Genetic and physiological characteristics of salt-tolerance in nine rice varieties at seedling stage
PDF

Keywords

proline
Na /K
SSR primer
salt-tolerant rice

How to Cite

1.
Nguyen Pham ND, Le PH, Tran ID, Tong TTT, Pham AT, Huynh K. Genetic and physiological characteristics of salt-tolerance in nine rice varieties at seedling stage. hueuni-jns [Internet]. 2025Dec.26 [cited 2025Dec.27];134(1S-3):151-6. Available from: https://jos.hueuni.edu.vn/index.php/hujos-ns/article/view/7954

Abstract

Climate change has caused severe saltwater intrusion, significantly affecting rice production in the Mekong Delta. This study aims to evaluate the genotypes and salt tolerance of nine rice varieties, including two control varieties, FL478 (salt-tolerant) and IR29 (salt-sensitive), and seven other varieties: ST3, Lua Tim Can Tho, Lua Tim Vinh Long, ST24, Jasmine85, TNN91, and Vin16. The experiments were conducted under artificial conditions with zero and 100 mM NaCl in the Yoshida nutrient solution for 21 days. The genotypes were analysed with the 15 SSR primer pairs linked to salt-tolerance quantitative trait loci identified in FL478. The measured physiological parameters included Na⁺ and K⁺ ion contents in shoots and roots, the Na⁺-to-K⁺ ratio, and the proline content. The results reveal that 8 SSR primer pairs identified salt-tolerant genotypes similar to FL478. Physiologically, the salt-tolerant varieties maintained a low Na⁺-to-K⁺ ratio and efficiently accumulated proline, although FL478 accumulated less proline than IR29. This indicates that FL478 utilises proline more effectively for osmotic regulation and protecting cells from oxidative stress. The Membership Function Value of Salt Tolerance analysis grouped the 9 rice varieties into three categories according to their salt tolerance levels, with ST3 clustered in the highly salt-tolerant group alongside FL478. The study confirms the correlation between genotype and salt tolerance, providing a scientific basis for breeding rice varieties adapted to increasingly severe salinity conditions in the Mekong Delta.

https://doi.org/10.26459/hueunijns.v134i1S-3.7954
PDF

References

  1. Phuong TT, Vien TD, Son CT, Thuy DT, Greiving S. Impact of climate change on agricultural production and Food Security: A case study in the Mekong River Delta of Vietnam. Sustainability. 2024;16(17):7776.
  2. Trung NH, Hong TT, Nguyen T, Luan NV. Assessing the effect of saline intrusion on agricutural farming models in Binh Dai district, Ben Tre province. Can Tho University Journal of Science. 2021;57:183-9.
  3. Giang LV. Impacts of sea level rise and salinity intrusion on water resources in the Mekong Delta. Environment Magazine. 2025;4:47-51. (in Vietnamese)
  4. Dat TT, Trang NT, Hoa DD, Nguyen TT, Nam TV. Assessing of of salinity intrusion on livihoods at Tan Phu Dong and Go Cong Dong districts of Tien Giang province and proposal solutions. Journal of Military Science and Technology. 2022(VITTEP):79-90.
  5. Rasheed A, Li H, Nawaz M, Mahmood A, Hassan MU, Shah AN, et al. Molecular tools, potential frontiers for enhancing salinity tolerance in rice: A critical review and future prospective. Frontiers in Plant Science. 2022;Volume 13 - 2022.
  6. Platten JD, Egdane JA, Ismail AM. Salinity tolerance, Na+ exclusion and allele mining of HKT1; 5 in Oryza sativa and O. glaberrima: many sources, many genes, one mechanism? BMC plant biology. 2013;13(1):32.
  7. Hoang TML, Tran TN, Nguyen TKT, Williams B, Wurm P, Bellairs S, et al. Improvement of salinity stress tolerance in rice: challenges and opportunities. Agronomy. 2016;6(4):54.
  8. Doyle JJ, Doyle JL. Isolation of plant DNA from fresh tissue. Focus. 1990;12(1):13-15.
  9. Maclean JL, Dawe DC, Institute IRR, Hettel GP. Rice Almanac: Source Book for the Most Important Economic Activity on Earth. Oxon: CABI Pub; 2002.
  10. Yoshida S. Fundamentals of rice crop science. Manila: IRRI; 1981.
  11. Iseki K, Marubodee R, Ehara H, Tomooka N. A rapid quantification method for tissue Na+ and K+ concentrations in salt-tolerant and susceptible accessions in Vigna vexillata (L.) A. Rich. Plant Production Science. 2017;20(1):144-8.
  12. Chen T, Zhang B. Measurements of proline and malondialdehyde content and antioxidant enzyme activities in leaves of drought stressed cotton. Bio-protocol. 2016;6(17):e1913.
  13. Chen X, Min D, Yasir TA, Hu YG. Evaluation of 14 morphological, yield-related and physiological traits as indicators of drought tolerance in Chinese winter bread wheat revealed by analysis of the membership function value of drought tolerance (MFVD). Field Crops Research. 2012;137:195-201.
  14. Afsar S, Bibi G, Ahmad R, Bilal M, Naqvi TA, Baig A, et al. Evaluation of salt tolerance in Eruca sativa accessions based on morpho-physiological traits. PeerJ. 2020;8:e9749.
  15. Wang Z, Chen Z, Cheng J, Lai Y, Wang J, Bao Y, et al. QTL analysis of Na+ and K+ concentrations in roots and shoots under different levels of NaCl stress in rice (Oryza sativa L.). PLOS ONE. 2012;7(12):e51202.
  16. Thomson MJ, de Ocampo M, Egdane J, Rahman MA, Sajise AG, Adorada DL, et al. Characterizing the Saltol quantitative trait locus for salinity tolerance in rice. Rice. 2010;3(2):148-60.
  17. Lin HX, Zhu MZ, Yano M, Gao JP, Liang ZW, Su WA, et al. QTLs for Na+ and K+ uptake of the shoots and roots controlling rice salt tolerance. Theoretical and Applied Genetics. 2004;108(2):253-60.
  18. Carballo Rivero G, Tremblay MF, Charest C, Laliberté S. Effect of nitrogen stress on growth, soluble metabolites, and glutamine synthetase activity of jack pine callus cultures. Journal of Plant Nutrition. 2002;25(3):443-55.
  19. Essa TA. Effect of salinity stress on growth and nutrient composition of three soybean (Glycine max L. Merrill) cultivars. Journal of Agronomy and Crop Science. 2002;188(2):86-93.
  20. Anschütz U, Becker D, Shabala S. Going beyond nutrition: regulation of potassium homoeostasis as a common denominator of plant adaptive responses to environment. Journal of Plant Physiology. 2014;171(9):670-87.
  21. Munns R, Tester M. Mechanisms of salinity tolerance. Annu Rev Plant Biol. 2008;59(Volume 59, 2008):651-81.
  22. Ren Z-H, Gao J-P, Li L-G, Cai X-L, Huang W, Chao D-Y, et al. A rice quantitative trait locus for salt tolerance encodes a sodium transporter. Nature Genetics. 2005;37(10):1141-6.
  23. Farooq M, Park JR, Jang YH, Kim EG, Kim KM. Rice cultivars under salt stress show differential expression of genes related to the regulation of Na+/K+ balance. Frontiers in Plant Science. 2021;Volume 12 - 2021.
  24. Rao PS, Mishra B, Gupta SR. Zinc/phosphorous ratio in shoot as an index of evaluating rice salt tolerance. African Journal of Agricultural Research. 2013;8(1):70-6.
  25. Ashraf MF, Foolad MR. Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany. 2007;59(2):206-16.
  26. Tahjib-Ul-Arif M, Sayed MA, Islam MM, Siddiqui MN, Begum SN, Hossain MA. Screening of rice landraces (Oryza sativa L.) for seedling stage salinity tolerance using morpho-physiological and molecular markers. Acta Physiologiae Plantarum. 2018;40(4):70.
  27. Ministry of Natural Resources and Environment (MONRE). Climate change and sea level rise scenarios for Viet Nam. Hanoi: MONRE; 2020.
  28. Bao N. Study on the economic impacts of climate change on the Mekong Delta. Tia Sang. 2024;13. (in Vietnamese)
Creative Commons License

This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.

Copyright (c) 2025 Array