Short-Term Pretreatment with Melatonin Increases the Resistance of Barley Plants to the Subsequent Action of Cadmium

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Abstract

The effect of short-term and long-term root treatment with melatonin on growth parameters, photochemical activity of PSII, content of basic photosynthetic pigments, lipid peroxidation, and accumulation of
inorganic ions in barley plants under the action of cadmium chloride
was studied. It was shown for the first time that the protective
effect of phytomelatonin during short-term treatment is manifested in
a decrease in the toxic effect of cadmium on the content of
photosynthetic pigments and the accumulation of cadmium ions in the
shoots and roots of barley plants. The protective effect of melatonin
is based on its ability to reduce the intensity of oxidative stress by
maintaining the level of carotenoids and increasing the activity of
antioxidant enzymes. The effectiveness of short-term use of melatonin
in a number of indicators exceeds its protective effect from long-term
exposure. The data obtained indicate the possibility of using
melatonin as a substance that induces the state of plant priming upon
subsequent exposure to cadmium.

About the authors

E. D. Danilova

National Research Tomsk State University

Email: nusy.l.d@gmail.com
Tomsk, Russia

I. E. Zlobin

National Research Tomsk State University; Timiryazev Institute of Plant Physiology, Russian Academy of Sciences

Email: nusy.l.d@gmail.com
Tomsk, Russia; Moscow, Russia

M. V. Efimova

National Research Tomsk State University

Author for correspondence.
Email: nusy.l.d@gmail.com
Tomsk, Russia

References

  1. Clemens S., Ma J.F. Toxic heavy metal and metalloid accumulation in crop plants and foods // Annu. Rev. Plant Biol. 2016. V. 67. P. 489. https://doi.org/10.1146/annurev-arplant-043015-112301
  2. Srivastava V., Sarkar A., Singh S., Singh P., de Araujo A.S.F., Singh R. Agroecological responses of heavy metal pollution with special emphasis on soil health and plant performances // Front. Environ. Sci. 2017. V. 5. P. 1. https://doi.org/10.3389/fenvs.2017.00064
  3. Danilova E.D., Zlobin I.E., Kuznetsov V.V., Efimova M.V. Exogenic melatonin reduces the toxic effect of polymetallic stress on barley plants // Dokl. Biochem. Biophys. 2021. V. 499. P. 228. https://doi.org/10.1134/S1607672921040049
  4. Asgher M., Khan M.I.R., Anjum N.A., Khan N.A. Minimising toxicity of cadmium in plants – role of plant growth regulators // Protoplasma. 2015. V. 252. P. 399. https://doi.org/10.1007/s00709-014-0710-4
  5. Muradoglu F., Gundogdu M., Ercisli S., Encu T., Balta F., Jaafar H., Zia-Ul-Haq M. Cadmium toxicity affects chlorophyll a and b content, antioxidant enzyme activities and mineral nutrient accumulation in strawberry // Biological Res. 2015. V. 48. P. 1. https://doi.org/10.1186/s40659-015-0001-3
  6. Cho U.H., Seo N.H. Oxidative stress in Arabidopsis thaliana exposed to cadmium is due to hydrogen peroxide accumulation // Plant Sci. 2005. V. 168. P. 113. https://doi.org/10.1016/j.plantsci.2004.07.021
  7. Hussain I., Iqbal M., Qurat-Ul-Ain S., Rasheed R., Mahmood S., Perveen F., Wahid A. Cadmium dose and exposure-time dependent alterations in growth and physiology of maize (Zea mays) // Int. J. Agric. Biol. 2012. V. 14. P. 959.
  8. El Rasafi T., Oukarroum A., Haddioui A., Song H., Kwon E.E., Bolan N., Tack F.M.G., Sebastian A., Prasad M.N.V., Rinklebe J. Cadmium stress in plants: a critical review of the effects, mechanisms, and tolerance strategies // Crit. Rev. Environ. Sci. Technol. 2020. P. 1. https://doi.org/10.1080/10643389.2020.183543
  9. Bian M., Zhou M., Sun D., Li C. Molecular approaches unravel the mechanism of acid soil tolerance in plants // Crop J. 2013. V. 1. P. 91. https://doi.org/10.1016/j.cj.2013.08.002
  10. Arnao M.B., Hernandez-Ruiz J. Functions of melatonin in plants: a review // J. Pineal Res. 2015. V. 59. P. 133. https://doi.org/10.1111/jpi.12253
  11. Zhang Y.P., Yang S.J., Chen Y.Y. Effects of melatonin on photosynthetic performance and antioxidants in melon during cold and recovery // Biol. Plant. 2017. V. 61. P. 571. https://doi.org/10.1007/s10535-017-0717-8
  12. Kholodova V.P., Vasil’ev S.V., Efimova M.V., Voronin P.Yu., Rakhmankulova Z.F., Danilova E.Yu., Kuznetsov Vl.V. Exogenous melatonin protects canola plants from toxicity of excessive copper // Russ. J. Plant Physiol. 2018. T. 65. P. 882. https://doi.org/10.1134/S1021443718060080
  13. Nawaz M.A., Jiao Y., Chen C., Shireen F., Zheng Z., Imtiaz M., Bie Z., Huang Y. Melatonin pretreatment improves vanadium stress tolerance of watermelon seedlings by reducing vanadium concentration in the leaves and regulating melatonin biosynthesis and antioxidant-related gene expression // J. Plant Physiol. 2018. V. 220. P. 115. https://doi.org/10.1016/j.jplph.2017.11.003
  14. Savvides A., Ali S., Tester M., Fotopoulos V. Chemical priming of plants against multiple abiotic stresses: mission possible? // Trends Plant Sci. 2016. V. 21. P. 329. https://doi.org/10.1016/j.tplants.2015.11.003
  15. Blamey F.P.C., Hernandez-Soriano M.C., Cheng M., Cheng M., Tang C., Paterson D.J., Lombi E., Wang W.H., Scheckel K.G., Kopittke P.M. Synchrotron-based techniques shed light on mechanisms of plant sensitivity and tolerance to high manganese in the root environment // Plant Physiol. 2015. V. 169. P. 2006. https://doi.org/10.1104/pp.15.00726
  16. Danilova E.D., Litvinovskaya R.P., Zlobin I.E., Kolomeichuk L.V., Murgan O.K., Sauchuk A.L., Khripach V.A., Kuznetsov V.V., Efimova M.V. Polymetallic stress changes the endogenous status of brassinosteroids and reduces the effectiveness of photochemical reactions photosystem II in barley plants // Dokl. Biochem. Biophys. 2022. V. 504. P. 123. https://doi.org/10.1134/S1607672922030024
  17. Kopittke P.M., Blamey F.P.C., Asher C.J., Menzies N.W. Trace metal phytotoxicity in solution culture: a review // J. Exp. Bot. 2010. V. 61. P. 945. https://doi.org/10.1093/jxb/erp385
  18. Li Z., Wang P., Menzies N.W., Kopittke P.M. Defining appropriate methods for studying toxicities of trace metals in nutrient solutions // Ecotoxicol. Environ. Saf. 2018. V.147. P. 872. https://doi.org/10.1016/j.ecoenv.2017.09.044
  19. Аникеев В.В., Кутузов Ф.Ф. Новый способ определения листовой поверхности у злаков // Физиология растений. 1961. Т. 8. С. 375.
  20. Buege J.A., Aust S.D. Microsomal lipid peroxidation // Biomembrans. 1978. V. 52. P. 302. https://doi.org/10.1016/s0076-6879(78)52032-6
  21. Lichtenthaler H.K. Chlorophylls and carotenoids: pigments of photosynthetic biomembranes // Plant Cell. 1987. P. 350. https://doi.org/10.1016/0076-6879(87)48036-1
  22. Bates L.S., Waldren R.P., Teare I.D. Rapid determination of free proline for water-stress studies // Plant Soil. 1973. V. 39. P. 205. https://doi.org/10.1007/BF00018060
  23. Beauchamp C., Fridovich I. Superoxide dismutase improved assays and an assay applicable to acrylamide gels // Anal. Biochem. 1971. V. 44. P. 276. https://doi.org/10.1016/0003-2697(71)90370-8
  24. Shevyakova N.I., Stetsenko L.A., Meshcheryakov A.B., Kuznetsov Vl.V. The activity of the peroxidase system in the course of stress-induced CAM development // Russ. J. Plant Physiol. 2002. V. 49. P. 598. https://doi.org/10.1023/A:1020224531599
  25. Esen A.A. Simple method for quantitative, semiquantitative, and qualitative assay of protein // Anal. Biochem. 1978. V. 89. P. 264. https://doi.org/10.1016/0003-2697(78)90749-2
  26. Ruban A.V. Nonphotochemical chlorophyll fluorescence quenching: mechanism and effectiveness in protecting plants from photodamage // Plant Physiol. 2016. V. 170. P. 1903. https://doi.org/10.1104/pp.15.01935
  27. Yan H., Jia S., Mao P. Melatonin priming alleviates aging-induced germination inhibition by regulating β-oxidation, protein translation, and antioxidant metabolism in oat (Avena sativa L.) seeds // Int. J. Mol. Sci. 2020. V. 21. P. 1. https://doi.org/10.3390/ijms21051898
  28. Mehta V., Kansara R., Srivashtav V., Savaliya P. A novel insight into phytoremediation of heavy metals through genetic engineering and phytohormones // J. Nanosci. Nanomed. Nanobio. 2021. V. 4. P. 1.
  29. Sadak M.S., Abdalla A.M., Abd Elhamid E.M., Ezzo M.I. Role of melatonin in improving growth, yield quantity and quality of Moringa oleifera L. plant under drought stress // Bull. Natl. Res. Cent. 2020. V. 44. P. 1.
  30. Danilova E.D., Efimova M.V., Kolomeichuk L.V., Kuznetsov V.V. Melatonin supports photochemical activity of assimilation apparatus and delays senescence of leaves of monocotyledonous plants // Dokl. Biochem. Biophys. 2020. V. 495. P. 271. https://doi.org/10.1134/S1607672920050051
  31. Wang L.Y., Liu J.L., Wang W.X., Sun Y. Exogenous melatonin improves growth and photosynthetic capacity of cucumber under salinity-induced stress // Photosynthetica. 2016. V. 54. P. 19. https://doi.org/10.1007/s11099-015-0140-3
  32. Zhang Y.P., Yang S.J., Chen Y.Y. Effects of melatonin on photosynthetic performance and antioxidants in melon during cold and recovery // Biol. Plant. 2017. V. 61. P. 571. https://doi.org/10.1007/s10535-017-0717-8
  33. Sharma A., Zheng B. Melatonin mediated regulation of drought stress: physiological and molecular aspects // Plants. 2019. V. 8. P. 1. https://doi.org/10.3390/plants8070190
  34. Hoqu M., Tahjib-Ul-Arif M., Hannan A., Sultana N., Akhter S., Hasanuzzaman M., Akter F., Hossain M.S., Sayed M.A., Hasan M.T., Skalicky M., Li X., Brestic M. Melatonin modulates plant tolerance to heavy metal stress: Morphological responses to molecular mechanisms // Int. J. Mol. Sci. 2021. V. 22. № 21. P. 1. https://doi.org/10.3390/ijms222111445
  35. Xu L., Zhang F., Tang M., Wang Y., Dong J., Ying J., Chen Y., Hu B., Li C., Liu L. Melatonin confers cadmium tolerance by modulating critical heavy metal chelators and transporters in radish plants // J. Pin. Res. 2020. V. 69. P. 1. https://doi.org/10.1111/jpi.12659
  36. Jiang M., Dai S., Wang B., Xie Z., Li J., Wang L., Li S., Tana Y., Tian B., Shu Q., Huang J. Gold nanoparticles synthesized using melatonin suppress cadmium uptake and alleviate its toxicity in rice // Enviro. Sci. Nano. 2021. V. 8. P. 1042.
  37. Amjadi Z., Namdjoyan S., Soorki A.A. Exogenous melatonin and salicylic acid alleviates cadmium toxicity in safflower (Carthamus tinctorius L.) seedlings // Ecotoxicol. 2021. V. 30. P. 387. https://doi.org/10.1007/s10646-021-02364-y
  38. Hasan M.K., Ahammed G.J., Sun S., Li M., Yin H., Zhou J. Melaton ininhibits cadmium translocation and enhances plant tolerance by regulating sulfur uptake and assimilation in Solanum lycopersicum L. // J. Agric. Food Chem. 2019. V. 67. P. 10563. https://doi.org/10.1021/acs.jafc.9b0240

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Copyright (c) 2023 Е.Д. Данилова, И.Е. Злобин, М.В. Ефимова

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