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Eliciting Plant Defense on Anthracnose Disease in Chili (Capsicum annuum Linn.) by Sodium Nitroprusside Solution

Received: 5 October 2014    Accepted: 25 October 2014    Published: 29 January 2015
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Abstract

The study on the induction of plant defense against to anthracnose disease of chili by sodium nitroprusside solution was investigated during pre- and post-harvest. Pre-harvest treatment was conducted by spraying the chili plants with sodium nitroprusside (SNP, nitric oxide donor) solution at 0 (control), 0.05 and 0.1 mM every 3 days for 9 times before inoculating with the spore suspension of Colletotrichum gloeosporioides (the causal agent of anthracnose disease) and then sprayed with SNP again 1 time after inoculating. The results revealed that 0.1 mM SNP was the best concentration to suppress anthracnose disease by reducing disease incidence and disease index on chili leaves, and showing the lowest loss of yield caused by anthracnose disease. This founding also showed that either pathogenic inoculation or SNP treatment had ability to induce the activities of peroxidase (POD) and phenylalanine ammonia lyase (PAL) of chili leaves, particularly the chili plant inoculated with pathogenic fungi followed by treated with 0.1 mM SNP showed the highest POD and PAL activities. Post-harvest treatment was done by inoculating the mature chilli fruit with C. capcisi for 4 h and followed by dipping in 0 (control) and 4 mM SNP. All fruit samples were kept at 13C for 15 days. The results showed that chili fruit dipped with 4 mM SNP reduced disease incidence, disease index, delayed weight loss, respiration rate, ethylene production, and also maintained the changes of fruit color (ΔE) better than non-treated fruit (control). The activities of chitinase (CHI) and β-1,3-glucanase (GLU) in chili fruit were induced by SNP with the highest peak on day 6 of storage but they were not significant different with the control fruit. These results indicated that SNP might potential leading to the reduction of anthracnose disease in chili by eliciting plant defense related enzymes in both pre- and post-harvest periods.

Published in Journal of Food and Nutrition Sciences (Volume 3, Issue 1-2)

This article belongs to the Special Issue Food Processing and Food Quality

DOI 10.11648/j.jfns.s.2015030102.14
Page(s) 20-27
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Chitinase, β-1,3-Glucanase, Peroxidase, Phenylalanine Ammonia Lyase, Nitric Oxide

References
[1] G.N. Agrios, Plant pathology (5th ed). Elsevier Press Burlington, MA, USA, 922 pp., 2005.
[2] M. Arasimowicz, and J. Floryszak-Wieczorek, “Nitric oxide as a bioactive signaling molecule in plant stress response,” J. Plant Science, 172, 876-887, 2007.
[3] J.A. Bailey, and M.J. Jeger, (Eds). Colletotrichum: Biology, pathology and control. Common Wealth Mycological Institute. Wallingford, 388 pp., 1992.
[4] J.N. Bates, M.T. Baker, Jr. Guerra, and D.G. Harrison, “Nitric oxide generation from nitroprusside by vascular tissue: evidence that reduction of the nitroprusside anion cyanide loss are required,” J. Biochemical Pharmacology, vol. 42 (Suppl.1), pp. S157-S165, 1991.
[5] M. Bradford, “A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding,” Analytical Biochemistry, col. 72, pp. 248-254, 1976.
[6] G. Cheng, E. Yang, W. Lu, Y. Jia, Y. Yiang, and X. Duan, “Effect of nitric oxide on ethylene synthesis and softening of banana fruit slice during ripening,” J. Agricultural and Food Chemistry, vol. 57, pp. 5799-5804, 2009.
[7] J. Durner, D. Wendehenne, and F.D. Klessig, “Defense gene induction in tobacco by nitric oxide, cyclic GMP and cyclic ADP-ribose,” J. Plant Biology, vol. 95(17), pp. 10328–10333, 1993.
[8] T.L. Graham, and M.Y. Graham, “Signaling in soybean phenylpropanoid response,” J. Plant Physiology, vol. 110, pp. 1123-1133, 1996.
[9] R. Gupta, R.K. Saxena, P. Chaturvedi, and J.S. Virdi, “Chitinase production by streptomyces virdificans: its potential in fungal cell walls lysis” J. Appllied Bacteriology, vol. 78, pp. 378-383, 1995.
[10] P.R. Johnston, and D. Jones, “Relationships among Colletotrichum isolates from fruit-rots assessed using rDNA sequences,” J. Mycologia, vol. 89(3), pp. 420-430, 1997.
[11] K.D. Kim, B.J. Oh, and J. Yang, “Differential interactions of a Colletotrichum gloeosporioides isolate with green and red pepper fruits,” J. Phytoparasitica, vol. 27, pp. 1-10, 1999.
[12] D. Lacan, and J.C. Baccou, “ Changes in lipids and electrolyte leakage during non-netted muskmelon ripening,” J. American Society for Horticultural Science, vol. 121, pp. 554–558, 1996.
[13] T. Lai, Y. Wang, B. Li, G. Qin, and S. Tian, “Defense responses of tomato fruit to exogenous nitric oxide during postharvest storage,” J. Postharvest Biology and Technology, vol. 62,pp. 127–132, 2011.
[14] L. Liu, J. Wang, L. Qu, S. Li, R. Wu, and K. Zheng, “Effect of nitric oxide treatment on storage quality of Glorious oranges,” Procedia Engineering, vol. 62, pp. 127–132, 2012.
[15] J.B. Manandhar, G.L. Hartman, and T.C. Wang, “Anthracnose development on pepper fruits inoculated with Colletotrichum gloeosporioides,” J. Plant Disease, vol. 79, pp. 380–383, 1995
[16] B.S-B. Marianne, S.P. Anne, A.B-V. Sandra, S.M. Leo, J.M. Peter, E. van den, and J.C.C. Ben, “Only specific tobacco (Nicotiana tabacum) chitinase and β-1,3-Glucanases exhibit antifungal activity,” J. Plant Physiology, vol. 101, pp. 857-863, 1993.
[17] X. Meng, B. Li, J. Liu, and S. Tian, “ Physiological responses and quality attributes of table grape fruit to chitosan preharvest spray and postharvest coating during storage,” J. Food Chemistry, vol. 106, pp. 501-508, 2008.
[18] L.V. Modolo, F.Q. Cunha, R.B. Maircia, and I. Salgado, “Nitric oxide synthase mediated phytoalexin accumulation in soybean cotyledons in response to the Diaporthe phaseolorum f. sp. Meridionallis elicitor,” J. Plant Physiology, vol. 130, pp. 1288-1297, 2002.
[19] H. Qian, W. Chen, J. Li, J. Wang, Z. Zhou, W. Liu, and Z. Fu, “ The effect of exogenous nitric oxide on alleviating herbicide damage in Cholrella vugaris,” J. Aquatic Toxicology, vol. 92, pp. 250–257, 2009.
[20] I.I. Salles, J.W. Blount, R.A. Dixon, and K. Schubert, “Phytoalexin induction and beta-1,3-glucanase activities in Colletotrichum trifolii infected leaves of alfalfa (Medicago sativa L.),” J. Physiological and Molecular Plant Pathology, vol. 61(2), pp. 89-101, 2002.
[21] P.N. Sharma, M. Kaur, O.P. Sharma, P. Sharma, and A. Pathania, “Morphological, pathological and molecular variability in Colletotrichum capsici, the cause of fruit rot of chillies in the subtropical region of north-western India,” J. Phytopathology, vol. 153(4), pp. 232-237, 2005.
[22] D. Sharp, K.S. Braithwaite, J.A.R. Irwin, and J.M. Manners, “Biochemical and cytochemical responses of Stylosanthes guianensis to infection by Colletotrichum gloeosporioides: association of callose deposition with resistance,” Canadian Journal of Botany, vol. 68, pp. 505-511, 1990.
[23] S.G. Shoutherton, and B.J. Deverall, “Changes in phenylalanine ammonia-lyase and peroxidase activites in wheat cultivars expressing resistance to the leaf-rust fungus,” J. Plant Pathology, vol. 39(2), pp. 223-230, 1990.
[24] J.H. Simmonds, “A study of the species of Colletotrichum causing ripe fruit rots in Queensland,” Queensland J. Agriculture and Animal Science, vol. 22, pp. 437–459, 1965.
[25] Y. Tada, T. Mori, T. Shinogi, N. Yao, S. Takahashi, and S. Betsuyaku, “Nitric oxide and reactive oxygen species do not elicit hypersensitive cell death but induce apoptosis in the adjacent cells during the defense response of oat,” Molecular Plant-Microbe Interactions J., vol. 17, pp. 245-253, 2004.
[26] L.C. van Loon, and E.A. van Strien, “The families of pathogenesis-related proteins, their activities and comparative analysis of PR-1 type proteins,” J. Physiology and Molecular Biology of Plants, vol. 55, pp. 85-97, 1999.
[27] L.C. van Loon, M. Rep, and C.M.J. Pietersen, “Significance of inducible defense-related proteins in infected plants,” Annual Review of Phytopathology, vol. 44, pp. 135-162, 2006.
[28] P. Vander, M.V. Kjell, A. Domard, N.E. El-Gueddari, and B.M. Moerschbacher, “Comparison of the ability of partially N-acetylated chitosans and oligosaccharides to elicit resistance in wheat leaves,” J. Plant Physiology, vol. 118, pp. 1353–1359, 1998.
[29] C.Y. Wang, “Physiological and biochemical responses of plants to chilling stress,” American Society for Horticultural Science, vol. 17(2), pp. 173-186, 1982.
[30] J. Yin, S. Bai, F. Wu, G. Lu, and H. Yang, “Effect of nitric oxide on the activity of phenylalanine ammonia-lyase and antioxidative response in sweet potato root in relation to wound-healing,” J. Postharvest Biology and Technology, vol. 74, pp. 125-131, 2012.
[31] Y.J. Yuan, C. Li, Z.D. Hu, J.C. Wu, and A.P. Zeng, “Fungal elicitor induces cell apoptosis in suspension cultures of Taxus chinensis var mairei for toxol production,” Process Biochemistry J., vol. 38, pp. 193-198, 2002.
[32] S.S. Zaharah, and Z. Singh, “Mode of action of nitric oxide in inhibiting ethylene biosynthesis and fruit softening during ripening and cool storage of ‘Kensington Pride’ mango,” J. Postharvest Biology and Technology, vol. 62, pp. 127-132, 2011.
[33] Y.H. Zhang, X.F. Yang, Q. Liu, D.W. Qiu, Y.L. Zhang, H.M. Zeng, J.J. Yuan, and J.J. Mao, “Purification of novel protein elicitor from Botrytis cinerea that induces disease resistance and drought tolerance in plants,” J. Microbiological Research, vol. 165, pp. 142-151, 2010.
[34] Y. Zheng, L. Shen, M. Yu, B. Fan, D. Zhao, L. Liu, and J. Sheng, “Nitric oxide synthase as a postharvest response in pathogen resistance of tomato fruit,” J. Postharvest Biology and Technology, vol. 60, pp. 38-46, 2011.
[35] S.H. Zhu, M.C. Liu, and J. Zhou, “Inhibition by nitric oxide of ethylene biosynthesis and lipoxygenase activity in peach fruit during storage,” J. Postharvest Biology and Technology, vol. 42, pp. 41-48, 2006.
[36] S.H. Zhu, J. Zhou, H. R. Shu, and L.L. Wang, “Effects of nitric oxide (NO) on ripening and senescence of strawberry,” J. Agricultural Science China, vol. 38, pp. 1418-1424, 2005.
[37] M. Zucker, “Light and enzymes,” Annual Review of Plant Physiology, vol. 23, pp. 133-156, 1972.
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    Vo Thi Thuong, Pongphen Jitareerat, Apiradee Uthairatanakij. (2015). Eliciting Plant Defense on Anthracnose Disease in Chili (Capsicum annuum Linn.) by Sodium Nitroprusside Solution. Journal of Food and Nutrition Sciences, 3(1-2), 20-27. https://doi.org/10.11648/j.jfns.s.2015030102.14

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    Vo Thi Thuong; Pongphen Jitareerat; Apiradee Uthairatanakij. Eliciting Plant Defense on Anthracnose Disease in Chili (Capsicum annuum Linn.) by Sodium Nitroprusside Solution. J. Food Nutr. Sci. 2015, 3(1-2), 20-27. doi: 10.11648/j.jfns.s.2015030102.14

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    AMA Style

    Vo Thi Thuong, Pongphen Jitareerat, Apiradee Uthairatanakij. Eliciting Plant Defense on Anthracnose Disease in Chili (Capsicum annuum Linn.) by Sodium Nitroprusside Solution. J Food Nutr Sci. 2015;3(1-2):20-27. doi: 10.11648/j.jfns.s.2015030102.14

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  • @article{10.11648/j.jfns.s.2015030102.14,
      author = {Vo Thi Thuong and Pongphen Jitareerat and Apiradee Uthairatanakij},
      title = {Eliciting Plant Defense on Anthracnose Disease in Chili (Capsicum annuum Linn.) by Sodium Nitroprusside Solution},
      journal = {Journal of Food and Nutrition Sciences},
      volume = {3},
      number = {1-2},
      pages = {20-27},
      doi = {10.11648/j.jfns.s.2015030102.14},
      url = {https://doi.org/10.11648/j.jfns.s.2015030102.14},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jfns.s.2015030102.14},
      abstract = {The study on the induction of plant defense against to anthracnose disease of chili by sodium nitroprusside solution was investigated during pre- and post-harvest. Pre-harvest treatment was conducted by spraying the chili plants with sodium nitroprusside (SNP, nitric oxide donor) solution at 0 (control), 0.05 and 0.1 mM every 3 days for 9 times before inoculating with the spore suspension of Colletotrichum gloeosporioides (the causal agent of anthracnose disease) and then sprayed with SNP again 1 time after inoculating. The results revealed that 0.1 mM SNP was the best concentration to suppress anthracnose disease by reducing disease incidence and disease index on chili leaves, and showing the lowest loss of yield caused by anthracnose disease. This founding also showed that either pathogenic inoculation or SNP treatment had ability to induce the activities of peroxidase (POD) and phenylalanine ammonia lyase (PAL) of chili leaves, particularly the chili plant inoculated with pathogenic fungi followed by treated with 0.1 mM SNP showed the highest POD and PAL activities. Post-harvest treatment was done by inoculating the mature chilli fruit with C. capcisi for 4 h and followed by dipping in 0 (control) and 4 mM SNP. All fruit samples were kept at 13C for 15 days. The results showed that chili fruit dipped with 4 mM SNP reduced disease incidence, disease index, delayed weight loss, respiration rate, ethylene production, and also maintained the changes of fruit color (ΔE) better than non-treated fruit (control). The activities of chitinase (CHI) and β-1,3-glucanase (GLU) in chili fruit were induced by SNP with the highest peak on day 6 of storage but they were not significant different with the control fruit. These results indicated that SNP might potential leading to the reduction of anthracnose disease in chili by eliciting plant defense related enzymes in both pre- and post-harvest periods.},
     year = {2015}
    }
    

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  • TY  - JOUR
    T1  - Eliciting Plant Defense on Anthracnose Disease in Chili (Capsicum annuum Linn.) by Sodium Nitroprusside Solution
    AU  - Vo Thi Thuong
    AU  - Pongphen Jitareerat
    AU  - Apiradee Uthairatanakij
    Y1  - 2015/01/29
    PY  - 2015
    N1  - https://doi.org/10.11648/j.jfns.s.2015030102.14
    DO  - 10.11648/j.jfns.s.2015030102.14
    T2  - Journal of Food and Nutrition Sciences
    JF  - Journal of Food and Nutrition Sciences
    JO  - Journal of Food and Nutrition Sciences
    SP  - 20
    EP  - 27
    PB  - Science Publishing Group
    SN  - 2330-7293
    UR  - https://doi.org/10.11648/j.jfns.s.2015030102.14
    AB  - The study on the induction of plant defense against to anthracnose disease of chili by sodium nitroprusside solution was investigated during pre- and post-harvest. Pre-harvest treatment was conducted by spraying the chili plants with sodium nitroprusside (SNP, nitric oxide donor) solution at 0 (control), 0.05 and 0.1 mM every 3 days for 9 times before inoculating with the spore suspension of Colletotrichum gloeosporioides (the causal agent of anthracnose disease) and then sprayed with SNP again 1 time after inoculating. The results revealed that 0.1 mM SNP was the best concentration to suppress anthracnose disease by reducing disease incidence and disease index on chili leaves, and showing the lowest loss of yield caused by anthracnose disease. This founding also showed that either pathogenic inoculation or SNP treatment had ability to induce the activities of peroxidase (POD) and phenylalanine ammonia lyase (PAL) of chili leaves, particularly the chili plant inoculated with pathogenic fungi followed by treated with 0.1 mM SNP showed the highest POD and PAL activities. Post-harvest treatment was done by inoculating the mature chilli fruit with C. capcisi for 4 h and followed by dipping in 0 (control) and 4 mM SNP. All fruit samples were kept at 13C for 15 days. The results showed that chili fruit dipped with 4 mM SNP reduced disease incidence, disease index, delayed weight loss, respiration rate, ethylene production, and also maintained the changes of fruit color (ΔE) better than non-treated fruit (control). The activities of chitinase (CHI) and β-1,3-glucanase (GLU) in chili fruit were induced by SNP with the highest peak on day 6 of storage but they were not significant different with the control fruit. These results indicated that SNP might potential leading to the reduction of anthracnose disease in chili by eliciting plant defense related enzymes in both pre- and post-harvest periods.
    VL  - 3
    IS  - 1-2
    ER  - 

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Author Information
  • Postharvest Technology Division, School of Bioresources and Technology, King Mongkut’s University of Technology Thonburi, Bangkok 10150, Thailand

  • Postharvest Technology Division, School of Bioresources and Technology, King Mongkut’s University of Technology Thonburi, Bangkok 10150, Thailand; Postharvest Technology Innovation Center, Commission of Higher Education, Bangkok 10400, Thailand

  • Postharvest Technology Division, School of Bioresources and Technology, King Mongkut’s University of Technology Thonburi, Bangkok 10150, Thailand; Postharvest Technology Innovation Center, Commission of Higher Education, Bangkok 10400, Thailand

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