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Associations

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Animal / dung saprobe
sporangiophore of Cunninghamella echinulata is saprobic in/on dung or excretions of dung of Equus caballus

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Morphology

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Cunninghamella echinulata (C. echinulata) has globose to subglobose zygospores that are ornamented with warts, hooks, or blunt projections. The zygospore is also held by suspensor cells than can be equal or slightly unequal shown in Fig. 2. Lunn and Shipton (1983) observed rhizoid-like structures and pointed spines ornamenting the sporangiola when isolating this species, which can be observed in Fig. 1. The sporangiola are hyaline, clustered together on vesicles, and can be on branched or unbranched sporangiophores (Webster and Weber, 2007).

Fig. 1

http://i451.photobucket.com/albums/qq238/RockNRollA3/Mycology/i_zpsdbrqxnpf.png

Fig. 2

http://i451.photobucket.com/albums/qq238/RockNRollA3/Mycology/h_zps21twsgq5.png

References

  • Lunn J, Shipton W (1983) Re-evaluation of taxonomic criteria in Cunninghamella. Trans Br Mycol Soc 81:2 303-312
  • Webster J, Weber R (2007) Introduction to fungi. Cambridge 196-197

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Lunn J, Shipton W (1983) Re-evaluation of taxonomic criteria in Cunninghamella. Trans Br Mycol Soc 81:2 303-312 Webster J, Weber R (2007) Introduction to fungi. Cambridge 196-197
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Cunninghamella echinulata

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Classification:

Fungi – Mucoromycota – Mucoromycotina – Mucorales – Cunninghamellaceae – Cunninghamella

Synonym(s):

Oedocephalum echinulate (1891) R. Thaxter

Cunninghamella echinulate (1905) R. Thaxter

Muratella elegans (1913) G. Bainier and A. Sartory

Cunninghamella verticillata (1927) F. S. Paine

Cunninghamella dalmatica (1929) P.A.Pispek

Cunninghamella echinata (1929) P. A. Pispek

Cunninghamella bainieri (1939) N.A. Naumov

Reference

Mycobank (2016) Cunninghamella echinulate. www.mycobank.org (accessed 15 Oct 2016)

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Mycobank (2016) Cunninghamella echinulate. www.mycobank.org (accessed 15 Oct 2016)
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Cunninghamella echinulata

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Cunninghamella are found in soil, plant and animal material, and are globally dispersed among the tropics, subtropics, and temperate zones (Discovery Life, 2016).This genus of fungi can be difficult for classifying species, which is indicative of C. echinulata as it has been reclassified throughout its known existence. First described by Roland Thaxter as Oedocephalum echinulate in 1891, this fungus has a coenocytic (non-partitioned) mycelium, is areolate, and has oval, ornamented conidia (Alcorn and Yeager, 1938). One interesting feature is that apart from forming zygospores, this species can also form chlamydospores. C. echinulata can also act as mycoparasite of Rhizopus arrhizus, which is another Mucorales (Webster and Weber, 2007). Like others in Mucorales, C. echinulata is used in industry and pharmaceutical production. It contains terminal vesicles, is associated with mammalian metabolism, and can be cultivated in a lab setting (Blakeslee, 1905).

Various studies have been conducted in regard to C. echinulata’s metabolic capabilities, especially toward xenobiotic (foreign to the body) factors and drug metabolism (Smith and Rosazza, 1983). Cunninghamella, in general, are able to metabolize xenobiotics similar in processing to mammalian enzymatic systems. Furthermore, C. echinulata, as well as several other Cunninghamella species, has been researched due to various antitumor compounds arising from their ability to structurally modify organic compounds via microbial transformation (Asha and Vidyavathi, 2009).

In relatively recent years, C. echinulata has gained attention for its potential utilization in single cell oil production arising from renewable carbon sources (Fakas et al, 2009). It is an oleaginous, filamentous fungus that can accumulate triglycerides and cytosolic lipid bodies in larger amount that could result in an alternative oil source (Mukhopadhyay et al, 2011).

References

  • Alcorn G, Yeager C.C (1938) A monograph of the genus Cunninghamella with additional descriptions of several common species. Mycologia 30:6 653-658
  • Asha S, Vidyavathi M (2009) Cunninghamella – a microbial model for drug metabolism studies – a review. Biotechnol Adv 27:1 16-29
  • Blakeslee A.F (1905) Two conidia-bearing fungi. Cunninghamella and thamnocephalis, n. gen. Bot Gaz 40:3 161-170
  • Discovery Life (2016)Cunninghamella echinulate. www.discoverlife.org (accessed 26 Oct 2016)
  • Fakas S, Papanikolaou S, Batsos A, Galiotou-Panayotou M, Mallouchos A, Aggelis G (2009) Evaluating renewable carbon sources as substrates for single cell oil production by Cunninghamella echinulata and Mortierella isabellina. Biomass Bioenergy 33:4 573-580
  • Mukhopadhyay M, Singh A, Banerjee R (2011) Oleaginous fungi: a solution to oil crisis. Springer 403-414
  • Smith R, Rosazza J (1983) Microbial models of mammalian metabolism. J Nat Prod 46:1 79-91
  • Webster J, Weber R (2007) Introduction to fungi. Cambridge 196-197

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Refer to citations
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Alcorn G, Yeager C.C (1938) A monograph of the genus Cunninghamella with additional descriptions of several common species. Mycologia 30:6 653-658 Asha S, Vidyavathi M (2009) Cunninghamella – a microbial model for drug metabolism studies – a review. Biotechnol Adv 27:1 16-29 Blakeslee A.F (1905) Two conidia-bearing fungi. Cunninghamella and thamnocephalis, n. gen. Bot Gaz 40:3 161-170 Discovery Life (2016)Cunninghamella echinulate. www.discoverlife.org (accessed 26 Oct 2016) Fakas S, Papanikolaou S, Batsos A, Galiotou-Panayotou M, Mallouchos A, Aggelis G (2009) Evaluating renewable carbon sources as substrates for single cell oil production by Cunninghamella echinulata and Mortierella isabellina. Biomass Bioenergy 33:4 573-580 Mukhopadhyay M, Singh A, Banerjee R (2011) Oleaginous fungi: a solution to oil crisis. Springer 403-414 Smith R, Rosazza J (1983) Microbial models of mammalian metabolism. J Nat Prod 46:1 79-91 Webster J, Weber R (2007) Introduction to fungi. Cambridge 196-197
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Cunninghamella echinulata causing fatally invasive fungal sinusitis.

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We report a fatal case of invasive fungal sinusitis caused by Cunninghamella echinulata in a febrile, neutropenic 15-year-old male with relapsing acute leukemia. The isolate was recovered from a nasal biopsy from the right middle meatus, and microscopic examination of the tissue revealed angioinvasion and necrosis. Human infection caused by this organism has not been well documented; however, this report alerts us to its life-threatening potential.(PubMed.gov 2013)

References

  • Division of Medical Microbiology, Department of Pathology, the Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. rleblan4@jhmi.edu
  • Diagn Microbiol Infect Dis. 2013 Aug;76(4):506-9. doi: 10.1016/j.diagmicrobio.2013.03.009. Epub 2013 Apr 18. (site accessed 16 June 2015, PubMed.gov.)

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LeBlanc RE1, Meriden Z, Sutton DA, Thompson EH, Neofytos D, Zhang SX.
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Societal Significance

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C. echinulata has several aspects that give it an important ecological and medical role. As mentioned earlier, this species can yield antitumor components, which could give rise to potentially very effective cancer drugs and therapeutic steroid derivatives (Betts et al, 1974). However, despite such advantages it can cause mucormycosis in patients with compromised immune systems, especially since some strains are resistant to antifungal therapies (LeBlanc et al, 2013).

Another significant aspect of C. echinulata is its potential to act as a biofuel because of its ability to produce oil from raw substrates and accumulate lipids rarely found in plants or animals. This could potentially be a starting point for bio-diesel as its oleaginous properties convert microbial oils (lipids) into bio-diesel (Fakas et al, 2009). This is important because alternative oil sources have been an ongoing conversation in leading society to environmentally friendly practices.

C. echinulata can also aid in wastewater treatment being an effective biosorbent agent. Morsy (2004) researched C. echinulata’s effectiveness in removing metal ions from polluted water, specifically in Egypt. They compared this species to other zygomycetes such as Rhizopus arrhizus, Absidia orchidis, etc. and found C. echinulata able to remove heavy metals effectively when alkali treated or when immobilized. This is significant because this could potentially improve water reuse and quality.

CulturedC. echinulata

http://i451.photobucket.com/albums/qq238/RockNRollA3/Mycology/h_zpsehezlxy7.png

References

  • Betts R, Walters D, Rosazza J (1974) Microbial transformations of antitumor compounds. 1 conversion of acronycine to 9-hydroxyacronycine by Cunninghamella echinulata. J Med Chem 17:6 599-602
  • LeBlanc R, Meriden Z, Sutton D, Thompson E, Neofytos D, Zhang S (2013) Cunninghamella echinulata causing fatally invasive fungal sinusitis. Diagn Microbiol Infect Dis 76:4 506-509
  • Morsy S (2004) Cunninghamella echinulata a new biosorbent of metal ions from polluted water in Egypt. Mycologia 96:6 1183-1189

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Refer to citations
bibliographic citation
Betts R, Walters D, Rosazza J (1974) Microbial transformations of antitumor compounds. 1 conversion of acronycine to 9-hydroxyacronycine by Cunninghamella echinulata. J Med Chem 17:6 599-602 Fakas S, Papanikolaou S, Batsos A, Galiotou-Panayotou M, Mallouchos A, Aggelis G (2009) Evaluating renewable carbon sources as substrates for single cell oil production by Cunninghamella echinulata and Mortierella isabellina. Biomass Bioenergy 33:4 573-580 LeBlanc R, Meriden Z, Sutton D, Thompson E, Neofytos D, Zhang S (2013) Cunninghamella echinulata causing fatally invasive fungal sinusitis. Diagn Microbiol Infect Dis 76:4 506-509 Morsy S (2004) Cunninghamella echinulata a new biosorbent of metal ions from polluted water in Egypt. Mycologia 96:6 1183-1189
author
Savannah Gentry
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EOL authors

Cunninghamella echinulata

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Cunninghamella echinulata is a fungal species in the genus Cunninghamella.[1] It is an asexually reproducing fungus and a mesophile, preferring intermediate temperature ranges.[1][2] C. echinulata is a common air contaminant,[3] and is currently of interest to the biotechnology industry due to its ability to synthesize γ-linolenic acid[4] as well as its capacity to bioconcentrate metals.[5] This species is a soil saprotroph that forms rhizoids,[3] preferring soils enriched in nitrogen, phosphorus and potassium.[2] It has been reported occasionally an agent of mucormycosis following the inhalation of fungal spores.[6] Czapek's agar is a suitable growth medium for the propagation of C. echinulata.[7]

Taxonomy, growth and morphology

Cunninghamella echinulata is a member of the family, Cunninghamellaceae (phylum Mucoromycota).[1][8] This species is closely related to C. elegans, and both species share highly similar characteristics of growth and morphology. Colonies tend to be rapidly growing on most growth media producing a dense, white or greyish aerial mycelium.[9] Cunninghamella echinulata reproduces asexually and solely via yellow-brown, spiny, single-spored sporangioles that, due to the nature of the sporangiospore being retained within the sporangium, appear to have a two-layered outer wall.[1][10][11] This fungus grows by means of filaments that lack septa.[6][12] This is a common feature of members if the Mucoromycota where the hyphal compartments are either fully divided by septa or are completely continuous (coenocytic) and multinucleate. Zygospores of this fungus are only produced following the fusion of gametangia of compatible mating strains, exemplifying a heterothallic mating system.[13] Sporangiophores of this species are irregularly branched and do not resemble the sporangiospores typical of most other members of the Mucoromycota encountered in similar habitats.[13][9] The sporangioles produced by this fungus are larger in size (10–20 μm) than those of the closely related species, C. elegans.[13]

Physiology

Cunninghamella echinulata and other species of Cunninghamellaceae can be selectively grown on Czapek's solution agar,[7] a property unique to this family of the Mucorales. However, depending on the nutrients the agar is supplemented with, different media can alter the oxidative metabolism profile of this fungus.[14] This species grows better on acetate than d-glucose.[2] Additionally, if grown in liquid, cultures of this fungus can be externally stimulated to increase oxygen consumption by adding 2% montmorillonite or kaolinite.[2]

While this fungus is a mesophilic (preferring intermediate growth temperatures), it is able to grow between 6 °C (43 °F) and 45 °C (113 °F) although the rate of growth near the extremes of temperature tolerance is minimal.[2][6] The optimal temperature for the development of zygospores is between 25 °C (77 °F) and 35 °C (95 °F).[2] This species exhibits different growth characteristic depending on environmental influences. At a pH of 5.5, the fungus grows in small dense pellets;[14] but a more typical, radiating growth pattern is achieved at a pH of 8.0,[14] The presence of indole-3-acetic acid in the growth medium stimulates linear growth.[2]

When grown on medium containing hydrolysed tomato residue, this fungus utilizes glucose to synthesize triacylglycerols (TAG) rich in GLA.[4] This fungus has been investigated for use in the production of single cell oils (SCO) and storage lipids (like GLA).[15] C. echinulata is also able to selectively take up and sequester metal contaminants from polluted waters, suggesting a potential use in bioremediation of polluted water.[5] However, its role as an agent of opportunistic disease may limit its use in environmental remediation. Cunninghamella echinulata is able to grow on orange rind and assimilate carbohydrates into necessary biomolecules,[15] where the fermented peel does not exhibit appreciable discolouration or odour.[15] Growth of this fungus on organic nitrogen leads yields lipids rich in γ-linolenic acid (GLA).[4] The presence of an active monooxygenase system allows this species to perform oxidative demethylation and hydroxylation.[2] The fungus possesses a p450 cytochrome system similar to that in humans, making it a potentially useful model for the study liver-mediated drug metabolism.[14]

This species is also able to stereoselectively biotransform rac-mexiletine into hydroxymethyl mexiletine (HMM) and p-hydroxymexiletine (PHM), two metabolites also produced in humans.[14] Cunninghamella echinulata grown in yeast extract broth, trypticase soy medium or peptone broth at a pH of 8 yielded 0 μg/ml of breakdown products from the metabolism of rac-mexiletine.[14] The production of maximal HMM is achieved in yeast extract broth at a pH of 7.0.[14] Metabolic activity diminishes with increasing pH up to a maximum pH of 8.0.[14] At increased pH, C. echinulata shows preferential production of S-HMM over R-HMM, the two stereoisomers, specifically enantiomers, of HMM.[14] In order to achieve the highest quantity of GLA, Cunninghamella echinulata grows preferentially on nitrogen-depleted media with a C/N (carbon:nitrogen) molar ratio of 169.[15]

The species has been reported to exhibit antibacterial effects against Staphylococcus aureus and Salmonella typhus,[2] common agents of skin infections and food poisoning respectively. It is also known to inhibit root growth in various grass species in vitro.[2] The fungus is not known to produce mycotoxins.[13]

Habitat and ecology

Cunninghamella echinulata is a saprotrophic resident of the soils in warmer regions of the world, particularly those enriched with NPK fertilizers (Nitrogen, Phosphorus and Potassium).[1][2] It has been reported from both cultivated and uncultivated soils,[9][16] including soils from greenhouses and forests[7] in the mediterranean and subtropical zones but is thought to be comparatively rare in temperate zones.[9][13] Soil depth and pH are not considered to be strongly influential on the growth properties of this fungus in vivo.[2] This species is able to cause rot in foods such as Kola nuts[13] and is a common air contaminant.[3] It can be parasitized by other fungi including species of Piptocephalis,[12] and Trichoderma viride.[2] Additionally, its growth is inhibited in vitro by the fungus, Memnoniella echinata.[2]

Human disease

Disease caused by this fungus and other species of Mucorales is referred to as mucormycosis characterized by a rapidly progressive and destructively invasive disease with relatively low survival.[6] Literature reporting this agent in healthy people is lacking. As a consequence, this species is thought to be exclusively an opportunistic pathogen, affecting individuals with pre-existing health conditions. People with underlying health conditions such as HIV infection and diabetes are at heightened risk for mucormycosis.[6] Infections by C. echinulata are thought to arise from inhalation of fungal spores and are not communicable.[6] Relatively few case reports implicating C. echinulata are available. Of those that are, one prototypical case from 2005 reported a fatal rhinocerebral infection in a 15-year-old boy suffering from acute leukaemia.[6] Biopsy of the infected nasal tissue showed signs of necrosis and vascular invasion.[6]

Cunninghamella echinulata, like other members of the genus, exhibit strong resistance to the antifungal polyene, amphotericin B with a MIC (Minimum Inhibitory Concentration) ranging from 4-16μg/mL that varies according to strain.[6] Strains of C. echinulata also display greater tolerance to itraconazole and posaconazole than other members of the Mucorales.[6] The antifungal agent terbinafine, typically restricted to the treatment of nail and skin infections, shows a relatively low MIC ranging from 0.06 to 0.125 μg/mL.[6]

Biotechnology

It is commonly cultivated for its ability to produce GLA,[4] preferentially synthesizing R-PHM and S-HMM.[14] The fungus is able to synthesize γ-linolenic acid.[4] It also possesses the ability to bioabsorb metals, with the highest levels of bioabsorpotion reported 5 to 15 minutes after contact with the metals.[5] Adding NaOH to this fungus before it bioabsorbs metals enhances the uptake of Pb, Cu and Zn.[5] These uptake rates also seem to be influenced by pH where at a pH of 7.1, Zn was the most highly absorbed metal,[5] at a pH of 4, Pb was the most highly absorbed metal[5] and at a pH of 5, Cu was the most highly absorbed metal.[5] Cunninghamella echinulata has been used to transform cortexolone to hydrocortisone.[17] Hydroxylation of biphenyl oxide has been studied in C. echinulata.[18]

References

  1. ^ a b c d e Webster, John (1980). Introduction to Fungi. Cambridge: Cambridge university press. pp. 230. ISBN 0-521-22888-3.
  2. ^ a b c d e f g h i j k l m n Domsch, Gams, Heidi-Anderson, K.H, W, Traute (1980). Compendium of Soil Fungi (Vol I). Academic Press. p. 238.{{cite book}}: CS1 maint: multiple names: authors list (link)
  3. ^ a b c Skinner, Charles (1947). Molds, Yeasts and Actinomycetes. New York: John Wiley & Sons. p. 92.
  4. ^ a b c d e De-Wei, Li (2016). Biology of Microfungi. Springer. p. 555. ISBN 9783319291376.
  5. ^ a b c d e f g El-Morsy, El-Sayed M. (2016-12-01). "Cunninghamella echinulata a new biosorbent of metal ions from polluted water in Egypt". Mycologia. 96 (6): 1183–1189. doi:10.2307/3762133. ISSN 0027-5514. JSTOR 3762133. PMID 21148940.
  6. ^ a b c d e f g h i j k LeBlanc, Robert E.; Meriden, Zina; Sutton, Deanna A.; Thompson, Elizabeth H.; Neofytos, Dionissios; Zhang, Sean X. (2013-08-01). "Cunninghamella echinulata causing fatally invasive fungal sinusitis". Diagnostic Microbiology and Infectious Disease. 76 (4): 506–509. doi:10.1016/j.diagmicrobio.2013.03.009. ISSN 1879-0070. PMID 23602784.
  7. ^ a b c Mycology Guidebook. Seattle and London: University of Washington press. 1974. pp. 94, 96, 97. ISBN 0-295-95313-6.
  8. ^ Hawker, Lilian (1966). Fungi. London: Hutchinson University library. p. 76.
  9. ^ a b c d L. O.Donnell, Kerry (1979). Zygomycetes in Culture. Dept. of Botany, University of Georgia. p. 236.
  10. ^ Khan (1975). "Wall Structure and Germination of Spores in Cunninghamella echinulata". Journal of General Microbiology. 90: 115–124. doi:10.1099/00221287-90-1-115.
  11. ^ Watanabe, Tsuneo (2010). Pictorial Atlas of Soil and Seed Fungi. New York: CRC press. p. 69.
  12. ^ a b Gwynne-Vaughan, Barnes, H.C.I, B. (1927). Structure and Development of the Fungi. New York: The Macmillan company. pp. 115, 116.
  13. ^ a b c d e f Pitt, Hocking, John, Ailsa (1999). Fungi and Food Spoilage (2nd ED). Springer. pp. 178–180. ISBN 978-0-387-92206-5.
  14. ^ a b c d e f g h i j Freitag, D. G; Foster, R. T; Coutts, R. T; Pickard, M. A; Pasutto, F. M (1997). "Stereoselective metabolism of rac-mexiletine by the fungus Cunninghamella echinulata yields the major human metabolites hydroxymethylmexiletine and p-hydroxymexiletine". Drug Metab Dispos. 25 (6): 685–692. PMID 9193869.
  15. ^ a b c d Gema, H.; Kavadia, A.; Dimou, D.; Tsagou, V.; Komaitis, M.; Aggelis, G. (2002). "Production of γ-linolenic acid by Cunninghamella echinulata cultivated on glucose and orange peel". Applied Microbiology and Biotechnology. 58 (3): 303–307. doi:10.1007/s00253-001-0910-7. ISSN 0175-7598. PMID 11935180. S2CID 2346913.
  16. ^ Dennis, R.W.G (1986). Fungi of the Hebrides. Kew: Royal Botanic Gardens. p. 231. ISBN 0-947643-02-8.
  17. ^ Manosroi, J.; Chisti, Y.; Manosroi, A. (2006). "Biotransformation of cortexolone to hydrocortisone by molds using a rapid color development assay". Prikladnaia Biokhimiia I Mikrobiologiia. 42 (5): 547–551. PMID 17066954.
  18. ^ Seigle-Murandi, F. M.; Krivobok, S. M. A.; Steiman, R. L.; Benoit-Guyod, J. L. A.; Thiault, G. A. (1991). "Biphenyl oxide hydroxylation by Cunninghamella echinulata". Journal of Agricultural and Food Chemistry. 39 (2): 428. doi:10.1021/jf00002a041.
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Cunninghamella echinulata: Brief Summary

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Cunninghamella echinulata is a fungal species in the genus Cunninghamella. It is an asexually reproducing fungus and a mesophile, preferring intermediate temperature ranges. C. echinulata is a common air contaminant, and is currently of interest to the biotechnology industry due to its ability to synthesize γ-linolenic acid as well as its capacity to bioconcentrate metals. This species is a soil saprotroph that forms rhizoids, preferring soils enriched in nitrogen, phosphorus and potassium. It has been reported occasionally an agent of mucormycosis following the inhalation of fungal spores. Czapek's agar is a suitable growth medium for the propagation of C. echinulata.

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