Ionomic and transcriptomic analyses of two cotton cultivars (Gossypium hirsutum L.) provide insights into the ion balance mechanism of cotton under salt stress
Autoři:
Huijuan Guo aff001; Shuangnan Li aff001; Wei Min aff001; Jun Ye aff001; Zhenan Hou aff001
Působiště autorů:
Department of Resources and Environmental Science, Shihezi University, Shihezi, Xinjiang, People’s Republic of China
aff001
Vyšlo v časopise:
PLoS ONE 14(12)
Kategorie:
Research Article
doi:
https://doi.org/10.1371/journal.pone.0226776
Souhrn
Soil salinity is a major abiotic stress factor that limits cotton production worldwide. To improve salt tolerance in cotton, an in-depth understanding of ionic balance is needed. In this study, a pot experiment using three levels of soil salinity (0%, 0.2%, and 0.4%, represented as CK, SL, and SH, respectively) and two cotton genotypes (salt-tolerant genotype: L24; salt-sensitive genotype: X45) was employed to investigate how sodium chloride (NaCl) stress effects cotton growth, ion distribution, and transport, as well as to explore the related mechanism. The results showed that SL treatment mainly inhibited shoot growth, while SH treatment caused more extensive impairment to roots and shoots. The growth inhibition ratio of NaCl stress on X45 was more marked than that of L24. Under NaCl stress, the Na concentration in the roots, stems and leaves significantly increased, whereas the K, Cu, B, and Mo concentration in roots, as well as Mg and S concentrations in the leaves, significantly decreased. Under salt stress conditions, salt-tolerant cotton plants can store Na in the leaves, and as a result, a larger amount of minerals (e.g., Cu, Mo, Si, P, and B) tend to transport to the leaves. By contrast, salt-sensitive varieties tend to accumulate certain minerals (e.g., Ca, P, Mg, S, Mn, Fe, Cu, B, Mo, and Si) in the roots. Most genes related to ion transport and homeostasis were upregulated in L24, but not in X45. The expression level of GhSOS1 in X45 was higher than L24, but GhNHX1 in L24 was higher than X45. Our findings suggest that the two varieties response to salt stress differently; for X45 (salt-sensitive), the response is predominantly governed by Na+ efflux, whereas for L24 (salt-tolerant), vacuolar sequestration of Na+ is the major mechanism. The expression changes of the genes encoding the ion transporters may partially explain the genotypic difference in leaf ion accumulation under salt stress conditions.
Klíčová slova:
Cotton – Gene expression – Homeostasis – Leaves – Plant resistance to abiotic stress – Root growth – Sodium – Transcriptome analysis
Zdroje
1. Akhtar SS, Andersen MN, Naveed M, Zahir ZA, Liu F. Interactive effect of biochar and plant growth-promoting bacterial endophytes on ameliorating salinity stress in maize. Functional Plant Biology. 2015; 42(8): 770–781.
2. Chen H, Diao J, Li Y, Chen Q, Kong B. The effectiveness of clove extracts in the inhibition of hydroxyl radical oxidation-induced structural and rheological changes in porcine myofibrillar protein. Meat Science. 2016; 111: 60–66. doi: 10.1016/j.meatsci.2015.08.017 26340742
3. Ahmad P, Azooz MM, Prasad MNV. Ecophysiology and responses of plants under salt stress. Springer, New York, 2013; pp, 25–87
4. Sall SN, Ndour NYB, Diédhiou-Sall S, Dick R, Chotte JL. Microbial response to salinity stress in a tropical sandy soil amended with native shrub residues or inorganic fertilizer. Journal of environmental management. 2015; 161: 30–37. doi: 10.1016/j.jenvman.2015.06.017 26143083
5. Abdelraheem A, Esmaeili NO’Connell M, Zhang J. Progress and perspective on drought and salt stress tolerance in cotton. Industrial Crops and Products. 2019; 130: 118–129.
6. Sairam RK, Tyagi A. Physiology and molecular biology of salinity stress tolerance in plants. Current Science. 2004; 86: 407–421.
7. Munns R, Tester M. Mechanisms of salinity tolerance. Annual Review of Plant Biology. 2008; 59: 651–681. doi: 10.1146/annurev.arplant.59.032607.092911 18444910
8. Munns R. Approaches to identifying genes for salinity tolerance and the importance of timescale. In Plant stress tolerance (pp. 25–38). Humana Press.2010.
9. Tavakkoli E, Rengasamy P, McDonald GK. The response of barley to salinity stress differs between hydroponic and soil systems. Functional Plant Biology. 2010; 37(7): 621–633.
10. Wu D, Shen Q, Cai S, Chen ZH, Dai F, Zhang G. Ionomic responses and correlations between elements and metabolites under salt stress in wild and cultivated barley. Plant and Cell Physiology. 2013; 54(12): 1976–1988. doi: 10.1093/pcp/pct134 24058150
11. Xu LH, Wang WY, Guo JJ, Qin J, Shi DQ, Li YL, et al. Zinc improves salt tolerance by increasing reactive oxygen species scavenging and reducing Na+ accumulation in wheat seedlings. Biologia plantarum. 2014; 58(4): 751–757.
12. Ali L, Ashraf M, Maqbool M, Ahmad R, Aziz A. Optimization of soil K:Na ratio for cotton (Gossypium hirsutum L.) nutrition under field conditions. Pakistan Journal of Botany. 2013; 45(1): 127–134.
13. Dogan I, Ozyigit II, Demir G. Mineral element distribution of cotton (Gossypium hirsutum L.) seedlings under different salinity levels. Pakistan Journal of Botany. 2012; 44: 15–20.
14. Severino LS, Lima RL, Castillo N, Lucena AM, Auld DL, Udeigwe TK. Calcium and magnesium do not alleviate the toxic effect of sodium on the emergence and initial growth of castor, cotton, and safflower. Industrial Crops and Products. 2014; 57: 90–97.
15. Habib F, Akram Z, Akhtar J, Hussain S, Mansoor M. Assessment of variations in growth and ionic concentration of salt tolerant and sensitive cotton genotypes. Scientia. 2014; 3(2): 105–110.
16. Dai JL, Duan LS, Dong HZ. Improved nutrient uptake enhances cotton growth and salinity tolerance in saline media. Journal of plant nutrition. 2014; 37(8): 1269–1286.
17. Salt DE, Baxter I, Lahner B. Ionomics and the study of the plant ionome. Annual Review of Plant Biology. 2008; 59: 709–733. doi: 10.1146/annurev.arplant.59.032607.092942 18251712
18. Singh UM, Sareen P, Sengar RS, Kumar A. Plant ionomics: a newer approach to study mineral transport and its regulation. Acta physiologiae plantarum. 2013; 35(9): 2641–2653.
19. Baxter I, Hermans C, Lahner B, Yakubova E, Tikhonova M, Verbruggen N, et al. Biodiversity of mineral nutrient and trace element accumulation in Arabidopsis thaliana. PLoS one. 2012; 7(4): e35121. doi: 10.1371/journal.pone.0035121 22558123
20. Xu J, Tian X, Eneji AE, Li Z. Functional characterization of GhAKT1, a novel Shaker-like K+ channel gene involved in K+ uptake from cotton (Gossypium hirsutum). Gene. 2014; 545(1): 61–71. doi: 10.1016/j.gene.2014.05.006 24802116
21. Zhu JK. Salt and drought stress signal transduction in plants. Annual review of plant biology. 2002; 53(1): 247–273.
22. Ishitani M, Liu J, Halfter U, Kim CS, Shi W, Zhu JK. SOS3 function in plant salt tolerance requires N-myristoylation and calcium binding. The Plant Cell. 2000; 12(9): 1667–1677. doi: 10.1105/tpc.12.9.1667 11006339
23. Sánchez-Barrena MJ, Martínez-Ripoll M, Zhu JK, Albert A. The structure of the Arabidopsis thaliana SOS3: molecular mechanism of sensing calcium for salt stress response. Journal of molecular biology. 2005; 345(5): 1253–1264. doi: 10.1016/j.jmb.2004.11.025 15644219
24. Wu CA, Yang GD, Meng QW, Zheng CC. The cotton GhNHX1 gene encoding a novel putative tonoplast Na+/H+ antiporter plays an important role in salt stress. Plant and Cell Physiology. 2004; 45(5): 600–607. doi: 10.1093/pcp/pch071 15169942
25. Song L, Ye W, Zhao Y, Wang J, Fan B, Wang D. Isolation and analysis of salt tolerance related gene (GhVP) from Gossypium hirsutum. Cotton Science. 2010; 22(3): 285–288.
26. Wang XC, Zhao QY, Ma CL, Zhang ZH, Cao HL, Kong YM, et al. Global transcriptome profiles of Camellia sinensis during cold acclimation. BMC genomics. 2013;14(1): 415.
27. Zeng A, Chen P, Korth K L, Ping J, Thomas J, Wu C, et al. RNA sequencing analysis of salt tolerance in soybean (Glycine max). Genomics. 2019; 111(4): 629–635. doi: 10.1016/j.ygeno.2018.03.020 29626511
28. Li G, Wu JL, Wang YZ, Liu LP. Field evaluation of suppressive effect of different rice varieties on weeds in paddy field. Scientia Agricultura Sinica. 2010; 43(5): 965–971. (In chinese)
29. Freitas VS, Alencar NLM, de Lacerda CF, Prisco JT, Gomes-Filho E. Changes in physiological and biochemical indicators associated with salt tolerance in cotton, sorghum and cowpea. African Journal of Biochemistry Research. 2011; 5(8): 264–271.
30. Abbas G, Saqib M, Akhtar J, Haq MAU. Interactive effects of salinity and iron deficiency on different rice genotypes. Journal of Plant Nutrition and Soil Science. 2015; 178(2): 306–311.
31. Akhtar J, Saqib ZA, Sarfraz M, Saleem I, Haq MA. Evaluating salt tolerant cotton genotypes at different levels of NaCl stress in solution and soil culture. Pakistan Journal of Botany. 2010; 42(4): 2857–2866.
32. Basal H. Response of cotton (Gossypium hirsutum L.) genotypes to salt stress. Pakistan Journal of Botany. 2010; 42(1): 505–511.
33. Munis MFH, Tu LILI, Ziaf K, Tan J, Deng FENGLIN, Zhang X. Critical osmotic, ionic and physiological indicators of salinity tolerance in cotton (Gossypium hirsutum L.) for cultivar selection. Pakistan Journal of Botany. 2010; 42(3): 1685–1694.
34. Hajer AS, Malibari AA, Al-Zahrani HS, Almaghrabi OA. Responses of three tomato cultivars to sea water salinity 1. Effect of salinity on the seedling growth. African Journal of Biotechnology. 2006; 5(10):855–861.
35. Qiu L, Wu DZ, Ali S, Cai SG, Dai F, Jin XL, et al. Evaluation of salinity tolerance and analysis of allelic function of HvHKT1 and HvHKT2 in Tibetan wild barley, Theor Appl Genet. 2011; 122: 695–703. doi: 10.1007/s00122-010-1479-2 20981400
36. Lokhande VH, Nikam TD, Patade VY, Ahire ML, Suprasanna P. Effects of optimal and supra-optimal salinity stress on antioxidative defence, osmolytes and in vitro growth responses in Sesuvium portulacastrum L. Plant Cell, Tissue and Organ Culture (PCTOC). 2011; 104(1): 41–49.
37. Bracci T, Minnocci A, Sebastiani L. In vitro olive (Olea europaea L.) cvs Frantoio and Moraiolo microshoot tolerance to NaCl. Plant Biosystems-An International Journal Dealing with all Aspects of Plant Biology. 2008; 142(3): 563–571.
38. Wang N, Qiao W, Liu X, Shi J, Xu Q, Zhou H, et al. Relative contribution of Na+/K+ homeostasis, photochemical efficiency and antioxidant defense system to differential salt tolerance in cotton (Gossypium hirsutum L.) cultivars. Plant Physiology and Biochemistry. 2017; 119: 121–131. doi: 10.1016/j.plaphy.2017.08.024 28866234
39. Basel S. Effect of salt stress (NaCl) on biomass and K+/Na+ ratio in cotton. Journal of Stress Physiology & Biochemistry. 2011; 7(4): 06–14.
40. Ozyigit II, Dogan I, Demir G, Yalcin IE. Mineral nutrient acquisition by cotton cultivars grown under salt stress. Communications in Soil Science and Plant Analysis. 2017; 48(8): 846–856.
41. Grattan SR, Grieve CM. Mineral nutrient acquisition and response by plants grown in saline environments. Handbook of plant and crop stress. 1999; 2: 203–229.
42. Blumwald E. Sodium transport and salt tolerance in plants. Current opinion in cell biology. 2000; 12(4): 431–434. doi: 10.1016/s0955-0674(00)00112-5 10873827
43. Yang C, Chong J, Li C, Kim C, Shi D, Wang D. Osmotic adjustment and ion balance traits of an alkali resistant halophyte Kochia sieversiana during adaptation to salt and alkali conditions. Plant and soil. 2007; 294(1–2): 263–276.
44. Tester M, Davenport R. Na+ tolerance and Na+ transport in higher plants. Annals of botany. 2003; 91(5): 503–527. doi: 10.1093/aob/mcg058 12646496
45. Shi H, Quintero FJ, Pardo JM, Zhu JK. The putative plasma membrane Na+/H+ antiporter SOS1 controls long-distance Na+ transport in plants. The Plant Cell, 2002; 14(2): 465–477. doi: 10.1105/tpc.010371 11884687
46. Banjara M, Zhu L, Shen G, Payton P, Zhang H. Expression of an Arabidopsis sodium/proton antiporter gene (AtNHX1) in peanut to improve salt tolerance. Plant biotechnology reports. 2012; 6(1): 59–67.
47. Chen LH, Zhang B, Xu ZQ. Salt tolerance conferred by overexpression of Arabidopsis vacuolar Na+/H+ antiporter gene AtNHX1 in common buckwheat (Fagopyrum esculentum). Transgenic Research. 2008; 17(1): 121. doi: 10.1007/s11248-007-9085-z 17541720
48. Ma Q, Li YX, Yuan HJ, Hu J, Wei L, Bao AK, et al. ZxSOS1 is essential for long-distance transport and spatial distribution of Na+ and K+ in the xerophyte Zygophyllum xanthoxylum. Plant and Soil. 2014; 374(1–2): 661–676.
49. Qiu QS, Guo Y, Dietrich MA, Schumaker KS, Zhu JK. Regulation of SOS1, a plasma membrane Na+/H+ exchanger in Arabidopsis thaliana, by SOS2 and SOS3. Proceedings of the National Academy of Sciences, 2002; 99(12): 8436–8441.
50. Lebaudy A, Véry AA, Sentenac H. K+ channel activity in plants: genes, regulations and functions. FEBS letters. 2007; 581(12): 2357–2366. doi: 10.1016/j.febslet.2007.03.058 17418142
51. Duan HR, Ma Q, Zhang JL, Hu J, Bao AK, Wei L, et al. The inward-rectifying K+ channel SsAKT1 is a candidate involved in K+ uptake in the halophyte Suaeda salsa under saline condition. Plant and soil. 2015; 395(1–2): 173–187.
52. Jafri AZ, Ahmad RAFIQ. Plant growth and ionic distribution in cotton (Gossypium hirsutum L.) under saline environment. Pakistan Journal of Botany. 1994; 26: 105–105.
53. Abbas W, Ashraf M, Akram NA. Alleviation of salt-induced adverse effects in eggplant (Solanum melongena L.) by glycinebetaine and sugarbeet extracts. Scientia horticulturae. 2010; 125(3): 188–195.
54. Gerard CJ, Hinojosa E. Cell Wall Properties of Cotton Roots as Influenced by Calcium and Salinity. Agronomy Journal. 1973; 65(4): 556–560.
55. Leidi EO, Nogales R, Lips SH. Effect of salinity on cotton plants grown under nitrate or ammonium nutrition at different calcium levels. Field Crops Research. 1991; 26(1): 35–44.
56. Leidi EO, Silberbush M, Soares MIM, Lips SH. Salinity and nitrogen nutrition studies on peanut and cotton plants. Journal of Plant Nutrition. 1992; 15(5): 591–604.
57. Martinez V, Läuchli A. Salt-induced inhibition of phosphate uptake in plants of cotton (Gossypium hirsutum L.). New Phytologist. 1994; 126(4): 609–614.
58. Qadir M, Shams M. Some agronomic and physiological aspects of salt tolerance in cotton (Gossypium hirsutum L.). Journal of Agronomy and Crop Science. 1997; 179(2): 101–106.
59. Meloni DA, Oliva MA, Ruiz HA, Martinez CA. Contribution of proline and inorganic solutes to osmotic adjustment in cotton under salt stress. Journal of Plant Nutrition. 2001; 24(3): 599–612.
60. Thomas JR. Osmotic and Specific Salt Effects on Growth of Cotton. Agronomy Journal. 1980; 72(3): 407–412.
61. Abd Ella M K, Shalaby EE. Cotton Response to Salinity and Different Potassium-Sodium Ratio in Irrigation Water. Journal of Agronomy and Crop Science. 1993; 170(1): 25–31.
62. Rathert G. Effects of high salinity stress on mineral and carbohydrate metabolism of two cotton varieties. Plant and Soil. 1983; 73(2): 247–256.
63. Ahmad S, Khan N, Iqbal MZ, Hussain A, Hassan M. Salt tolerance of cotton (Gossypium hirsutum L.). Asian Journal of Plant Sciences. 2002; 1(6): 715–719.
64. Zhang L, Ma H, Chen T, Pen J, Yu S, Zhao X. Morphological and physiological responses of cotton (Gossypium hirsutum L.) plants to salinity. PLoS One. 2014; 9(11): e112807. doi: 10.1371/journal.pone.0112807 25391141
65. Hirayama O. Characterization of membrane lipids of high plants, different in salt tolerance. Agricultural and Biolgical Chemistry. 1987; 51: 3215–3321
66. Rabhi M, Farhat N, Msilini N, Rajhi H, Smaoui A, Abdelly C, et al. Physiological responses of Carthamus tinctorius to CaCl2 salinity under Mg-sufficient and Mg-deficient conditions. Flora. 2018; 96–101.
67. El-Fouly M M, Mobarak Z M, Salama ZA. Micronutrients (Fe, Mn, Zn) foliar spray for increasing salinity tolerance in wheat Triticum aestivum L. African Journal of Plant Science. 2011; 5(5): 314–322.
68. Iqbal MN, Rasheed R, Ashraf MY, Ashraf MA, Hussain I. Exogenously applied zinc and copper mitigate salinity effect in maize (Zea mays L.) by improving key physiological and biochemical attributes. Environmental Science and Pollution Research. 2018; 1–14.
69. Karimi G, Ghorbanli M, Heidari H, Nejad RK, Assareh MH. The effects of NaCl on growth, water relations, osmolytes and ion content in Kochia prostrata. Biologia Plantarum. 2005; 49(2): 301–304.
70. Li H, Zhu Y, Hu Y, Han W, Gong H. Beneficial effects of silicon in alleviating salinity stress of tomato seedlings grown under sand culture. Acta physiologiae plantarum. 2015; 37(4): 71.
Článek vyšel v časopise
PLOS One
2019 Číslo 12
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