A mycoparasite is an organism with the ability to parasitize fungi.
Mycoparasites might be biotrophic or necrotrophic, depending on the type of interaction with their host.[1]
Types of mycoparasitic organisms
editMyco-heterotrophy
editVarious plants may be considered mycoparasites, in that they parasitize and acquire most of their nutrition from fungi during a part or all of their life cycle. These include many orchid seedlings, as well as some plants that lack chlorophyll such as Monotropa uniflora. Mycoparasitic plants are more precisely described as myco-heterotrophs.
Mycoparasitic bacteria
editSome bacteria live on or within fungal cells as parasites or symbionts.
Mycoparasitic viruses
editSome viruses, called mycoviruses live on or within fungal cells as parasites or symbionts.
Mycoparasitic fungi
editMany mycoparasites are fungi, though not all fungicolous fungi are parasites (some are commensals or saprobes.[2]) Biotrophic mycoparasites acquire nutrients from living host cells. Necrotrophic mycoparasites rely on dead host cells, which they might first kill with toxins or enzymes (saprophytic growth).[2][3]
Kinds of mycoparasitic interactions
editBiotrophic and necrotrophic mycoparasites
editBiotrophic mycoparasites get nutrients from living host cells and growth of these parasites is greatly influenced by the metabolism of the host.[4] Biotrophic mycoparasites tend to show high host specificity, and often form specialized infection structures.[5] Necrotrophic mycoparasites can be aggressively antagonistic, invading the host fungus and killing, then digesting components of its cells. Necrotrophic parasites tend to have low host specificity, and are relatively unspecialized in their mechanism of parasitism.[5]
Balanced and destructive mycoparasites
editBalanced mycoparasites have little or no destructive effect on the host, whereas destructive mycoparasites have the opposite effect.[6] Biotrophic mycoparasites are generally considered to be balanced mycoparasites; necrotrophic mycoparasites use toxins or enzymes to kill host cells, therefore necrotrophic mycoparasites are usually considered to be destructive mycoparasites. However, in some combinations, the parasite may live during its early development as a biotroph, then kill its host and act more like destructive mycoparasites in late stages of parasitization.[4][6]
Mechanisms of Mycoparasitism
editThe four main steps of mycoparasitism include target location; recognition; contact and penetration; and nutrient acquisition.[7]
Target location
editMany research indicate that hyphal growth direction, spore germination, and bud tube elongation of mycoparasitic fungi may exhibit tropism in response to detection of a potential host.[8] This tropic recognition reaction is thought to arise from detection of signature chemicals of the host; the direction of the concentration gradient determines the growth direction of the parasite.[9] As the mycoparasitic interaction is host-specific and not merely a contact response, it is likely that signals from the host fungus are recognized by mycoparasites such as Trichoderma and provoke transcription of mycoparasitism-related genes.[10][11]
Recognition
editWhen mycoparasites contact their fungal host, they will recognize each other. This recognition between mycoparasites and their host fungi may be related to the agglutinin on the cell surface of the mycohost. Carbohydrate residues on the cell wall of mycoparasites might bind to lectins on the surface of the host fungi to achieve mutual recognition.[12]
Contact and penetration
editOnce a mycoparasitic fungus and its host recognize each other, both may exhibit changes in external form and internal structure.[13][14] Different mycoparasitic fungi form different structures when interacting with their hosts. For example, the hyphae of some mycoparasitic fungi form specialized contact cells resembling haustoria on the hyphae of their hosts; others may coil around the hyphae of their host fungus or penetrate then grow inside host hyphae.[15] Nectrophic mycoparasites may kill host hyphae with toxins or enzymes before invading them.[3]
Application
editMycoparasitic fungi can be important controls of plant disease fungi in natural systems and in agriculture, and may play a role in integrated pest management (IPM) as biological controls [16]
Some Trichoderma species have been developed as biocontrols of a range of commercially important diseases,[7] and have been applied in the United States, India, Israel, New Zealand, Sweden, and other countries to control plant diseases caused by Rhizoctonia solani, Botrytis cinerea, Sclerotium rolfsii, Sclerotinia sclerotiorum, Pythium spp., and Fusarium spp. as a promising alternative to chemical pesticides.[17][18]
Further study of mycoparasitism may drive discovery off more bioactive compounds including biopesticides and biofertilizers.[19]
| Commercial products | Bioagents used | Name of the manufacturer |
|---|---|---|
| AQ10 biofungicide | Ampelomyces quisqualis
isolate M-10 |
Ecogen, Inc. Israel |
| Anti-Fungus | Trichoderma spp. | Grondortsmettingen De Cuester, Belgium |
| Biofungus | Trichoderma spp. | Grondortsmettingen De
Cuester n. V.Belgium |
| Bas-derma | Trichoderma viride | Basarass Biocontrol Res.
Lab., India |
| Binab T | Trichoderma harzianum
(ATCC 20476) and (ATCC 20475) |
Bio-Innovation AB, UK |
| Bioderma | Trichoderma viride/T. harzianum | Biotech International Ltd., India |
| Biofox C | Fusarium oxysporum (Non- pathogenic) | S. I. A. P. A., Italy |
| Prestop, Prirnastop | Gliocladium catenulatum | Kemira Agro. Oy, Finland |
| Root Pro, Root Prota to Soilgard | Trichoderma harzianum/Gliocladium virens strain
GL-21 |
Efal Agr, Israel Thermo Trilogy, USA |
| Root shield, Plant shield,
T-22 Planter box |
Trichoderma harzianum Rifai strain KRL-AG
(T-22) |
Bioworks Inc., USA |
| Supresivit | Trichoderma harzianum | Borregaard and Reitzel, Czech Republic |
| T-22 G, T-22 HB | Trichoderma harzianum
strain KRL-AG2 |
THT Inc., USA |
| Trichodex, Trichopel | Trichoderma harzianum | Makhteshim Chemical Works Ltd., USA |
| Trichopel, Trichoject, Trichodowels, Trichoseal | Trichoderma harzianum
and Trichoderma viride |
Agrimm Technologies Ltd., New Zealand |
| Trichopel | Trichoderma harzianumand Trichoderma viride | Agrimm Technologies Ltd., New Zealand |
| Trichoderma 2000 | Trichoderma sp. | Myocontrol Ltd., Israel |
| Tri-control | Trichoderma spp. | Jeypee Biotechs, India |
| Trieco | Trichoderma viride | Ecosense Labs Pvt. Ltd.,
Mumbai, India |
| TY | Trichoderma sp. | Mycocontrol, Israel |
References
edit- ^ Boosalis, M G (1964). "Hyperparasitism". Annual Review of Phytopathology. 2 (1): 363–376. doi:10.1146/annurev.py.02.090164.002051. ISSN 0066-4286.
- ^ a b Hawksworth, D.L.; Kirk, P.M.; Sutton, B.C.; Pegler, D.N. (1995). Ainsworth & Bisby's Dictionary of the Fungi. Wallingford, UK: CAB International.
- ^ a b Barnett, H.L. (1963). "The nature of mycoparasitism by fungi". Annu. Rev. Microbiol. 17: 1–14. doi:10.1146/annurev.mi.17.100163.000245.
- ^ a b JEFFRIES, PETER (1985). "Mycoparasitism within the Zygomycetes". Botanical Journal of the Linnean Society. 91 (1–2): 135–150. doi:10.1111/j.1095-8339.1985.tb01140.x. ISSN 0024-4074.
- ^ a b c Ashraf, Shabbir; Zuhaib, Mohammad (2013), "Fungal Biodiversity: A Potential Tool in Plant Disease Management", Management of Microbial Resources in the Environment, Springer Netherlands, pp. 69–90, doi:10.1007/978-94-007-5931-2_4, ISBN 9789400759305
- ^ a b H.L., Barnett; F.L., Binde (1973). "The Fungal Host-Parasite Relationship". Annual Review of Phytopathology. 11 (1): 273–292. doi:10.1146/annurev.py.11.090173.001421.
- ^ a b Ojha, S.; Chatterjee, N. C. (2011). "Mycoparasitism of Trichoderma spp. in biocontrol of fusarial wilt of tomato". Archives of Phytopathology and Plant Protection. 44 (8): 771–782. doi:10.1080/03235400903187444. ISSN 0323-5408. S2CID 86656967.
- ^ Chet, I.; Harman, G. E.; Baker, R. (1981). "Trichoderma hamatum: Its hyphal interactions withRhizoctonia solani and Pythium spp". Microbial Ecology. 7 (1): 29–38. doi:10.1007/bf02010476. ISSN 0095-3628. PMID 24227317. S2CID 35220790.
- ^ Barak, R.; Elad, Y.; Mirelman, D.; Chet, I. (1985). "Lectins: a possible basis for specific recognition in the interaction of Trichoderma and Sclerotium rolfsii". Phytopathology. 75 (4): 458–462. doi:10.1094/phyto-75-458.
- ^ Druzhinina, Irina S.; Seidl-Seiboth, Verena; Herrera-Estrella, Alfredo; Horwitz, Benjamin A.; Kenerley, Charles M.; Monte, Enrique; Mukherjee, Prasun K.; Zeilinger, Susanne; Grigoriev, Igor V. (2011-09-16). "Trichoderma: the genomics of opportunistic success" (PDF). Nature Reviews Microbiology. 9 (10): 749–759. doi:10.1038/nrmicro2637. ISSN 1740-1526. PMID 21921934. S2CID 11046734.
- ^ Karlsson, Magnus; Durling, Mikael Brandström; Choi, Jaeyoung; Kosawang, Chatchai; Lackner, Gerald; Tzelepis, Georgios D.; Nygren, Kristiina; Dubey, Mukesh K.; Kamou, Nathalie (2015-01-08). "Insights on the Evolution of Mycoparasitism from the Genome of Clonostachys rosea". Genome Biology and Evolution. 7 (2): 465–480. doi:10.1093/gbe/evu292. ISSN 1759-6653. PMC 4350171. PMID 25575496.
Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
- ^ Inbar, Jacob; Menendez, Ana; Chet, Ilan (1996). "Hyphal interaction between Trichoderma harzianum and Sclerotinia sclerotiorum and its role in biological control". Soil Biology and Biochemistry. 28 (6): 757–763. doi:10.1016/0038-0717(96)00010-7. ISSN 0038-0717.
- ^ Zeilinger, Susanne; Brunner, Kurt; Peterbauer, Clemens K.; Mach, Robert L.; Kubicek, Christian P.; Lorito, Matteo (2003-07-01). "The Nag1 N-acetylglucosaminidase of Trichoderma atroviride is essential for chitinase induction by chitin and of major relevance to biocontrol". Current Genetics. 43 (4): 289–295. doi:10.1007/s00294-003-0399-y. ISSN 0172-8083. PMID 12748812. S2CID 22135834.
- ^ Troian, Rogério Fraga; Steindorff, Andrei Stecca; Ramada, Marcelo Henrique Soller; Arruda, Walquiria; Ulhoa, Cirano José (2014-06-26). "Mycoparasitism studies of Trichoderma harzianum against Sclerotinia sclerotiorum: evaluation of antagonism and expression of cell wall-degrading enzymes genes". Biotechnology Letters. 36 (10): 2095–2101. doi:10.1007/s10529-014-1583-5. ISSN 0141-5492. PMID 24966041. S2CID 254278907.
- ^ Goh, Yit Kheng; Vujanovic, Vladimir (2010). "Biotrophic mycoparasitic interactions betweenSphaerodes mycoparasiticaand phytopathogenicFusariumspecies". Biocontrol Science and Technology. 20 (9): 891–902. doi:10.1080/09583157.2010.489147. ISSN 0958-3157. S2CID 85250682.
- ^ Karlsson, Magnus; Durling, Mikael Brandström; Choi, Jaeyoung; Kosawang, Chatchai; Lackner, Gerald; Tzelepis, Georgios D.; Nygren, Kristiina; Dubey, Mukesh K.; Kamou, Nathalie (2015-01-08). "Insights on the Evolution of Mycoparasitism from the Genome of Clonostachys rosea". Genome Biology and Evolution. 7 (2): 465–480. doi:10.1093/gbe/evu292. ISSN 1759-6653. PMC 4350171. PMID 25575496.
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- ^ Howell, C. R. (2003). "Mechanisms Employed by Trichoderma Species in the Biological Control of Plant Diseases: The History and Evolution of Current Concepts". Plant Disease. 87 (1): 4–10. doi:10.1094/pdis.2003.87.1.4. ISSN 0191-2917. PMID 30812698. S2CID 44803233.
- ^ Vinale, Francesco; Sivasithamparam, Krishnapillai; Ghisalberti, Emilio L.; Marra, Roberta; Woo, Sheridan L.; Lorito, Matteo (2008). "Trichoderma–plant–pathogen interactions". Soil Biology and Biochemistry. 40 (1): 1–10. doi:10.1016/j.soilbio.2007.07.002. ISSN 0038-0717.