Effect of Fungi Isolated from the Chenopodiaceae Family on the Growth Characteristics and Increasing Phosphorus Absorption of Barley (Hordeum vulgare) Plant

Document Type : Research Article

Authors

1 Ph.D. Student, Department of Biotechnology and Plant Breeding, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran

2 Department of Biotechnology and Plant Breeding, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran

3 Department of Plant Protection, Faculty of Agriculture, Ferdowsi University of Mashhad, Mashhad, Iran

4 Department of Soil Science, Faculty of Agriculture, Bu-Ali Sina University, Hamedan, Iran

Abstract

Introduction
Plant endophytes are microorganisms that live in healthy plant organs but do not cause disease symptoms, and the endophyte lifestyle plays an important role in plant growth, fitness, and diversity. Dark septate endophytic are a group of endophytic fungi that have special hyphae that form dark colonies in agar culture. In this stuy, the effect of these fungi on germination indicators, growth characteristics and increasing the amount of phosphorus in barley (Hordeum vulgare) plants was investigated, in order to investigate the possibility of using these fungi as biofertilizers in laboratory and greenhouse conditions.
Materials and Methods
In this study, seven endogenous fungal isolates were obtained from plants belonging to the Chenopodiaceae family including Aspergillus terreus, Penicillium sp., Curvularia spicifera, Alternaria alternaria, Fusarium solani, Fusarium brachigibbosum and Acremonium consortialis, which were identified in previous researches, were investigated. Piriformospora indica was used as a known fungal species. Yousef cultivar barley seeds were obtained from Khorasan Razavi Agricultural Research Center. The experiments were carried out as a completely randomized design with four replications in two sections: germination in the laboratory and planting in pots at the greenhouse of the faculty of agriculture of Ferdowsi university. To check the germination indicators, the seeds were stored on moist paper towels inside a sterile petri dish for one week at 28°C in an incubator. Sterile distilled water was used as control. After one week, germination speed, germination percentage, germination value, and vigor index were assessed. For the greenhouse study, the soil mixture (three parts sand and one part soil) was sterilized at 105°C for 48 hours. Pots measuring 20 x 20 cm were used. Seed inoculation was performed in a manner consistent with the germination test. Twelve seeds were sown in each pot, and at the two-leaf stage, the seedlings were thinned to eight plants per pot. After 28 days, the plants were evaluated for leaf area index, chlorophyll content, shoot phosphorus levels, dry weight, and fungal colonization percentage in the roots.
 Results and Discussion
The percentage of colonization in all fungi except A. alternaria (%19.60) was above %30. The germination rate in the treatment with A. terreus (2.95 seed day-1) was significantly higher than the control and other fungi. Also, the germinationn rate in the treatment with A. alternaria, C. spicifera, A. consortialis, F. brachibosum and Penicilium sp. was more than control. Germination percentage in A. terreus (%95), Penicillium sp. (%90), C. spicifera (%85) and A. alternaria (%80) were higher than the control (α=%5). Considering that the viability of the selected seeds was low (control germination percentage %50) and the mentioned fungi were able to increase the germination percentage in these seeds, these fungi are a suitable option for sowing seeds with low germination percentage. The value of germination in the treatment with A. terreus (3.735) was higher than the control and other treatments. Treatment with Penicillium sp., A. alternaria and C. spicifera fungi was more than the control. The vigour index of treatment with A. terreus (13.65), C. spicifera (13.23) and A. alternaria (11.53) in one group and at a significant level of %5 were higher than treatment with other fungi. A. terreus treatment improved all germination indices and this increase was higher than the control species (P. indica). The amount of leaf phosphorus in the treatment with A. terreus (%0.516) and P. indica (%0.499) was higher than other fungal and control treatments. The leaf surface area in the treatment with A. terreus (9.97 cm2) was higher than the treatment with other fungi and the control fungus (9.84 cm2). In addition to A. terreus, the treatment with A. consortialis (10.06 cm2), C. spicifera (9.91 cm2) and P. indica (9.84cm2) was significantly higher than the control . Chlorophyll a and b were the highest in the treatment with A. terreus and P.indica. In addition, the treatment with C. spicifera and A. alternaria had more chlorophyll a and b at a significant level of 5% than the control treatment . The dry weight of shoot with the treatment of A. terreus (6.40 mg g-1) and P. indica (6.10 mg g-1) increased the most compared to the treatment with other fungi.
 Conclusion
Considering the ability of A. terreus in improving the germination characteristics, the plant growth conditions observed in this study. It is suggested to the next works should pay attention to the effect of this fungi on the environment and the ecosystem of other organisms and plants so that it can be used as a biological fertilizer.
 Acknowledgement
We thank ferdowsi university of mashhad for providing the necessary facilities for the implementation of the project, Ferdowsi University Department of Plant Medicine and Soil Science for providing the control strain and the necessary equipment, and the expert on breeding barley cultivars at Khorasan Razavi Agricultural and Natural Resources Research Center.

Keywords

Main Subjects


©2024 The author(s). This is an open-access article distributed under Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, sharing, adaptation, distribution, and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source.

  1. Ahadi, N., Safari Sinegani, A. A., & Aletaha, R. S. (2021). Evaluation of capability of fifteen isolates of mycorrhiza-like endophytic fungi on release of phosphorous from phosphorite mineral in the aquatic culture medium. Applied Soil Research, 9(2), 87-101.
  2. Ahmadvand, G., & Hajinia, S. (2018) Effect of endophytic fungus Piriformospora indica on yield and some physiological traits of millet (Panicum miliaceum) under water stress. Crop and Pasture Science, 69(6), 594-605. https://doi.org/10.1071/CP17364
  3. Aktar, M. W., Sengupta, D., & Chowdhury, A. (2009). Impact of pesticides use in agriculture: Their benefits and hazards. Interdiscip Toxicol, 2, 1-12. https://doi.org/10.2478/v10102-009-0001-7
  4. Aletaha, R., Safari Sinegani, A. A., & Zafari, D. )2018(. A survey on endophytic fungi within roots of Chenopodiaceae species under different environmental conditions. Mycosphere, 9(4), 618-634. https://doi.org/5943/mycosphere/9/4/1
  5. Aletaha, R., & Sinegani, A. A. S. (2020). Water availability in soil affect performance of different root fungal colonizers on metabolism of wheat. Iranian Journal of Science and Technology, Transactions A: Science, 44(4), 919-931.
  6. Aly, A. H., Debbab, A., & Proksch, P. (2011). Fungal endophytes: unique plant inhabitants with great promises. Applied Microbioly and Biotechnology, 90, 1829-45. https://doi.org/10.5943/mycosphere/9/4/1
  7. Bader, A. N., Salerno, G. L., Covacevich, F., & Consolo, V. F. (2020). Native Trichoderma harzianum strains from Argentina produce indole-3 acetic acid and phosphorus solubilization, promote growth and control wilt disease on tomato (Solanum lycopersicum ). Journal of King Saud University-Science, 32(1), 867-873. https://doi.org/10.1016/j.jksus.2019.04.002
  8. Baron, N ., Costa, N. T. A., Mochi, D. A., & Rigobelo, E. C. )2018(. First report of Aspergillus sydowii and Aspergillus brasiliensis as phosphorus solubilizers in maize. Annals of Microbiology, 68(12), 863-870. https://doi.org/10.1007/s13213-018-1392-5
  9. Bouzouina, M., Kouadria, R., & Lotmani, B. (2021). Fungal endophytes alleviate salt stress in wheat in terms of growth, ion homeostasis and osmoregulation. Journal of Applied Microbiology, 130(3), 913-925. https://doi.org/10.1111/jam.14804
  10. Brazhnikova, Y. V., Shaposhnikov, A. I., & Sazanova, A. L. (2022). Phosphate mobilization by culturable fungi and their capacity to increase soil P availability and promote barley growth. Current Microbiology, 79, 240 https://doi.org/10.1007/s00284-022-02926-1
  11. Cao, M. A., Liu, R. C., Xiao, Z. Y., Hashem, A., Abd_Allah, E. F., Alsayed, M. F., Harsonowati, W., & Wu, Q. S. (2022). Symbiotic fungi alter the acquisition of phosphorus in Camellia oleifera through regulating root architecture, plant phosphate transporter gene expressions and soil phosphatase activities. Journal of Fungi, 8, 800. https://doi.org/10.3390/jof8080800
  12. Card, S., Johnson, L., Teasdale, S., & Caradus, J. (2016). Deciphering endophyte behaviour: The link between endophyte biology and efficacious biological control agents. FEMS Microbiology Ecology, 92(8), 19. https://doi.org/10.1093/femsec/fiw114
  13. Dasila, H., Sah, V. K., Jaggi, V., Kumar, A., Tewari, L., Taj, G., ... & Sahgal, M. (2023). Cold-tolerant phosphate-solubilizing Pseudomonas strains promote wheat growth and yield by improving soil phosphorous (P) nutrition status. Frontiers in Microbiology, 14, 1135693.
  14. Diene, O., Wang, W., & Narisawa, K. (2013). Pseudosigmoidea ibarakiensis nov., a dark septate endophytic fungus from a cedar forest in Ibaraki, Japan. Journal of Microbes and Environments, 13002, 387. https://doi.org/10.1264/jsme2.ME13002
  15. Ferreira, A. P., dos Santos Oliveira, J. A., Polonio, J. C., Pamphile, J. A., & Azevedo, J. L. (2023). Recombinants of Alternaria alternata endophytes enhance inorganic phosphate solubilization and plant growth hormone production. Biocatalysis and Agricultural Biotechnology. 51: 102784. https://doi.org/10.1016/j.bcab.2023.102784
  16. Ghoniemy, E. A., El-Khawaga, M. A., El-Aziz, A., Marwa, A., & Abulila, H. I. (2020). Biosynthesis of Plant Growth Hormones (Indol Acetic Acid and Gibberellin) By Salt-Tolerant Endophytic Fungus Aspergillus terreus SQU14026. Egyptian Academic Journal of Biological Sciences, G. Microbiology, 12(2), 111-129. http://doi.org/10.21608/eajbsg.2020.214043
  17. Gu, K., Chen, C. Y., Selvaraj, P., Pavagadhi, S., Yeap, Y. T., Swarup, S., & Naqvi, N. I. (2023). Penicillium citrinum provides transkingdom growth benefits in choy sum (Brassica rapa var. parachinensis). Journal of Fungi, 9(4), 420.
  18. Habibi, S., Maskarbashi, M., & Farzaneh, M. (2015). Effect of mycorrhizal fungus (Glomus spp) on wheat (Triticum aestivum) yield and yield components with regard to irrigation water quality. Iranian Journal of Field Crops Research, 14(3), 85-100. (in Persian with English abstract). https://doi.org/10.22067/gsc.v13i3.51155
  19. Hardoim, P. R., van Overbeek, L. S., Berg, G., Pirttila, A. M., Compant, S., Campisano, A., Doring, M., & A. (2015). The hidden world within plants: ecological and evolutionary considerations for defining functioning of microbial endophytes. Microbiology and Molecular Biology Reviews, 79(3), 293-320. https://doi.org/10.1128/mmbr.00050-14
  20. Jahandideh, A., Barani Motlagh, M., Dordipoor, E., Ghorbani Nasr Abadi, R., &Nazari, T. (2019). The effects of Co-application of Humic acid and phosphorous fertilizer on vegetative growth indices and phosphorous availability in canola. Applied Soil Research, 8, 68-78. https://doi.org/10.1007/BF00000098
  21. Jiang, H. J., Zhao, Y. , & Pan, Y. T. (2022). The endophytic fungus Phomopsis liquidambaris promotes phosphorus uptake by Arachis hypogaea L. by regulating host auxin, gibberellins, and cytokinins signaling pathways. J Journal of Soil Science and Plant Nutrition, 22, 4913-4927. https://doi.org/10.1007/s42729-022-00970-1
  22. Khare, E. J., & Mishra, N. K. (2018). Multifaceted interactions between endophytes and plant: Developments and prospects. Frontier of Microbiology, 9, 1-12. https://doi.org/10.3389/fmicb.2018.02732
  23. Knapp, D. G., Kovács, G. M., Zajta, E., Groenewald, J. Z., & Crous, P. W. (2015). Dark septate endophytic pleosporalean genera from semiarid areas. Molecular Phylogeny and Evolution of Fungi, 35, 87. https://doi.org/10.3767/003158515X687669
  24. Kobae, Y., & Ohtomo, R. (2015). An improved method for brightfield imaging of arbuscular mycorrhizal fungi in plant roots. Soil Science and Plant Nutrition, 62(1), 27-30. https://doi.org/10.1080/00380768.2015.1106923
  25. Kumar A., Maurya, B. M., & Raghuwanshi, R. (2021). The microbial consortium of indigenous rhizobacteria improving plant health, yield and nutrient content in wheat (Triticum aestivum). Journal of Plant Nutrition, 44, 1942-1956. https://doi.org/10.1080/01904167.2021.1884706
  26. Marschner, H., & Dell, B. )1994(. Nutrient uptake in mycorrhizal symbiosis. Plant and Soil, 159, 89-102. https://doi.org/10.1007/BF00000098
  27. Mathur, P., Chaturvedi, P., & Sharma, C. (2022). Improved seed germination and plant growth mediated by compounds synthesized by endophytic Aspergillus niger (isolate 29) isolated from Albizia lebbeck (L.) Benth. 3 Biotech 12, 271. https://doi.org/10.1007/s13205-022-03332-x
  28. Ortega-Garcia, J. G., Montes-Belmont, R., Rodriguez-Monroy, M., Ramirez-Trujillo, J. , Suarez-Rodriguez, R., & Sepulveda-Jimenez, G. )2015(. Effect of trichoderma asperellum applications and mineral fertilization on growth promotion and the content of phenolic compounds and flavonoids in onions. Scientia Horticulturae (Amsterdam), 195, 8-16. https://doi.org/10.1016/j.scienta.2015.08.027
  29. Pahalvi, H. N., Rafiya, L., & Rashid, S. (2021). Chemical fertilizers and their impact on soil health. In: GH Dar, KR Hakeem, MA Mehmood, & RA Bhat (eds.). Microbiota and Biofertilizers, Vol 2. New York: Springer, New York. 1–20. https://doi.org/10.1007/978-3-030-61010-4_1
  30. Qi, S., Wang, J., Wan, L., Dai, Z., da Silva Matos, D. M., Du, D., Egan, S., Bonser, S. P., Thomas, T., & Moles, A. T. (2022). Arbuscular mycorrhizal fungi contribute to phosphorous uptake and allocation strategies of solidago canadensis in a phosphorous−deficient environment. Frontiers in Plant Science, 13, 831654. https://doi.org/10.3389/fpls.2022.831654
  31. Rana, K. L., Kour, D., Kaur, T., Devi, R., Yadav, A. N., Yadav, N., Dhaliwal, H. S., & Saxena, A. K.(2020). Endophytic microbes: biodiversity, plant growth-promoting mechanisms and potential applications for agricultural sustainability. Antonie Van Leeuwenhoek International Journal of General and Molecular Microbiology, 113(8), 1075-1107. https://doi.org/10.1007/s10482-020-01429-
  32. Sadeghi, A., Farsi, M., Taheri, P., & Safari Sanjani, A. (2022). Priming of barley seeds with filtered culture of fungal species to increase tolerance to salinity (sodium chloride) in the germination stage. 8th International Knowledge Conference and Technology of Agricultural Sciences, Natural Resources and Environment of Iran, Tehran. (in Persian with English abstract). https://civilica.com/doc/1651909
  33. Sembiring, M. (2017). Bacterial and fungi phosphate solubilization effect to increase nutrient uptake and potatoes (Solanum tuberosum ) production on Andisol Sinabung area. Journal Agronomy, 16, 131-137. https://doi.org/10.3923/ja.2017.131.137
  34. Vujanovic, V., St-Arnaud, M., Barabe, D., & Thibeault, G. (2000). Viability testing of orchid seed and the promotion of colouration and germination. Annals of. Botany, 86, 79-86. https://doi.org/10.3390/plants8010005
  35. Waqas, M., Khan, A. L., Hamayun, M., Kamran, M., Kang, S. M., Kim, Y. H., & Lee, I. J. (2012). Assessment of endophytic fungi cultural filtrate on soybean seed germination. African Journal of Biotechnology, 11(85), 15135-15143.
  36. Weggler- Beaton, R. D., & Graham, M. J. (2003(. The influence of low rates of arid- dried on yield and phosphorus and zinc nutrition of wheat and barley. Australian Journal of Soil Research, 41, 293-308. https://doi.org/10.1071/SR02074
  37. Yoo, S., Shin, D., Won, H., Song, J., & Sang, M.(2018)Aspergillus terreus JF27 promotes the growth of tomato plants and induces resistance against Pseudomonas syringae tomato. Mycobiology, 46(2), 147-153. https://doi.org/10.1080/12298093.2018.1475370
  38. Zeng, Q., Dong, J., Lin, X., Zhou, X., & Xu, H. (2024). Isolation and Identification of Acer truncatum Endophytic Fungus Talaromyces verruculosus and evaluation of its effects on insoluble phosphorus absorption capacity and growth of cucumber seedlings. Journal of Fungi, 10(2), 136. https://doi.org/10.3390/jof10020136
  39. Zhao, G., & Zhong, T. (2013). Influence of exogenous IAA and GA on seed germination, vigor and their endogenous levels in Cunninghamia lanceolata. Scandinavian Journal of Forest Research, 28(6), 511-517. https://doi.org/10.1080/02827581.2013.783099
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Volume 22, Issue 4 - Serial Number 76
January 2025
Pages 359-371
  • Receive Date: 29 December 2023
  • Revise Date: 13 March 2024
  • Accept Date: 20 May 2024
  • First Publish Date: 07 December 2024