Identification of potential morpho-biochemical determinants conferring salt tolerance in wheat (Triticum aestivum L.) through seedling- and -reproductive stage phenotyping
DOI:
https://doi.org/10.14719/pst.2988Keywords:
Salinity screening, phenotyping, leaf cutting, seedling stage salt tolerance, reproductive stage salt tolerance, oxidative stress, stress indicesAbstract
To optimize a reproductive-stage-specific phenotyping protocol and isolate potential determinants conferring salinity tolerance in wheat, two consecutive experiments were conducted using salt-tolerant varieties (Binagom-1 and BARI Gom 25) and a sensitive variety (BARI Gom 20). In the first experiment, seedlings were grown hydroponically, and 14-day-old seedlings were subjected to two different levels of salt stress (EC=12 dS/m and 16 dS/m) for 7 days. Based on the results of tolerant and susceptible varieties, parameters such as root and shoot weight, shoot Na+/K+ ratio, chlorophyll content, proline content, methylglyoxal content, H2O2 content and lipid peroxidation content and the activities of enzymes such as ascorbate peroxidase, peroxidase, and glyoxalase I were considered as potential determinants of salt tolerance. The second experiment employed four leaf cutting treatments under both control and salinity stress conditions. Seedlings were grown in perforated pots filled with field soil, and at the heading stage, plants were subjected to salt stress (12 dS/m) after trimming as indicated. The combined analysis of control and salt stress data obtained from setup B reflected a significant decrease in yield and yield-attributing traits; however, a lesser decrease was observed in tolerant varieties. Correlation studies revealed that grain yield per spike exhibited a significant positive correlation with the number of seeds per spike, spike weight, plant height, and days to first flowering under both stress and control conditions. Additionally, different stress tolerance indices also supported the results of reproductive stage phenotyping. However, further studies will be required to tag the genes/QTLs controlling salinity tolerance in wheat at various growth phases.
Downloads
References
Arzani A, Ashraf M. Cultivated ancient wheats (Triticum spp.): A potential source of health-beneficial food products. Comprehensive Reviews in Food Science and Food Safety. 2017;16:477-88. https://doi.org/10.1111/1541-4337.12262.
Barma NC, Hossain A, Hakim MA, Mottaleb KA, Alam MA, Reza MM, Rohman MM. Progress and challenges of wheat production in the era of climate change: A Bangladesh perspective. In: Hasanuzzaman M, Nahar K, Hossain MA (Eds.) Wheat Production in Changing Environments. Springer, Singapore. 2019; p. 615-79. https://doi.org/10.1007/978-981-13-6883-7.
Salehin M, Chowdhury MMA, Clarke D, Mondal S, Nowreen S, Jahiruddin M, Haque A. Mechanisms and drivers of soil salinity in Coastal Bangladesh. In: Nicholls R, Hutton CW, Adger W, Hanson S, Rahman M, Salehin M (Eds.) Ecosystem Services for Well-being in Deltas. Cham: Palgrave Macmillan. 2018; p. 333-47. http://doi.org/10.1007/978-3-319-71093-8_18.
Su Q, Zheng X, Tian Y, Wang C. Exogenous brassinolide alleviates salt stress in Malus hupehensis Rehd. by regulating the transcription of NHX-Type Na+ (K+)/H+ antiporters. Frontiers in Plant Science. 2020;11:38. https://doi.org/10.3389/fpls.2020.00038.
Mostofa MG, Hossain MA, Fujita M. Trehalose pretreatment induces salt tolerance in rice (Oryza sativa L.) seedlings: Oxidative damage and co-induction of antioxidant defense and glyoxalase systems. Protoplasma. 2015;252:461-75. doi:10.1007/s00709-014-0691-3 .
Gupta BK, Sahoo KK, Ghosh A, Tripathi AK, Anwar K, Das P et al. Manipulation of glyoxalase pathway confers tolerance to multiple stresses in rice. Plant, Cell and Environment. 2018;41:1186-200. doi:10.1111/pce.12968.
Hu L, Liang W, Yin C, Cui X, Zheng J, Wang X et al. Rice MADS3 regulates ROS homeostasis during late anther development. The Plant Cell. 2011;23:515-33. doi: 10.1105/tpc.110.074369 .
Hasan A, Hafiz HR, Siddiqui N, Khatun M, Islam R, Madman AA. Evaluation of wheat genotypes for salt tolerance based on some physiological traits. Journal of Crop Science and Biotechnology. 2015;18:333-40. http://doi.org/10.1007/s12892-015-0064-2.
Hossain A, Skalicky M, Brestic M, Maitra S, Alam MA, Syed MA et al. Consequences and mitigation strategies of abiotic stresses in wheat (Triticum aestivum L.) under the changing climate. Agronomy. 2021;11:241. https://doi.org/10.3390/agronomy11020241.
Tao R, Ding J, Li C, Zhu X, Guo W, Zhu M. Evaluating and screening of agro-physiological indices for salinity stress tolerance in wheat at the seedling stage. Frontiers of Plant Science. 2021;12:646175. http://doi.org/10.3389/fpls.2021.646175.
Genc Y, Oldach K, Taylor J, Lyons GH. Uncoupling of sodium and chloride to assist breeding for salinity tolerance in crops. New Phytologist. 2016;210:145-56. https://doi.org/10.1111/nph.13757.
Hossain MA, Hasanuzzaman M, Fujita M. Up-regulation of antioxidant and glyoxalase systems by exogenous glycine betaine and proline in mung bean confer tolerance to cadmium stress. Physiology and Molecular Biology of Plant. 2010;26:259-72. http://doi.org/10.1007/s12298-010-0028-4.
Horie T, Karahara I, Katsuhara M. Salinity tolerance mechanisms in glycophytes: An overview with the central focus on rice plants. Rice. 2012;5:1-8. doi:10.1186/1939-8433-5-11.
Hossain MA, Bhattacharjee, Armin SM, Qian P, Xin W, Li HY et al. Hydrogen peroxide-priming modulates abiotic oxidative stress tolerance: insights from ROS detoxification and scavenging. Frontiers in Plant Science. 2015;6:420. https://doi.org/10.3389/fpls.2015.00420.
Hoque TS, Hossain MA, Mostofa MG, Burritt DJ, Fujita M, Tran L-SP. Methylglyoxal: An emerging signaling molecule in plant abiotic stress responses and tolerance. Frontiers of Plant Science. 2016;7:1341. doi: 10.3389/fpls.2016.01341.
Zheng Y, Wang Z, Sun X, Jia A, Jiang G, Li Z. Higher salinity tolerance cultivars of winter wheat relieved senescence at reproductive stage. Environmental and Experimental Botany. 2008;62:129-38. doi:10.1016/j.envexpbot.2007.07.011.
Singh RK, Kota S, Flowers TJ. Salt tolerance in rice: Seedling and reproductive stage QTL mapping come of age. Theoretical and Applied Genetics. 2021;134:3495-533. https://doi.org/10.1007/s00122-021-03890-3.
El-Hendawy SE, Hassan WM, Al-Suhaibani NA, Refay Y, Abdella KA. Comparative performance of multivariable agro-physiological parameters for detecting salt tolerance of wheat cultivars under simulated saline field growing conditions. Frontiers in Plant Science. 2017;8:435. https://doi.org/10.3389/fpls.2017.00435.
Ahmadizadeh M, Vispo NA, Calapit-Palao CDO, Pangaan ID, Viña CD, Singh RK. Reproductive stage salinity tolerance in rice: A complex trait to phenotype. Indian Journal of Plant Physiology. 2016;21(4):528-36. doi:10.1007/s40502-016-0268-6.
Uddin MS, Hossain KMW. Screening of wheat genotypes against salinity at early vegetative stage in pot culture. Bangladesh Journal of Botany. 2018;47:381-87. doi:10.3329/bjb.v47i3.38655.
Lichtenthaler HK, Langsdorf G, Lenk S, Bushmann C. Chlorophyll fluorescence imaging of photosynthetic activity with the flesh lamp fluorescence imaging system. Phtosynthetica. 2005;43:355-69. doi: 10.1007/s11099-005-0060-8.
Rohman MM, Talukder MZ, Hossain MG, Uddin MS, Amiruzzaman M, Biswas A et al. Saline sensitivity leads to oxidative stress and increases the antioxidants in presence of proline and betaine in maize (Zea mays L.) inbred. Plant Omics. 2016;9:35-47.
Brown JG, Lilleland O. Rapid determination of potassium and sodium in plant materials and soil extracts by flame photometry. In: Proceedings of the American Society for Horticultural Science. 1946;48:341-46. Accession: 013806306.
Islam MNA, Paul N, Rahman MM, Haque MA, Rohman MM, Mostofa MG. Salicylic acid application mitigates oxidative damage and improves the growth performance of barley under drought stress. Phyton-International Journal of Experimental Botany. 2023;92(5):1513-37. https://doi.org/10.32604/phyton.2023.025175.
Hemeda HM, Klein BP. Effects of naturally occurring antioxidants on peroxidase activity of vegetable extracts. Journal of Food Science. 1990A;55:184-85. https://doi.org/10.1111/j.1365-2621.1990.tb06048.x.
Rahman MM, Jahan I, Noor MMA, Tuzzohora MF, Sohag AAM, Raffi SA et al. Potential determinants of salinity tolerance in rice (Oryza sativa L.) and modulation of tolerance by exogenous ascorbic acid application. Journal of Phytology. 2020;12:86-98. doi:10.25081/jp.2020.v12.6535.
Saddiq MS, Iqbal S, Hafeez MB, Ibrahim AM, Raza A, Fatima EM et al. Effect of salinity stress on physiological changes in winter and spring wheat. Agronomy. 2021;11:1193. https://doi.org/10.3390/agronomy11061193.
Rasel M, Tahjib-Ul-Arif M, Hossain MA, Sayed MA, Hassan L. Discerning of rice landraces (Oryza sativa L.) for morpho-physiological, antioxidant enzyme activity and molecular markers responses to induced salt stress at the seedling stage. Journal of Plant Growth Regulation. 2019;39:41-59. doi:10.1007/s00344-019-09962-5.
Oney-Birol S. Exogenous L-Carnitine promotes plant growth and cell division by mitigating genotoxic damage of salt stress. Scientific Reports. 2019;9:17229. doi: 10.1038/s41598-019-53542-2.
Irshad A, Ahmed RI, Rehman SU, Sun G, Ahmad F, Sher MA et al. Characterization of salt tolerant wheat genotypes by using morpho-physiological, biochemical and molecular analysis. Frontiers in Plant Science. 2022;13:956298. doi: 10.3389/fpls.2022.956298.
Kobayashi NI, Yamaji N, Yamamoto H, Okubo K, Ueno H, Costa A et al. OsHKT1;5 mediates Na+ exclusion in the vasculature to protect leaf blades and reproductive tissues from salt toxicity in rice. The Plant Journal. 2017;91:657-70. doi: 10.1111/tpj.13595.
Theerawitaya C, Tisarum R, Samphumphuang T, Takabe T, Cha-um S. Expression levels of the Na+/K+ transporter OsHKT2;1 and vacuolar Na+/H+ exchanger OsNHX1, Na enrichment, maintaining the photosynthetic abilities and growth performances of indica rice seedlings under salt stress. Physiology and Molecular Biology of Plants. 2020a;26:513-23. https://doi.org/10.1007/s12298-020-00769-3.
Gurmani AR, Khan SU, Mabood F, Ahmed Z, Butt SJ, Din J et al. Screening and selection of synthetic hexaploid wheat germplasm for salinity tolerance based on physiological and biochemical characters. International Journal of Agriculture and Biology. 2014;16:681-90. doi:13H–015/2014/16–4–681–690.
Chookhampaeng S. The effect of salt stress on growth, chlorophyll content proline content and antioxidative enzymes of pepper (Capsicum annuum L.) seedling. European Journal of Scientific Research. 2011;49:103-09.
Zhang S, Song J, Wang H, Feng G. Effect of salinity on seed germination, ion content and photosynthesis of cotyledons in halophytes or xerophyte growing in Central Asia. Journal of Plant Ecology. 2010;3:259-67. https://doi.org/10.1093/jpe/rtq005.
Yassin M, Fara SA, Hossain A, Saneoka H, Sabagh AE. Assessment of salinity tolerance bread wheat genotypes: Using stress tolerance indices. Fresenius Environmental Bulletin and Advances in Food Sciences. 2019;28:4199-217.
El-Shabrawi H, Kumar B, Kaul T, Reddy MK, Singla-pareek SL. Redox homeostasis, antioxidant defense and methylglyoxal detoxification as markers for salt tolerance in Pokkali rice. Protoplasma. 2010;24:85-96. doi:10.1007/s00709-010-0144-6.
Haouari CC, Nasraoui AH, Carrayol E, Gouia H. Response of two wheat genotype to long-term salinity stress in relation to oxidative stress and osmolyte concentration. Cereal Research Communications. 2013;41(3):388-99. doi: 10.1556/CRC.2013.0020.
Vighi IL, Benitez LC, Amaral MN, Moraes GP, Auler PA, Rodrigues GS, Braga EJB. Functional characterization of the antioxidant enzymes in rice plants exposed to salinity stress. Biologia Plantarum. 2017;1:540-50. doi: 10.1007/s10535-017-0727-6.
Li JT, Qiu ZB, Zhang XW, Wang LS. Exogenous hydrogen peroxide can enhance tolerance of wheat seedlings to salt stress. Acta Physiologiae Plantarum. 2011;33:835-42. doi:10.1007/s11738-010-0608-5.
Chernane H, Latique S, Mansori M, Kaoua ME. Salt stress tolerance and antioxidative mechanisms in wheat plants (Triticum durum L.) by seaweed extracts application. IOSR Journal of Agriculture and Veterinary Science. 2013;8(3):36-44. doi:10.9790/2380-08313644.
Yang G, Wang Y, Xia D et al. Overexpression of a GST gene (ThGSTZ1) from Tamarix hispida improves drought and salinity tolerance by enhancing the ability to scavenge reactive oxygen species. Plant Cell Tissue and Organ Culture. 2014;117:99-112. https://doi.org/10.1007/s11240-014-0424-5.
Hossain MA, Hossain MZ, Fujita M. Stress induced changes of methylglyoxal leveland Glyoxalase I activity in pumpkin seedlings and cDNA cloning of glyoxalase I gene. Australian Journal of Crop Science. 2009;3:53-64.
Calapit-Palao CD, Vina CB, Gregorio GB, Singh RK. A new phenotyping technique for salinity tolerance at the productive stage in rice. ORYZA. 2013;50(3):199-207.
Abou-Khalifa AB, Mishra AN, Salem KM. Effect of leaf cutting on physiological traits and yield of two rice cultivars. African Journal of Plant Science. 2008;2:147-50.
Sabagh AE, Islam MS, Skalicky M, Raza MA, Singh K, Hossain MA et al. Salinity stress in wheat (Triticum aestivum L.) in the changing climate: Adaptation and management strategies. Frontiers in Agronomy. 2021;3:661932. doi: 10.3389/fagro.2021.661932.
Hussain N, Ghaffar A, Zafar ZU, Javed M, Shah KH, Noreen S. Identification of novel source of salt tolerance in local bread wheat germplasm using morpho-physiological and biochemical attributes. Scientific Reports. 2021;11:1-12. doi: 10.1038/s41598-021-90280-w.
Dadshani S, Sharma RC, Baum M, Ogbonnaya FC, Léon J, Ballvora A. Multi-dimensional evaluation of response to salt stress in wheat. PLoS ONE. 2019;14:e0222659. doi: 10.1371/journal.pone.0222659.
Sharbatkhari M, Shobbar ZS, Galeshi S, Nakhoda B. Wheat stem reserves and salinity tolerance: Molecular dissection of fructan biosynthesis and remobilization to grains. Planta. 2016;244:191-202. doi: 10.1007/s00425-016-2497-3.
Al-Ashkar I, Alderfasi A, El-Hendawy S, Al-Suhaibani N, El-Kafafi S, Seleiman MF. Detecting salt tolerance in doubled haploid wheat lines. Agronomy. 2019;9:211. https://doi.org/10.3390/agronomy9040211.
Mohsin T, Khan N, Naqvi FN. Heritability, phenotypic correlation and path coefficient studies for some agronomic characters in synthetic elite lines of wheat. Journal of Food Agriculture and Environment. 2009;7:278-82.
Haider Z, Khan AS, Zia S. Correlation and path coefficient analysis of yield components in rice (Oryza sativa L.) under simulated drought stress condition. American-Eurasian Journal of Agricultural Environment Science. 2012;12:100-04.
Krishnamurthy SL, Gautam RK, Sharma PC, Sharma DK. Effect of different salt stresses on agro-morphological traits and utilisation of salt stress indices for reproductive stage salt tolerance in rice. Field Crop Research. 2016;190:26-33. https://doi.org/10.1016/j.fcr.2016.02.018.
Rosielle AA, Hamblin J. Theoretical aspects of selection for yield in stress and non-stress environments. Crop Science. 1981;21:943-46. http://dx.doi.org/10.2135/cropsci1981.0011183X002100060033x.
Bouslama M, Schapaugh WT. Stress tolerance in soybeans: Evaluation of three screening techniques for heat and drought tolerance. Crop Science. 1984;24(5):933-37. https://doi.org/10.2135/cropsci1984.0011183X002400050026x.
Downloads
Published
Versions
- 20-05-2024 (2)
- 30-04-2024 (1)
How to Cite
Issue
Section
License
Copyright (c) 2024 Shahnaj Akter, Shafiul Islam, Noushin Chowdhury, Sheikh Mahfuja Khatun, Md. Motiar Rohman, Lutful Hassan, Mohammad Anwar Hossain
This work is licensed under a Creative Commons Attribution 4.0 International License.
Copyright and Licence details of published articles
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
Open Access Policy
Plant Science Today is an open access journal. There is no registration required to read any article. All published articles are distributed under the terms of the Creative Commons Attribution License (CC Attribution 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited (https://creativecommons.org/licenses/by/4.0/). Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).