Evaluation of pigment types and pigment contents in different rice growth stage of Taichung Native 1 with leaf crude rice ragged stunt disease
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Published:
Feb 15, 2021
Keywords:
Rice ragged stunt virus (RRSV) Brown planthopper (Nilaparvata lugens Stål) Taichung Native 1 rice plant plant pigment contents
Main Article Content
Abstract
Rice ragged stunt disease is one of the major rice viral disease in rice cultivation process of the central and lower northern-irrigated rice field of Thailand. Rice ragged stunt virus (RRSV) infected rice plants caused physiological and pathological changes due to virus invasion and affecting the plant photosynthesis. This research aimed to evaluate the interaction of RRSV-infected period on the various pigment types and contents of standard susceptible variety Taichung Native 1 (TN 1) rice plant leaves. The experiment was 3´9 factorial in completely randomized design with 3 replications. Factor A were tested rice plant population from the sap-sucking of the brown planthopper (BPH, Nilaparvata lugens Stål) including: non-sucking, non-viruliferous, and viruliferous BPH sucking, respectively, and factor B were the period of RRSV infection in rice plants at various plant ages between 10 and 90 days. The research showed that the pigment contents from the viruliferous BPH sucked rice plant were the most decrease when compared to the non-sucking and non-viruliferous BPH sucked rice plant, respectively. The different infectious periods in tested rice plants affected the increasing contents of primary pigment, whereas the secondary pigment decreased, respectively. The interaction of infectious periods in tested rice plants to the pigment types and contents were non–significant statistical interaction (P³0.05) to chlorophyll A (Chl-A), chlorophyll B (Chl-B), total chlorophyll (TChl), carotenoid (Cx+c), and TChl/Cx+c, but significant statistical interaction (P£0.05) to Chl-A/B, and phaeophytin (P), respectively. These results demonstrated that the rice plants afforded to improve and recover after the different viral-infectious periods of vegetative growth, reproductive growth, and ripening growth stage, respectively. These research results are the important preliminary information to be used to influence of RRSV to pigment contents and plant resistant assessment due to virus-pathogenesis to biochemical processes, and a rice plant variety improving to resist the virus and insect vector disruption.
Article Details
How to Cite
Na Phatthalung, T. ., & Tangkananond, W. . (2021). Evaluation of pigment types and pigment contents in different rice growth stage of Taichung Native 1 with leaf crude rice ragged stunt disease. Khon Kaen Agriculture Journal, 49(1), 130–143. retrieved from https://li01.tci-thaijo.org/index.php/agkasetkaj/article/view/249323
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บทความวิจัย (research article)
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
References
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Na Phatthalung, T., W. Rattanakarn, and W. Tangkananond. 2017. The application of chlorophyll absorbents to enhance efficiency of Rice ragged stunt virus detection in plant sap by Dot-immunobinding assay. King Mongkut's Agricultural Journal. 35: 104-115.
Na Phatthalung, T., W. Tangkananond, and W. Rattanakarn. 2017. The efficiency of Rice ragged stunt virus detection in the brown planthoppers by dot-immunobinding assay. Thai Journal of Science and Technology. 6: 236-246.
Oelmuller, R. 2008. Photoxidative destruction of chloroplasts and its effect on nuclear gene expression and extraplastidic enzyme levels. Photochemistry and Photobiology. 49: 229-239.
Otulak-Koziel, K., E. Koziel, and B.E.L. Lockhart. 2018. Plant cell wall dynamics in compatible and incompatible potato response to infection caused by Potato virus Y (PVYNTN). International Journal of Molecular Science. 19: 1-23.
Parejarearn, A., and H. Hibino. 1985. Distribution of Rice ragged stunt virus (RSV) in infected TN1 plants. International Rice Research Notes. 10: 12.
Parejarearn, A., and H. Hibino. 1987a. Ragged stunt virus (RSV) concentration in tolerant rice. International Rice Research Notes. 12: 14.
Parejarearn, A., and H. Hibino. 1987b. Symptoms and yield reduction in tolerant varieties infected with ragged stunt virus (RSV). International Rice Research Notes. 12: 14-15.
Ronen, R., and M. Galun. 1984. Pigment extraction from lichens with dimethyl sulfoxide (DMSO) and estimation of chlorophyll degradation. Environmental and Experimental Botany. 24: 239-245.
Rungreangsri, U., N. Rungreangsri, and S. Pongjareankit. 2008. Histopathogenesis of Rice ragged stunt virus and viral evolution implication. Maejo University, Chiang Mai.
Russin, W.A., R.F. Evert, P.J. Vanderveer, T.D. Sharkey, and S.P. Briggs. 1996. Modification of a specific class of plasmodesmata and loss of sucrose export ability in the sucrose export defective1 Maize Mutant. Plant Cell. 8: 645-658.
Schommer, C., J.F. Palatnik, P. Aggarwal, A. Chetelat, P. Cubas, E.E. Farmer, U. Nath, and D. Weigel. 2008. Control of jasmonate biosynthesis and senescence by miR319 targets. PLoS Biology. 6: 1991-2001.
Shen, J., L. Song, K. Müller, Y. Hu, Y. Song, W. Yu, H. Wang, and J. Wu. 2016. Magnesium alleviates adverse effects of lead on growth, photosynthesis, and ultrastructural alterations of Torreya grandis seedlings. Frontiers in Plant Science. 7: 1-11.
Shi, B., L. Lin, S. Wang, Q. Guo, H. Zhou, L. Rong, J. Li, J. Peng, Y. Lu, H. Zheng, Y. Yang, Z. Chen, J. Zhao, T. Jiang, B. Song, J. Chen, and F. Yan. 2016. Identification and regulation of host genes related to Rice stripe virus symptom production. New Phytologist. 209: 1106-1119.
Sogawa, K. 1982. The rice brown planthopper: feeding physiology and host plant interactions. Annual Review of Entomology. 27: 49-73.
Srivastava, A., L. Agrawal, R. Raj, M. Jaidi, S.K. Raj, S. Gupta, R. Dixit, P.C. Singh, T. Tripathi, O.P. Sidhu, B.N. Singh, S. Shukla, P.S. Chauhan, and S. Kumar. 2017. Ageratum enation virus infection induces programmed cell death and alters metabolite biosynthesis in Papaver somniferum. Frontiers in Plant Science. 8: 1-15.
Sumanta, N., C. Haque, J. Nishika, and R. Suprakash. 2014. Spectrophotometric analysis of chlorophylls and carotenoids from commonly grown fern species by using various extracting solvents. Research Journal of Chemical Sciences. 4: 63-69.
Taylor, A.O., and A.S. Craig. 1971. Plants under climatic stress: II. low temperature, high light effects on chloroplast ultrastructure. Plant Physiology. 47: 719-725.
Taylor, A.O., and J.A. Rowley. 1971. Plants under climatic stress: I. low temperature, high light effects on photosynthesis. Plant Physiology. 47: 713-718.
Tromas, N., M.P. Zwart, G. Lafforgue, and S.F. Elena. 2014. Within-host spatiotemporal dynamics of plant virus infection at the cellular level. PLoS Genetics. 10: 1-14.
Vuorinen, A.L., J. Kelloniemi, and J.P. Valkonen. 2011. Why do viruses need phloem for systemic invasion of plants?. Plant Science. 181: 355-363.
Zhang, Y., X. Chen, F. Yang, L. Zhang, and W. Liu. 2016. miRNA: A novel link between Rice ragged stunt virus and Oryza sativa. Indian Journal of Microbiology. 56: 219-224.
Zhou, G., D. Xu, D. Xu, and M. Zhang. 2013. Southern rice black-streaked dwarf virus: a white-backed planthopper-transmitted Fijivirus threatening rice production in Asia. Frontiers in Microbiology. 4: 1-19.
Zhu, S., F. Gao, X. Cao, M. Chen, G. Ye, C. Wei, and Y. Li. 2005. The Rice dwarf virus P2 protein interacts with ent-kaurene oxidases in vivo, leading to reduced biosynthesis of gibberellins and rice dwarf symptoms. Plant Physiology. 139: 1935-1945.
Almasi, A., D. Apatini, K. Bóka, B. Böddi, and R. Gáborjányi. 2000. BSMV infection inhibits chlorophyll biosynthesis in barley plants. Physiological and Molecular Plant Pathology. 56: 227-233.
Almasi, A., A. Harsanyi, and R. Gaborjanyi. 2001. Photosynthetic alterations of virus infected plants. Acta Phytopathologica et Entomologica Hungarica. 36: 15-29.
Bhogale, S., A.S. Mahajan, B. Natarajan, M. Rajabhoj, H.V. Thulasiram, and A.K. Banerjee. 2014. MicroRNA156: a potential graft-transmissible microRNA that modulates plant architecture and tuberization in Solanum tuberosum ssp. andigena. Plant Physiology. 164: 1011-1027.
Cabauatan, P.Q., and K.C. Ling. 1978. A study of vein-swellings of rice plants infected with ragged stunt. International Rice Research Notes. 3: 9-10.
Chen, S., W. Li, X. Huang, B. Chen, T. Zhang, and G. Zhou. 2019. Symptoms and yield loss caused by Rice stripe mosaic virus. Virology Journal. 16: 145.
Disthaporn, S., H.D. Catling, D. Chettanachit, and M. Putta. 1985. Effect of time of infection of Rice ragged stunt virus on deepwater rice. International Journal of Tropical Plant Diseases. 3: 19-25.
Helina, S., S. Sulandari, S. Hartono, and A. Trisyono. 2018. Detection and transmission of rice stunt virus on Ciherang and Situ Bagendit varieties. Jurnal Hama dan Penyakit Tropika. 18: 169-176.
Hibino, H., N. Saleh, and M. Roecha. 1979. Reovirus-like particles associated with Rice ragged stunt diseased rice and insect vector cells. Annals of the Phytopathological Society of Japan. 45: 228-239
Huang, H.-J., Y.-Y. Bao, S.-H. Lao, X.-H. Huang, Y.-Z. Ye, J.-X. Wu, H.-J. Xu, X.-P. Zhou, and C.-X. Zhang. 2015. Rice ragged stunt virus-induced apoptosis affects virus transmission from its insect vector, the brown planthopper to the rice plant. Scientific Reports. 5: 11413.
Huang, H.-J., C.-W. Liu, Y.-F. Cai, M.-Z. Zhang, Y.-Y. Bao, and C.-X. Zhang. 2015. A salivary sheath protein essential for the interaction of the brown planthopper with rice plants. Insect Biochemistry and Molecular Biology. 66: 77-87.
Jones, J.D.G., and J.L. Dangl. 2006. The plant immune system. Nature. 444: 323-329.
Kana, R., M. Spundova, P. Ilıik, D. Lazar, K. Klem, P. Tomek, J. Naus, and O. Prasil. 2004. Effect of herbicide clomazone on photosynthetic processes in primary barley (Hordeum vulgare L.) leaves. Pesticide Biochemistry and Physiology. 78: 161-170.
Inderjit, S.K. 2006. Phytotoxicity of selected herbicides to mung bean (Phaseolus aureus Roxb.). Environmental and Experimental Botany. 55: 41-48.
Ling, K.C. 1977. Rice ragged stunt disease. International Rice Research Notes. 2: 6-7.
Liu, H., X. Wang, K. Ren, K. Li, M. Wei, W. Wang, and X. Sheng. 2017. Light deprivation-induced inhibition of chloroplast biogenesis does not arrest embryo morphogenesis but strongly reduces the accumulation of storage reserves during embryo maturation in Arabidopsis. Frontiers in Plant Science. 8: 1287.
Lu, G., T. Zhang, Y. He, and G. Zhou. 2016. Virus altered rice attractiveness to planthoppers is mediated by volatiles and related to virus titre and expression of defence and volatile-biosynthesis genes. Scientific Reports. 6: 38581.
Luttmann, W., K. Bratke, M. Kupper, and D. Myrtek. 2006. Immunology. 1st Edition, Academic Press, MA.
Manassero, N.G., I.L. Viola, E. Welchen, and D.H. Gonzalez. 2013. TCP transcription factors: architectures of plant form. Biomolecular Concepts. 4: 111-127.
Milne, R.G., E. Luisoni, L.K. Zhou, and K.C. Ling. 1981. Morphological and serological similarities of rice ragged stunt samples from China and the Philippines. International Rice Research Notes. 6: 11-12.
Miyazaki, N., T. Uehara-Ichiki, L. Xing, L. Bergman, A. Higashiura, A. Nakagawa, T. Omura, and R.H. Cheng.. 2008. Structural evolution of Reoviridae revealed by Oryzavirus in acquiring the second capsid shell. Journal of Virology. 82: 11344-11353.
Na Phatthalung, T. 2014. Comparison of one-step RT-PCR and DIBA for diagnosis of Rice ragged stunt virus. M. S. Thesis. Thammasat University, Rangsit Centre, Pathum Thani.
Na Phatthalung, T., W. Rattanakarn, and W. Tangkananond. 2017. The application of chlorophyll absorbents to enhance efficiency of Rice ragged stunt virus detection in plant sap by Dot-immunobinding assay. King Mongkut's Agricultural Journal. 35: 104-115.
Na Phatthalung, T., W. Tangkananond, and W. Rattanakarn. 2017. The efficiency of Rice ragged stunt virus detection in the brown planthoppers by dot-immunobinding assay. Thai Journal of Science and Technology. 6: 236-246.
Oelmuller, R. 2008. Photoxidative destruction of chloroplasts and its effect on nuclear gene expression and extraplastidic enzyme levels. Photochemistry and Photobiology. 49: 229-239.
Otulak-Koziel, K., E. Koziel, and B.E.L. Lockhart. 2018. Plant cell wall dynamics in compatible and incompatible potato response to infection caused by Potato virus Y (PVYNTN). International Journal of Molecular Science. 19: 1-23.
Parejarearn, A., and H. Hibino. 1985. Distribution of Rice ragged stunt virus (RSV) in infected TN1 plants. International Rice Research Notes. 10: 12.
Parejarearn, A., and H. Hibino. 1987a. Ragged stunt virus (RSV) concentration in tolerant rice. International Rice Research Notes. 12: 14.
Parejarearn, A., and H. Hibino. 1987b. Symptoms and yield reduction in tolerant varieties infected with ragged stunt virus (RSV). International Rice Research Notes. 12: 14-15.
Ronen, R., and M. Galun. 1984. Pigment extraction from lichens with dimethyl sulfoxide (DMSO) and estimation of chlorophyll degradation. Environmental and Experimental Botany. 24: 239-245.
Rungreangsri, U., N. Rungreangsri, and S. Pongjareankit. 2008. Histopathogenesis of Rice ragged stunt virus and viral evolution implication. Maejo University, Chiang Mai.
Russin, W.A., R.F. Evert, P.J. Vanderveer, T.D. Sharkey, and S.P. Briggs. 1996. Modification of a specific class of plasmodesmata and loss of sucrose export ability in the sucrose export defective1 Maize Mutant. Plant Cell. 8: 645-658.
Schommer, C., J.F. Palatnik, P. Aggarwal, A. Chetelat, P. Cubas, E.E. Farmer, U. Nath, and D. Weigel. 2008. Control of jasmonate biosynthesis and senescence by miR319 targets. PLoS Biology. 6: 1991-2001.
Shen, J., L. Song, K. Müller, Y. Hu, Y. Song, W. Yu, H. Wang, and J. Wu. 2016. Magnesium alleviates adverse effects of lead on growth, photosynthesis, and ultrastructural alterations of Torreya grandis seedlings. Frontiers in Plant Science. 7: 1-11.
Shi, B., L. Lin, S. Wang, Q. Guo, H. Zhou, L. Rong, J. Li, J. Peng, Y. Lu, H. Zheng, Y. Yang, Z. Chen, J. Zhao, T. Jiang, B. Song, J. Chen, and F. Yan. 2016. Identification and regulation of host genes related to Rice stripe virus symptom production. New Phytologist. 209: 1106-1119.
Sogawa, K. 1982. The rice brown planthopper: feeding physiology and host plant interactions. Annual Review of Entomology. 27: 49-73.
Srivastava, A., L. Agrawal, R. Raj, M. Jaidi, S.K. Raj, S. Gupta, R. Dixit, P.C. Singh, T. Tripathi, O.P. Sidhu, B.N. Singh, S. Shukla, P.S. Chauhan, and S. Kumar. 2017. Ageratum enation virus infection induces programmed cell death and alters metabolite biosynthesis in Papaver somniferum. Frontiers in Plant Science. 8: 1-15.
Sumanta, N., C. Haque, J. Nishika, and R. Suprakash. 2014. Spectrophotometric analysis of chlorophylls and carotenoids from commonly grown fern species by using various extracting solvents. Research Journal of Chemical Sciences. 4: 63-69.
Taylor, A.O., and A.S. Craig. 1971. Plants under climatic stress: II. low temperature, high light effects on chloroplast ultrastructure. Plant Physiology. 47: 719-725.
Taylor, A.O., and J.A. Rowley. 1971. Plants under climatic stress: I. low temperature, high light effects on photosynthesis. Plant Physiology. 47: 713-718.
Tromas, N., M.P. Zwart, G. Lafforgue, and S.F. Elena. 2014. Within-host spatiotemporal dynamics of plant virus infection at the cellular level. PLoS Genetics. 10: 1-14.
Vuorinen, A.L., J. Kelloniemi, and J.P. Valkonen. 2011. Why do viruses need phloem for systemic invasion of plants?. Plant Science. 181: 355-363.
Zhang, Y., X. Chen, F. Yang, L. Zhang, and W. Liu. 2016. miRNA: A novel link between Rice ragged stunt virus and Oryza sativa. Indian Journal of Microbiology. 56: 219-224.
Zhou, G., D. Xu, D. Xu, and M. Zhang. 2013. Southern rice black-streaked dwarf virus: a white-backed planthopper-transmitted Fijivirus threatening rice production in Asia. Frontiers in Microbiology. 4: 1-19.
Zhu, S., F. Gao, X. Cao, M. Chen, G. Ye, C. Wei, and Y. Li. 2005. The Rice dwarf virus P2 protein interacts with ent-kaurene oxidases in vivo, leading to reduced biosynthesis of gibberellins and rice dwarf symptoms. Plant Physiology. 139: 1935-1945.
