In Cameroon, tomato yields remain low due to attacks by pathogens and insects. Fusarium oxysporum f.sp. lycopersici (FOL) is a fungus responsible for Fusarium wilt, a disease responsible for important economic losses. To contribute to the control of this pathogen, the stimulatory effect of the tomato defence system of extracts of plants in the tomato/FOL interaction was evaluated. Tomato plants were treated with the aqueous extracts (AE) of Callistemon citrinus (C. citrinus), Cymbopogon citratus (C. citratus), and Oxalis barrelieri (O. barrelieri) at 10% (W/V). After 4 days of spraying with the extracts, the plants were inoculated with a virulent strain of Fusarium oxysporum f.sp. lycopersici (FOL) in pots experiments. Tomato roots were used to determine the contents of phenols, proteins, carbohydrates, amino acids (AA) and proline. The activities of antioxidant enzymes were evaluated: ascorbate peroxidase (APX), catalase (CAT), guaiacol peroxidase (GPX) and superoxide dismutase (SOD). The results showed that treatment of tomato plants with extracts and their infection with FOL induced an increase in the contents of phenols, proteins, carbohydrates, lipids, amino acids and proline in tomato roots, an increase in APX, GPX, SOD activities and a reduction in CAT activity. Our results suggest that the increase and reduction of enzymatic activities, and the increase in the synthesis of some metabolites could mitigate the oxidative damage that takes place during the expansion of the pathogen. Aqueous extracts of C. citrinus, C. citratus and O. barrelieri could be used as natural products to stimulate the tomato defence system against FOL.
Published in | Plant (Volume 11, Issue 3) |
DOI | 10.11648/j.plant.20231103.11 |
Page(s) | 82-93 |
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), 2023. Published by Science Publishing Group |
Tomato, Fusarium Wilt, Plant Extracts, Defence System
[1] | Abdelkhalek, A., Al-Askar, A. A., Alsubaie, M. M., and Behiry, S. I. 2021. First report of protective activity of Paronychia argentea extract against Tobacco Mosaic Virus infection. Plant Theory, 10, 2435. |
[2] | Ahmad, A and Singh, L. 2007. Effect of staking and row spacing on the yield of tomato (Lycopersicon esculentum Mill.) cultivar “Roma VF” in the Sokoto Fadama, Nigeria, Nigerian Journal of Horticultural Science, 10, 94–98. |
[3] | Agarwal, P. C., Carmen Mortensen, N. and Mathur, S. B. 1989. Seed-borne diseases and seed health testing of rice. Technical Bulletin N° 3 and Phytopathological Papers N° 30. Danish Government Institute of Seed Pathology for Developing Countries, Copenhagen, Denmark and CAB International Mycological Institute, Kew, Surrey, United Kingdom, 106p. |
[4] | Akladious A., Isaac, G. S. and Abu-Tahon, M. A. 2015. Induction and resistance against Fusarium wilt disease of tomato by using sweet basil (Ocimum basilicum L.) extract. Canadian. Journal of Plant Science, 95, 689-701. |
[5] | Anjum, S. A., Farooq, M., Xie, X. Y., Lie, X. J. and Ijaz, M. F. 2012. Antioxidant defence system and proline accumulation enable hot pepper to perform better under drought. Science Horticulture, 140, 66-73. |
[6] | Bates, L. S., Waldren, R. P. and Teare, I. D. 1973. Rapid determination of the free proline in water stress studies. Plant soil, 38, 205-208. |
[7] | Beauchamp, C. and Fridovich, I. 1971. Superoxide dismutase: improved assays and an assay applicable to acrylamide gels. Annal of Biochemistry, 44, 276-286. |
[8] | Behiry, S. I., Al-Askar, A. A., Soliman, S. A., Alotibi, F. O., Basile; A., Abdelkhalek, A., Elsharkawy, M. M., Salem, M. Z. M., Hafez, E. E. and Heflish, A. A. 2022. Plantago lagopus extract as a green fungicide induces systemic resistance against Rhizoctonia root rot disease in tomato plants. Frontiers in Plant Science, 13, 966929. |
[9] | Boudjeko, T., Djocgoue, P. F., Nankeu, D. J., Mbouobda, H. D., Omokolo, D. N. and El Hadrami I. 2007. Luteolin derivatives and heritability of resistance to Phytophtora megakaria in Theobroma cacao L. Australian Plant Pathology, 36, 56-61. |
[10] | Bradford, M. M. 1976. A rapid and sensitive method for the quantification of micrograms of quantities of protein utilizing the principle of protein-dye binding. Annal of Biochemistry, 72, 248-254. |
[11] | Cakmak, I. and Marschner, H. 1992. Magnesium deficiency and high light intensity enhance the activities of superoxide dismutase, ascorbate peroxidase, and glutathione reductase in bean leaves. Plant Physiology, 98, 1222-1227. |
[12] | Cassab, G. I 1998. Plant cell wall proteins. Annual Review of Plant Physiology and Plant Molecular Biology, 49, 281-309. |
[13] | Chance, B. and Maehly, A. C. 1955. Assay of catalase and peroxidases, Methods Enzymology, 2, 764-765. |
[14] | Couée, I., Sulmon, C., Gouesbet, G. and El Amrani, A. 2006. Involvement of soluble sugars in reactive oxygen species balance and responses to oxidative stress in plants. Journal of Experimental Botany, 57, 449-459. |
[15] | Dakole, D. C., Nguefack, J., Dongmo, L. B. J., Galani, Y. J. H., Azah, U. R., Somda, I and Amvam Z. P. H. 2016. Antifungal potential of essential oils, aqueous and ethanol extracts of thirteen plants against Fusarium oxysporum f. sp lycopersici and Phytophtora infestans (Mont.) de Bary as major tomato pathogens in Cameroon. International Journal of Current Research, 19 (2), 128-145. |
[16] | Djocgoue, P. F., Boudjeko, T., Mbouobda, H. D., Nankeu, D. J., El Hadrami, I. and Omokolo, N. D. 2007. Heritability of phenols in resistance of Theobroma cacao against Phytophtora megakaria, the causal agent of black pod disease. Journal of Phytopathology, 155, 519-525. |
[17] | Fangue, G. Y., Mouafo R. A., Fomekong K M., Effa O M. P and Djocgoue, P. F. 2021. Allelopathic Effect of Three Wild Plants (Azadirachta indica, Tithonia diversifolia and Thevetia peruviana) on Tomato (Lycopersicum esculentum Mill.) Growth and Stimulation of Metabolites Involved in Plant Resistance. American Journal of Plant Sciences, 12, 285-299. |
[18] | FAOSTAT. 2019. Food and Agriculture Organization of the United Nations. https://faostat3.Fao.org/download/Q/QC/E. Consulted on 10-9-2022. |
[19] | Foleh, J., Less M., Solune and Stanley, G. 1957. A simple method for the isolation and purification of total lipids from animal tissues. Journal of Biology and Chemistry, 226, 497-509. |
[20] | Konje, C. N., Abdulai, A. N., Tange, D. A., Nsobinenyui, D., Tarla, D. N. and Tita, M. A. 2019. Identification and management of pests and diseases of garden crops in Santa Cameroon. Journal of Agriculture and Ecology Research International, 18, 1-9. |
[21] | Li, B., Wei, J., Wei, X., Tang, K., Liang, Y., Shu, K. and Wang, B. 2008. Effect of sound wave stress on antioxidant enzyme activities and lipid peroxidation of Dendrobium candidum. Colloids and Surfaces. Biointerfaces, 63, 269-275. |
[22] | Li, Z. G., Ding, X. J. and Du, P. F. 2013. Hydrogen sulfide donor sodium hydrosulfide-improved heat tolerance in maize and involvement of proline. Journal of Plant Physiology, 170, 741-747. |
[23] | Macheix, J. J., Billot, J. and Fleuriet, A. 1990. Fruits Phenolics (1st Edition). CR Press, Inc: Boca. Raton, FL, 149-237. |
[24] | Mandal, S. and Mitra, A. 2008. Accumulation of cell wall-bound phenolic metabolites and their upliftment in hairy root cultures of tomato (Lycopersicon esculentum Mill.). Biotechnology Letters, 30, 1253–1258. |
[25] | Mandal, S., Kar, I., Mukherjee, A. K. and Acharya, P. 2013. Elicitor-Induced Defence Responses in Solanum lycopersicum against Ralstonia solanacearum. The Scientific World Journal, 1-9. |
[26] | Mathur, S. B. and Kongsdal, O. 2003. Common laboratory seed health testing methods for detecting fungi. (1st Edtion). Bassersdorf: International Testing Association, 425p. |
[27] | Mbouobda, H. D., Boudjeko, T., Djocgoue, P. F., Tsafack T. J. J. and Omokolo, D. N. 2007. Morphological characterisation and agronomic evaluation of cocoyam (Xanthosoma sagittifolium (L.) Schott germplasm in Cameroon. Journal of Biological Sciences, 7 (1), 27-33. |
[28] | Mbouobda, H. D. 2013. Stimulation of defence mechanism system by chitosan (CHT) and Benzo-(1, 2, 3)-thiadiazole-7-carbothionic acid-S-méthyl ester acid (BTH) in Xanthosoma sagittifolium (macabo) / Pythium myriotylum interaction. PhD thesis. University of Yaounde 1, 142p. |
[29] | Mbouobda, H. D., Fotso, Djocgoue, P. F., Omokolo, D. N., El Hadrami, I. and Boudjeko, T. 2010. Benzo-(1, 2, 3)-thiadiazole-7-carbothionic acid-S-methyl ester (BTH) stimulates defence reactions in Xanthosoma sagittifolium. Phytoparasitica, 38, 71-79. |
[30] | Mekam, P. N., Martini, S., Nguefack, J., Tagliazucchi, D., Mangoumou, G. N. and Stefani, E. 2019. Activity of extracts from three tropical plants towards fungi pathogenic to tomato (Solanum lycopersicum). Phytopathologia Mediterranea, 58 (3), 573-586. |
[31] | Moore, S. and Stein, W. H. 1948. Photometric method for use in the chromatography of amino acids. Journal of Biology, 176, 367-388. |
[32] | Nakano, Y., and Asada, K. 1981. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiology, 22, 867-880. |
[33] | Nelson, N. 1944. A photometric adaptation of Somogyi's method for the determination of reducing sugar. Analytic Chemistry, 31, 426-428. |
[34] | Omokolo, N. D. and Boudjeko, T. 2005. Comparative analyses of alterations in carbohydrates, amino acids, phenols and lignin in roots of five cultivars of Xanthosoma sagittifolium infected by Pythium myriotylum. South African Journal of Botany, 71 (3-4), 432-440. |
[35] | Ramadan A. A., Said M. K., Dalia I. T., Svein Ø. S., and Mohamed T. R. 2022. Leaf Extracts from Resistant Wild Tomato Can Be Used to Control Late Blight (Phytophthora infestans) in the Cultivated Tomato. Plants, 11, 1-16. |
[36] | Samir K B., HG Prakesh, H. G., Ram, P. and Javed B. 2019. Induced synthesis of defence molecules in tomato (Solamum lycopersicum L.) against Fusarium wilt through plant extracts Bangladesh Journal of. Botany, 48, 169-175. |
[37] | Zinkakuba, L. V., Mwanyikag, G., Ntwenga, J. E. and James, A. 2019. Pesticide regulations and their malpractice implications on food and environment safety. Food Science and Technology, 5, 1601544. |
APA Style
Dakole Daboy Charles, Dongmo Lekagne Joseph Blaise, Fonkoua Martin, Nguefack Julienne, Irénée Somda. (2023). Callistemon Citrinus, Cymbopogon Citratus, and Oxalis Barrelieri Extracts Stimulate Defence of Tomato Against Fusarium Wilt. Plant, 11(3), 82-93. https://doi.org/10.11648/j.plant.20231103.11
ACS Style
Dakole Daboy Charles; Dongmo Lekagne Joseph Blaise; Fonkoua Martin; Nguefack Julienne; Irénée Somda. Callistemon Citrinus, Cymbopogon Citratus, and Oxalis Barrelieri Extracts Stimulate Defence of Tomato Against Fusarium Wilt. Plant. 2023, 11(3), 82-93. doi: 10.11648/j.plant.20231103.11
AMA Style
Dakole Daboy Charles, Dongmo Lekagne Joseph Blaise, Fonkoua Martin, Nguefack Julienne, Irénée Somda. Callistemon Citrinus, Cymbopogon Citratus, and Oxalis Barrelieri Extracts Stimulate Defence of Tomato Against Fusarium Wilt. Plant. 2023;11(3):82-93. doi: 10.11648/j.plant.20231103.11
@article{10.11648/j.plant.20231103.11, author = {Dakole Daboy Charles and Dongmo Lekagne Joseph Blaise and Fonkoua Martin and Nguefack Julienne and Irénée Somda}, title = {Callistemon Citrinus, Cymbopogon Citratus, and Oxalis Barrelieri Extracts Stimulate Defence of Tomato Against Fusarium Wilt}, journal = {Plant}, volume = {11}, number = {3}, pages = {82-93}, doi = {10.11648/j.plant.20231103.11}, url = {https://doi.org/10.11648/j.plant.20231103.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.plant.20231103.11}, abstract = {In Cameroon, tomato yields remain low due to attacks by pathogens and insects. Fusarium oxysporum f.sp. lycopersici (FOL) is a fungus responsible for Fusarium wilt, a disease responsible for important economic losses. To contribute to the control of this pathogen, the stimulatory effect of the tomato defence system of extracts of plants in the tomato/FOL interaction was evaluated. Tomato plants were treated with the aqueous extracts (AE) of Callistemon citrinus (C. citrinus), Cymbopogon citratus (C. citratus), and Oxalis barrelieri (O. barrelieri) at 10% (W/V). After 4 days of spraying with the extracts, the plants were inoculated with a virulent strain of Fusarium oxysporum f.sp. lycopersici (FOL) in pots experiments. Tomato roots were used to determine the contents of phenols, proteins, carbohydrates, amino acids (AA) and proline. The activities of antioxidant enzymes were evaluated: ascorbate peroxidase (APX), catalase (CAT), guaiacol peroxidase (GPX) and superoxide dismutase (SOD). The results showed that treatment of tomato plants with extracts and their infection with FOL induced an increase in the contents of phenols, proteins, carbohydrates, lipids, amino acids and proline in tomato roots, an increase in APX, GPX, SOD activities and a reduction in CAT activity. Our results suggest that the increase and reduction of enzymatic activities, and the increase in the synthesis of some metabolites could mitigate the oxidative damage that takes place during the expansion of the pathogen. Aqueous extracts of C. citrinus, C. citratus and O. barrelieri could be used as natural products to stimulate the tomato defence system against FOL.}, year = {2023} }
TY - JOUR T1 - Callistemon Citrinus, Cymbopogon Citratus, and Oxalis Barrelieri Extracts Stimulate Defence of Tomato Against Fusarium Wilt AU - Dakole Daboy Charles AU - Dongmo Lekagne Joseph Blaise AU - Fonkoua Martin AU - Nguefack Julienne AU - Irénée Somda Y1 - 2023/07/06 PY - 2023 N1 - https://doi.org/10.11648/j.plant.20231103.11 DO - 10.11648/j.plant.20231103.11 T2 - Plant JF - Plant JO - Plant SP - 82 EP - 93 PB - Science Publishing Group SN - 2331-0677 UR - https://doi.org/10.11648/j.plant.20231103.11 AB - In Cameroon, tomato yields remain low due to attacks by pathogens and insects. Fusarium oxysporum f.sp. lycopersici (FOL) is a fungus responsible for Fusarium wilt, a disease responsible for important economic losses. To contribute to the control of this pathogen, the stimulatory effect of the tomato defence system of extracts of plants in the tomato/FOL interaction was evaluated. Tomato plants were treated with the aqueous extracts (AE) of Callistemon citrinus (C. citrinus), Cymbopogon citratus (C. citratus), and Oxalis barrelieri (O. barrelieri) at 10% (W/V). After 4 days of spraying with the extracts, the plants were inoculated with a virulent strain of Fusarium oxysporum f.sp. lycopersici (FOL) in pots experiments. Tomato roots were used to determine the contents of phenols, proteins, carbohydrates, amino acids (AA) and proline. The activities of antioxidant enzymes were evaluated: ascorbate peroxidase (APX), catalase (CAT), guaiacol peroxidase (GPX) and superoxide dismutase (SOD). The results showed that treatment of tomato plants with extracts and their infection with FOL induced an increase in the contents of phenols, proteins, carbohydrates, lipids, amino acids and proline in tomato roots, an increase in APX, GPX, SOD activities and a reduction in CAT activity. Our results suggest that the increase and reduction of enzymatic activities, and the increase in the synthesis of some metabolites could mitigate the oxidative damage that takes place during the expansion of the pathogen. Aqueous extracts of C. citrinus, C. citratus and O. barrelieri could be used as natural products to stimulate the tomato defence system against FOL. VL - 11 IS - 3 ER -