Ultraviolet-C irradiation of wheat grains induces seedling resistance to leaf rust and powdery mildew disease

Published: 19 October 2023
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Authors

  • Marian Thabet Department of Plant Pathology, Faculty of Agriculture, Ain Shams University, Cairo, Egypt.
  • Mohamed A. Abou-Zeid m.abouzeid@arc.sci.eg Wheat Diseases Research Department, Agricultural Research Center, Plant Pathology Research Institute, Giza, Egypt.
  • Fatmah A. Safhi Department of Biology, College of Science, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
  • Khairiah M. Alwutayd Department of Biology, College of Science, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
  • Walaa Khalifa Department of Plant Pathology, Faculty of Agriculture, Ain Shams University, Cairo, Egypt.

Ultraviolet-C (UV-C) irradiation of grains activated the antioxidant system and wheat seedlings’ resistance to leaf rust and powdery mildew disease under greenhouse conditions. Two wheat cultivars (Gemmeiza-12 and Sids-1) with dry and germinated grains were treated with UV-C at three exposure times (5, 10, and 15 minutes). The results indicated that the percentages of disease severity and infection type for leaf rust and powdery mildew on wheat seedlings were significantly reduced when exposed to UVC at all exposure times compared to the untreated control. The most effective treatments for both cultivars were obtained in seedlings grown from germinated grains treated with UV-C for 10 minutes. Furthermore, UV-C irradiation treatments improved plant resistance to infection by activating certain defense genes, thereby increasing the production of resistance compounds that support defense mechanisms against pathogens. Our results demonstrated that UV-C for 10 minutes can induce resistance in wheat seedlings while also increasing total chlorophyll, total phenolic compounds, phenylalanine ammonia-lyase, and peroxidase activity. In addition, phenylalanine ammonia-lyase mRNA expression levels were significantly increased in seedlings growing from germinated grains treated with UV-C for 10 minutes, as compared to both infected and uninfected controls. These findings demonstrate the potential for additional UV-C radiation treatments to enhance disease resistance.

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Aarrouf J, Urban L, 2020. Flashes of UVC light: an innovative method for stimulating plant defences. PLoS One 15:e0235918. DOI: https://doi.org/10.1371/journal.pone.0235918
Aboul Fotouh MM, Maha HM, Moawad FG, Tag El-Din MA, Srour HAM, 2019. Enhancement of resistance against Rhizoctonia solani by glycine betaine and UV-C radiation in green bean (Phaseolus vulgaris L.). Arab Univ. J. Agric. Sci. 27:1829-41. DOI: https://doi.org/10.21608/ajs.2019.15060.1063
Arab SA, El Shal MH, Eissa ST, Abou-Zeid MA, 2021. Assessment of some wheat genotypes for resistance to some diseases and their effect on yield and yield components. PCBMB. 22:73-8.
Araujo SS, Paparella S, Dondi D, Bentivoglio A, Carbonera D, Balestrazzi A, 2016. Physical methods for seed invigoration: Advents and challenges in seed technology. Front. Plant Sci. 7:646. DOI: https://doi.org/10.3389/fpls.2016.00646
Atia AM, El-Khateeb EA, El-Maksoud RMA, Abou-Zeid MA, Salah A, Abdel-Hamid AME, 2021. Mining of leaf rust resistance genes content in Egyptian bread wheat collection. Plants 10:1378. DOI: https://doi.org/10.3390/plants10071378
Biles CL, Martyn RD, 1993. Peroxidase, polyphenoloxidase and shikimate dehydrogenase isozymes in relation to tissue type, maturity and pathogen induction of watermelon seedling. Plant Physiol. Biochem. 31:499-506.
Brown JE, Lu TY, Stevens C, Khan VA, Lu JY, Wilson CL, Collins DJ, Wilson MA, Igwegbe ECK, Chalutz E, Droby S, 2001. The effect of low dose ultraviolet light-C seed treatment on induced resistance in cabbage to black rot (Xanthomonas campestris pv. campestris). Crop Protect. 20:873-83. DOI: https://doi.org/10.1016/S0261-2194(01)00037-0
Castronuovo D, Sofo A, Lovelli S, Candido V, Scopa A, 2017. Effects of UV-C radiation on common dandelion and purple coneflower: first results. Int. J. Plant Biol. 8:7255. DOI: https://doi.org/10.4081/pb.2017.7255
Chandrasekaran M, Belachew ST, Yoon E, Chun SC, 2017. Expression of β-1,3-glucanase (GLU) and phenylalanine ammonia-lyase (PAL) genes and their enzymes in tomato plants induced after treatment with Bacillus subtilis CBR05 against Xanthomonas campestris pv. vesicatoria. J. Gen. Plant Pathol. 83:7-13. DOI: https://doi.org/10.1007/s10327-016-0692-5
Conrath U, 2011. Molecular aspects of defence priming. Trends Plant Sci. 16:524-31. DOI: https://doi.org/10.1016/j.tplants.2011.06.004
Dixon RA, Achnine L, Kota P, Liu CJ, Reddy MSS, Lang LJ, 2002. The phenylpropanoid pathway and the plant defence: a genomic perspective. Mol. Plant Pathol. 3:371-90. DOI: https://doi.org/10.1046/j.1364-3703.2002.00131.x
Draz IS, Esmail SM, Abou-Zeid MA, Essa TA, 2019. Powdery mildew susceptibility of spring wheat cultivars as a major constraint on grain yield. Ann. Agric. Sci. 64:39-45. DOI: https://doi.org/10.1016/j.aoas.2019.05.007
Duncan BD, 1955. Multiple ranges and multiple F test. Biometrics 11:1-42. DOI: https://doi.org/10.2307/3001478
El-Orabey WM, Nagwa I, El-Malik A, Ashmawy MA, Abou-Zeid MA, 2017. Reduction of bread wheat grain yield caused by leaf rust infection in common wheat varieties. Minufiya J. Plant Prot. 2:71-81. DOI: https://doi.org/10.21608/mjapam.2017.125383
El-Shamy MM, Emara HM, Mohamed ME, 2016. Virulence analysis of wheat powdery mildew (Blumeria graminis f. sp. tritici) and effective genes in Middle Delta, Egypt. Plant Dis. 100:1927-30. DOI: https://doi.org/10.1094/PDIS-01-16-0130-RE
El-Shamy MM, Sallam MEA, Awad HMF, 2012. Powdery mildew infection on some Egyptian bread wheat cultivars in relation to environmental conditions. J. Plant Prot. Path. Mansoura Univ. 3:363-72. DOI: https://doi.org/10.21608/jppp.2012.83777
Elshafei AA, El-Orabey WM, Fathallah FB, Esmail RM, Abou-Zeid MA, 2021. Phenotyping and validation of molecular markers associated with rust resistance genes in wheat cultivars in Egypt. Mol. Biol. Rep. 49:1903-15. DOI: https://doi.org/10.1007/s11033-021-07002-8
Falconí CE, Yánez‐Mendizábal V, 2018. Efficacy of UV‐C radiation to reduce seedborne anthracnose (colletotrichum Acutatum) from andean lupin (lupinus Mutabilis). Plant Pathol. 67:831-8. DOI: https://doi.org/10.1111/ppa.12793
Gao H, Niu J, Li S, 2018. Impact of wheat powdery mildew on grain yield & quality and its prevention and control methods. Ame. J. Agric. Forestry 6:141-7. DOI: https://doi.org/10.11648/j.ajaf.20180605.14
Glazenner JA, 1982. Accumulation of phenolic compounds in cells and formation of lignin-like polymers in cell walls of young tomato fruits after inoculation with Botrytis cinerea. Physiol. Plant Pathol. 20:11-25. DOI: https://doi.org/10.1016/0048-4059(82)90019-4
Gogoi R, Singh DV, Srivastava KD, 2001. Phenols as a biochemical basis of resistance in wheat against karnal bunt. Plant Pathol. 50:470-6. DOI: https://doi.org/10.1046/j.1365-3059.2001.00583.x
Govindaraj M, Masilamani P, Albert AV, Bhaskaran M, 2017. Effect of physical seed treatment on yield and quality of crops: a review. Agric. Rev. 38:1-14. DOI: https://doi.org/10.18805/ag.v38i03.8977
Hammerschmidt R, 2005. Phenols and plant-pathogeninteractions: the saga continues. Physiol. Mol. Plant P. 66:77-8. DOI: https://doi.org/10.1016/j.pmpp.2005.08.001
Hernandez-Aguilar C, Dominguez-Pacheco A, Tenango MP, Valderrama-Bravo C, Hernández MS, Cruz-Orea A, Ordonez-Miranda J, 2021. Characterization of bean seeds, germination, and phenolic compounds of seedlings by UV-C radiation. J. Plant. Growth. Regul. 40:642-55. DOI: https://doi.org/10.1007/s00344-020-10125-0
Huerta-Espino J, Singh RP, German S, McCallum BD, Park RF, Chen WQ, Bhardwaj SC, Goyeau H, 2011. Global status of wheat leaf rust caused by Puccinia triticina. Euphytica 179:143-60. DOI: https://doi.org/10.1007/s10681-011-0361-x
Kacharava N, Chanishvili SS, Badridze GS, Chkhubianishvili E, Janukashvili N, 2009. Effect of seed irradiation on the content of antioxidants in leaves of kidney bean, cabbage and beet cultivars. Aust. J. Crop Sci. 3:137-45.
Khan MH, Asifa B, Zahoor AD, Syed MR, 2013. Status and strategies in breeding for rust resistance in wheat. Agric. Sci. 4:292-301. DOI: https://doi.org/10.4236/as.2013.46042
Kobayashi M, Kanto T, Fujikawa T, Yamada M, Ishiwata M, Satou M, Hisamatsu T, 2013. Supplemental UV radiation controls rose powdery mildew disease under the greenhouse conditions. Environ. Control. Biol. 51:157-63. DOI: https://doi.org/10.2525/ecb.51.157
Korotkova I, Semenov A, Sakhno T, 2020. The ultraviolet radiation: disinfection and stimulation processes. Lambert: Academic Publishing, Saarbruecken, Saarland, Germany.
Li H, Wang X, Song F, Wu C, Wu X, Zhang N, Zhon Y, Zhang X, 2011. Response to powdery mildew and detection of resistance genes in wheat cultivars from China. Acta Agron. Sin. 37:943-54. DOI: https://doi.org/10.3724/SP.J.1006.2011.00943
Li X, He Y, Xie C, Zu Y, Zhan F, Mei X, Xia Y, Li Y, 2018. Effects of UV-B radiation on the infectivity of Magnaporthe oryzae and rice disease resistant physiology in Yuanyang terraces. Photoch. Photobio. Sci. 17:8-17. DOI: https://doi.org/10.1039/c7pp00139h
Liu F, Wei F, Wang L, Liu H, Zhu X, Liang Y, 2010. Riboflavin activates defense responses in tobacco and induces resistance against Phytophthora parasitica and Ralstonia solanacearum. Physiol. Mol. Plant P. 74:330-6. DOI: https://doi.org/10.1016/j.pmpp.2010.05.002
Long DL, Roelfs AP, Leonard KJ, Roberts JJ, 1994. Virulence and diversity of Puccinia recondite f.sp. tritici in the United States in 1992. Plant Dis. 78:901-6. DOI: https://doi.org/10.1094/PD-78-0901
Ma P, Xu H, Luo Q, Qie Y, Zhou Y, Xu Y, Han H, Li L, An D, 2014. Inheritance and genetic mapping of a gene for seedling resistance to powdery mildew in wheat line X39862. Euphytica 200:149-57. DOI: https://doi.org/10.1007/s10681-014-1178-1
Mariz-Ponte N, Mendes RJ, Sario S, Melo P, Santos C, 2018. Moderate UV-A supplementation benefits tomato seed and seedling invigoration: a contribution to the use of UV in seed technology. Sci. Hortic. 235:357-66. DOI: https://doi.org/10.1016/j.scienta.2018.03.025
McLay ER, Pontaroli AC, Wargent JJ, 2020. UV-B induced flavonoids contribute to reduced biotrophic disease susceptibility in lettuce seedlings. Front. Plant Sci. 11:594681. DOI: https://doi.org/10.3389/fpls.2020.594681
Middleton EM, Teramura AH, 1993. The role of flavonol glycosides and carotenoids in protecting soybean from ultraviolet-B damage. Plant Physiol. 103:741-52. DOI: https://doi.org/10.1104/pp.103.3.741
Monje OA, Bugbee B, 1992. Inherent limitation of nondestructive chlorophyll meters. A comparison of two types of meters. HortScience 27:69-71. DOI: https://doi.org/10.21273/HORTSCI.27.1.69
Najeeb KMA, Thabet M, Negm SS, EL-Deeb SH, 2019. Monitoring of Puccinia triticina Erikss. physiologic races and effectiveness of Lr-genes in Egyptian wheat during 2014-2016 growing seasons. Int. J. Agric. Technol. 15:35-54.
Novichonok EV, Novichonok AO, Kurbatova JA, Markovskaya EF, 2016. Use of the atLEAF plus chlorophyll meter for a nondestructive estimate of chlorophyll content. Photosynthetica 54:130-7. DOI: https://doi.org/10.1007/s11099-015-0172-8
Omar HS, Al Mutery A, Osman NH, Reyad NEA, Abou-Zeid MA, 2021. Genetic diversity, antifungal evaluation and molecular docking studies of Cu-chitosan nanoparticles as prospective stem rust inhibitor candidates among some Egyptian wheat genotypes. PLoS One 16:e0257959. DOI: https://doi.org/10.1371/journal.pone.0257959
Ouhibi C, Attia H, Rebah F, Msilini N, Chebbi M, Aarrouf J, Urban L, Lachaal M, 2014. Salt stress mitigation by seed priming with UV-C in lettuce plants: growth, antioxidant activity and phenolic compounds. Plant Physiol. Biochem. 83:126-33. DOI: https://doi.org/10.1016/j.plaphy.2014.07.019
Peterson RF, Campbell AB, Hannah AE, 1948. A Diagrammatic scale for estimating rust intensity on leaves and stem of cereals. Can. J. Res. 26c:496-500. DOI: https://doi.org/10.1139/cjr48c-033
Pombo MA, Rosli HG, Martínez GA, Civello PM, 2010. UV-C treatment affects the expression and activity of defense genes in strawberry fruit (Fragaria × ananassa, Duch.). Postharvest Biol. Tec. 59:94-102. DOI: https://doi.org/10.1016/j.postharvbio.2010.08.003
Rao MV, Paliyath G, Ormrod DP, 1996. Ultraviolet ‐B‐ and ozone‐induced biochemical changes in antioxidant enzymes of Arabidopsis thaliana. Plant Physiol. 110:125-36. DOI: https://doi.org/10.1104/pp.110.1.125
Rice-Evans C, Miller N, Paganga G, 1997. Antioxidant properties of phenolic compounds. Trends Plant Sci. 2:152-9. DOI: https://doi.org/10.1016/S1360-1385(97)01018-2
Rifna EJ, Ramanan KR, Mahendran R, 2019. Emerging technology applications for improving seed germination. Trends Food Sci. Tech. 86:95-108. DOI: https://doi.org/10.1016/j.tifs.2019.02.029
Rivera-Pastrana DM, Gardea AA, Yahia EM, Martınez-Tellez MA, Gonzalez-Aguilar GA, 2014. Effect of UV-C irradiation and low temperature storage on bioactive compounds, antioxidant enzymes and radical scavenging activity of papa fruit. J. Food Sci. Technol. 51:3821-9. DOI: https://doi.org/10.1007/s13197-013-0942-x
Rupiasih NN, Vidyasagar PB, 2016. Effect of UV-C radiation and hypergravity on germination, growth and content chlorophyll of wheat seedlings. AIP Conf. Proc. 1719, 030035. DOI: https://doi.org/10.1063/1.4943730
Sadeghianfar P, Nazari M, Backes G, 2019. Exposure to ultraviolet (UV-C) radiation increases germination rate of Maize (Zea maize L.) and sugar beet (Beta vulgaris) seeds. Plants 8:49. DOI: https://doi.org/10.3390/plants8020049
Scott G, Almasrahi A, Mansoorkhani FM, Ru-par M, Dickinson M, Shama G, 2019. Hormetic UV-C seed treatments for the control of tomato diseases. Plant Pathol. 68:700-7. DOI: https://doi.org/10.1111/ppa.12987
Scott G, Dickinson M, Shama G, Rupar M, 2018. A comparison of the molecular mechanisms underpinning high-intensity, pulsed polychromatic light and low-intensity UV-C hormesis in tomato fruit. Postharvest Biol. Tec. 137:46-55. DOI: https://doi.org/10.1016/j.postharvbio.2017.10.017
Semenov A, Korotkova I, Sakhno T, Marenych M, Нanhur V, Liashenko V, Kaminsky V, 2020. Effect of UV-C radiation on basic indices of growth process of winter wheat (Triticum aestivum L.) seeds in pre-sowing treatment. Acta Agric. Slov. 116:49-58. DOI: https://doi.org/10.14720/aas.2020.116.1.1563
Semenov A, Sakhno T, Hordieieva O, Sakhno Y, 2021. Pre-sowing treatment of vetch hairy seeds, viсia villosa using ultraviolet irradiation. Global J. Environ. Sci. Manag. 7:555-64.
Semenov AO, Kozhushko GM, Sakhno TV, 2017. Analysis of the role of UV radiation on the development and productivity of different cultures. Light Eng. Electricity 2:3-16. [Article in Ukrainian].
Sharma P, Jha AB, Dubey RS, Pessarakli M, 2012. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J. Bot. 2012:217037. DOI: https://doi.org/10.1155/2012/217037
Shin DH, Choi M, Kim K, Bang G, Cho M, Choi SB, 2013. HY5 regulates anthocyanin biosynthesis by inducing the transcriptional activation of the MYB75/PAP1 transcription factor in Arabidopsis. FEBS Lett. 587:1543-7. DOI: https://doi.org/10.1016/j.febslet.2013.03.037
Siddiqui A, Dawar S, Zaki MJ, Hamiid N, 2011. Role of ultraviolet (UV-C) radiation in the control of root infecting fungi on groundnut and mungbean. Pak. J. Bot. 43:2221-4.
Smith LM, 2008. Mapping of drought tolerance and leaf rust resistance in wheat. Degree Diss., Kansas State University, Manhattan, Kansas, USA.
Solecka D, Kacperska A, 2003. Phenylpropanoid deficiency affects the course of plant acclimation to cold. Physiol. Plantarum 119:253-62. DOI: https://doi.org/10.1034/j.1399-3054.2003.00181.x
Stakman EC, Stewart DM, Loegering WQ, 1962. Identification of physiologic races of Puccinia graminis var. tritici. United States Department of Agriculture, Agricultural Research Service, Washington DC, USA.
Sukthavornthum W, Bodhipadma K, Noichinda S, Phanomchai S, Deelueak U, Kachonpadungkitti Y, Leung DW, 2018. UV-C irradiation induced alterations in shoot proliferation and in vitro flowering in plantlets developed from encapsulated and non-encapsulated microshoots of Persian violet. Sci. Hortic. 233:9-13. DOI: https://doi.org/10.1016/j.scienta.2018.01.027
Swain T, Hallis WE, 1955. The phenolic constituents of Prunus domestica. I. The quantative analysis of phenolic constituent. J. Sci. Food Agr.10:63-8. DOI: https://doi.org/10.1002/jsfa.2740100110
Sztatelman O, Grzyb J, Gabrys H, Banas AK, 2015. The effect of UV-B on Arabidopsis leaves depends on light conditions after treatment. BMC Plant Biol. 15:281. DOI: https://doi.org/10.1186/s12870-015-0667-2
Tervet I, Cassel RC, 1951. The use of cyclone separation in race identification of cereal rust. Phytopathology 41:282-5.
Thabet M, Najeeb KMA, 2017. Impact of wheat leaf rust severity on grain yield losses in relation to host resistance for some Egyptian wheat cultivars. Middle East J. Agric. Res. 4:1501-9.
Thomas DT, Puthur JT, 2017. UV radiation priming: a means of amplifying the inherent potential for abiotic stress tolerance in crop plants. Environ. Exp. Bot. 138:57-66. DOI: https://doi.org/10.1016/j.envexpbot.2017.03.003
Turtoi M, 2013. Ultraviolet light treatment of fresh fruits and vegetables surface: a review. J. Agroaliment. Processes Technol. 19:325-37.
Urban L, Charles F, de Miranda MRA, Aarrouf J, 2016. Understanding the physiological effects of UV-C light and exploiting its agronomic potential before and after harvest. Plant Physiol. Biochem. 105:1-11. DOI: https://doi.org/10.1016/j.plaphy.2016.04.004
Vanhaelewyn L, Van Der Straeten D, De Coninck B, Vandenbussche F, 2020. Ultraviolet radiation from a plant perspective: the plant-microorganism context. Front. Plant Sci. 11:597642. DOI: https://doi.org/10.3389/fpls.2020.597642
Vlase L, Benedec D, Hanganu D, Madian G, Csillag I, Sevastre B, Tilea I, 2014. Evaluation of antioxidant and antimicrobial activities and phenolic profile for Hyssopus officinalis, Ocimum basilicum and Teucrium chamaedrys. Molecules 19:5490-507. DOI: https://doi.org/10.3390/molecules19055490
Wang H, Qin F, Cheng P, Ma Z, Wang H, 2018. Effects of UV-B radiation intensity and timing on epidemiological components of wheat stripe rust. J. Integr. Agr. 17:2704-13. DOI: https://doi.org/10.1016/S2095-3119(18)62020-9
Wang ZL, Li LH, He ZH, Duan XY, Zhou YL, Chen XM, Lillemo M, Singh RP, Wang H, Xia XC, 2005. Seedling and adult plant resistance to powdery mildew in Chinese bread wheat cultivars and lines. Plant Dis. 89:457-63. DOI: https://doi.org/10.1094/PD-89-0457
Windram O, Madhou P, McHattie S, Hill C, Hickman R, Cooke E, 2012. Arabidopsis defense against Botrytis cinerea: chronology and regulation deciphered by high-resolution temporal transcriptomic analysis. Plant Cell 24:3530-57. DOI: https://doi.org/10.1105/tpc.112.102046
Xu Y, Charles MT, Luo Z, Mimee B, Tong Z, Véronneau P, Roussel D, Rolland D, 2019. Ultraviolet‐C priming of strawberry leaves against subsequent Mycosphaerella fragariae infection involves the action of reactive oxygen species, plant hormones, and terpenes. Plant Cell Environ. 42:815-31. DOI: https://doi.org/10.1111/pce.13491
Yongmei H, Xiang L, Fangdong Z, Chunmei X, Yanqun Z, Yuan L, Ming Y, 2018. Resistance-related physiological response of rice leaves to the compound stress of enhanced UV-B radiation and Magnaportheoryzae. J. Plant Interact. 13:321-8. DOI: https://doi.org/10.1080/17429145.2018.1478007
Zhang RQ, Sun BX, Chen AZ, Xing LP, Feng YG, Lan CX, Chen PD, 2016. Pm55, a developmental-stage and tissue-specific powdery mildew resistance gene introgressed from Dasypyrum villosum into commom wheat. Theor. Appl. Genet. 129:1975-84. DOI: https://doi.org/10.1007/s00122-016-2753-8
Zhang Y, Bai Y, Wu G, Zou S, Chen Y, Gao C, Tang D, 2017. Simultaneous modification of three homoeologs of TaEDR1 by genome editing enhances powdery mildew resistance in wheat. Plant J. 91:714-24. DOI: https://doi.org/10.1111/tpj.13599
Zu YG, Wei XX, Yu JH, Li DW, Pang HH, Tong L, 2011. Responses in the physiology and biochemistry of Korean pine (Pinus koraiensis) under supplementary UV-B radiation. Photosynthetica 49:448-58. DOI: https://doi.org/10.1007/s11099-011-0057-4

How to Cite

Thabet, M., Abou-Zeid, M. A., Safhi, F. A., Alwutayd, K. M., & Khalifa, W. (2023). Ultraviolet-C irradiation of wheat grains induces seedling resistance to leaf rust and powdery mildew disease. Italian Journal of Agronomy, 18(3). https://doi.org/10.4081/ija.2023.2201