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]
Various 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.
Some bacteria live on or within fungal cells as parasites or symbionts.
Some viruses, called mycoviruses live on or within fungal cells as parasites or symbionts.
Many 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]
Biotrophic 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 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]
The four main steps of mycoparasitism include target location; recognition; contact and penetration; and nutrient acquisition. [7]
Many 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]
When 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]
Once 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]
Mycoparasitic 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 |
Plant pathology is the scientific study of diseases in plants caused by pathogens and environmental conditions. Organisms that cause infectious disease include fungi, oomycetes, bacteria, viruses, viroids, virus-like organisms, phytoplasmas, protozoa, nematodes and parasitic plants. Not included are ectoparasites like insects, mites, vertebrate, or other pests that affect plant health by eating plant tissues and causing injury that may admit plant pathogens. Plant pathology also involves the study of pathogen identification, disease etiology, disease cycles, economic impact, plant disease epidemiology, plant disease resistance, how plant diseases affect humans and animals, pathosystem genetics, and management of plant diseases.
Botrytis cinerea is a necrotrophic fungus that affects many plant species, although its most notable hosts may be wine grapes. In viticulture, it is commonly known as "botrytis bunch rot"; in horticulture, it is usually called "grey mould" or "gray mold".
An arbuscular mycorrhiza (AM) is a type of mycorrhiza in which the symbiont fungus penetrates the cortical cells of the roots of a vascular plant forming arbuscules. Arbuscular mycorrhiza is a type of endomycorrhiza along with ericoid mycorrhiza and orchid mycorrhiza.
Glomeromycota are one of eight currently recognized divisions within the kingdom Fungi, with approximately 230 described species. Members of the Glomeromycota form arbuscular mycorrhizas (AMs) with the thalli of bryophytes and the roots of vascular land plants. Not all species have been shown to form AMs, and one, Geosiphon pyriformis, is known not to do so. Instead, it forms an endocytobiotic association with Nostoc cyanobacteria. The majority of evidence shows that the Glomeromycota are dependent on land plants for carbon and energy, but there is recent circumstantial evidence that some species may be able to lead an independent existence. The arbuscular mycorrhizal species are terrestrial and widely distributed in soils worldwide where they form symbioses with the roots of the majority of plant species (>80%). They can also be found in wetlands, including salt-marshes, and associated with epiphytic plants.
Mycoviruses, also known as mycophages, are viruses that infect fungi. The majority of mycoviruses have double-stranded RNA (dsRNA) genomes and isometric particles, but approximately 30% have positive-sense, single-stranded RNA (+ssRNA) genomes.
Trichoderma is a genus of fungi in the family Hypocreaceae that is present in all soils, where they are the most prevalent culturable fungi. Many species in this genus can be characterized as opportunistic avirulent plant symbionts. This refers to the ability of several Trichoderma species to form mutualistic endophytic relationships with several plant species. The genomes of several Trichoderma specieshave been sequenced and are publicly available from the JGI.
Thielaviopsis basicola is the plant-pathogen fungus responsible for black root rot disease. This particular disease has a large host range, affecting woody ornamentals, herbaceous ornamentals, agronomic crops, and even vegetable crops. Examples of susceptible hosts include petunia, pansy, poinsettia, tobacco, cotton, carrot, lettuce, tomato, and others. Symptoms of this disease resemble nutrient deficiency but are truly a result of the decaying root systems of plants. Common symptoms include chlorotic lower foliage, yellowing of plant, stunting or wilting, and black lesions along the roots. The lesions along the roots may appear red at first, getting darker and turning black as the disease progresses. Black root lesions that begin in the middle of a root can also spread further along the roots in either direction. Due to the nature of the pathogen, the disease can easily be identified by the black lesions along the roots, especially when compared to healthy roots. The black lesions that appear along the roots are a result of the formation of chlamydospores, resting spores of the fungus that contribute to its pathogenicity. The chlamydospores are a dark brown-black color and cause the "discoloration" of the roots when they are produced in large amounts.
Pythium ultimum is a plant pathogen. It causes damping off and root rot diseases of hundreds of diverse plant hosts including corn, soybean, potato, wheat, fir, and many ornamental species. P. ultimum belongs to the peronosporalean lineage of oomycetes, along with other important plant pathogens such as Phytophthora spp. and many genera of downy mildews. P. ultimum is a frequent inhabitant of fields, freshwater ponds, and decomposing vegetation in most areas of the world. Contributing to the widespread distribution and persistence of P. ultimum is its ability to grow saprotrophically in soil and plant residue. This trait is also exhibited by most Pythium spp. but not by the related Phytophthora spp., which can only colonize living plant hosts.
Fungivory or mycophagy is the process of organisms consuming fungi. Many different organisms have been recorded to gain their energy from consuming fungi, including birds, mammals, insects, plants, amoebas, gastropods, nematodes, bacteria and other fungi. Some of these, which only eat fungi, are called fungivores whereas others eat fungi as only part of their diet, being omnivores.
A fungus is any member of the group of eukaryotic organisms that includes microorganisms such as yeasts and molds, as well as the more familiar mushrooms. These organisms are classified as a kingdom, separately from the other eukaryotic kingdoms, which, by one traditional classification, includes Plantae, Animalia, Protozoa, and Chromista.
The Zoopagomycotina are a subdivision of the fungal division Zygomycota sensu lato. It contains 5 families and 20 genera. Relationships among and within subphyla of Zygomycota are poorly understood, and their monophyly remains in question, so they are sometimes referred to by the informal name zygomycetes.
Chaetomium cupreum is a fungus in the family Chaetomiaceae. It is able to decay in manufactured cellulosic materials, and is known to antagonize a wide range of soil microorganisms. This species is component of the biocontrol agent, Ketomium, a commercial biofungicide. It has also been investigated for use in the production of natural dyes. Chaetomium cupreum is mesophilic and known to occur in harsh environments and can rapidly colonize organic substrates in soil. Laboratory cultures of C. cupreum can be propagated on a range of common growth media including potato dextrose at ambient or higher than ambient temperature producing cottony white colonies with a reddish reverse.
Ampelomyces quisqualis is an anamorphic fungus that is a hyperparasite of powdery mildews. This parasitism reduces growth and may eventually kill the mildew. These mycoparasites can live up to 21 days on mildew-free host plant surfaces, attacking powdery mildew structures as soon as they appear. A. quisqualis is used as the active ingredient in a commercial fungicide.
Mycetophagites is an extinct fungal genus of mycoparasitic in the order Hypocreales. A monotypic genus, it contains the single species Mycetophagites atrebora.
Entropezites is an extinct monotypic genus of [hypermycoparasitic] fungus in the order Hypocreales. At present it contains the single species Entropezites patricii.
The root microbiome is the dynamic community of microorganisms associated with plant roots. Because they are rich in a variety of carbon compounds, plant roots provide unique environments for a diverse assemblage of soil microorganisms, including bacteria, fungi and archaea. The microbial communities inside the root and in the rhizosphere are distinct from each other, and from the microbial communities of bulk soil, although there is some overlap in species composition.
Orchid mycorrhizae are endomycorrhizal fungi which develop symbiotic relationships with the roots and seeds of plants of the family Orchidaceae. Nearly all orchids are myco-heterotrophic at some point in their life cycle. Orchid mycorrhizae are critically important during orchid germination, as an orchid seed has virtually no energy reserve and obtains its carbon from the fungal symbiont.
Hemibiotrophs are the spectrum of plant pathogens, including bacteria, oomycete and a group of plant pathogenic fungi that keep its host alive while establishing itself within the host tissue, taking up the nutrients with brief biotrophic-like phase. It then, in later stages of infection switches to a necrotrophic life-style, where it rampantly kills the host cells, deriving its nutrients from the dead tissues.
Fungal effectors are proteins or non-proteinaceous molecules secreted by pathogenic fungi into a host organism in order to modulate the host's immune response.
Trichoderma atroviride is a filamentous fungal species commonly found in the soil. This fungal species is of particular interest to researchers due to the plethora of secondary metabolites it makes which are used in industry The genus Trichoderma is known for its ubiquity in almost all soils and being easy to culture. Many Trichoderma's are also avirulent plant symbionts.