Wikipedia

Mycorrhiza helper bacteria

Mycorrhiza helper bacteria (MHB) are a group of organisms that form symbiotic associations with both ectomycorrhiza and arbuscular mycorrhiza.[1] MHBs are diverse and belong to a wide variety of bacterial phyla including both Gram-negative and Gram-positive bacteria.[1] Some of the most common MHBs observed in studies belong to the genera Pseudomonas and Streptomyces.[1] MHBs have been seen to have extremely specific interactions with their fungal hosts at times, but this specificity is lost with plants.[2] MHBs enhance mycorrhizal function, growth, nutrient uptake to the fungus and plant, improve soil conductance, aid against certain pathogens, and help promote defense mechanisms.[1] These bacteria are naturally present in the soil, and form these complex interactions with fungi as plant root development starts to take shape.[2] The mechanisms through which these interactions take shape are not well-understood and needs further study.[1][2][3]

General association and effects of MHBs with mycorrhizal fungi.

Taxonomy

edit

MHBs consist of a diverse group of bacteria, often gram-negative and gram-positive bacteria. Most of the bacteria are associated with both ectomycorrhiza and arbuscular mycorrhiza, but some show specificity to a particular type of fungus.[1] The common phyla that MHB belong to will be addressed in the following sections, as well as common genera.

Pseudomonadota

edit

The Pseudomonadota (formerly Proteobacteria) are a large and diverse group of gram-negative bacteria containing five classes. Pseudomonas is in the gammaproteobacteria class. Specific bacteria within this genus are strongly associated as being MHBs in the rhizosphere of both ectomycorrhiza and arbuscular mycorrhiza.[1] Pseudomonas fluorescens has been examined in several studies to understand how they work in benefiting the mycorrhiza and plant.[1] In one study, they found that the bacteria helped ectomycorrhizal fungi promote a symbiotic relationship with the plant by examining an increase in formation of mycorrhiza when Pseudomonas fluorescens was applied to the soil.[4] Some bacteria improve root colonization and plant growth when associated with arbuscular mycorrhiza.[5] It has been hypothesized that MHBs aid the plant in pathogenic defense by improving the nutrient uptake from the soil, allowing plants to allocate more resources to broad defense mechanisms.[6] However, the mechanism these species use to help both fungi is still unknown and needs to be further investigated.[5]

Actinomycetota

edit
 
The branching shape of Streptomyces, a very common soil bacteria that often aids in the plant-mycorhiza relationship.

Actinomycetota are gram-positive bacteria and are naturally found in the soil. In this phylum, Streptomyces is the largest genus of bacteria, and are often associated with MHBs.[1] Streptomyces have been a model organism of study in biological research on MHBs. In one study, it has been reported that Streptomyces are responsible for increasing root colonization, plant biomass growth, mycorrhizal colonization, and fungal growth.[7][8] However, there is not just a single mechanism that the MHBs participate in.[1][7][8] It has also been found that Streptomyces interact with ectomycorrhiza and arbuscular mycorrhiza.[1] While these interactions need further understanding, they seem to be extremely common in natural soil.[8]

Bacillota

edit

Bacillota are gram-positive bacteria, many of which have a low GC content in their DNA. There are a few genera that act as MHBs, but one of the most common is Bacillius.[1] Bacillius belong to the class Bacilli, and are rod-shaped organisms that can be free-living or pathogenic. However, in the presence of mycorrhiza some species can be beneficial and are considered to be MHBs.[1] Since they are common, they can form a relationship with ectomycorrhiza and arbuscular mycorrhiza, similar to the previous genera.[1] Bacillius aids in the establishment and growth of mycorrhiza, and helps with the fixation of nitrogen in the rhizosphere.[9][10][11]

Impact

edit

MHBs are known to have several functions when interacting with the roots of plants and growth of fungi. In several studies it has been reported that MHBs can help fungi by increasing mycelial growth and aid in nutrient intake.[3] The mycelial increase allows for fungi to absorb more nutrients, increasing its surface area.[9]

Growth promoted by nutrients

edit

Some MHBs are known to help break down molecules to a more usable form.[1] MHBs can obtain both inorganic and organic nutrients in the soil through a direct process known as mineral-weathering which aids in the recycling of nutrients throughout the environment.[12] The process of mineral-weathering releases protons and iron into the soil.[12] This results in a lowering of the pH.[12] A diverse group of bacteria can participate in the mineral- weathering process, such as Pseudomonas, Burkholderia, and Collimonas.[12] The acidification of the soil by MHBs is hypothesized to be linked to their glucose metabolism.[12]

MHBs also help gather unavailable phosphorus from the surrounding soil.[13] Phosphate solubilizing rhizobacteria are the most common MHB that aids in phosphorus uptake.[13] The bacteria are involved in this process by releasing phosphate-degrading compounds in the soil to break down organic and inorganic phosphate.[14] As a result, the MHB create a pool of phosphate that the mycorrhiza then use.[14][15] The bacteria work in phosphorus-limited conditions to help the mycorrhiza establish and grow.[13] Streptomyces can assist arbuscular mycorrhiza in phosphorus-limited conditions through a similar process.[8][13]

MHBs in the rhizosphere often have the capability to acquire nitrogen that the plant can use. The MHBs are able to fix nitrogen in the soil, and create pools of available nitrogen.[16] However, MHBs do not cause plant modifications as legumes do, to help with nitrogen-fixation.[16] Nitrogen-fixation is done only in the surrounding soil in relation to the mycorrhiza.[16] In one study, researchers reported that a Bacillius MHB contributed to the nitrogen-fixation, and among other factors helped the plant grow when inoculated with a fungus.[11]

Plant growth hormones

edit

It has been proposed (Kaska et al., 1994) that MHBs induce growth hormones in a plant, which helps the mycorrhiza interact with the lateral roots in soil.[17] An increase of root formation was also observed when Pseudomonas putida produced growth hormones, and was inoculated with the arbuscular mycorrhiza Gigaspora rosea on a cucumber plant.[18] The inoculation of both the MHB and the fungus allowed for an increase in root elongation and growth in the soil, similar to the previous study.[18] In another study, it was found that MHB can release gaseous compounds to attract and aid in the growth of fungi.[19] The introduction of growth hormones and gaseous compounds produced by MHBs was only discovered recently, and requires further study on how MHBs influence the mycorrhiza symbiotic relationship and root growth.

Alteration of fungal genes aiding in growth

edit
 
An example of cell-signaling, a proposed method for communication between MHBs and their fungal hosts allowing for recognition and co-colonization of plants.

Researchers have reported that fungal genes can be altered in the presence of an MHB.[20] In one study, it was hypothesized that in the presence of a fungus, an MHB will promote an increase in the expression of a gene that helps to promote growth in the fungus.[20] The fungus changes its genes expression after the MHB has promoted growth of the fungus, thus the alteration of the gene is an indirect effect.[20] This is likely the cause of certain compounds or signals released by the MHBs, and further analysis is needed to better understand this communication.[20]

Interactions with specific fungi

edit

Only certain bacteria are specific to mycorrhizal fungi groups.[15] Results have shown that the indigenous arbuscular mycorrhizal fungi of the clover plant could only grow in the presence Pseudomonas putida, but in fact, the plant could grow with the presence of multiple bacteria.[15] It has been hypothesized that rhizosphere helper bacteria, in the soil, have developed traits to aid them in competition for inoculating fungi in their environment.[8] Thus, it is plausible that MHBs select for certain fungi and developed some specificity towards a fungus that favors the bacteria.[8][1]

Detoxifying soil

edit

MHBs help mycorrhiza establish symbiotic associations in stressful environments such as those high in toxic metals.[21] In harsh environments, the bacteria assist in acquiring more nutrients such as nitrogen and phosphorus.[22][23] MHBs help to prevent the uptake of toxic metals including lead, zinc, and cadmium.[22][23] The bacteria decrease the amount of metals taken up by the plant through blockade mechanisms.[22][23] The blockade of the toxic metals by the bacteria allows the fungus to form a stronger symbiotic association with the plant, and promotes the growth of both.[22][23] Another proposed mechanism of MHBs in toxic environments is that the bacteria aid the mycorrhiza by compensating for the negative effects the toxic metal imposed.[24] The MHBs help by increasing the plant nutrition uptake, and creating a balance between the macronutrients and micronutrients.[23][24] Thus, MHBs have mechanisms to help the plant tolerate harsh and otherwise unsuitable environments. This relationship makes them great candidates for bioremediation.

With pathogenic fungi

edit
 
Pathogenic fungi, able to harm other fungi or plants.

In the presence of a pathogenic fungus, most studies show that MHBs aid in fighting off pathogens.[2] However, there have been a few cases where MHBs help to promote pathogenic effects of a fungus.[2]

Assisting pathogenic fungi

edit

There have been a few studies that have found that MHBs aid pathogenic fungi. One study showed that MHBs aided in colonization of a type of fungal pathogen because the surrounding environment was unsuitable for the symbiotic mycorrhiza.[25] Thus the MHB became more harmful under certain conditions to increase their own fitness.[25][2]  Researchers have also found that MHBs help the pathogenic fungus to colonize on the surface of the plant.[25] This has a negative effect on the plant, by increasing the deleterious effects of the fungus. Another proposed mechanism is that MHBs alter the defense mechanism of the plant, by shutting off degrading peroxidase enzymes, and allowing the pathogenic fungus to inoculate the plant.[26]

Defending against pathogenic fungi

edit

In several studies, researchers have proposed numerous ways MHBs defend against pathogens. In one experiment researchers observed that MHBs produced acid in the surrounding environment, which helped to fight off various pathogens.[27] It has also been hypothesized that the defense mechanism against pathogens is from a combination of both fungi and plant.[27] Another study found that MHBs release antifungal metabolites into the soil.[28] The anti-fungal metabolites produce antagonistic effects towards the pathogenic fungi.[28] However, MHBs can help defend a pathogen depending on the nutrient availability and space in the rhizosphere.[1][27] Further research is still necessary to understand the mechanism of how MHBs aid mycorrhiza in order to defeat pathogens, and if this role is symbiotic or more mutualistic in nature.

References

edit
  1. ^ a b c d e f g h i j k l m n o p q Frey-Klett, P.; Garbaye, J.; Tarkka, M. (2007-10-01). "The mycorrhiza helper bacteria revisited". New Phytologist. 176 (1): 22–36. doi:10.1111/j.1469-8137.2007.02191.x. ISSN 1469-8137. PMID 17803639.
  2. ^ a b c d e f Rigamonte, T; Pylro, V (2010). "The role of mycorrhization helper bacteria in the establishment and action of ectomycorrhizae associations". Brazilian Journal of Microbiology. 41 (4): 832–840. doi:10.1590/S1517-83822010000400002. PMC 3769757. PMID 24031563.
  3. ^ a b Pivato, Barbara; Offre, Pierre; Marchelli, Sara; Barbonaglia, Bruno; Mougel, Christophe; Lemanceau, Philippe; Berta, Graziella (2009-02-01). "Bacterial effects on arbuscular mycorrhizal fungi and mycorrhiza development as influenced by the bacteria, fungi, and host plant". Mycorrhiza. 19 (2): 81–90. doi:10.1007/s00572-008-0205-2. ISSN 0940-6360. PMID 18941805.
  4. ^ Founoune, Hassna; Duponnois, Robin; Meyer, Jean Marie; Thioulouse, Jean; Masse, Dominique; Chotte, Jean Luc; Neyra, Marc (2002-07-01). "Interactions between ectomycorrhizal symbiosis and fluorescent pseudomonads on Acacia holosericea: isolation of mycorrhiza helper bacteria (MHB) from a Soudano-Sahelian soil". FEMS Microbiology Ecology. 41 (1): 37–46. doi:10.1111/j.1574-6941.2002.tb00964.x. PMID 19709237.
  5. ^ a b Gamalero, Elisa; Trotta, Antonio; Massa, Nadia; Copetta, Andrea; Martinotti, Maria Giovanna; Berta, Graziella (2004-06-01). "Impact of two fluorescent pseudomonads and an arbuscular mycorrhizal fungus on tomato plant growth, root architecture and P acquisition". Mycorrhiza. 14 (3): 185–192. doi:10.1007/s00572-003-0256-3. PMID 15197635.
  6. ^ Basu, Muthuramalingam; Santhaguru, Karuppagnaniar (2009-06-01). "Impact of Glomus Fasciculatum and Fluorescent Pseudomonas on Growth Performance of Vigna Radiata (L.) Wilczek Challenged with Phytopathogens". Journal of Plant Protection Research. 49 (2): 190–194. CiteSeerX 10.1.1.599.7665. doi:10.2478/v10045-009-0028-y.
  7. ^ a b Abdel-Fattah, G. M.; Mohamedin, A. H. (2000-12-01). "Interactions between a vesicular-arbuscular mycorrhizal fungus (Glomus intraradices) and Streptomyces coelicolor and their effects on sorghum plants grown in soil amended with chitin of brawn scales". Biology and Fertility of Soils. 32 (5): 401–409. doi:10.1007/s003740000269.
  8. ^ a b c d e f Franco-Correa, Marcela; Quintana, Angelica; Duque, Christian; Suarez, Christian; Rodríguez, Maria X.; Barea, José-Miguel (2010). "Evaluation of actinomycete strains for key traits related with plant growth promotion and mycorrhiza helping activities". Applied Soil Ecology. 45 (3): 209–217. doi:10.1016/j.apsoil.2010.04.007.
  9. ^ a b Toro, M.; Azcon, R.; Barea, J. (1997-11-01). "Improvement of Arbuscular Mycorrhiza Development by Inoculation of Soil with Phosphate-Solubilizing Rhizobacteria To Improve Rock Phosphate Bioavailability ((sup32)P) and Nutrient Cycling". Applied and Environmental Microbiology. 63 (11): 4408–4412. doi:10.1128/AEM.63.11.4408-4412.1997. PMC 1389286. PMID 16535730.
  10. ^ Mamatha, G.; Bagyaraj, D.; Jaganath, S. (2002-12-01). "Inoculation of field-established mulberry and papaya with arbuscular mycorrhizal fungi and a mycorrhiza helper bacterium". Mycorrhiza. 12 (6): 313–316. doi:10.1007/s00572-002-0200-y. PMID 12466919.
  11. ^ a b Chanway, C. P.; Holl, F. B. (1991-03-01). "Biomass increase and associative nitrogen fixation of mycorrhizal Pinus contorta seedlings inoculated with a plant growth promoting Bacillus strain". Canadian Journal of Botany. 69 (3): 507–511. doi:10.1139/b91-069.
  12. ^ a b c d e Uroz, S.; Calvaruso, C.; Turpault, M. P.; Pierrat, J. C.; Mustin, C.; Frey-Klett, P. (2007-05-01). "Effect of the Mycorrhizosphere on the Genotypic and Metabolic Diversity of the Bacterial Communities Involved in Mineral Weathering in a Forest Soil". Applied and Environmental Microbiology. 73 (9): 3019–3027. doi:10.1128/aem.00121-07. ISSN 0099-2240. PMC 1892860. PMID 17351101.
  13. ^ a b c d Barea, JM; Azcón, R; Azcón-Aguilar, C (August 2002). "Mycorrhizosphere interactions to improve plant fitness and soil quality". Antonie van Leeuwenhoek. 81 (1–4): 343–51. doi:10.1023/A:1020588701325. PMID 12448732.
  14. ^ a b Kucey, R.M.N.; Janzen, H.H.; Leggett, M.E. (1989). "Microbially Mediated Increases in Plant-Available Phosphorus". Advances in Agronomy Volume 42. Advances in Agronomy. Vol. 42. pp. 199–228. doi:10.1016/s0065-2113(08)60525-8. ISBN 9780120007424.
  15. ^ a b c Artursson, Veronica; Finlay, Roger D.; Jansson, Janet K. (2006-01-01). "Interactions between arbuscular mycorrhizal fungi and bacteria and their potential for stimulating plant growth". Environmental Microbiology. 8 (1): 1–10. doi:10.1111/j.1462-2920.2005.00942.x. PMID 16343316.
  16. ^ a b c Antoun, Hani; Prévost, Danielle (2005). PGPR: Biocontrol and Biofertilization. Springer, Dordrecht. pp. 1–38. doi:10.1007/1-4020-4152-7_1. ISBN 9781402040023.
  17. ^ Kaska, D. D.; Myllylä, R.; Cooper, J. B. (1999-04-01). "Auxin transport inhibitors act through ethylene to regulate dichotomous branching of lateral root meristems in pine". New Phytologist. 142 (1): 49–57. doi:10.1046/j.1469-8137.1999.00379.x. ISSN 1469-8137.
  18. ^ a b Gamalero, Elisa; Berta, Graziella; Massa, Nadia; Glick, Bernard R.; Lingua, Guido (2008-06-01). "Synergistic interactions between the ACC deaminase-producing bacterium Pseudomonas putida UW4 and the AM fungus Gigaspora rosea positively affect cucumber plant growth". FEMS Microbiology Ecology. 64 (3): 459–467. doi:10.1111/j.1574-6941.2008.00485.x. ISSN 0168-6496. PMID 18400004.
  19. ^ Duponnois, Robin; Kisa, Marija (2006-06-01). "The possible role of trehalose in the mycorrhiza helper bacterium effect". Canadian Journal of Botany. 84 (6): 1005–1008. doi:10.1139/b06-053. ISSN 0008-4026.
  20. ^ a b c d Schrey, Silvia D.; Schellhammer, Michael; Ecke, Margret; Hampp, Rüdiger; Tarkka, Mika T. (2005-10-01). "Mycorrhiza helper bacterium Streptomyces AcH 505 induces differential gene expression in the ectomycorrhizal fungus Amanita muscaria". New Phytologist. 168 (1): 205–216. doi:10.1111/j.1469-8137.2005.01518.x. ISSN 1469-8137. PMID 16159334.
  21. ^ Bonfante, Paola; Anca, Iulia-Andra (2009-09-08). "Plants, Mycorrhizal Fungi, and Bacteria: A Network of Interactions". Annual Review of Microbiology. 63 (1): 363–383. doi:10.1146/annurev.micro.091208.073504. hdl:2318/99264. PMID 19514845.
  22. ^ a b c d Vivas, A; Azcón, R; Biró, B; Barea, J. M.; Ruiz-Lozano, J. M. (2003-10-01). "Influence of bacterial strains isolated from lead-polluted soil and their interactions with arbuscular mycorrhizae on the growth of Trifolium pratense L. under lead toxicity". Canadian Journal of Microbiology. 49 (10): 577–588. doi:10.1139/w03-073. PMID 14663492.
  23. ^ a b c d e Vivas, A.; Barea, J. M.; Biró, B.; Azcón, R. (2006-03-01). "Effectiveness of autochthonous bacterium and mycorrhizal fungus on Trifolium growth, symbiotic development and soil enzymatic activities in Zn contaminated soil". Journal of Applied Microbiology. 100 (3): 587–598. doi:10.1111/j.1365-2672.2005.02804.x. PMID 16478498.
  24. ^ a b Vivas, A.; Barea, J. M.; Azcón, R. (2005). "Interactive effect of Brevibacillus brevis and Glomus mosseae, both isolated from Cd contaminated soil, on plant growth, physiological mycorrhizal fungal characteristics and soil enzymatic activities in Cd polluted soil". Environmental Pollution. 134 (2): 257–266. doi:10.1016/j.envpol.2004.07.029. PMID 15589653.
  25. ^ a b c Dewey, F. M.; Wong, Y. L.; Seery, R.; Hollins, T. W.; Gurr, S.J. (27 August 1999). "Bacteria associated with Stagonospora (Septoria) nodorum increase pathogenicity of the fungus". New Phytol. 144 (3): 489–497. doi:10.1046/j.1469-8137.1999.00542.x.
  26. ^ Lehr, Nina A.; Schrey, Silvia D.; Bauer, Robert; Hampp, Rüdiger; Tarkka, Mika T. (2007-06-01). "Suppression of plant defence response by a mycorrhiza helper bacterium". New Phytologist. 174 (4): 892–903. doi:10.1111/j.1469-8137.2007.02021.x. ISSN 1469-8137. PMID 17504470.
  27. ^ a b c Schelkle, M.; Peterson, R. L. (1997-02-01). "Suppression of common root pathogens by helper bacteria and ectomycorrhizal fungi in vitro". Mycorrhiza. 6 (6): 481–485. doi:10.1007/s005720050151. ISSN 0940-6360.
  28. ^ a b Dwivedi, Deepti; Johri, B. N. (2003). "Antifungals from fluorescent pseudomonads: Biosynthesis and regulation". Current Science. 85 (12): 1693–1703. JSTOR 24109974.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Mycorrhiza_helper_bacteria&oldid=1250140519"