The Mycorrhizal Network: Difference between revisions

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The engineering of symbiotic fungal species using clustered regularly interspaced short palindromic repeats (CRISPR)/Cas-mediated genome editing tools are of interest for increasing the nutritional benefits of mycorrhizal fungi for agricultural development <ref>Song, R., Zhai, Q., Sun, L. et al. CRISPR/Cas9 genome editing technology in filamentous fungi: progress and perspective . <i>Appl Microbiol Biotechnol</i> 103, 6919–6932 (2019). https://doi.org/10.1007/s00253-019-10007-w</ref><ref>Shelake RM, Pramanik D, Kim JY. Exploration of Plant-Microbe Interactions for Sustainable Agriculture in CRISPR Era. <i>Microorganisms.</i> 2019 Aug 17;7(8):269. doi: 10.3390/microorganisms7080269. PMID: 31426522; PMCID: PMC6723455.</ref>
The engineering of symbiotic fungal species using clustered regularly interspaced short palindromic repeats (CRISPR)/Cas-mediated genome editing tools are of interest for increasing the nutritional benefits of mycorrhizal fungi for agricultural development <ref>Song, R., Zhai, Q., Sun, L. et al. CRISPR/Cas9 genome editing technology in filamentous fungi: progress and perspective . <i>Appl Microbiol Biotechnol</i> 103, 6919–6932 (2019). https://doi.org/10.1007/s00253-019-10007-w</ref><ref>Shelake RM, Pramanik D, Kim JY. Exploration of Plant-Microbe Interactions for Sustainable Agriculture in CRISPR Era. <i>Microorganisms.</i> 2019 Aug 17;7(8):269. doi: 10.3390/microorganisms7080269. PMID: 31426522; PMCID: PMC6723455.</ref>
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Studies have analyzed the effect of the addition of AMF into the soil of agricultural plants and found increased nutrient acquisition and plant growth with the utilization of this symbiosis<ref name = aaa>[Kothari, S. K., Marschner, H., & Römheld, V. (1991). Contribution of the VA mycorrhizal hyphae in the acquisition of phosphorus and zinc by maize grown in a calcareous soil. <i>Plant and Soil, 131</i>(2), 177–185. doi: 10.1007/BF00009447]</ref><ref name = aac>[Azaizeh, H. A., Marschner, H., Römheld, V., & Wittenmayer, L. (1995). Effects of a vesicular-arbuscular mycorrhizal fungus and other soil microorganisms on growth, mineral nutrient acquisition, and root exudation of soil-grown maize plants.<i> Mycorrhiza, 5</i>(5), 321–327. doi: 10.1007/BF00207404]</ref><ref name = aac>[Arines, J., Vilarino, A., & Sainz, M. (1989). Effect of Different Inocula of Vesicular-Arbuscular Mycorrhizal Fungi on Manganese Content and Concentration in Red Clover (Trifolium pratense L.) Plants. <i>The New Phytologist, 112</i>(2), 215-219. Retrieved April 17, 2021, from http://www.jstor.org/stable/2556903]</ref>. One study demonstrated the effectiveness of arbuscular mycorrhizae with the growth of soil-grown maize plants, showing a significant increase in shoot dry weight and the shoot: root ratio of the maize plants after only 6 weeks of infection with AMF compared to the control plants<ref name=aac/>. After six weeks of infection, it was also shown that there were significant increases in nutrient concentrations of zinc, copper, nitrogen, and phosphorus in both the shoots and roots of the maize plants<ref name=aac/>. Another study found similar results, studying the acquisition of P and Zn by maize plants inoculated with AMF, demonstrating a 1.3 to 3-fold increase of P concentration in the maize roots and shoots, as well as a 1.7 to 3.8-fold increase of Zn concentration in shoots after AMF inoculation<ref name = aaa/>. The study by Arines et al (1989) also demonstrated a significant decrease in manganese concentrations within the plants, an essential nutrient for plant growth, but can be toxic in high concentrations<ref name=aac/><ref name = aad>[S. V., . K. V. H., & . S. J. (2007). Characterization of manganese toxicity and its influence on nutrient uptake, antioxidant enzymes and biochemical parameters in tea. <i>Research Journal of Phytochemistry, 1</i>(2), 52–60. doi: 10.3923/rjphyto.2007.52.60]</ref><ref name = aae>[Millaleo, R., Reyes- Diaz, M., Ivanov, A. G., Mora, M. L., & Alberdi, M. (2010). Manganese as essential and toxic element for plants: transport, accumulation and resistance mechanisms.<i> Journal of Soil Science and Plant Nutrition, 10</i>(4), 470–481. doi: 10.4067/S0718-95162010000200008]</ref>.  It is deduced that the decrease in Mn concentration may be related to the AMF decreasing the amount of Mn-reducing bacteria, or the increase of Mn-oxidizing bacteria<ref name=aac/><ref name = aaf>[Posta, K., Marschner, H., & Römheld, V. (1994). Manganese reduction in the rhizosphere of mycorrhizal and nonmycorrhizal maize. <i>Mycorrhiza, 5</i>(2), 119–124. doi: 10.1007/BF00202343]</ref>.
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<b>Water Absorption</b>
<b>Water Absorption</b>

Revision as of 03:44, 17 April 2021

This is a curated page. Report corrections to Microbewiki.


By Freya Beinart


Introduction

Fungal colonization of a plant's rhizosphere representing a mycorrhizal symbiosis. [1].

A mycorrhiza is the symbiotic relationship between fungi and plants. Mycelium, the vegetative part of a fungus, extends in a branching network of hyphae that secrete enzymes, breaking down organic material into nutrients. The vast mycelial branches of the fungi are made of branching networks of hyphae which, in a mycorrhizal association, colonize the root systems of many plant species, greatly increasing the surface area of a plant’s rhizosphere in which it collects water and essential nutrients [1] [2]. In exchange for these nutrients, the plants provide the fungi with carbohydrates that the fungi cannot produce on its own, being heterotrophic. The hyphae of soil fungi colonize the root system of plants, providing the photosynthetic organisms with nutrients and water in exchange for carbohydrates that the heterotrophic fungi cannot produce on its own. This colonization may be intracellular as endomycorrhizal fungi which trade nutrients via a signal transduction pathway, or extracellular as ectomycorrhizal fungi that envelop plant roots [3][4].

About 10% of identified fungal species are known to occur in mycorrhizal symbioses, these fungi are most species of the Glomeromycota, and many species of the Ascomycota and Basidiomycota [5]. The fungal symbionts assist host plants to be less susceptible to pathogens and environmental stresses such as lack of nutrient density, drought, and high salinity [6][1][7][8][9]. The vast underground networks of hyphae increase nutrient cycling, erosion resistance, air permeability, and water permeability within the soil itself. Including and maintaining these associations between fungi and plants has proven to be highly beneficial for agricultural health and biogeochemical cycling [10][7][11][12][9][13].

Types of Mycorrhizal Symbioses

Figure 1. Diagram of different types of mycorrhizal associations on the cellular level. [2].

Characterization of mycorrhizal association is dependent upon the location of fungal colonization and is specific to both the plant species and their fungal symbionts.

Endomycorrhizae

Endomycorrhizal symbioses occur when the mycorrhizal fungi colonizes a host plant intracellularly.

Arbuscular Mycorrhizae

Fungi of the phylum Glomeromycota that forms mutualistic symbioses, called arbuscular mycorrhizae, with vascular plants are referred to as arbuscular mycorrhizal fungi, or AMF. These fungi are associated with 90% of vascular plant species. AMF are unable to live without the presence of the host plants, as they depend on the transfer of carbohydrates from the plant tissue, making the fungi obligate biotrophs [14]. Plant taxa that are observed to exhibit this relationship are bryophyta, pteridophyta, gymnosperms, and angiosperms][15].

Hyphae from a germinating spore infect the host root, passing the epidermis and penetrating cortical cells which form arbuscules - the structure from which the name of these fungi originated <[14]. The arbuscules are networks of extremely fine clustered hyphae within the host cells where nutrient transfer is centralized [16].The hyphae may also form vesicles between or within the root cells, acting as an organ for storage with a thickened cell wall which aids in the establishment of new colonies [1] [17]. The mycelium which extends from the plant root is called the extraradical mycelium, which connects from plant to plant, forming a continuum of nutrient and water exchange [18].

Ericoid mycorrhizae

Ericoid mycorrhizae are usually found in environments with high acidity and free-draining soils susceptible to droughts. These associations involve a mycorrhizal fungus in the Ascomycota and a host plant of the Ericideae family [2][4][19]. The hyphal coils are where nutrient transfer occurs within ericoid mycorrhizae. Experimentation of ericoid mycorrhizal fungi growth in axenic has revealed a range of saprotrophic capabilities, allowing the fungi to feed on decaying organic matter [20].

Ectomycorrhizae

Figure 2. Light micrograph of ectomycorrhizal roots with penetrating fungal hyphae forming the Hartig net structure. [3].

Fungi that form ectomycorrhizae are majorly Basidiomycota, as well as some Ascomycota and Zygomycetes of the genus Endogone. These associations differ from AM symbioses in the way that the fungi does not penetrate the root cells, instead, it grows intercellularly. Hyphae grow between epidermal and cortical cells of the plant, forming a structure called the Hartig net where nutrient transfer is localized [4]. Hyphae of ectomycorrhizal fungi create sheathes which envelop the exterior of the plant root, called mantle. The hyphae extend outward from the plant root to extend the surface area of the plant root, forming a structure called a rhizomorph. The rhizomorphs’ increased ability to uptake water and nutrients from the soil makes up for the suppression of root hairs by the mantle [21].

Ectomycorrhizae occur in about 10% of plant species, specifically woody plants in certain families of gymnosperms and angiosperms [22]. These fungi form fruiting bodies, unlike AMF which only reproduce asexually. Examples of these fruiting bodies are mushrooms of the genus Amanita and genus Tuber.

Ectendomycorrhizae

Ectendomycorrhizal fungi form Hartig net and mantle structures akin to Ectomycorrhizal fungi. Ectendomycorrhizal symbioses differ from ectomycorrhizae as the hyphae penetrate the cortical cells of plant roots, forming an intracellular Hartig net. One type of ectendomycorrhiza is arbutoid mycorrhiza, which is a symbiosis between basidiomycetes and some plant species of the Ericaceae family [23].

Evolution of Mycorrhizae

Figure 3. Fossilized hyphae and spores from the Ordovician period (A, B, C, E, F, G) and spores formed by extant glomalean fungi (D and H). [4].
Figure 4. Fossil ectomycorrhizae associated with Pinus roots [5].

Fossil records indicate that mycorrhizal fungi predate the evolution of vascular plants, about 460 million years ago in the Ordovician period [24]. The most ancestral mycorrhizal fungi has been identified as arbuscular, penetrating the root cortical cells in most extant plant taxa. The phylum of fungi that associates with land plants as AMF is that of Glomeromycota [25] The presence of these fungi were involved in the development of soil and the evolution and colonization of vascular land plants, specifically by aiding the non-vascular plants with acquisition of nutrients through fungal hyphae, as the “soil” lacked a significant amount of nutrients for terrestrial plants to survive without their fungal symbionts [26]. As the fungi cycles nutrients such as nitrogen, phosphorus, and sulfur to the plants, the fungus receives and fixes carbon into the ground, assisting in the lowering of atmospheric CO2 leading to the oxygenation of the atmosphere during the development of terrestrial plants [27] [28].

In a study by Krings et al (2007) fossil evidence from the Rhynie chert sediment of the Early Devonian period suggests that fungal endophytes, specifically those which colonize the rhizoids of Nothia aphylla, actively influenced the evolution of these plants due to observed host responses. The responses to fungal infection in N. aphylla - rhizoid bulging, separation of infected cells via thickening of cell walls, and the motile inhibition of hypha - suggests its susceptibility to colonization by fungi at least 400 million years ago, advancing selection between plant species with the increasing complexity of interspecies interactions [29].

The other form of mycorrhiza associated with the intercellular colonization of fungal symbionts within plants, ectomycorrhiza, evolved much later than its ancestor AMF. Fossil records suggest that ectomycorrhizal fungi may have evolved at least 156 million years ago, as the oldest known extant plant family associated with ectomycorrhizal fungi, Pinaceae, appear to have evolved in that time period [30]. Another study shows the morphological identification of ectomycorrhizal fungi based on apparent Hartig net, mantle, and hyphal structures on fossils of Pinus roots dating back 50 million years, clearly representing the established ectomycorrhizal associations (Fig. 4) [31].

Biogeochemical Cycles

Figure 5. Amount of carbon stored in plant biomass in vegetation of different mycorrhizal types (Mt C per-grid cell of 15 arcmin). a Arbuscular mycorrhizal plants, b ectomycorrhizal plants, c ericoid mycorrhizal plants, d non-mycorrhizal plants. [6].

Carbon Storage

Carbon is an extremely important element as it is the primary component of organic compounds and macromolecules. Major amounts of carbon stores are located within the soil, containing more soil than the atmosphere and vegetation combined [32]. Saprotrophic fungi play an extremely important role in the carbon cycle as they decompose organic matter, releasing nutrients into the soil. It was believed that most of the carbon found in terrestrial ecosystems was stored in vegetative remains, or leaf litter, however recent studies suggest that most of the stored carbon is derived from the mycelium of mycorrhizal fungi [33][34].

Figure 6. Effects of fertilization of Brachypodium distachyon with Rhizophagus irregularis and soil microbes. [7].

Nitrogen Fixation

Nitrogen is an extremely important nutrient for all living organisms as it is essential for amino acid synthesis and therefore the formation of proteins. Despite its importance, nitrogen cannot be used by many organisms until it has been heavily reduced into ammonia [35]. This anabolic process is very energy-intensive, and therefore many organisms do not possess the ability to fix nitrogen [36] [37]. Organisms that can fix atmospheric nitrogen are known as diazotrophs - bacteria and archaea that do not require fixed nitrogen for their growth or survival [38].

Root nodule symbiosis between plants and nitrogen-fixing bacteria is apparent in plants of the Fabaceae, also known as the legume family[39]. Legumes have a symbiotic relationship with rhizobia, single-celled, Gram-negative bacteria [39] [40]. The mutualism between the legumes and rhizobia allows the bacteria to take up atmospheric nitrogen, feeding it to the plant. In return, the plant provides carbohydrates to the bacteria as it is essential for their metabolic processes and growth [36]. Although mycorrhizal symbionts do not possess the metabolism required for nitrogen fixation, studies have shown that mycorrhizae may indirectly affect nitrogen fixation as they increase root nodulation [39] [40][41].

The legume symbiotic signaling (SYM) pathway has been studied in relation to arbuscular mycorrhizal symbiosis [3] [41]. The SYM pathway controls both nodulation of legumes and the mycorrhization of land plants, and is suggested to evolve first in legumes and adapted for arbuscular mycorrhizal symbiosis [42]. This pathway is characterized by its use of calcium as a second messenger, regulating both arbuscular mycorrhizal symbiosis and rhizobial symbiosis. Due to the SYM pathway evolutionary phylogeny, it is believed that legumes demonstrating root nodule symbiosis adapted the use of AMF to increase their uptake of nitrogen [9].

Unlike legumes which maintain root nodule symbiosis, AMF have limited accessibility to acquire atmospheric nitrogen. A study has shown that the arbuscular mycorrhizal association between the fungus Rhizophagus irregularis and rhizobia communities increase nitrogen acquisition in the mycorrhizal grass species Brachypodium distachyon [43]. Growth of Brachypodium distachyon fertilized with Rhizophagus irregularis spores acquired two to threefold more nitrogen from organic matter than from the Brachypodium distachyon control without fertilization with AMF or soil microbial communities (Fig. 6)[43]. Brachypodium distachyon fertilized with both Rhizophagus irregularis and soil microbial communities acquired ten to twelvefold more nitrogen from organic matter than the control (Fig. 6)[43]. The increased uptake of organic nitrogen in host plants with AM symbiosis represents the extreme degree of importance that AM symbiosis has on nutrient cycles within global ecosystems.

Phosphorus Transport

Applications

There has been plenty of research pertaining to the efficacy of introducing fungal spores into crop fertilizer, specifically to utilize and maintain mycorrhizal symbiosis between plants and fungi [13]. The branching networks of mycelium that the fungi form increase the absorption of water within the soil as well as aerate the soil to aid in plant growth and colonization. Introducing hyphae into environments has the ability to promote plant growth and diversity upon other forms of agricultural intervention.

Nutrient Cycling
The engineering of symbiotic fungal species using clustered regularly interspaced short palindromic repeats (CRISPR)/Cas-mediated genome editing tools are of interest for increasing the nutritional benefits of mycorrhizal fungi for agricultural development [44][45]

Studies have analyzed the effect of the addition of AMF into the soil of agricultural plants and found increased nutrient acquisition and plant growth with the utilization of this symbiosis[46][47][47]. One study demonstrated the effectiveness of arbuscular mycorrhizae with the growth of soil-grown maize plants, showing a significant increase in shoot dry weight and the shoot: root ratio of the maize plants after only 6 weeks of infection with AMF compared to the control plants[47]. After six weeks of infection, it was also shown that there were significant increases in nutrient concentrations of zinc, copper, nitrogen, and phosphorus in both the shoots and roots of the maize plants[47]. Another study found similar results, studying the acquisition of P and Zn by maize plants inoculated with AMF, demonstrating a 1.3 to 3-fold increase of P concentration in the maize roots and shoots, as well as a 1.7 to 3.8-fold increase of Zn concentration in shoots after AMF inoculation[46]. The study by Arines et al (1989) also demonstrated a significant decrease in manganese concentrations within the plants, an essential nutrient for plant growth, but can be toxic in high concentrations[47][48][49]. It is deduced that the decrease in Mn concentration may be related to the AMF decreasing the amount of Mn-reducing bacteria, or the increase of Mn-oxidizing bacteria[47][50].

Water Absorption

Conclusion

Although many people commonly associate fungi with disease or death, filamentous fungi demonstrate remarkable benefits for terrestrial organisms and the global environment.

References

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Authored for BIOL 238 Microbiology, taught by Joan Slonczewski, 2021, Kenyon College.