COINOCULATION WITH Bradyrhizobium AND Trichoderma ALLEVIATES THE EFFECTS OF SALT STRESS IN COWPEA
DOI:
https://doi.org/10.1590/1983-21252019v32n206rcKeywords:
Salinity. Osmoprotectants. Plant growth-promoting fungi.Abstract
The deleterious effects of salt stress can be mitigated by the use of beneficial microorganisms. The aims of this study were to evaluate whether coinoculation with Bradyrhizobium and Trichoderma asperelloides alleviates salt stress in cowpea. The experiment was conducted in a greenhouse using pots filled with sterile soil. Seeds were sown and inoculated with Bradyrhizobium or coinoculated with Bradyrhizobium and T. asperelloides. At 15 days after sowing (DAS), the nitrogen-free nutritive solution was supplemented with 50 or 100 mmol L-1 sodium chloride (NaCl) to induce salinity. Uninoculated plants and irrigated with solution without NaCl were used as absolute control. At 35 DAS, plants were collected and nodules were excised for use in the determinations. The absolute controls did not show root nodules. Salt stress decreased plant biomass and growth, especially in cowpea inoculated with Bradyrhizobium. The stem diameter increased in cowpea coinoculated with Bradyrhizobium and T. asperelloides, mainly in plants subjected to salt stress at 100 mmol L-1 NaCl. Cowpea coinoculated with Bradyrhizobium and T. asperelloides maintained a higher content of free ammonia and organic compounds in its nodules even under salt stress. We concluded that the coinoculation of cowpea with Bradyrhizobium and T. asperelloides induces an increase in the concentration of organic solutes in the root nodules, especially when cowpeas are cultivated under salinity. Therefore, the use of coinoculation with Bradyrhizobium and T. asperelloides alleviates the negative effects of salt stress in cowpea.
References
AHMAD, P. et al. Role of Trichoderma harzianum in mitigating NaCl stress in Indian mustard (Brassica juncea L.) through antioxidative defense system. Frontiers in Plant Science, v. 6, s/n., p. 1-15, 2015.
ALCÁNTARA, C. et al. The free-living rhizosphere fungus Trichoderma hamatum GD12 enhances clover productivity in clover-ryegrass mixtures. Plant and Soil, v. 398, n. 1, p. 165-180, 2016.
BABU, S. et al. Synergistic action of PGP agents and Rhizobium spp. for improved plant growth, nutrient mobilization and yields in different leguminous crops. Biocatalysis and Agricultural Biotechnology, v. 4, n. 4, p. 456-464, 2015.
BATES, L.; WALDREN, P. P.; TEARE, J. D. Rapid determination of free proline of water stress studies. Plant and Soil, v. 39, n. 1, p. 205-207, 1973.
BRADFORD, M. M. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, v. 722, n. 1-2, p. 248-254, 1976.
BYRT, C. S. et al. Root cell wall solutions for crop plants in saline soils. Plant Science, v. 269, s/n., p. 47-55, 2018.
CHAGAS, L. F. B. et al. Trichoderma asperellum efficiency in soybean yield components. Comunicata Scientiae, v. 8, n. 1, p. 165-169, 2017.
CHINNASWAMY, A. et al. A nodule endophytic Bacillus megaterium strain isolated from Medicago polymorpha enhances growth, promotes nodulation by Ensifer medicae and alleviates salt stress in alfalfa plants. Annals of Applied Biology, v. 172, n. 3, p. 295-308, 2018.
DUBOIS, M. et al. Colorimetric method for determination of sugars and related substances. Analytical Chemistry, v. 28, n. 3, p. 350-356, 1956.
EGAMBERDIEVA, D. et al. Endophytic bacteria improve plant growth, symbiotic performance of chickpea (Cicer arietinum L.) and induce suppression of root rot caused by Fusarium solani under salt stress. Frontiers in Microbiology, v. 8, s/n., p. 1-13, 2017.
EVANS, J. S. B. Interpretation and matching bias in a reasoning task. Quarterly Journal of Experimental Psychology, v. 24, n. 2, p. 193-199, 1972.
FIGUEIREDO, M. V. B. et al. Plant growth-promoting rhizobacteria: key mechanisms of action. In: CHOUDHARY, D. K.; VARMA, A. (Eds.) Microbial-mediated Induced Systemic Resistance in Plants. Singapore: Springer, 2016. p. 23-37.
FREIRE-FILHO, F. R. et al. Produção, melhoramento genético e potencialidades do feijão-caupi no Brasil. 1. ed. Teresina, PI: Embrapa Meio-Norte, 2011. 84 p.
HANEY, C. H. et al. Associations with rhizosphere bacteria can confer an adaptive advantage to plants. Nature Plants, v. 1, s/n., p. 1-9, 2015.
HASHEM, A. et al. Arbuscular mycorrhizal fungi enhances salinity tolerance of Panicum turgidum Forssk by altering photosynthetic and antioxidant pathways. Journal of Plant Interaction, v. 10, n. 1, p. 230-242, 2015.
HOAGLAND, D.; ARNON, D. I. The water culture method for growing plants without soil. 1. ed. California, EUA: Agriculture Experimental Station Circular, 1950. 347 p.
JAGADEESH, V. et al. Effect of biological seed coating on pigeon pea seedling vigour. International Journal of Current Microbiology and Applied Sciences, v. 6, n. 8, p. 843-854, 2017.
MASSON-BOIVIN, C.; SACHS, J. L. Symbiotic nitrogen fixation by rhizobia: the roots of a success story. Current Opinion in Plant Biology, v. 44, s/n., p. 7-15, 2018.
MORAES, N. J. et al. Bradyrhizobium sp. inoculation ameliorates oxidative protection in cowpea subjected to long-term composted tannery sludge amendment. European Journal of Soil Biology, v. 76, s/n., p. 35-45, 2016.
MUNNS, R.; GILLIHAM, M. Salinity tolerance of crops–what is the cost? New Phytologist, v. 208, n. 3, p. 668-673, 2015.
MWEETWA, A. M.; CHILOMBO, G.; GONDWE, B. M. Nodulation, nutrient uptake and yield of common bean inoculated with Rhizobia and Trichoderma in an acid soil. Journal of Agricultural Science, v. 8, n. 12, p. 61-71, 2016.
NUMAN, M. et al. Plant growth promoting bacteria as an alternative strategy for salt tolerance in plants: A review. Microbiological Research, v. 209, s/n., p. 21-32, 2018.
O’CALLAGHAN, M. Microbial inoculation of seed for improved crop performance: issues and opportunities. Applied Microbiology and Biotechnology, v. 100, n. 13, p. 5729-5746, 2016.
PEREG, L.; MCMILLAN, M. Scoping the potential uses of beneficial microorganisms for increasing productivity in cotton cropping systems. Soil Biology & Biochemistry, v. 80, s/n., p. 349-358, 2015.
PÉREZ-MONTAÑO, F. et al. Plant growth promotion in cereal and leguminous agricultural important plants: from microorganism capacities to crop production. Microbiological Research, v. 169, n. 5-6, p. 325-336, 2014.
POOLE, P. P.; RAMACHANDRAN, V.; TERPOLILLI, J. Rhizobia: from saprophytes to endosymbionts. Nature Reviews Microbiology, v. 18, n. 5, p. 291-303, 2018.
RODRIGUES, A. C. et al. Metabolism of nitrogen and carbon: optimization of biological nitrogen fixation and cowpea development. Soil Biology & Biochemistry, v. 67, p. 226-234, 2013.
RODRIGUES, A. C. et al. Rhizobium tropici exopolysaccharides as carriers improve the symbiosis cowpea-Bradyrhizobium-Paenibacillus. African Journal of Microbiology Research, v. 9, n. 37, p. 2037-2050, 2015.
RUBIO, M. B. et al. The Combination of Trichoderma harzianum and chemical fertilization leads to the deregulation of phytohormone networking, preventing the adaptive responses of tomato plants to salt stress. Frontiers in Plant Science, v. 8, s/n., p. 1-14, 2017.
SANTOS, A. A. et al. Changes induced by co-inoculation in nitrogen–carbon metabolism in cowpea under salinity stress. Brazilian Journal of Microbiology, v. 49, n. 4, p. 685-694, 2018.
SHARMA, R. L. et al. Evaluation of chickpea varieties treated with bio inoculants for yield performance, disease resistance and adaptability to climatic conditions of Gariyaband district in Chhattisgarh. Legume Research, v. 41, n. 1, p. 57-59, 2018.
SILVEIRA, J. A. G. et al. Phosfoenolpyruvate carboxylase and glutamine synthetase activities in relation to nitrogen fixation in cowpea nodules. Revista Brasileira de Fisiologia Vegetal, v. 10, n. 1, p. 19-23, 1998.
VAN HANDEL, E. Direct microdetermination of sucrose. Analytical Biochemical, v. 22, n. 2, p. 280-283, 1968.
WEATHERBURN, M. W. Phenol-hypochlorite reaction for determination of ammonia. Analytical Chemistry, v. 39, n. 8, p. 971-974, 1967.
XAVIER, G. R. et al. Especificidade simbiótica entre rizóbios e acessos de feijão-caupi de diferentes nacionalidades. Revista Caatinga, v. 19, n. 1, p. 25-33, 2006.
YASMEEN, R.; SIDDIQUI, Z. S. Ameliorative effects of Trichoderma harzianum on monocot crops under hydroponic saline environment. Acta Physiologiae Plantarum, v. 40, n. 4, p. 1-14, 2018.
YEMM, E. W.; COCKING, E. C. The Determination of Amino Acids with Ninhydrin. Analyst, v. 80, n. 948, p. 209-213, 1955.
YOUNG, E. G.; CONWAY, C. F. On the estimation of allantoin by the Rimini-Schryver reaction. Journal of Biological Chemistry, v. 142, n. 4, p. 839-853, 1942.
ZHANG, F. et al. Biocontrol potential of Trichoderma harzianum isolate T-aloe against Sclerotinia sclerotiorum in soybean. Plant Physiology and Biochemistry, v. 100, s/n., p. 64-74, 2016.
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