Nuclear Physics and Atomic Energy

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Nuclear Physics and Atomic Energy

  ISSN: 1818-331X (Print), 2074-0565 (Online)
  Publisher: Institute for Nuclear Research of the National Academy of Sciences of Ukraine
  Languages: Ukrainian, English
  Periodicity: 4 times per year

  Open access peer reviewed journal


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Nucl. Phys. At. Energy 2026, volume 27, issue 3, pages 265-273.
Section: Radiobiology and Radioecology.
Received: 27.12.2025; Accepted: 31.08.2026; Published online: 29.09.2026.
PDF Full text (ua)
https://doi.org/10.15407/jnpae2026.03.265

The effect of low doses of X-ray irradiation on wheat resistance to phytopathogens

I. Zhuk*, J. Shylina

Institute of Cell Biology and Genetic Engineering, National Academy of Sciences of Ukraine, Kyiv, Ukraine

*Corresponding author. E-mail address: ivzhukvi@gmail.com

Abstract: The effect of low-dose X-ray irradiation (10 and 20 Gy) of winter wheat seeds of the cultivars Sofiia Kyivska and Shchedrivka Kyivska on plant resistance to phytopathogenic pressure was investigated. Seed infestation by the phytopathogens Fusarium sp., Aspergillus, and Mucor was identified. It is shown that in both cultivars, both irradiation doses suppressed the development of phytopathogens; however, the 20 Gy dose had a more pronounced effect on infection development. Changes in the hydrogen peroxide content during the experimental period were also sensitive to phytopathogenic pressure and to the cultivar-specific adaptive potential of the plants. Changes in the contents of chlorophylls and carotenoids indicate the functional integrity of leaves following exposure of wheat grains to low doses of X-ray radiation and the compensation of the detrimental effects of the Fusarium pathogen on the photosynthetic apparatus of plants.

Keywords: wheat, X-rays, photosynthetic pigments, hydrogen peroxide, Fusarium, Mucor, Aspergillus.

References:

1. M. Hassine et al. Screening of the effect of mutation breeding on biotic stress tolerance and quality traits of durum wheat. Gesunde Pflanzen 75 (2023) 837. https://doi.org/10.1007/s10343-022-00750-y

2. J. Wang et al. Ionizing radiation: Effective physical agents for economic crop seed priming and the underlying physiological mechanisms. Int. J. Mol. Sci. 23 (2022) 15212. https://doi.org/10.3390/ijms232315212

3. D. Kiani et al. Application of gamma irradiation on morphological, biochemical, and molecular aspects of wheat (Triticum aestivum L.) under different seed moisture contents. Sci. Rep. 12 (2022) 11082. https://doi.org/10.1038/s41598-022-14949-6

4. V.V. Zhuk, O.M. Mikheev, L.G. Ovsyannikova. Effect of X-ray irradiation of pea seeds on plant resistance to UV-C. Nucl. Phys. At. Energy 26 (2025) 256. (Ukr) https://doi.org/10.15407/jnpae2025.03.256

5. H. Kashtoh, M.F. Rabbee, K.-H. Baek. New insights into plant signaling mechanisms in biotic and abiotic stress. Plants 14(13) (2025) 1953. https://doi.org/10.3390/plants14131953

6. S. Mishra et al. Complexity of responses to ionizing radiation in plants, and the impact on interacting biotic factors. Sci. Total. Environ. 924 (2024) 17156. https://doi.org/10.1016/j.scitotenv.2024.171567

7. H.K. Lichtenthaler. Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes. Methods Enzymol. 148 (1987) 350. https://doi.org/10.1016/0076-6879(87)48036-1

8. L.-M. Chen, C.-H. Kao. Effect of excess copper on rice leaves: evidence for involvement of lipid peroxidation. Bot. Bull. Acad. Sin. 40 (1999) 283. https://ejournal.sinica.edu.tw/bbas/content/1999/4/bot404-05.html

9. Yu.V. Shylina, O.S. Molozhava, M.I. Hushcha. Methodological Guidelines for Practical Classes in the Course "Phytoimmunology". O.P. Dmytriiev (Ed.) (Kyiv: Kondor, 2019) 40 p. (Ukr) Book

10. M. Kamran, P. Burdiak, S. Karpiński. Crosstalk between abiotic and biotic stresses responses and the role of chloroplast retrograde signaling in the cross-tolerance phenomena in plants. Cells 14(3) (2025) 176. https://doi.org/10.3390/cells14030176

11. N.A. Zulkifli et al. Advances in irradiation technology for plant resistance: A review. Agric. Rev. 45(1) (2024) 25. https://doi.org/10.18805/ag.RF-284

12. D. Legland et al. Synchrotron based X-ray microtomography reveals cellular morphological features of developing wheat grain. Appl. Sci. 12(7) (2022) 3454. https://doi.org/10.3390/app12073454

13. S. Cheng et al. Plant chloroplast stress response: insights from mass spectrometry metabolites analysis. Front. Plant Sci. 16 (2025) 1549156. https://doi.org/10.3389/fpls.2025.1549156

14. Z. Katanić et al. Photosynthetic efficiency in flag leaves and ears of winter wheat during fusarium head blight infection. Agronomy 11(12) (2021) 2415. https://doi.org/10.3390/agronomy11122415

15. K. Sunic et al. Fusarium head blight infection induced responses of six winter wheat varieties in ascorbate-glutathione pathway, photosynthetic efficiency and stress hormones. Plants 12 (2023) 3720. https://doi.org/10.3390/plants12213720

16. F. Rocher et al. Unravelling ecophysiological and molecular adjustments in the photosynthesis-respiration balance during Fusarium graminearum infection in wheat spikes. Physiol. Plant. 177(2) (2025) e70150. https://doi.org/10.1111/ppl.70150

17. J. Chrpová et al. Potential role and involvement of antioxidants and other secondary metabolites of wheat in the infection process and resistance to Fusarium spp. Agronomy 11 (2021) 2235. https://doi.org/10.3390/agronomy11112235

18. K.O. Karpenko, T.O. Rozhkova, V.A. Vlasenko. Black point and fusarium of winter wheat seeds (literature review). Myronivskyi Visnyk 1 (2015) 170. (Ukr) Article

19. T.O. Rozhkova. Harmfulness of Fusarium sp. from mycobiota of winter wheat seeds. Bulletin of Sumy National Agrarian University. The series: Agronomy and Biology 47(1) (2022) 119. (Ukr) https://doi.org/10.32845/agrobio.2022.1.16

20. D.M. Ostrovskiy, V.M. Zotsenko, V.A. Gryshko. Microscopic fungi of wheat grain in the Polissya zone. Ukr. J. Vet. Agric. Sci. 6(2) (2023) 19. https://doi.org/10.32718/ujvas6-2.04

21. M. Shiju. A review on the effect of fungi on the wheat grain under post harvest storage ecology. Food Environ. Saf. J. 9(2) (2010) 87. https://fens.usv.ro/index.php/FENS/article/view/414

22. C. Deligeorgakis et al. Fungal and toxin contaminants in cereal grains and flours: Systematic review and meta-analysis. Foods 12 (2023) 4328. https://doi.org/10.3390/foods12234328

23. Y. Li et al. Effect of UV-C irradiation treatment on mycotoxins production in Fusarium species inoculated wheat seeds during wheat germination. Food Chem. 467 (2025) 142369. https://doi.org/10.1016/j.foodchem.2024.142369

24. R. Abdi et al. Surface disinfection of wheat kernels using gas phase hydroxyl-radical processes: Effect on germination characteristics, microbial load, and functional properties. J. Food Sci. 89(2) (2024) 1154. https://doi.org/10.1111/1750-3841.16883

25. Á. Iglesias-Ganado et al. Improvement of wheat and barley cultivation through seed priming with UV, ozone, and nutripriming (Fe, Zn, and B). Appl. Sci. 15 (2025) 9988. https://doi.org/10.3390/app15189988

26. S. Paulikienė, R. Žvirdauskienė. Evaluation of hydrothermal treatment of winter wheat grain with ozonated water. Plants 12 (2023) 3267. https://doi.org/10.3390/plants12183267

27. M.J. Hong et al. Biological effect of gamma rays according to exposure time on germination and plant growth in wheat. Appl. Sci. 12 (2022) 3208. https://doi.org/10.3390/app12063208