Effect of Glomus intraradices spore abundance of the inoculum on percent mycorrhizal colonization and growth of Vigna mungo (L.) Hepper
DOI:
https://doi.org/10.14719/pst.1653Keywords:
Blackgram Glomus intraradices, Arbuscular mycorrhizal fungal spore, Percent mycorrhizal colonization, Plant growthAbstract
Arbuscular mycorrhizal (AM) fungi are well known symbiotic microorganism found to improve the growth of host plant by mobilizing immobile nutrients, mainly phosphorus, from the soil. However, the effect of AM fungi on host plant growth depends on the percentage mycorrhizal colonization, whereas it is not clear that the percent mycorrhization impacts by AM fungal spore abundance of the inoculum. Therefore, the current investigation was conducted to know the effect of percent mycorrhization of Glomus intraradices on the growth of blackgram inoculated with varied numbers of AM fungal spores via seed biotization (1 to 10 AM fungal spores per seed). Percent mycorrhizal colonization and plant growth characteristics of blackgram were recorded after 10, 20 and 30 days of sowing (DOS). Our results are revealed that the percentage of mycorrhizal colonization significantly influenced based on the availability of AM fungal spore richness of the biotized seeds, which leads to altered crop growth. Percent mycorrhizal colonization in the roots of blackgram increased with increasing AM fungal spore abundance per seed and it ranges from 10 to 70 %. Moreover, mycorrhizal colonized plants recorded higher shoot and root length, leaf area, leaf area index, shoot and root biomass production as well as chlorophyll content over control, conversely it was increased further with increasing percent mycorrhizal colonization, which is directly proportional to the richness of the AM fungal spores per seed. Therefore, AM fungal spore abundance is one of the governing factors that influence percent mycorrhizal colonization in roots of plants besides AM fungal and plant species and soil condition.
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Saeed SMG, Ali SA, Ali R, Sayeed SA, Mobin L, Ahmed R. Exploring the potential of blackgram (Vigna mungo) flour as a fat replacer in biscuits with improved physicochemical, microstructure, phytochemicals, nutritional and sensory attributes. SN Applied Sciences. 2020; 2(12):1-17. https://doi.org/10.1007/s42452-020-03797-6
Sarangapani C, Devi RY, Thirumdas R, Trimukhe AM, Deshmukh RR, Annapure US. Physico-chemical properties of low-pressure plasma treated black gram. LWT-Food Science and Technology. 2017;79:102-10. https://doi.org/10.1016/j.lwt.2017.01.017
Allito BB, Ewusi-Mensah N, Logah V, Hunegnaw DK. Legume-rhizobium specificity effect on nodulation, biomass production and partitioning of faba bean (Vicia faba L.). Scientific Reports. 2021;11(1):1-13. https://doi.org/10.1038/s41598-021-83235-8
Muthini M, Awino R, Kirui KC, Koech K, Jalloh AA, Njeru EM. Optimizing Rhizobium-legume symbiosis in smallholder agroecosystems. In: Guleria P, Kumar V, Lichtfouse E (eds) Sustainable Agriculture Reviews 45. Springer, Cham. 2020;159-77. https://doi.org/10.1007/978-3-030-53017-4_8
Sindhu SS, Sharma R, Sindhu S, Sehrawat A. Soil fertility improvement by symbiotic rhizobia for sustainable agriculture. In: Panpatte D, Jhala Y (editors) Soil fertility management for sustainable development. Springer, Singapore. 2019; 101-66. https://doi.org/10.1007/978-981-13-5904-0_7
Sharma K. Impact of different Rhizobial strains on physiological responses and seed yield of Mungbean [Vigna radiata (L.) Wilczek] under field conditions. Legume Research: An International Journal. 2021;44(6):679-83. https://doi.org/10.18805/LR-4339
Stella M, Sharma R, Nema S, Ramakrishnan R, Kumar A. Genetic characterization and diversity of Rhizobia isolated from root nodules of green gram (Vigna radiata L.) found in Central Plateau of India. Legume Research: An International Journal. 2021;44(3):353-61.
Wang X, Feng H, Wang Y, Wang M, Xie X, Chang H, Wang E. Mycorrhizal symbiosis modulates the rhizosphere microbiota to promote rhizobia–legume symbiosis. Molecular Plant. 2021;14(3):503-16. https://doi.org/10.1016/j.molp.2020.12.002
Smith S, Read D. Mycorrhizal symbiosis. 3rd edition Academic Press. San Diego. CA. 2008.
Chandrasekaran M. A meta-analytical approach on arbuscular mycorrhizal fungi inoculation efficiency on plant growth and nutrient uptake. Agriculture. 2020;10(9):370. https://doi.org/10.3390/agriculture10090370
Kim SJ, Eo JK, Lee EH, Park H, Eom AH. Effects of arbuscular mycorrhizal fungi and soil conditions on crop plant growth. Mycobiology. 2017;45(1):20-24. https://doi.org/10.5941/MYCO.2017.45.1.20
Qi S, Wang J, Wan L, Dai Z, Du D, Egan S, Moles AT. Arbuscular mycorrhizal fungi contribute to phosphorous uptake and allocation strategies of Solidago canadensis in a phosphorous-deficient environment. Frontiers in Plant Science. 2022; 13: 831654-831654. https://doi.org/10.3389/fpls.2022.831654
Basyal B, Emery SM. An arbuscular mycorrhizal fungus alters switchgrass growth, root architecture and cell wall chemistry across a soil moisture gradient. Mycorrhiza. 2021;31(2):251-58. https://doi.org/10.1007/s00572-020-00992-6
Allen MF. Mycorrhizal fungi: highways for water and nutrients in arid soils. Vadose Zone Journal. 2007;6(2):291-97. https://doi.org/10.2136/vzj2006.0068
Zhang F, Wang P, Zou YN, Wu QS, Ku?a K. Effects of mycorrhizal fungi on root-hair growth and hormone levels of taproot and lateral roots in trifoliate orange under drought stress. Archives of Agronomy and Soil Science. 2019;65(9):1316-30. https://doi.org/10.1080/03650340.2018.1563780
Zhang J, Bi Y, Song Z, Xiao L, Christie P. Arbuscular mycorrhizal fungi alter root and foliar responses to fissure-induced root damage stress. Ecological Indicators. 2021;127:107800. https://doi.org/10.1016/j.ecolind.2021.107800
Balestrini R, Brunetti C, Chitarra W, Nerva L. Photosynthetic traits and nitrogen uptake in crops: which is the role of arbuscular mycorrhizal fungi ? Plants. 2020;9(9):1105. https://doi.org/10.3390/plants9091105
Manoharan P, Pandi M, Shanmugaiah V, Gomathinayagam S, Balasubramanian N. Effect of vesicular arbuscular mycorrhizal fungus on the physiological and biochemical changes of five different tree seedlings grown under nursery conditions. African Journal of Biotechnology. 2008;7(9):3431-36.
Juntahum S, Ekprasert J, Boonlue S. Efficiency of arbuscular mycorrhizal fungi for the growth promotion of sugarcane under pot conditions. Sugar Tech. 2022; 1-10. https://doi.org/10.1007/s12355-022-01129-z
Moustakas M, Bayçu G, Sperdouli I, Ero?lu H, Eleftheriou EP. Arbuscular mycorrhizal symbiosis enhances photosynthesis in the medicinal herb Salvia fruticosa by improving photosystem II photochemistry. Plants. 2020;9(8):962. https://doi.org/10.3390/plants9080962
Wu YH, Wang H, Liu M, Li B, Chen X, Ma YT, Yan ZY. Effects of native arbuscular mycorrhizae isolated on root biomass and secondary metabolites of Salvia miltiorrhiza Bge. Frontiers in Plant Science. 2021;12:66. https://doi.org/10.3389/fpls.2021.617892
Shamizi N, Yarnia M, Mohebalipour N, Fara-marzi A, Ajalli J. The effect of mycorrhizal species on the growth, essential oils, yield and morpho-physiological parameters of Lemon Balm (Melissa officinalis L.) under water-deficit conditions in Tabriz region. Plant Science Today. 2022;9(2):228-35. https://doi.org/10.14719/pst.1338
Adeyemi NO, Atayese MO, Sakariyawo OS, Azeez JO, Sobowale SPA, Olubode A, Adeoye S. Alleviation of heavy metal stress by arbuscular mycorrhizal symbiosis in Glycine max (L.) grown in copper, lead and zinc contaminated soils. Rhizosphere. 2021;18:100325. https://doi.org/10.1016/j.rhisph.2021.100325
Chen J, Zhang H, Zhang X, Tang M. Arbuscular mycorrhizal symbiosis mitigates oxidative injury in black locust under salt stress through modulating antioxidant defence of the plant. Environmental and Experimental Botany. 2020;175:104034. https://doi.org/10.1016/j.envexpbot.2020.104034
Fiorilli V, Vannini C, Ortolani F, Garcia-Seco D, Chiapello M, Novero M, Bagnaresi P. Omics approaches revealed how arbuscular mycorrhizal symbiosis enhances yield and resistance to leaf pathogen in wheat. Scientific Reports. 2018;8(1):1-18. https://doi.org/10.1038/s41598-018-27622-8
Rivero J, Lidoy J, Llopis-Giménez Á, Herrero S, Flors V, Pozo MJ. Mycorrhizal symbiosis primes the accumulation of antiherbivore compounds and enhances herbivore mortality in tomato. Journal of Experimental Botany. 2021;72(13):5038-50. https://doi.org/10.1093/jxb/erab171
Chen M, Arato M, Borghi L, Nouri E, Reinhardt D. Beneficial services of arbuscular mycorrhizal fungi from ecology to application. Frontiers in Plant Science. 2018;9:1270. https://doi.org/10.3389/fpls.2018.01270
Hussain HA, Qingwen Z, Hussain S, Hongbo L, Waqqas A, Li Z. Effects of arbuscular mycorrhizal fungi on maize growth, root colonization and root exudates varied with inoculum and application method. Journal of Soil Science and Plant Nutrition. 2021;21(2):1577-90. https://doi.org/10.1007/s42729-021-00463-7
Mangan SA, Eom AH, Adler GH, Yavitt JB, Herre EA. Diversity of arbuscular mycorrhizal fungi across a fragmented forest in Panama: insular spore communities differ from mainland communities. Oecologia. 2004;141(4):687-700. https://doi.org/10.1007/s00442-004-1684-2
Sielaff AC, Polley HW, Fuentes-Ramirez A, Hofmockel K, Wilsey BJ. Mycorrhizal colonization and its relationship with plant performance differs between exotic and native grassland plant species. Biological Invasions. 2019;21(6):1981-91. https://doi.org/10.1007/s10530-019-01950-w
Rubio R, Borie F, Schalchli C, Castillo C, Azcón R. Occurrence and effect of arbuscular mycorrhizal propagules in wheat as affected by the source and amount of phosphorus fertilizer and fungal inoculation. Applied Soil Ecology. 2003;23(3):245-55. https://doi.org/10.1016/S0929-1393(03)00045-3
Khakpour O, Khara J. Spore density and root colonization by arbuscular mycorrhizal fungi in some species in the northwest of Iran. International Research Journal of Applied and Basic Sciences. 2012;3(5):977-82.
Gerdemann JW, Nicolson TH. Spores of mycorrhizal endogone species extracted from soil by wet sieving and decanting. Transactions of the British Mycological Society. 1963; 46: 235-44. https://doi.org/10.1016/S0007-1536(63)80079-0
Arnon DI. Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiology. 1949;24(1):1. https://doi.org/10.1104/pp.24.1.1
Phillips JM, Hayman D. Improved procedures for clearing roots and staining parasitic and vesicular-arbuscular mycorrhizal fungi for rapid assessment of infection. Transactions of the British Mycological Society. 1970;55(1):158-61. https://doi.org/10.1016/S0007-1536(70)80110-3
Dhumal KC, Shinde BP. Impact of chemical properties of soil on spore density, colonization and distribution of native arbuscular mycorrhizal fungi associated with Capsicum annuum L. Journal of Applied Biology and Biotechnology. 2020;8(05):59-67.
Sivakumar N. Effect of edaphic factors and seasonal variation on spore density and root colonization of arbuscular mycorrhizal fungi in sugarcane fields. Annals of Microbiology. 2013;63(1):151-60. https://doi.org/10.1007/s13213-012-0455-2
Louis I, Lim G. Spore density and root colonization of vesicular-arbuscular mycorrhizas in tropical soil. Transactions of the British Mycological Society. 1987;88(2):207-12. https://doi.org/10.1016/S0007-1536(87)80216-4
Treseder KK. The extent of mycorrhizal colonization of roots and its influence on plant growth and phosphorus content. Plant and Soil. 2013;371(1):1-13. https://doi.org/10.1007/s11104-013-1681-5
Wang J, Fu Z, Ren Q, Zhu L, Lin J, Zhang J, Yue J. Effects of arbuscular mycorrhizal fungi on growth, photosynthesis and nutrient uptake of Zelkova serrata (Thunb.) Makino seedlings under salt stress. Forests. 2019;10(2):186. https://doi.org/10.3390/f10020186
Weraduwage SM, Chen J, Anozie FC, Morales A, Weise SE, Sharkey TD. The relationship between leaf area growth and biomass accumulation in Arabidopsis thaliana. Frontiers in Plant Science. 2015;6:167. https://doi.org/10.3389/fpls.2015.00167
Shao YD, Zhang DJ, Hu XC, Wu QS, Jiang CJ, Xia TJ, Ku?a K. Mycorrhiza-induced changes in root growth and nutrient absorption of tea plants. Plant, Soil and Environment. 2018;64(6):283-89. https://doi.org/10.17221/126/2018-PSE
Liese R, Leuschner C, Meier IC. The effect of drought and season on root life span in temperate arbuscular mycorrhizal and ectomycorrhizal tree species. Journal of Ecology. 2019;107(5):2226-39. https://doi.org/10.1111/1365-2745.13181
Cesaro P, Massa N, Cantamessa S, Todeschini V, Bona E, Berta G, Lingua G. Tomato responses to Funneliformis mosseae during the early stages of arbuscular mycorrhizal symbiosis. Mycorrhiza. 2020;30 (5):601-10. https://doi.org/10.1007/s00572-020-00973-9
Birhane E, Gebretsadik KF, Taye G, Aynekulu E, Rannestad MM, Norgrove L. Effects of forest composition and disturbance on arbuscular mycorrhizae spore density, arbuscular mycorrhizae root colonization and soil carbon stocks in a dry afromontane forest in Northern Ethiopia. Diversity. 2020;12 (4):133. https://doi.org/10.3390/d12040133
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