans and animals (2. ed.). New York [u.a.]: Dekker. ISBN  0-8247-0683-8.
  5. ^ a b c d e f g h de Hoog, G.S.; Guarro, J; Gene, J; Figueras, M.J. (1995). Atlas of Clinical Fungi (2nd ed.). Amer Society for Microbiology.
  6. ^ a b Woo, Patrick C. Y.; Ngan, Antonio H. Y.; Tsang, Chris C. C.; Ling, Ian W. H.; Chan, Jasper F. W.; Leung, Shui-Yee; Yuen, Kwok-Yung; Lau, Susanna K. P. (January 2013). "Clinical Spectrum of Exophiala Infections and a Novel Exophiala Species, Exophiala hongkongensis". Journal of Clinical Microbiology. 51 (1): 260–267. doi: 10.1128/JCM.02336-12. PMC  3536265. PMID  23152554.
  7. ^ a b Zeng, J. S.; Sutton, D. A.; Fothergill, A. W.; Rinaldi, M. G.; Harrak, M. J.; de Hoog, G. S. (27 June 2007). "Spectrum of Clinically Relevant Exophiala Species in the United States". Journal of Clinical Microbiology. 45 (11): 3713–3720. doi: 10.1128/JCM.02012-06. PMC  2168524. PMID  17596364.
  8. ^ a b c d e f g h i Matsumoto, T.; Padhye, A.A.; Ajello, L.; McGinnis, M.R. (January 1986). "a new dematiaceous hyphomycete". Medical Mycology. 24 (5): 395–400. doi: 10.1080/02681218680000601. PMID  3783362.
  9. ^ a b c Matos, T.; Haase, G; Gerrits van den Ende, A.H.G; deHoog, G (2003). "Molecular diversity of oligotrophic and neurotropic members of the black yeast genus Exophiala, with accent on E. dermatitidis". Antonie van Leeuwenhoek. 83 (4): 293–303. doi: 10.1023/A:1023373329502. PMID  12777065. S2CID  4849346.
  10. ^ a b c Uijthof; Van Belkum; De Hoog; Haase (25 July 2008). "Exophiala dermatitidis and Sarcinomyces phaeomuriformis: ITS1-sequencing and nutritional physiology". Medical Mycology. 36 (3): 143–151. doi: 10.1111/j.1365-280X.1998.00143.x. PMID  9776827.
  11. ^ a b Rogers, Everett Smith Beneke, Alvin Lee (1996). Medical mycology and human mycoses. Belmont, Calif.: Star Pub. Co. ISBN  0-89863-175-0.{{ cite book}}: CS1 maint: multiple names: authors list ( link)
  12. ^ Haase, G.; Sonntag, L.; van de Peer, Y.; Uijthof, J. M. J.; Podbielski, A.; Melzer-Krick, B. (March 1995). "Phylogenetic analysis of ten black yeast species using nuclear small subunit rRNA gene sequences". Antonie van Leeuwenhoek. 68 (1): 19–33. doi: 10.1007/BF00873289. PMID  8526477. S2CID  2819521.
  13. ^ K June; Wang (1990). Identification manual for fungi from utility poles in the eastern United States. Rockville, Md.: American Type Culture Collection. pp.  356. ISBN  9780930009311.
  14. ^ a b Döğen, Aylin; Ilkit, Macit; de Hoog, G. Sybren (October 2013). "Black yeast habitat choices and species spectrum on high altitude creosote-treated railway ties". Fungal Biology. 117 (10): 692–696. doi: 10.1016/j.funbio.2013.07.006. PMID  24119407.
  15. ^ a b Kwon-Chung, K.J.; Bennett, John E. (1992). Medical mycology. Philadelphia: Lea & Febiger. ISBN  0-8121-1463-9.
  16. ^ a b Packeu, A.; Lebecque, P.; Rodriguez-Villalobos, H.; Boeras, A.; Hendrickx, M.; Bouchara, J.-P.; Symoens, F. (11 May 2012). "Molecular typing and antifungal susceptibility of Exophiala isolates from patients with cystic fibrosis". Journal of Medical Microbiology. 61 (Pt_9): 1226–1233. doi: 10.1099/jmm.0.042317-0. PMID  22580912.
  17. ^ Lebecque, Patrick; Leonard, Anissa; Huang, Daniel; Reychler, Grégory; Boeras, Anca; Leal, Teresinha; Symoens, Françoise (November 2010). "Exophiala (Wangiella) dermatitidis and cystic fibrosis – Prevalence and risk factors". Medical Mycology. 48 (O1): S4–S9. doi: 10.3109/13693786.2010.495731. PMID  21067329.
  18. ^ Rivard, Robert G.; McCall, Suzanne; Griffith, Matthew E.; Hawley, Joshua S.; Ressner, Roseanne A.; Borra, Himabindu; Moon, James E.; Beckius, Miriam L.; Murray, Clinton K.; Hospenthal, Duane R. (January 2007). "Efficacy of caspofungin and posaconazole in a murine model of disseminated infection". Medical Mycology. 45 (8): 685–689. doi: 10.1080/13693780701390157. PMID  17885951.
From Wikipedia, the free encyclopedia

Exophiala phaeomuriformis
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Fungi
Division: Ascomycota
Class: Eurotiomycetes
Order: Chaetothyriales
Family: Herpotrichiellaceae
Genus: Exophiala
Species:
E. phaeomuriformis
Binomial name
Exophiala phaeomuriformis
Matos (2003)
Synonyms
  • Sarcinomyces phaeomuriformis T. Matsumoto (1986)

Exophiala phaeomuriformis is thermophilic fungus belonging to the genus Exophiala and the family Herpotrichiellaceae. [1] [2] it is a member of the group of fungi known as black yeasts, and is typically found in hot and humid locations, such as saunas, bathrooms, and dishwashers. [3] This species can cause skin infections [4] and is typically classified as a Biosafety Risk Group 2 agent. [5]

History

Exophiala phaeomuriformis is a member of the genus Exophiala, described in 1952 based on E. jeanselmei. [1] Thirty species of Exophiala are currently recognized [6] amongst which Exophiala (Wangiella) dermatitidis is the most common. [7] When studying samples of E. dermatitidis, Tadahiko Matsumoto and colleagues observed strains with a granular colonial form and distinctive microscopic morphology. [8] Based on the resemblance of these strains to the genus Sarcinomyces, they proposed the new name, S. phaeomuriformis. [8] This taxon was transferred to the genus Exophiala by Tiago Matos and co-workers in 2003 because of its yeast-like morphology (rather than the meristematic form characteristic to members of the genus Sarcinomyces), and its closer DNA homology to the genus Exophiala. [9]

Exophiala phaeomuriformis is a dematiceous (darkly pigmented) fungus and member of the group of fungi known as the black yeasts. [10] [11] Black yeasts are an unrelated category of fungi that share yeast-like morphology and possess darkly melanized cell walls. [5] Although their DNA sequences are distinctive, E. phaeomuriformis and E. dermatitidis are so closely related that the two cannot be reliably differentiated morphologically or physiologically. [5] [12] Antigenic cross-reactivity suggests that E. phaeomuriformis may have originated as multicellular variant of E. dematitidis. [10]

Growth and morphology

Like many other black yeasts, Exophiala phaeomuriformis is known only by its asexual form and no sexual form has been found. [4] [5] [8] It is a thermophilic fungus preferring temperatures between 37–42 °C (99–108 °F) [2] but growing at any temperature between 15–42 °C (59–108 °F). [3] Exophilala phaeomuriformis is more sensitive than other black yeasts to salt, incapable of growth at concentrations of sodium chloride exceeding 17%. [3] Like other members of the genus Exophiala, it is able to tolerate a wide range of pH (2.5–12.5). [3]

Colonies of E. phaeomuriformis are hyaline, mycoid, and smooth when young [9] but become black, dry, crumbly, raised, and mulberry-like in texture with age. [4] [8] Some strains fail to undergo this morphological switch and remain yeast-like in age. [5] [8] By contrast, many strains of E. dermatitidis become mycelial with age. [8] Hyphal growth has not been observed in E. phaeomuriformis. [8] Instead, colonies develop from loosely packed, single, and rounded budding yeast cells that are either scattered or aggregated in groups. [5] [8] Vegetative cells can either by unicellular or muriform (septate in all planes) or become divided by transverse septa only. [4] [8] Yeast cells are thick-walled and spherical or near-spherical in shape. [4] [5] Budding cells can have broad bases, occur in chains, and be multilateral, budding in different directions. [9]

Physiology

Like other member of the genus Exophiala, E. phaeomuriformis is saprotrophic, obtaining its energy exclusively from non-living organic materials. [6] When inoculated on a suitable growth medium under optimal conditions, the growth of E. phaeomuriformis is initiated in roughly 3 days; [3] however, when subject to competition, the cells may remain in a stationary state for many weeks prior to the development of visible growth. [3] Similar to E. dematitidis, E. phaeomuriformis is unable to assimilate nitrate, nitrite and melibiose; however it differs in it that some strains are unable to metabolize D-gluconate, D-glucuronate, D-galacturonate and glucono-δ-lactone. [10]

Habitat and ecology

Exophiala phaeomuriformis has a proclivity for environments rich in mono- and polyaromatic compounds, such as hydrocarbons, where it uses these compounds as sources of energy. [3] The species is plurivorous, occurring on a wide range of materials from contaminated soils and toluene rich environments to wild berries and animal feces. [3] It is also found in environments containing the preservative creosote, such as railroad ties where it is an important agent of biodeterioration. [3] [13] In indoor environments, E. phaeomuriformis occurs in warm and moist environments such as toilets, saunas, or dishwashers. [2] This species is found world-wide. [14]

Human disease

Exophiala phaeomuriformis is a rare causative agent of phaeohyphomycosis [15] in cutaneous, subcutaneous and deep tissues, [4] and is responsible for 6.4% of infections caused by black yeasts. [7] Infection usually occurs following skin abrasion or penetrating injuries. [11] Exophiala phaeomuriformis can also cause corneal infection following eye exposure to contaminated water. [1] People with cystic fibrosis (CF) are considered abnormally susceptible to Exophiala infections, including E. phaeomuriformis. [14] [16] It has been suggested that differences in the microbiota profiles of CF patients may be responsible for this predisposition. [17] Treatment of E. phaeomuriformis involves a combination of surgical debridement and antifungal therapy. [15] A range of antifungal agents including caspofungin, voriconazole, itraconazole, posaconazole, and amphotericin B are active against this species. [16] [18] Due to its pathogenic potential, E. phaeomuriformis is regarded as a Biosafety Risk Group 2 agent in the laboratory. [5]

References

  1. ^ a b c Aggarwal, Shruti; Yamaguchi, Takefumi; Dana, Reza; Hamrah, Pedram (October 2015). "Exophiala phaeomuriformis Fungal Keratitis". Eye & Contact Lens: Science & Clinical Practice. 43 (2): e4–e6. doi: 10.1097/ICL.0000000000000193. PMID  26513718.
  2. ^ a b c Ozhak-Baysan, B.; O unc, D.; Do en, A.; Ilkit, M.; de Hoog, G. S. (6 April 2015). "MALDI-TOF MS-based identification of black yeasts of the genus Exophiala". Medical Mycology. 53 (4): 347–352. doi: 10.1093/mmy/myu093. PMID  25851261.
  3. ^ a b c d e f g h i Döğen, Aylin; Kaplan, Engin; Ilkit, Macit; de Hoog, G. Sybren (3 November 2012). "Massive Contamination of Exophiala dermatitidis and E. phaeomuriformis in Railway Stations in Subtropical Turkey". Mycopathologia. 175 (5–6): 381–386. doi: 10.1007/s11046-012-9594-z. PMID  23124309. S2CID  16726797.
  4. ^ a b c d e f Howard, Dexter H., ed. (2003). Pathogenic fungi in humans and animals (2. ed.). New York [u.a.]: Dekker. ISBN  0-8247-0683-8.
  5. ^ a b c d e f g h de Hoog, G.S.; Guarro, J; Gene, J; Figueras, M.J. (1995). Atlas of Clinical Fungi (2nd ed.). Amer Society for Microbiology.
  6. ^ a b Woo, Patrick C. Y.; Ngan, Antonio H. Y.; Tsang, Chris C. C.; Ling, Ian W. H.; Chan, Jasper F. W.; Leung, Shui-Yee; Yuen, Kwok-Yung; Lau, Susanna K. P. (January 2013). "Clinical Spectrum of Exophiala Infections and a Novel Exophiala Species, Exophiala hongkongensis". Journal of Clinical Microbiology. 51 (1): 260–267. doi: 10.1128/JCM.02336-12. PMC  3536265. PMID  23152554.
  7. ^ a b Zeng, J. S.; Sutton, D. A.; Fothergill, A. W.; Rinaldi, M. G.; Harrak, M. J.; de Hoog, G. S. (27 June 2007). "Spectrum of Clinically Relevant Exophiala Species in the United States". Journal of Clinical Microbiology. 45 (11): 3713–3720. doi: 10.1128/JCM.02012-06. PMC  2168524. PMID  17596364.
  8. ^ a b c d e f g h i Matsumoto, T.; Padhye, A.A.; Ajello, L.; McGinnis, M.R. (January 1986). "a new dematiaceous hyphomycete". Medical Mycology. 24 (5): 395–400. doi: 10.1080/02681218680000601. PMID  3783362.
  9. ^ a b c Matos, T.; Haase, G; Gerrits van den Ende, A.H.G; deHoog, G (2003). "Molecular diversity of oligotrophic and neurotropic members of the black yeast genus Exophiala, with accent on E. dermatitidis". Antonie van Leeuwenhoek. 83 (4): 293–303. doi: 10.1023/A:1023373329502. PMID  12777065. S2CID  4849346.
  10. ^ a b c Uijthof; Van Belkum; De Hoog; Haase (25 July 2008). "Exophiala dermatitidis and Sarcinomyces phaeomuriformis: ITS1-sequencing and nutritional physiology". Medical Mycology. 36 (3): 143–151. doi: 10.1111/j.1365-280X.1998.00143.x. PMID  9776827.
  11. ^ a b Rogers, Everett Smith Beneke, Alvin Lee (1996). Medical mycology and human mycoses. Belmont, Calif.: Star Pub. Co. ISBN  0-89863-175-0.{{ cite book}}: CS1 maint: multiple names: authors list ( link)
  12. ^ Haase, G.; Sonntag, L.; van de Peer, Y.; Uijthof, J. M. J.; Podbielski, A.; Melzer-Krick, B. (March 1995). "Phylogenetic analysis of ten black yeast species using nuclear small subunit rRNA gene sequences". Antonie van Leeuwenhoek. 68 (1): 19–33. doi: 10.1007/BF00873289. PMID  8526477. S2CID  2819521.
  13. ^ K June; Wang (1990). Identification manual for fungi from utility poles in the eastern United States. Rockville, Md.: American Type Culture Collection. pp.  356. ISBN  9780930009311.
  14. ^ a b Döğen, Aylin; Ilkit, Macit; de Hoog, G. Sybren (October 2013). "Black yeast habitat choices and species spectrum on high altitude creosote-treated railway ties". Fungal Biology. 117 (10): 692–696. doi: 10.1016/j.funbio.2013.07.006. PMID  24119407.
  15. ^ a b Kwon-Chung, K.J.; Bennett, John E. (1992). Medical mycology. Philadelphia: Lea & Febiger. ISBN  0-8121-1463-9.
  16. ^ a b Packeu, A.; Lebecque, P.; Rodriguez-Villalobos, H.; Boeras, A.; Hendrickx, M.; Bouchara, J.-P.; Symoens, F. (11 May 2012). "Molecular typing and antifungal susceptibility of Exophiala isolates from patients with cystic fibrosis". Journal of Medical Microbiology. 61 (Pt_9): 1226–1233. doi: 10.1099/jmm.0.042317-0. PMID  22580912.
  17. ^ Lebecque, Patrick; Leonard, Anissa; Huang, Daniel; Reychler, Grégory; Boeras, Anca; Leal, Teresinha; Symoens, Françoise (November 2010). "Exophiala (Wangiella) dermatitidis and cystic fibrosis – Prevalence and risk factors". Medical Mycology. 48 (O1): S4–S9. doi: 10.3109/13693786.2010.495731. PMID  21067329.
  18. ^ Rivard, Robert G.; McCall, Suzanne; Griffith, Matthew E.; Hawley, Joshua S.; Ressner, Roseanne A.; Borra, Himabindu; Moon, James E.; Beckius, Miriam L.; Murray, Clinton K.; Hospenthal, Duane R. (January 2007). "Efficacy of caspofungin and posaconazole in a murine model of disseminated infection". Medical Mycology. 45 (8): 685–689. doi: 10.1080/13693780701390157. PMID  17885951.

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