Innate resistance linked to non-enzymatic biochemical alteration of rice plants in response to Pyricularia oryzae
DOI:
https://doi.org/10.61308/LCVB8867Keywords:
rice blast, reactive oxygen species (ROS), antioxidants, flavonoid, disease incidence (%), principal component analysis (PCA)Abstract
Blast disease of rice caused by the fungus Pyricularia oryzae Cavara is one of the most destructive diseases, which causes about 10% to 30% yield loss. Utilization of innate host resistance has been the best way to manage the disease, for which understanding the innate immunity of our popular rice genotypes is necessary. To measure non-enzymatic biochemical alterations of rice genotypes against P. oryzae, an experiment was conducted and repeated once in the next year following a factorial completely randomized design at Plant Protection and Plant Breeding laboratory of Agrotechnology Discipline of Khulna University. BRRI dhan74, BRRI dhan33 and BRRI dhan75 along with IR 64 (resistant check line) showed minimum disease incidence (%) and maximum synthesis of total flavonoids, antioxidants, protein and sugar. These genotypes also maintained a balanced ROS (H2O2; O2-) production at later disease developmental stages (96 and 120 HAI). Pearson correlation revealed that H2O2 and O2- were positively, whereas antioxidant, flavonoid, protein and sugar was negatively associated with disease incidence. Principal component analysis (PCA) showed 91.7% total variability and indicated that total antioxidant, flavonoid, protein, sugar and H2O2 contributed more to the variation. Notably, BRRI dhan74, BRRI dhan33 and BRRI dhan75 sustained higher synthesis levels of resistance-related non-enzymatic compounds with lower disease incidence indicating a robust defense response against P. oryzae.
References
Agati, G., Azzarello, E., Pollastri, S. & Tattini, M. (2012). Flavonoids as antioxidants in plants: Location and functional significance. Plant Science, 196, 67 - 76. https://doi.org/10.1016/j.plantsci.2012.07.014. DOI: https://doi.org/10.1016/j.plantsci.2012.07.014
Ahmed, D., Khan, M. M. & Saeed, R. (2015). Comparative analysis of phenolics, flavonoids, and antioxidant and antibacterial potential of methanolic, hexanic and aqueous extracts from Adiantum caudatum leaves. Antioxidants, 4(2), 394 - 409. https://doi.org/10.3390/antiox4020394. DOI: https://doi.org/10.3390/antiox4020394
Ahamed, S. & Jahiruddin, M. (2018). Fertilizer Recommendation Guide - 2018. Bangladesh Agricultural Research Council (BARC), 223.
Ashfaq, B., Arshad, H. M., Atiq, M., Yousaf, S., Saleem, K. & Arshad, A. (2021). Biochemical profiling of resistant phenotypes against Bipolaris oryzae causing brown spot disease in rice. Frontiers in Agronomy, 3, 675895. https://doi.org/10.3389/fagro.2021.675895. DOI: https://doi.org/10.3389/fagro.2021.675895
Asibi, A. E., Chai, Q. & Coulter, J. A. (2019). Rice blast: A disease with implications for global food security. Agronomy, 9(8), 451. https://doi.org/10.3390/agronomy9080451. DOI: https://doi.org/10.3390/agronomy9080451
Biswas, S. K., Srivastava, K. D., Aggarwal, R. Praveen, S. & Singh, D. V. (2003). Biochemical changes in wheat induced by Chaetomium globosum against spot blotch pathogen. Indian Phytopathology, 56, 374 - 379.
Bradford, M. N. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem., 72(1-2), 248 - 254. https://doi.org/10.1016/0003-2697(76)90527-3. DOI: https://doi.org/10.1016/0003-2697(76)90527-3
Carvalho, D., Anastacio, Q. & Luciana, M. (2006). Proteins and isozymes electrophoresis in seeds of Desti (Leguminosae caesalpinioidea) artificially aged. Revista Árvore, 30, 19 - 21. doi: 10.1590/S0100-67622006000100003. DOI: https://doi.org/10.1590/S0100-67622006000100003
Chhabra, R., Kaur, N. & Bala, A. (2022). Biochemical and anatomical characteristics of basmati and non-basmati rice (Oryza sativa L.) for resistance to foot rot. Bangladesh Journal of Botany, 51(1), 29 - 36. https://doi.org/10.3329/bjb.v51i1.58817. DOI: https://doi.org/10.3329/bjb.v51i1.58817
Dean, R., Van Kan, J. a. L., Pretorius, Z. A., Hammond‐kosack, K. E., Di Pietro, A., Spanu, P. D., Rudd, J. J., Dickman, M., Kahmann, R., Ellis, J. & Foster, G. D. (2012). The Top 10 fungal pathogens in molecular plant pathology. Molecular Plant Pathology, 13(4), 414 - 430. https://doi.org/10.1111/j.1364-3703.2011.00783.x. DOI: https://doi.org/10.1111/j.1364-3703.2011.00783.x
Debona, D., Rodrigues, F. Á., Rios, J. A. & Nascimento, K. J. T. (2012). Biochemical changes in the leaves of wheat plants infected by Pyricularia oryzae. Phytopathology, 102(12), 1121 - 1129. https://doi.org/10.1094/phyto-06-12-0125-r. DOI: https://doi.org/10.1094/PHYTO-06-12-0125-R
Di Meo, S., Reed, T. T., Venditti, P. & Victor, V. M. (2016). Harmful and beneficial role of ROS. Oxidative Medicine and Cellular Longevity, 2016(1), 7909186. https://doi.org/10.1155/2016/7909186. DOI: https://doi.org/10.1155/2016/7909186
Dubois, M., Gilles, K., Hamilton, J. K., Rebers, P. A. & Smith, F. (1951). A colorimetric method for the determination of sugars. Nature, 168(4265), 167. https://doi.org/10.1038/168167a0. DOI: https://doi.org/10.1038/168167a0
Fink, W., Liefland, M. & Mendgen, K. (1988). Chitinases and β-1,3-Glucanases in the apoplastic compartment of oat leaves (Avena sativa L.). Plant Physiology, 88(2), 270 - 275. https://doi.org/10.1104/pp.88.2.270. DOI: https://doi.org/10.1104/pp.88.2.270
Giberti, S., Bertea, C. M., Narayana, R., Maffei, M. E. & Forlani, G. (2011). Two phenylalanine ammonia lyase isoforms are involved in the elicitor-induced response of rice to the fungal pathogen Magnaporthe oryzae. Journal of Plant Physiology, 169(3), 249 - 254. https://doi.org/10.1016/j.jplph.2011.10.008. DOI: https://doi.org/10.1016/j.jplph.2011.10.008
Gill, M. B., Zeng, F., Shabala, L., Zhang, G., Yu, M., Demidchik, V., Shabala, S. & Zhou, M. (2019). Identification of QTL related to ROS formation under hypoxia and their association with waterlogging and salt tolerance in barley. International Journal of Molecular Sciences, 20(3), 699. https://doi.org/10.3390/ijms20030699. DOI: https://doi.org/10.3390/ijms20030699
Gupta, D. R., Khanom, S., Rohman, M. M., Hasanuzzaman, M., Surovy, M. Z., Mahmud, N. U., Islam, M. R., Shawon, A. R., Rahman, M., Abd-Elsalam, K. A. & Islam, T. (2021). Hydrogen peroxide detoxifying enzymes show different activity patterns in host and non-host plant interactions with Magnaporthe oryzae - Triticum pathotype. Physiology and Molecular Biology of Plants, 27(9), 2127 - 2139. https://doi.org/10.1007/s12298-021-01057-4. DOI: https://doi.org/10.1007/s12298-021-01057-4
Høj, P. B., Hartman, D. J., Morrice, N. A., Doan, D. N. P. & Fincher, G. B. (1989). Purification of (1→3)-β-glucan endohydrolase isoenzyme II from germinated barley and determination of its primary structure from a cDNA clone. Plant Molecular Biology, 13(1), 31 - 42. https://doi.org/10.1007/bf00027333. DOI: https://doi.org/10.1007/BF00027333
Jiang, L., Wu, P., Yang, L., Liu, C., Guo, P., Wang, H., Wang, S., Xu, F., Zhuang, Q., Tong, X., Liu, P. & Luo, L. (2021). Transcriptomics and metabolomics reveal the induction of flavonoid biosynthesis pathway in the interaction of Stylosanthes-Colletotrichum gloeosporioides. Genomics, 113(4), 2702 - 2716. https://doi.org/10.1016/j.ygeno.2021.06.004. DOI: https://doi.org/10.1016/j.ygeno.2021.06.004
Khan, M. A. I., Sen, P. P., Bhuiyan, R., Kabir, E., Chowdhury, A. K., Fukuta, Y., Ali, A. & Latif, M. A. (2014). Phenotypic screening and molecular analysis of blast resistance in fragrant rice for marker assisted selection. Comptes Rendus Biologies, 337(5), 318 - 324. https://doi.org/10.1016/j.crvi.2014.02.007. DOI: https://doi.org/10.1016/j.crvi.2014.02.007
Kumawat, G. L., Biswas, S. K. & Srivastava, S. S. L. (2008). Biochemical evidence of defence response in plant induced by bio-agents against brown leaf spot pathogen. Indian Phytopathology, 61(2), 197 - 203.
Laha, G. S., Singh, R. & Ladhalakshmi, D. (2017). Importance and Management of Rice Diseases: A Global Perspective. In: Chauhan, B., Jabran, K., Mahajan, G. (eds) Rice Production Worldwide. Springer, Cham. 330 - 360. https://doi.org/10.1007/978-3-319-47516-5_13. DOI: https://doi.org/10.1007/978-3-319-47516-5_13
Laxa, M., Liebthal, M., Telman, W., Chibani, K. & Dietz, K. (2019). The role of the plant antioxidant system in drought tolerance. Antioxidants, 8(4), 94. https://doi.org/10.3390/antiox8040094. DOI: https://doi.org/10.3390/antiox8040094
Long, L., Liu, J., Gao, Y., Xu, F., Zhao, J., Li, B. & Gao, W. (2019). Flavonoid accumulation in spontaneous cotton mutant results in red coloration and enhanced disease resistance. Plant Physiology and Biochemistry, 143, 40 - 49. https://doi.org/10.1016/j.plaphy.2019.08.021. DOI: https://doi.org/10.1016/j.plaphy.2019.08.021
Mir, S. A. (2014). Optimized pyrogallol based superoxide scavenging assays for testing antioxidants. International Journal of PharmTech Research., 7, 266 – 274.
Mittler, R. (2016). ROS are good. Trends in Plant Science, 22(1), 11 - 19. https://doi.org/10.1016/j.tplants.2016.08.002. DOI: https://doi.org/10.1016/j.tplants.2016.08.002
Morkunas, I. & Ratajczak, L. (2014). The role of sugar signaling in plant defense responses against fungal pathogens. Acta Physiologiae Plantarum, 36(7), 1607 - 1619. https://doi.org/10.1007/s11738-014-1559-z. DOI: https://doi.org/10.1007/s11738-014-1559-z
Nasser, W., De Tapia, M. & Burkard, G. (1990). Maize pathogenesis-related proteins: characterization and cellular distribution of 1,3-β-glucanases and chitinases induced by brome mosaic virus infection or mercuric chloride treatment. Physiological and Molecular Plant Pathology, 36(1), 1 - 14. https://doi.org/10.1016/0885-5765(90)90087-e. DOI: https://doi.org/10.1016/0885-5765(90)90087-E
Nath, M., Bhatt, D., Bhatt, M. D., Prasad, R. & Tuteja, N. (2018). Microbe-Mediated enhancement of nitrogen and phosphorus content for crop improvement. In: Elsevier eBooks, 293 - 304. https://doi.org/10.1016/b978-0-444-63987-5.00014-1. DOI: https://doi.org/10.1016/B978-0-444-63987-5.00014-1
Poudel, A., Navathe, S., Chand, R., Mishra, V. K., Singh, P. K. & Joshi, A. K. (2019). Hydrogen peroxide prompted lignification affects pathogenicity of hemi-biotrophic pathogen Bipolaris sorokiniana to wheat. The Plant Pathology Journal, 35(4), 287 - 300. https://doi.org/10.5423/ppj.oa.09.2018.0180. DOI: https://doi.org/10.5423/PPJ.OA.09.2018.0180
Prieto, P., Pineda, M. & Aguilar, M. (1999). Spectrophotometric quantitation of antioxidant capacity through the formation of a phosphomolybdenum complex: Specific application to the determination of vitamin E. Analytical Biochemistry, 269(2), 337 - 341. https://doi.org/10.1006/abio.1999.4019. DOI: https://doi.org/10.1006/abio.1999.4019
Sahu, P. K., Sao, R., Choudhary, D. K., Thada, A., Kumar, V., Mondal, S., Das, B. K., Jankuloski, L. & Sharma, D. (2022). Advancement in the breeding, biotechnological and genomic tools towards development of durable genetic resistance against the rice blast disease. Plants, 11(18), 2386. https://doi.org/10.3390/plants11182386. DOI: https://doi.org/10.3390/plants11182386
Samal, P. & Babu, S. (2018). The shape of rice agriculture towards 2050. 2018 Conference, July 28-August 2, 2018, Vancouver, British Columbia. https://doi.org/10.22004/ag.econ.277550.
Sharma, T. R., Rai, A. K., Gupta, S. K., Vijayan, J., Devanna, B. N. & Ray, S. (2012). Rice blast management through host-plant resistance: Retrospect and prospects. Agricultural Research, 1(1), 37 - 52. https://doi.org/10.1007/s40003-011-0003-5. DOI: https://doi.org/10.1007/s40003-011-0003-5
Shetty, N. P., Mehrabi, R., Lütken, H., Haldrup, A., Kema, G. H. J., Collinge, D. B. & Jørgensen, H. J. L. (2007). Role of hydrogen peroxide during the interaction between the hemibiotrophic fungal pathogen Septoria tritici and wheat. New Phytologist, 174(3), 637 - 647. https://doi.org/10.1111/j.1469-8137.2007.02026.x. DOI: https://doi.org/10.1111/j.1469-8137.2007.02026.x
Simkhada, K. & Thapa, R. (2022). Rice Blast, a major threat to the rice production and its various management techniques. Turkish Journal of Agriculture - Food Science and Technology, 10(2), 147 - 157. https://doi.org/10.24925/turjaf.v10i2.147-157.4548. DOI: https://doi.org/10.24925/turjaf.v10i2.147-157.4548
Singla, P., Bhardwaj, R. D., Kaur, S. & Kaur, J. (2019). Antioxidant potential of barley genotypes inoculated with five different pathotypes of Puccinia striiformis f. sp. hordei. Physiology and Molecular Biology of Plants, 25(1), 145 - 157. https://doi.org/10.1007/s12298-018-0614-4. DOI: https://doi.org/10.1007/s12298-018-0614-4
Velikova, V., Yordanov, I. & Edreva, A. (2000). Oxidative stress and some antioxidant systems in acid rain-treated bean plants. Plant Science, 151(1), 59 - 66. https://doi.org/10.1016/s0168-9452(99)00197-1. DOI: https://doi.org/10.1016/S0168-9452(99)00197-1
Younas, M. U., Wang, G., Du, H., Zhang, Y., Ahmad, I., Rajput, N., Li, M., Feng, Z., Hu, K., Khan, N. U., Xie, W., Qasim, M., Chen, Z. & Zuo, S. (2023). Approaches to reduce rice blast disease using knowledge from host resistance and pathogen pathogenicity. International Journal of Molecular Sciences, 24(5), 4985. https://doi.org/10.3390/ijms24054985. DOI: https://doi.org/10.3390/ijms24054985
Zandalinas, S. I., Fritschi, F. B. & Mittler, R. (2019). Signal transduction networks during stress combination. Journal of Experimental Botany, 71(5), 1734 - 1741. https://doi.org/10.1093/jxb/erz486. DOI: https://doi.org/10.1093/jxb/erz486
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