Lentinus crinitus

{{Short description|Species of fungus}}

{{Speciesbox

| image = Lentinus crinitus.jpg

| genus = Lentinus

| species = crinitus

| authority = (L.) Fr. (1825)

| synonyms_ref = {{cite web | url=https://eol.org/pages/1004828/names | title=Lentinus crinitus (L.) Fr. 1825 names - Encyclopedia of Life }}

| synonyms =

{{plainlist|

  • Agaricus crinitus L. (1763)
  • Agaricus essequeboensis G. Mey. (1818)
  • Lentinus chaetoloma Fr. (1851)
  • Agaricus crinitus var. crinitus L. Fr. (1825)
  • Lentinus essequeboensis G. Mey. Fr. (1825)
  • Panus crinitus (L.) Singer (1951)
  • Panus wrightii Berk. & M. A. Curtis (1868)
  • Pocillaria chaetoloma Fr. Kuntze (1891)
  • Polyporus phyllostipes D. Kruger (2004)

}}

}}

Lentinus crinitus is a basidiomycete species of fungus.

Taxonomy

It is in the subdivision Agaricomycotina, the order Polyporales and in the family Polyporaceae, within the group Polyporellus. There are many synonyms including Agaricus essequeboensis, Lentinus chaetoloma, L. essequeboensis, L. microloma, L. rigidulus, L. subcervinus, Curtis, L. wrightii, Panus crinitus, Panus wrightii, Polyporus phyllostipes, and Agaricus crinitus. The common name is the fringed sawgill.{{Cite journal |last1=Filho |first1=José Rivaldo dos Santos |last2=Santos |first2=Éverton da Silva |last3=Linde |first3=Giani Andrea |last4=Colauto |first4=Nelson Barros |last5=Gonçalves |first5=Regina Aparecida Correia |last6=de Oliveira |first6=Arildo José Braz |date=2023-10-01 |title=Lentinus crinitus: Traditional use, phytochemical and pharmacological activities, and industrial and biotechnological applications |url=https://www.sciencedirect.com/science/article/abs/pii/S096399692300724X |journal=Food Research International |volume=172 |pages=113179 |doi=10.1016/j.foodres.2023.113179 |pmid=37689932 |issn=0963-9969}}

This fungus was first described by Carl Linnaeus, and reported and identified by Elias Magnus Fries in 1825.

The closest relative is to L. crinitus is Lentinus swartzii and the closest genus is Polyporus with Ganoderma being closely related as well.

It has been included in multiple phylogenetic studies.{{Cite journal |last=Grand |first=Edward |date=2004-01-01 |title=Systematics and species concepts in the genera Lentinus Fr. and Panus Fr., with emphasis on the Lentinus tigrinus, L. crinitus and Panus lecomtei complexes |url=https://www.academia.edu/87639087}}{{Cite journal |last1=Grand |first1=Edward A. |last2=Hughes |first2=Karen W. |last3=Petersen |first3=Ronald H. |date=2011-11-01 |title=Relationships within Lentinus subg. Lentinus (Polyporales, Agaricomycetes), with emphasis on sects. Lentinus and Tigrini |url=https://link.springer.com/article/10.1007/s11557-010-0711-4 |journal=Mycological Progress |language=en |volume=10 |issue=4 |pages=399–413 |doi=10.1007/s11557-010-0711-4 |bibcode=2011MycPr..10..399G |issn=1861-8952|url-access=subscription }}

Lentinus crinitus appears to form a single mating group. In fungi, a single mating group means that a species has one mating type, or that it is homothallic. This means that the species can mate with itself, or reproduce asexually.

Description

The fruiting bodies commonly grow in irregular, clustered formations. The cap is {{convert|2–5|cm|frac=4}} wide{{Cite book |last=Audubon |title=Mushrooms of North America |publisher=Knopf |year=2023 |isbn=978-0-593-31998-7 |pages=277}} and ranges in shape from flat or slightly convex to depressed in the center or funnel-shaped (infundibuliform). Its surface is whitish when young, maturing to yellowish-brown. It is covered with a brownish scruff which can wear away. The margin is often rolled inward when young and flattens with age.

The stipe can be 2–4.5 cm long and 2–6 mm thick, usually having a small bulb at the base. The stipe is not hollow, has a somewhat roughened surface and a leathery feel. The stipe is lighter in color than the cap but the same color profile. The gills extend slightly down the stem (decurrent), are narrow, somewhat forked, and finely toothed (denticulate), with a glandular surface. They appear in shades from pale to dark fuscous, sometimes featuring yellowish-brown hairs along the edges. The stipe, measuring 1–4.5 cm long, can be central or off-center (eccentric) in relation to the cap, cylindrical, and leathery in texture, with a covering of light yellow scaly hairs (squamulose) and darker scales (squamules).{{Cite book |last1=Elliott |first1=Todd F. |url=https://books.google.com/books?id=WyZeDgAAQBAJ&dq=Elliott%2C+T.+F.%2C+%26+Stephenson%2C+S.+L.+%282018%29.+Mushrooms+of+the+Southeast.+Timber+Press.&pg=PP1 |title=Mushrooms of the Southeast |last2=Stephenson |first2=Steven L. |date=2018-01-24 |publisher=Timber Press |isbn=978-1-60469-837-4 |language=en}}

The basidiospores are white in and usually range between 5.5 and 8.0 × 1.8–3.0. The spores are rounded but may have a subtle point on one end that is off center and pointing right or left. The spores are not textured/smooth. These spores do not react with Meltzer's reagent. The spore print is white.{{Cite book |url=http://dx.doi.org/10.7560/322727 |title=Polypores and Similar Fungi of Eastern and Central North America |date=2021 |publisher=University of Texas Press |isbn=978-1-4773-2273-4 |doi=10.7560/322727}}

L. crinitus has a monomitic hyphae system with clamp connections. This fungi has generative hyphae and skeleton-ligators which differs from skeletal hyphae. Skeletal hyphae are generally thick-walled, non-septate and unbranched or sparsely branched while skeletal-ligators are highly branched and more flexible but still provide more structure and rigidity than generative hyphae alone. Skeletal-ligative hyphae help with connecting and binding other hyphal types, contributing to both strength and flexibility.

Habitat and distribution

Lentinus crinitus is a white rot fungus so it is saprotrophic and is able to break down lignin and cellulose and use it for energy. It can be found on decaying logs in open areas, in tropical forest and in mixed oak-dominated forest. Known hosts of L. crinitus include dead wood from Nerium oleander, Hevea spp., Hippomane spp.,  Quercus spp., Barringtonia spp., Nyssa spp., Salix spp., Rhizophora mangle.{{Cite web|url=https://www.discoverlife.org/20/q?search=Lentinus+crinitus|title=Lentinus crinitus -- Discover Life}}

Lentinus crinitus is distributed across 27 countries. In South America, it can be found in Brazil, Colombia, Peru, Ecuador, Venezuela, French Guiana, Guyana, and Argentina. In North America, it occurs in the United States and Mexico. Its range in Central America includes the Dominican Republic, Belize, Costa Rica, Bahamas, Jamaica, Cuba, Haiti, Martinique, Guatemala, Panama, Honduras, Nicaragua, Trinidad and Tobago, and the Cayman Islands. It is also found in Africa, specifically in the Congo and Ethiopia, as well as in Asia, in the Philippines. They are typically found at an altitude of {{Convert|50–2800|m}} above sea level, though there have been many observations of this species from Florida.

It is most often found in April to July in the Northern Hemisphere, and from September to December in the Southern Hemisphere. This means that this fungi is best suited to warmer and wetter climates so it is found in the summer months during the rainy season.{{Cite web |title=Lentinus crinitus |url=https://shroom.id/n/Lentinus_crinitus |access-date=2024-11-06 |website=ShroomID |language=en}}

Ecology

It is known to be a potential host of the parasitic fungus Hypomyces aurantius (Pers.) Fuckel 1870, Hypomyces aurantius is known to parasitize many species in the family Polyporaceae.{{Cite web |title=Lentinus crinitus (L.) Fr. 1825 |url=https://eol.org/pages/1004828}}

There are potential interactions with animals which may be attracted to the mushroom for food. Squirrels have been seen to eat this fungi.

Some have reported insects using it for food and habitat.

Uses

= Culinary =

{{More citations needed section|date=February 2025}}

Many indigenous communities have utilized L. crinitus in their diets. The Amazonian communities of the Yanomami and Txicó in Brazil, the Uitoto, Muinane, and Andoke (Caquetá) in Colombia, the rural Loreto in Peru, and the Hotï in Venezuela use mushrooms, including Lentinus crinitus, as a staple food. The indigenous Uitoto people of Colombia use L.crinitus while they are young since adult specimens are tough and leathery and therefore are unpleasant. They eat it roasted on yarumo leaves and in broth. It is reportedly used as a postpartum strength-boosting medication in Mexico.{{Cite journal |last1=Vargas-Isla |first1=Ruby |last2=Ishikawa |first2=Noemia Kazue |date=June 2008 |title=Optimal conditions of in vitro mycelial growth of Lentinus strigosus, an edible mushroom isolated in the Brazilian Amazon |url=http://dx.doi.org/10.1007/s10267-007-0404-2 |journal=Mycoscience |volume=49 |issue=3 |pages=215–219 |doi=10.1007/s10267-007-0404-2 |issn=1340-3540|url-access=subscription }}{{Cite web |title=Lentinus crinitus (L.) Fr. {{!}} Colombian Fungi made accessible |url=https://colfungi.org/taxon/urn:lsid:indexfungorum.org:names:262317/general-information |access-date=2024-11-06 |website=Plants of the World Online |language=en}}

The species can be cultivated in various substrates that yield differing nutritional values.{{Cite journal |last1=Fabros |first1=JA |last2=Dulay |first2=RMR |last3=De Leon |first3=AM |last4=Kalaw |first4=SP |last5=Reyes |first5=RG |date=2022 |title=Distribution, cultivation, nutritional composition, and bioactivities of Lentinus (Polyporaceae, Basidiomycetes): A review |url=http://dx.doi.org/10.5943/cream/12/1/13 |journal=Current Research in Environmental & Applied Mycology |volume=12 |issue=1 |pages=170–219 |doi=10.5943/cream/12/1/13 |issn=2229-2225|doi-access=free }}

It comprises 3.4% mineral matter, 26% crude fiber, and 1.5% ether extract. Compared to many edible mushrooms that are sold commercially, this fungus has a higher fiber content. Its protein levels are correlated with its nitrogen concentration, which is 2.24%. Significant amounts of other minerals are also found, including calcium (0.53%), phosphorus (0.19%), potassium (0.50%), magnesium (0.10%), and sulfur (0.18%). Copper is at 10 ppm, manganese is at 28 ppm, zinc is at 31 ppm, cobalt is at 0.11 ppm, sodium is at 109 ppm, and molybdenum is at 0.5 ppm.{{Cite journal |last1=Silva Neto |first1=Carlos de Melo e |last2=Pinto |first2=Diogo de Souza |last3=Santos |first3=Leovigildo Aparecido Costa |last4=Calaça |first4=Francisco J. Simões |date=2019-11-28 |title=Bromatological aspects of Lentinus crinitus mushroom (Basidiomycota: Polyporaceae) in agroforestry in the Cerrado |url=https://www.scielo.br/j/cta/a/GyhtRKbpsHYRDhB4K86QrRd/?lang=en |journal=Food Science and Technology |language=en |volume=40 |issue=3 |pages=659–664 |doi=10.1590/fst.14719 |issn=0101-2061 |doi-access=free}} Wild specimens of L. crinitus presented content of 14.42% protein which is similar to other commercial mushrooms. Lentinus citrinus cultivated on cupuaçu exocarp (Theobroma grandiflorum) mixed with litter (CE + LI) can have up to 27% protein.{{Cite journal |last1=Machado |first1=A. R. |last2=Teixeira |first2=M. F. |last3=De Souza Kirsch |first3=L. |last4=Campelo |first4=M. D. |last5=De Aguiar Oliveira |first5=I. M. |date=2015 |title=Nutritional value and proteases of Lentinus citrinus produced by solid state fermentation of lignocellulosic waste from tropical region |journal=Saudi Journal of Biological Sciences |volume=23 |issue=5 |pages=621–627 |doi=10.1016/j.sjbs.2015.07.002 |pmc=4992099 |pmid=27579012}} 27% protein is very high for commercial and this is especially important for those trying to build and retain muscle on a vegan diet.

The ability of the L. crinitus mycelium to convert agricultural waste to substrate with high protein, fiber, and nitrogen content may make it suitable for use as a beneficial soil amendment or as animal feed.{{Cite journal |last1=Dávila G |first1=Lina R. |last2=Murillo A |first2=Walter |last3=Zambrano F |first3=Cristian J. |last4=Suárez M |first4=Héctor |last5=Méndez A |first5=Jonh J. |date=March 2020 |title=Evaluation of nutritional values of wild mushrooms and spent substrate of Lentinus crinitus (L.) Fr |journal=Heliyon |volume=6 |issue=3 |pages=e03502 |doi=10.1016/j.heliyon.2020.e03502 |doi-access=free |pmid=32181387 |pmc=7062765 |issn=2405-8440}}

Lentinus crinitus basidiocarp pileus and stipe have high antioxidant activity due to high amounts of antioxidant compounds such as malic acid, p-hydroxybenzoic acids and β-tocopherol.{{Cite journal |last1=Bertéli |first1=Míria B. D. |last2=Oliveira Filho |first2=Olavo B. Q. |last3=Freitas |first3=Janyeli D. S. |last4=Bortolucci |first4=Wanessa C. |last5=Silva |first5=Gustavo R. |last6=Gazim |first6=Zilda C. |last7=Lívero |first7=Francislaine A. R. |last8=Lovato |first8=Evellyn C. W. |last9=Valle |first9=Juliana S. |last10=Linde |first10=Giani A. |last11=Barros |first11=Lillian |last12=Reis |first12=Filipa S. |last13=Ferreira |first13=Isabel C. F. R. |last14=Paccola-Meirelles |first14=Luzia D. |last15=Colauto |first15=Nelson B. |date=2021-04-10 |title=Correction to: Lentinus crinitus basidiocarp stipe and pileus: chemical composition, cytotoxicity and antioxidant activity |url=http://dx.doi.org/10.1007/s00217-021-03733-x |journal=European Food Research and Technology |volume=247 |issue=6 |pages=1367 |doi=10.1007/s00217-021-03733-x |issn=1438-2377}} The buildup of reactive oxygen species(free radicals) in the body causes oxidative stress, which seems to be linked to a number of clinical conditions, including aging, cancer, cardiovascular disease, and neurological illnesses, antioxidant compounds may provide relief to that but research is still limited and inconclusive.{{Cite journal |last1=Yoshihara |first1=Daisaku |last2=Fujiwara |first2=Noriko |last3=Suzuki |first3=Keiichiro |date=October 2010 |title=Antioxidants: Benefits and risks for long-term health |url=http://dx.doi.org/10.1016/j.maturitas.2010.05.001 |journal=Maturitas |volume=67 |issue=2 |pages=103–107 |doi=10.1016/j.maturitas.2010.05.001 |pmid=20627629 |issn=0378-5122|url-access=subscription }}

The pileus has a high concentration of protein, ash, tocopherols, and organic acids, particularly malic and oxalic acids. The stipe contains a lot of carbohydrates, energy, soluble sugars, and phenolic acids, primarily p-hydroxybenzoic acid. Trehalose is the major soluble sugar found in the basidiocarp pileus and stipe.

= Other uses =

Polysaccharides extracted from L. crinitus basidiocarps shown antiproliferative action in breast carcinoma cells . After treatment, these polysaccharides may activate J774 macrophages, as evidenced by an increase in the production of tumor necrosis factor alpha (TNFα) and nitric acid, which induces tumor cell death. These chemicals may improve anticancer activity.{{Cite journal |last1=López-Legarda |first1=Xiomara |last2=Arboleda-Echavarría |first2=Carolina |last3=Parra-Saldívar |first3=Roberto |last4=Rostro-Alanis |first4=Magdalena |last5=Alzate |first5=Juan F. |last6=Villa-Pulgarín |first6=Janny A. |last7=Segura-Sánchez |first7=Freimar |date=December 2020 |title=Biotechnological production, characterization and in vitro antitumor activity of polysaccharides from a native strain of Lentinus crinitus |url=http://dx.doi.org/10.1016/j.ijbiomac.2020.08.191 |journal=International Journal of Biological Macromolecules |volume=164 |pages=3133–3144 |doi=10.1016/j.ijbiomac.2020.08.191 |pmid=32860792 |issn=0141-8130|url-access=subscription }}

The majority of the chemicals found in L. crinitus are documented for the first time in the genus. These studies demonstrated that the fungus produces a variety of physiologically active secondary metabolites. The findings discovered extracts included phytochemical 1,13,4-di-O-Caffeoylquinic which was shown to have potential for inhibiting the Zika virus.{{Cite web |last1=Fonseca |first1=Aluísio Marques da |last2=Soares |first2=Neidelenio Baltazar |last3=Colares |first3=Regilany Paulo |last4=Coelho |first4=Ethanielda de Lima |last5=Ribeiro |first5=Paulo Riceli Vasconcelos |last6=de Souza |first6=João Sammy Nery |last7=Alexandre |first7=Jeferson Yves Nunes Holanda |last8=Sousa |first8=Cleiton |last9=Marinho |first9=Emmanuel Silva |date=2021-10-29 |title=In Silico Study of The Potential of Naturally Caffeoylquinic Acids From Lentinus Crinitus Basidiocarp With Zika Virus Inhibition Targets |url=http://dx.doi.org/10.21203/rs.3.rs-1011019/v1 |access-date=2024-11-06 |doi=10.21203/rs.3.rs-1011019/v1 }}

L. crinitus can be used as a biological control against plant pathogenic fungi and bacteria since it has shown antimicrobial activity against 11 species of microorganisms, with greater activity against Aspergillus niger (spores), Aspergillus flavus (spores), and Mucor rouxii (spores){{Cite journal |last1=ABATE |first1=DAWIT |last2=ABRAHAM |first2=WOLF-RAINER |date=1994 |title=Antimicrobial metabolites from Lentinus crinitus. |url=http://dx.doi.org/10.7164/antibiotics.47.1348 |journal=The Journal of Antibiotics |volume=47 |issue=11 |pages=1348–1350 |doi=10.7164/antibiotics.47.1348 |issn=0021-8820 |pmid=8002403}}

It has potential to fight foodborne illness and food spoilage because extracts 1-desoxyhypnophylline (1) and 6,7-epoxy-4(15)-hirsuteno-5-ol (3), from the basidiocarp of L. crinitus basidiocarp showed antimicrobial activity against bacteria such as Escherichia coli, Listeria monocytogenes, Micrococcus luteus, P. aeruginosa, Staphylococcus aureus, Salmonella enterica, Bacillus cereus, and Enterobacter cloacae; and fungi such as Aspergillus fumigatus, A. niger, A. versicolor, Penecillium. ochrochloron, Talaromyces funiculosus, and T. virens, and two fungal food isolates A. ochraceus and Penicillium aurantiogriseum.{{Cite journal |last1=Bertéli |first1=Míria Benetati Delgado |last2=Barros |first2=Lillian |last3=Reis |first3=Filipa S. |last4=Ferreira |first4=Isabel C. F. R. |last5=Glamočlija |first5=Jasmina |last6=Soković |first6=Marina |last7=Valle |first7=Juliana Silveira do |last8=Linde |first8=Giani Andrea |last9=Ruiz |first9=Suelen Pereira |last10=Colauto |first10=Nelson Barros |date=2021 |title=Antimicrobial activity, chemical composition and cytotoxicity ofLentinus crinitusbasidiocarp |url=http://dx.doi.org/10.1039/d1fo00656h |journal=Food & Function |volume=12 |issue=15 |pages=6780–6792 |doi=10.1039/d1fo00656h |issn=2042-6496 |pmid=34109332 |hdl-access=free |hdl=10198/24303}}

Potential to be cultivated in active agroforestry plantations as another source of income. Cultivation of this fungi provides nutritional alternatives in a growing world that has an increasing demand for food sources.

References

{{Reflist}}

{{Taxonbar|from=Q10557052}}

Category:Polyporaceae

Category:Fungus species