Research article

Differential metabolic rearrangements improve biomass and enhance the tolerance of two dwarf cashew (Anacardium occidentale L.) genotypes to salt stress

  • Received: 30 January 2024 Revised: 22 March 2024 Accepted: 26 March 2024 Published: 10 May 2024
  • Salinity is one of the abiotic stresses that affect crop productivity and plant development the most. We aimed to analyze the physiological and biochemical responses of dwarf cashew (A. occidentale L.) genotypes subjected to salt stress. The experiment was carried out in a greenhouse with a completely randomized design in a 5 × 2 factorial scheme, with five salinity levels (0, 25, 50, 75, and 100 mM NaCl) and 2 dwarf cashew genotypes (Embrapa51 and CCP76). There was no significant effect of salinity on plant height, leaf number, and stem diameter; however, the dry biomass was significantly reduced. Chlorophylls, starch, and total free amino acids decreased with salt stress, mainly with 75 and 100 mM NaCl. The CCP76 genotype salt-stressed increased carotenoids, anthocyanins, total soluble carbohydrates, reducing sugars, sodium, and potassium ions compared to Embrapa51. Free proline was increased in response to salt stress in dwarf cashew genotypes. Interestingly, sucrose declined in Embrapa51 and increased in CCP76 in response to salinity. When submitted to 75 and 100 mM NaCl, i.e., under severe stress, CCP76 presented more sucrose than Embrapa51. Our results indicated that sucrose accumulation plays an important role in the acclimation of CCP76 to salinity. This disaccharide induces metabolic rearrangements, mostly in the levels of soluble carbohydrates and amino acids, which contribute to rebalancing the osmotic potential and help to maintain favorable plant metabolism under salt stress. Overall, the dwarf cashew CCP76 was more tolerant to salinity than Embrapa51.

    Citation: Francisco dos Santos Farias, Vicente Paulo da Costa Neto, Cleriston Correia da Silva Souza, Daniela Vieira Chaves, Aurenivia Bonifácio. Differential metabolic rearrangements improve biomass and enhance the tolerance of two dwarf cashew (Anacardium occidentale L.) genotypes to salt stress[J]. AIMS Molecular Science, 2024, 11(2): 206-220. doi: 10.3934/molsci.2024012

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  • Salinity is one of the abiotic stresses that affect crop productivity and plant development the most. We aimed to analyze the physiological and biochemical responses of dwarf cashew (A. occidentale L.) genotypes subjected to salt stress. The experiment was carried out in a greenhouse with a completely randomized design in a 5 × 2 factorial scheme, with five salinity levels (0, 25, 50, 75, and 100 mM NaCl) and 2 dwarf cashew genotypes (Embrapa51 and CCP76). There was no significant effect of salinity on plant height, leaf number, and stem diameter; however, the dry biomass was significantly reduced. Chlorophylls, starch, and total free amino acids decreased with salt stress, mainly with 75 and 100 mM NaCl. The CCP76 genotype salt-stressed increased carotenoids, anthocyanins, total soluble carbohydrates, reducing sugars, sodium, and potassium ions compared to Embrapa51. Free proline was increased in response to salt stress in dwarf cashew genotypes. Interestingly, sucrose declined in Embrapa51 and increased in CCP76 in response to salinity. When submitted to 75 and 100 mM NaCl, i.e., under severe stress, CCP76 presented more sucrose than Embrapa51. Our results indicated that sucrose accumulation plays an important role in the acclimation of CCP76 to salinity. This disaccharide induces metabolic rearrangements, mostly in the levels of soluble carbohydrates and amino acids, which contribute to rebalancing the osmotic potential and help to maintain favorable plant metabolism under salt stress. Overall, the dwarf cashew CCP76 was more tolerant to salinity than Embrapa51.



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    Acknowledgments



    The authors are grateful to the National Council for Scientific and Technological Development (CNPq) and National Council for the Improvement of Higher Education (CAPES), Brazilian research-funding agencies, for financial support (CNPq-Universal n° 426655/2018-4).

    Conflict of interest



    The authors declare no conflicts of interest.

    [1] Munns R, Passioura JB, Colmer TD, et al. (2020) Osmotic adjustment and energy limitations to plant growth in saline soil. New Phytol 225: 1091-1096. https://doi.org/10.1111/nph.15862
    [2] Dias AS, Lima GS, Sá FV, et al. (2018) Gas exchanges and photochemical efficiency of West Indian cherry cultivated with saline water and potassium fertilization. Rev Bras Eng Agric Ambient 22: 628-633. https://doi.org/10.1590/1807-1929/agriambi.v22n9p628-633
    [3] Guilherme EA, Lacerda CF, Bezerra MA, et al. (2021) Development of adult cashew plants in response to irrigation with saline water. Rev Bras Eng Agric Ambient 9: 253-257.
    [4] Flowers TJ, Munns R, Colmer TD (2015) Sodium chloride toxicity and the cellular basis of salt tolerance in halophytes. Ann Botany 115: 419-431. https://doi.org/10.1093/aob/mcu217
    [5] Sheldon AR, Dalal RC, Kirchhof G, et al. (2017) The effect of salinity on plant-available water. Plant Soil 418: 477-491. https://doi.org/10.1007/s11104-017-3309-7
    [6] Bonifacio A, Carvalho FEL, Martins MO, et al. (2016) Silenced rice in both cytosolic ascorbate peroxidases displays pre-acclimation to cope with oxidative stress induced by 3-aminotriazole-inhibited catalase. J Plant Physiol 201: 17-27. https://doi.org/10.1016/j.jplph.2016.06.015
    [7] Negrão S, Schmöckel SM, Tester M (2017) Evaluating physiological responses of plants to salinity stress. Ann Bot 119: 1-11. https://doi.org/10.1093/aob/mcw191
    [8] Menezes RV, Azevedo Neto AD, Ribeiro MO, et al. (2017) Growth and contents of organic and inorganic solutes in amaranth under salt stress. Pesq Agropecu Trop 47: 22-30. https://doi.org/10.1590/1983-40632016v4742580
    [9] Karimi S, Karimi H, Mokhtassi A, et al. (2018) Inducing drought tolerance in greenhouse grown Juglans regia by imposing controlled salt stress: The role of osmotic adjustment. Sci Hortic 239: 181-192. https://doi.org/10.1016/j.scienta.2018.05.029
    [10] Nascimento IB, Medeiros JF, Alves SSV, et al. (2015) Initial development of Bell Pepper crop influenced by irrigation water salinity in two soil types. ACSA 11: 37-43.
    [11] Kaur G, Asthir B (2015) Proline: A key player in plant abiotic stress tolerance. Biol Plant 59: 609-619. https://doi.org/10.1007/s10535-015-0549-3
    [12] Sahie LBC, Soro D, Kone KY, et al. (2023) Some processing steps and uses of cashew apples: A review. Food Nutr Sci 14: 38-57. https://doi.org/10.4236/fns.2023.141004
    [13] Kyei SK, Akaranta O, Darko G, et al. (2019) Extraction, characterization and application of cashew nut shell liquid from cashew nut shells. Chem Sci Int J 28: 1-10. https://doi.org/10.9734/CSJI/2019/v28i330143
    [14] Ferreira-Silva SL, Voigt EL, Silva EN, et al. (2011) High temperature positively modulates oxidative protection in salt-stressed cashew plants. Environ Exp Bot 74: 162-170. https://doi.org/10.1016/j.envexpbot.2011.05.015
    [15] Lima GS, Silva JB, P. Souza L, et al. (2020) Tolerance of precocious dwarf cashew clones to salt stress during rootstock formation stage. Rev Bras Eng Agríc Ambient 24: 474-481. https://doi.org/10.1590/1807-1929/agriambi.v24n7p474-481
    [16] Hoagland DR, Arnon DI (1950) The water-culture method for growing plants without soil.California Agricultural Experiment Station, California. Available from: http://hdl.handle.net/2027/uc2.ark:/13960/t51g1sb8j
    [17] Lichtenthaler HK, Wellburn AR (1983) Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochem Soc Trans 11: 591-592. https://doi.org/10.1042/bst0110591
    [18] Gitelson AA, Merzlyak MN, Chivkunova OB (2001) Optical properties and nondestructive estimation of anthocyanin content in plant leaves. Photochem Photobiol 74: 38-45. https://doi.org/10.1562/0031-8655(2001)0740038OPANEO2.0.CO2
    [19] Viégas RA, Silveira JAG, Lima Junior AR, et al. (2001) Effects of NaCl-salinity on growth and inorganic solute accumulation in young cashew plants. Rev Bras Eng Agríc Ambient 5: 216-222. https://doi.org/10.1590/S1415-43662001000200007
    [20] Dubois M, Gilles KA, Hamilton JK, et al. (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28: 350-356. https://doi.org/10.1021/ac60111a017
    [21] Yemm EW, Cocking EF, Ricketts RE (1955) The determination of amino-acids with ninhydrin. Analyst 80: 209-214. https://doi.org/10.1039/an9558000209
    [22] Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water stress studies. Plant Soil 39: 205-207. https://doi.org/10.1007/BF00018060
    [23] Van Handel E (1968) Direct microdetermination of sucrose. Anal Biochem 22: 280-283. https://doi.org/10.1016/0003-2697(68)90317-5
    [24] McCready RM, Guggolz J, Silveira V, et al. (1950) Determination of starch and amylase in vegetables. Anal Chem 22: 1156-1158. https://doi.org/10.1021/ac60045a016
    [25] P. Souza L, Nobre RG, Silva EM, et al. (2016) Formation of ‘Crioula’ guava rootstock under saline water irrigation and nitrogen doses. Rev Bras Eng Agríc Ambient 20: 739-745. https://doi.org/10.1590/1807-1929/agriambi.v20n8p739-745
    [26] Alam A, Ullah H, Attia A, et al. (2020) Effects of salinity stress on growth, mineral nutrient accumulation and biochemical parameters of seedlings of three citrus rootstocks. Int J Fruit Sci 20: 786-804. https://doi.org/10.1080/15538362.2019.1674762
    [27] Bader B, Aissaoui F, Kmicha I, et al. (2015) Effects of salinity stress on water desalination, olive tree (Olea europaea L. cvs ‘Picholine’, ‘Meski’and ‘Ascolana’) growth and ion accumulation. Desalination 364: 46-52. https://doi.org/10.1016/j.desal.2015.01.002
    [28] Sayyad-Amin P, Jahansooz MR, Borzouei A, et al. (2016) Changes in photosynthetic pigments and chlorophyll-a fluorescence attributes of sweet-forage and grain sorghum cultivars under salt stress. J Biol Phys 42: 601-620. https://doi.org/10.1007/s10867-016-9428-1
    [29] Cavalcante AR, Santos JA, Furtado GDF, et al. (2019) Gas exchanges and photochemical efficiency of hydroponic bell pepper under salinity and plant density. Rev Bras Eng Agríc Ambient 23: 3-8. https://doi.org/10.1590/1807-1929/agriambi.v23n1p3-8
    [30] Dantas M, Lima GS, Gheyi HR, et al. (2021) Gas exchange and photosynthetic pigments of West Indian cherry under salinity stress and salicylic acid. Comunicata Scientiae 12: e3664.
    [31] Rêgo Meneses JR, Oliveira Lopes ÁL, Setubal IS, et al. (2022) Inoculation of Trichoderma asperelloides ameliorates aluminum stress-induced damages by improving growth, photosynthetic pigments and organic solutes in maize. 3 Biotech 12: 246. https://doi.org/10.1007/s13205-022-03310-3
    [32] Voitsekhovskaja OV, Tyutereva EV (2015) Chlorophyll b in angiosperms: Functions in photosynthesis, signaling and ontogenetic regulation. J Plant Physiol 189: 51-64. https://doi.org/10.1016/j.jplph.2015.09.013
    [33] Tyutereva EV, Evkaikina AI, Ivanova AN, et al. (2017) The absence of chlorophyll b affects lateral mobility of photosynthetic complexes and lipids in grana membranes of Arabidopsis and barley chlorina mutants. Photosynth Res 133: 357-370. https://doi.org/10.1007/s11120-017-0376-9
    [34] Cova AMW, Azevedo Neto AD, Ribas RF, et al. (2016) Effect of salt stress on growth and contents of organic and inorganic compounds in noni (Morinda citrifolia L.). Afr J Biotechnol 15: 2401-2410.
    [35] Akbari M, Mahna N, Ramesh K, et al. (2018) Ion homeostasis, osmoregulation, and physiological changes in the roots and leaves of pistachio rootstocks in response to salinity. Protoplasma 255: 1349-1362. https://doi.org/10.1007/s00709-018-1235-z
    [36] Yu J, Sun L, Fan N, et al. (2015) Physiological factors involved in positive effects of elevated carbon dioxide concentration on Bermudagrass tolerance to salinity stress. Environ Exp Bot 115: 20-27. https://doi.org/10.1016/j.envexpbot.2015.02.003
    [37] Li C, Li Y, Chu P, et al. (2022) Effects of salt stress on sucrose metabolism and growth in Chinese rose (Rosa chinensis). Biotechnol Biotec Eq 36: 706-716. https://doi.org/10.1080/13102818.2022.2116356
    [38] Kim JY, Lee SJ, Min WK, et al. (2022) COP1 controls salt stress tolerance by modulating sucrose content. Plant Signal Behav 17: 2096784. https://doi.org/10.1080/15592324.2022.2096784
    [39] Cardoso MN, Araújo AG, Oliveira LAR, et al. (2019) Proline synthesis and physiological response of cassava genotypes under in vitro salinity. Ciênc Rural 49: e20170175. https://doi.org/10.1590/0103-8478cr20170175
    [40] Ahmadi F, Samadi A, Sepehr E, et al. (2023) Potassium homeostasis and signaling as a determinant of Echinacea species tolerance to salinity stress. Environ Exp Bot 206: 105148. https://doi.org/10.1016/j.envexpbot.2022.105148
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