Arthrobotrys oligospora | |
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Scientific classification | |
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Species: | A. oligospora
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Binomial name | |
Arthrobotrys oligospora
Georg Fresenius (1850)
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Synonyms | |
Arthrobotrys oligospora was discovered in Europe in 1850 by Georg Fresenius. [1] [2] 'A. oligospora' is the model organism for interactions between fungi and nematodes. [2] It is the most common nematode capturing fungus, [3] [4] [5] and most widespread nematode capturing fungus. [2] [6] It was the first species of fungi that was identified as a nematode trapping fungus. [6] [2] The species name, oligospora, derives from the greek words ολιγο 'oligo' meaning few and σπορά 'spora' meaning spore.
This fungus undergoes reproduction using 2 cell pear-shaped conidia, of unequal size, [7] [4] on conidiophores. [7] The germ tube erupts from the smaller cell. [7] In environments rich with nematodes, the spores range from 22-32 by 12-20 micrometers, [7] [4] though the spores are smaller in environments devoid of nematodes. [7] [4] Conidium germination has a success rate of 100% but the formation of trapping organs are not always observed. [6] Conidia have been found to disintegrate both in the air and on impact with an agar plate. [8] Condiophores and conidia grow from hyphae sprouted outside of a trapped dead nematode, [2] and condiophores have been found to change and grow into art of the adhesive net. [2] A fungal colony can grow as large as 3.8-6.5cm in diameter, [6] and appear to be transparent, pale pink or yellow in color. [6] The optimal growth temperature for the fungus in a nematode free environment and a nematode infested environment is 20 °C (68 °F) and 25 °C (77 °F), respectively. [6] Growth was found to be less continuous in darkness than in light. [6]
A. oligospora is considered a saprobe and is more saprotrophic than other nematode capturing fungi. [6] [2] At first the fungus was considered largely saprophytic in nature but this was later determined to be untrue. [4] Saprophytic growth uses D-xylose, D-mannose, and cellobiose. [6] The fungus uses nitrite, nitrate, and ammonium for its nitrogen sources and uses pectin, cellulose, and chitin for its carbon sources. [6] When predating on nematodes, the fungus uses cellobiose, L-asparagine, L-arginine, DL glutamic acid for its carbon and nitrogen sources. [6]
Predation of nematodes occurs in low nitrogen environments, [9] as the nematode becomes the main nitrogen source for the fungi. [2] It has been found that the presence of ammonium causes a higher decrease of predation when compared to presence of nitrate or nitrite. [3] Adding green manure or carbohydrates has been found to increase nematode trapping behaviors. [6] A complex 3 dimensional net of hyphae is formed to trap the nematodes in a pH 4.9-8.1 and temperature less than 37 °C (99 °F). [6] [9] [8] [5] Nematodes and nemin (nematode extract) were found to stimulate net formation. [6] [2] Nematodes are not as attracted to A. oligospora without traps as A. Oligospora with traps indicating nematode attracting pheromones were likely used. [9] [10]
A full net is not needed to catch nematodes as smaller nematodes can be caught with a single loop. [2] Lectins are used in attaching nematode to fungi [9] The entire surface of net is covered in adhesive material. [8] [2] Strong adhesion keeps the nematode trapped and when the nematode struggles, it often results in multiple points of adhesion of the nematode to the net. [10] [8] It was even found that the adhesion of the nematode to the fungus remained under washing of agar plate with water. [8] The net is flexible which results in 'hyphal drag' tiring the nematode. [8] Multiple points of adhesion and 'hyphal drag' allow the net to be capable of catching both large and small nematodes easily. [8] In vitro, bait nematodes are consumed often leaving Bunonema nematodes. [8]
A substance found in paralyzed nematodes was found to be capable of paralyzing healthy nematodes, [6] [8] and it was later determined that a paralyzing substance, Subtilisin (A serine protease), [11] is excreted into nematode. [8] [2] An unstable toxin was thought to be made by the fungus, [6] [8] and it was later found that toxic levels of linoleic acid for nematodes (lethal dose of linoleic acid for C. elegans is 5–10 μg/ml) [12] were found in the fungus. [12] [5] Enzymatic hyphal invasion, likely using collagenases which are found in 'Arthrobotrys', [2] of a trapped nematode is followed by the digestion of contents of the nematode. [9] [8] Shortly after hyphal invasion, a hyphal bulb appears where hyphae grow outwards from the bulb along the entire body of the nematode. [8]
Not all nematodes are caught by the net as the nematode needs to be in contact with the net for a short period of time in order for adhesion to occur. [8] Nematodes were found to quickly move away from any net followed by curling if instantaneous contact occurs. [8] [13] The nematode then proceeds to move forward until out of the area of the net and unless prolonged contact is made the nematode is safe. [8] This means one or several instantaneous contacts are not enough for adhesion between the nematode and net to occur. [8]
No competing fungi or bacteria are found in nematodes which are being consumed by the fungus which means it is possible an antibiotic is released inside the nematode. [8] In 1993, secondary metabolites (oligosporon, oligosporol A, and oligosporal B) which can act as antibiotics were found in the fungus. [2] [12] Oligosporon, oligosporol A, oligosporal B have hemolytic effects and are cytotoxic to nematodes, however they are not toxic to the C. elegans. [12] Other oligosporon-type secondary metabolites also found in A. oligospora include (4S,5R,6R)-4′,5′- dihydrooligosporon, (4S,5R,6R)-hydroxyoligosporon, and (4S,5R,6R)-10′11 ′-epoxyoligosporon. [12]
A branch of hyphae grows out of a vegetative hyphae eventually arching back to the parent hyphae and fuses with it to make a loop. [8] [7] [3] This process repeats from any hyphae along any existing branches or a new parent hyphae. [8] [3] The nets are immediately adhesive [8], and hyphae in the loop have different organelles to trap nematodes which are not found in vegetative cells. [2]
A. oligospora has been found in many different geographical regions which include Asia, Africa, North America & South America and Australasia. [2] Some countries it has been found in include Turkmenistan, Azerbaijan, Poland, Canada, New Zealand, and India. [6] The presence of insects infected by nematodes increased presence of A. oligospora but not other nematode capturing fungi. [2]
The fungus can be found in soil in grassland, shrubland, plantations, sheep and cattle yards, [6] and domesticated and non-domesticated animal feces [2]. It colonizes forest steppe soil, mixed forest soil, and Mediterranean brown soil (pH 6.9-8.0) where the pH can be as low as 4.5, but is typically above 5.5. [6] The fungus has also been found in aquatic environments, [2] and heavily polluted areas, specifically heavy metal poisoned mines, fungicide, or nematicide infested soil, [2] [5] decayed plant material, leaves, roots, moss, [6] and in the rhizosphere of various bean plants, barley, [6] [2] and the tomato plant. [2] Larger populations of the fungus can be found in late spring and summer. [5]
The fungus is a biological indicator of nematodes. [2] The annual global cost of plant-parasitic nematodes is approximately 100 billion USD. [12] Nematode capturing fungi such as the A. oligospora can be used to control growth of nematodes. [6] [5] This means that they can be potentially used as a bio-control agent to protect crops against nematode infestations. [2] This may not be feasible since the nematodes occasionally eat the fungi. [6]
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Arthrobotrys oligospora | |
---|---|
Scientific classification | |
Kingdom: | |
Division: | |
Subdivision: | |
Class: | |
Order: | |
Family: | |
Genus: | |
Species: | A. oligospora
|
Binomial name | |
Arthrobotrys oligospora
Georg Fresenius (1850)
| |
Synonyms | |
Arthrobotrys oligospora was discovered in Europe in 1850 by Georg Fresenius. [1] [2] 'A. oligospora' is the model organism for interactions between fungi and nematodes. [2] It is the most common nematode capturing fungus, [3] [4] [5] and most widespread nematode capturing fungus. [2] [6] It was the first species of fungi that was identified as a nematode trapping fungus. [6] [2] The species name, oligospora, derives from the greek words ολιγο 'oligo' meaning few and σπορά 'spora' meaning spore.
This fungus undergoes reproduction using 2 cell pear-shaped conidia, of unequal size, [7] [4] on conidiophores. [7] The germ tube erupts from the smaller cell. [7] In environments rich with nematodes, the spores range from 22-32 by 12-20 micrometers, [7] [4] though the spores are smaller in environments devoid of nematodes. [7] [4] Conidium germination has a success rate of 100% but the formation of trapping organs are not always observed. [6] Conidia have been found to disintegrate both in the air and on impact with an agar plate. [8] Condiophores and conidia grow from hyphae sprouted outside of a trapped dead nematode, [2] and condiophores have been found to change and grow into art of the adhesive net. [2] A fungal colony can grow as large as 3.8-6.5cm in diameter, [6] and appear to be transparent, pale pink or yellow in color. [6] The optimal growth temperature for the fungus in a nematode free environment and a nematode infested environment is 20 °C (68 °F) and 25 °C (77 °F), respectively. [6] Growth was found to be less continuous in darkness than in light. [6]
A. oligospora is considered a saprobe and is more saprotrophic than other nematode capturing fungi. [6] [2] At first the fungus was considered largely saprophytic in nature but this was later determined to be untrue. [4] Saprophytic growth uses D-xylose, D-mannose, and cellobiose. [6] The fungus uses nitrite, nitrate, and ammonium for its nitrogen sources and uses pectin, cellulose, and chitin for its carbon sources. [6] When predating on nematodes, the fungus uses cellobiose, L-asparagine, L-arginine, DL glutamic acid for its carbon and nitrogen sources. [6]
Predation of nematodes occurs in low nitrogen environments, [9] as the nematode becomes the main nitrogen source for the fungi. [2] It has been found that the presence of ammonium causes a higher decrease of predation when compared to presence of nitrate or nitrite. [3] Adding green manure or carbohydrates has been found to increase nematode trapping behaviors. [6] A complex 3 dimensional net of hyphae is formed to trap the nematodes in a pH 4.9-8.1 and temperature less than 37 °C (99 °F). [6] [9] [8] [5] Nematodes and nemin (nematode extract) were found to stimulate net formation. [6] [2] Nematodes are not as attracted to A. oligospora without traps as A. Oligospora with traps indicating nematode attracting pheromones were likely used. [9] [10]
A full net is not needed to catch nematodes as smaller nematodes can be caught with a single loop. [2] Lectins are used in attaching nematode to fungi [9] The entire surface of net is covered in adhesive material. [8] [2] Strong adhesion keeps the nematode trapped and when the nematode struggles, it often results in multiple points of adhesion of the nematode to the net. [10] [8] It was even found that the adhesion of the nematode to the fungus remained under washing of agar plate with water. [8] The net is flexible which results in 'hyphal drag' tiring the nematode. [8] Multiple points of adhesion and 'hyphal drag' allow the net to be capable of catching both large and small nematodes easily. [8] In vitro, bait nematodes are consumed often leaving Bunonema nematodes. [8]
A substance found in paralyzed nematodes was found to be capable of paralyzing healthy nematodes, [6] [8] and it was later determined that a paralyzing substance, Subtilisin (A serine protease), [11] is excreted into nematode. [8] [2] An unstable toxin was thought to be made by the fungus, [6] [8] and it was later found that toxic levels of linoleic acid for nematodes (lethal dose of linoleic acid for C. elegans is 5–10 μg/ml) [12] were found in the fungus. [12] [5] Enzymatic hyphal invasion, likely using collagenases which are found in 'Arthrobotrys', [2] of a trapped nematode is followed by the digestion of contents of the nematode. [9] [8] Shortly after hyphal invasion, a hyphal bulb appears where hyphae grow outwards from the bulb along the entire body of the nematode. [8]
Not all nematodes are caught by the net as the nematode needs to be in contact with the net for a short period of time in order for adhesion to occur. [8] Nematodes were found to quickly move away from any net followed by curling if instantaneous contact occurs. [8] [13] The nematode then proceeds to move forward until out of the area of the net and unless prolonged contact is made the nematode is safe. [8] This means one or several instantaneous contacts are not enough for adhesion between the nematode and net to occur. [8]
No competing fungi or bacteria are found in nematodes which are being consumed by the fungus which means it is possible an antibiotic is released inside the nematode. [8] In 1993, secondary metabolites (oligosporon, oligosporol A, and oligosporal B) which can act as antibiotics were found in the fungus. [2] [12] Oligosporon, oligosporol A, oligosporal B have hemolytic effects and are cytotoxic to nematodes, however they are not toxic to the C. elegans. [12] Other oligosporon-type secondary metabolites also found in A. oligospora include (4S,5R,6R)-4′,5′- dihydrooligosporon, (4S,5R,6R)-hydroxyoligosporon, and (4S,5R,6R)-10′11 ′-epoxyoligosporon. [12]
A branch of hyphae grows out of a vegetative hyphae eventually arching back to the parent hyphae and fuses with it to make a loop. [8] [7] [3] This process repeats from any hyphae along any existing branches or a new parent hyphae. [8] [3] The nets are immediately adhesive [8], and hyphae in the loop have different organelles to trap nematodes which are not found in vegetative cells. [2]
A. oligospora has been found in many different geographical regions which include Asia, Africa, North America & South America and Australasia. [2] Some countries it has been found in include Turkmenistan, Azerbaijan, Poland, Canada, New Zealand, and India. [6] The presence of insects infected by nematodes increased presence of A. oligospora but not other nematode capturing fungi. [2]
The fungus can be found in soil in grassland, shrubland, plantations, sheep and cattle yards, [6] and domesticated and non-domesticated animal feces [2]. It colonizes forest steppe soil, mixed forest soil, and Mediterranean brown soil (pH 6.9-8.0) where the pH can be as low as 4.5, but is typically above 5.5. [6] The fungus has also been found in aquatic environments, [2] and heavily polluted areas, specifically heavy metal poisoned mines, fungicide, or nematicide infested soil, [2] [5] decayed plant material, leaves, roots, moss, [6] and in the rhizosphere of various bean plants, barley, [6] [2] and the tomato plant. [2] Larger populations of the fungus can be found in late spring and summer. [5]
The fungus is a biological indicator of nematodes. [2] The annual global cost of plant-parasitic nematodes is approximately 100 billion USD. [12] Nematode capturing fungi such as the A. oligospora can be used to control growth of nematodes. [6] [5] This means that they can be potentially used as a bio-control agent to protect crops against nematode infestations. [2] This may not be feasible since the nematodes occasionally eat the fungi. [6]
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has extra text (
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