Abstract
Antifungal activity of plant-derived compounds can be exploited in disease management systems to improve sustainability and replace synthetic molecules. In this study, four crude hydroethanolic extracts of leaves, collected from Italian Solanum spp. landraces, were selected to evaluate their ability to suppress Sclerotinia minor Jagger, a great threat to lettuce production worldwide. In vitro fungal development was inhibited by Solanum melongena L. and S. aethiopicum L. extracts showing a dose-dependent correlation. At the highest concentration tested in the current experiments (45 mg mL−1) antifungal activity caused up to 90% growth reduction. The exposure of the fungus to S. aethiopicum extracts incited pronounced changes in the hyphal morphology as observed under light microscopy. Consistently, under laboratory conditions, in planta application of the active extracts on lettuce significantly reduced Sclerotinia drop disease in comparison to non-treated controls. Phytochemical composition was determined by liquid chromatography/mass spectrometry (LC/MS) analyses. Four secondary metabolites differentially present in the extracts, identified as n-caffeoylputrescine, chlorogenic acid, isoquercitrin and solasodoside A, are hypothesized to play a crucial role in mechanisms underlying biological effects of extracts. PCA analysis showed positive correlations of these compounds with the overall control ability of the extracts. The results indicated that foliar material from cultivated eggplant could be suitable to produce biological-based remedies for controlling plant diseases.
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Abdel-Monaim, M. F., Abo-Elyousr, K. A. M., & Morsy, K. M. (2011). Effectiveness of plant extracts on suppression of damping-off and wilt diseases of lupine (Lupinus termis Forsik). Crop Protection, 30, 185–191.
Ahmad, A., Shafique, S., & Shafique, S. (2013). Cytological and physiological basis for tomato varietal resistance against Alternaria alternata. Journal of the Science of Food and Agriculture, 93, 2315–2322.
Chen, H., Jones, A. D., & Howe, G. A. (2006). Constitutive activation of the jasmonate signalling pathway enhances the production of secondary metabolites in tomato. FEBS Letters, 580, 2540–2546.
Chen, Y., Gao, X., Chen, Y., Qin, H., Huang, L., & Han, Q. (2014). Inhibitory efficacy of endophytic Bacillus subtilis EDR4 against Sclerotinia sclerotiorum on rapeseed. Biological Control, 78, 67–76.
Cipollini, M. L., & Levey, D. J. (1997). Antifungal activity of Solanum fruit glycoalkaloids: implications for frugivory and seed dispersal. Ecology, 78, 799–809.
Cruz-Cruz, C. A., Ramírez-Tec, G., García-Sosa, K., Escalante-Erosa, F., Hill, L., Osbourn, A. E., & Peña-Rodríguez, L. M. (2010). Phytoanticipins from banana (Musa acuminate cv. Grande Naine) plants, with antifungal activity against Mycosphaerella fijiensis, the causal agent of black Sigatoka. European Journal of Plant Pathology, 126, 459–463.
da Cruz Cabral, L., Fernández Pinto, V., & Patriarca, A. (2013). Application of plant derived compounds to control fungal spoilage and mycotoxin production in foods. International Journal of Food Microbiology, 166, 1–14.
Das, J., Prasad Lahan, J., & Srivastava, R. B. (2010). Solanum melongena: a potential source of antifungal agent. Indian Journal of Microbiology, 50, 62–69.
De Corato, U., Pane, C., Bruno, G. L., Cancellara, F. A., & Zaccardelli, M. (2015). Co-products from a biofuel production chain in crop disease management: a review. Crop Protection, 68, 12–26.
Delledonne, M., Dal Molin, A., Minio, A., Ferrarini, A., Tononi, P., Zamperin, G., Toppino, L., Sala, T., Barchi, L., Comino, C., Acquadro, A., Portis, E., Rinaldi, R., Scaglione, D., Francese, G., D’Alessandro, A., Mennella, G., Fantini, E., Pietrella, M., Sulli, M., Lanteri, S., Rotino, G. L., & Giuliano, G. (2014). A high quality eggplant (Solanum melongena L.) genome draft and its use for mapping metabolic QTLs. Proceedings of the 11th Solanaceae Conference, SOL 2014. November 2–6, 2014 Porto Seguro–Bahia, Brazil. pp 99
Dias, C., Domínguez-Pereles, R., Aires, A., Teixeira, A., Rosa, E., Barros, A., & Saavedra, M. J. (2015). Phytochemistry and activity against digestive pathogens of grape (Vitis vinifera L.) stem’s (poly)phenolic extracts. LWT–Food Science and Technology, 61, 25–32.
Elsherbiny, E. A., Amin, B. H., & Baka, Z. A. (2016). Efficiency of pomegranate (Punica granatum L.) peels extract as a high potential natural tool towards Fusarium dry rot on potato tubers. Postharvest Biology and Technology, 111, 256–263.
Gahukar, R. T. (2012). Evaluation of plant-derived products against pests and diseases of medicinal plants: a review. Crop Protection, 42, 202–209.
Gatto, M. A., Ippolito, A., Linsalata, V., Cascarano, N. A., Nigro, F., Vanadia, S., & Di Venere, D. (2011). Activity of extracts from wild edible herbs against postharvest fungal diseases of fruit and vegetables. Postharvest Biology and Technology, 61, 72–82.
Hashem, M. (2011). Antifungal properties of crude extracts of five egyptian medicinal plants against dermatophytes and emerging fungi. Mycopathologia, 172, 37–46.
Jasso de Rodríguez, D., Trejo-González, F. A., Rodríguez-García, R., Díaz-Jimenez, M. L. V., Sáenz-Galindo, A., Hernández-Castillo, F. D., Villareal-Quintanilla, J. A., & Peña-Ramos, F. M. (2015). Antifungal activity in vitro of Rhus muelleri against Fusarium oxysporum f. Sp. lycopersici. Industrial Crops and Products, 75, 150–158.
Jones, E. E., Mead, A., & Whipps, J. M. (2014). Effect of inoculum type and timing of application of Coniothyrium minitans on Sclerotinia sclerotiorum: control of sclerotinia disease in glasshouse lettuce. Plant Pathology, 53, 611–620.
Martins, N., Barros, L., Henriques, M., Silva, S., & Ferreira, I. C. F. R. (2015). Activity of phenolic compounds from plant origin against Candida species. Industrial Crops and Products, 74, 648–670.
Mennella, G., Rotino, G. L., Fibiani, M., D’Alessandro, A., Francese, G., Toppino, L., Cavallanti, F., Acciarri, N., & Lo Scalzo, R. (2010). Characterization of health-related compounds in eggplant (Solanum melongena L.,) lines derived from introgression of allied species. Journal of Agricultural and Food Chemistry, 58, 7597–7603.
Muthukumar, A., Eswaran, A., Nakkeeran, S., & Sangeetha, G. (2010). Efficacy of plant extracts and biocontrol agents against Pythium aphanidermatum inciting chili damping-off. Crop Protection, 29, 1483–1488.
Nguefack, J., Wulff, G. E., Lekagne Dongmo, J. B., Fouelefack, F. R., Fotio, D., Mbo, J., & Torp, J. (2013). Effect of plant extracts and an essential oil on the control of brown spot disease, tillering, number of panicles and yield increase in rice. European Journal of Plant Pathology, 137, 871–882.
Ono, M., Nishimura, K., Suzuki, K., Fukushima, T., Igoshi, K., Yoshimitsu, H., Ikeda, T., & Nohara, T. (2006). Steroidal glycosides from the underground parts of Solanum sodomaeum. Chemical and Pharmaceutical Bulletin, 54, 230–233.
Pane, C., Villecco, D., Pentangelo, A., Lahoz, E., & Zaccardelli, M. (2012). Integration of soil solarisation with Brassica carinata seed meals amendment in a greenhouse lettuce production system. Acta Agriculturae Scandinavica-Section B, Soil Plant Science, 62, 291–299.
Pane, C., Villecco, D., Roscigno, G., De Falco, E., & Zaccardelli, M. (2013). Screening of plant derived antifungal substances useful for the control of seedborne pathogens. Archives of Phytopathology and Plant Protection, 46, 1533–1539.
Pane, C., Fratianni, F., Caputo, M., Parisi, M., Nazzaro, F., & Zaccardelli, M. (2015). Antifungal activity of wild Capsicum foliar extracts containing polyphenols against the phytopathogens Alternaria alternata, Rhizoctonia solani, Sclerotinia minor and Verticillium dahliae. In A. Mendez-Vilas (Ed.), Multidisciplinary approach for studying and combating microbial pathogens (pp. 34–38). Boca Raton: BrownWalker Press.
Pane, C., Fratianni, F., Parisi, M., Nazzaro, F., & Zaccardelli, M. (2016). Control of Alternaria post-harvest infections on cherry tomato fruits by wild pepper phenolic-rich extracts. Crop Protection, 84, 81–87.
Plodpai, P., Chuenchitt, S., Petcharat, V., Chakthong, S., & Voravuthikunchai, S. P. (2013). Anti-Rhizoctonia solani activity by Desmos chinensis extracts and its mechanism of action. Crop Protection, 43, 65–71.
Pusztahelyi, T., Holb, I. J., & Pócsi, I. (2015). Secondary metabolites in fungus-plant interactions. Frontiers in Plant Science, 6, 573. doi:10.3389/fpls.2015.00573.
Roddick, J. G., Rijnenberg, A. L., & Weissenberg, M. (1990). Membrane-disrupting properties of the steroidal glycoalkaloids solasonine and solamargine. Phytochemistry, 29, 1513–1518.
Rosado-Álvarez, C., Molinero-Ruiz, L., Rodríguez-Arcos, R., & Basallote-Ureba, M. J. (2014). Antifungal activity of asparagus extracts against phytopathogenic Fusarium oxysporum. Scientia Horticulturae, 171, 51–57.
Ruelas, C., Tiznado-Hernández, M. E., Sánchez-Estrada, A., Robles-Burgueno, M. R., & Troncoso-Rojas, R. (2006). Changes in phenolic acid content during Alternaria alternate infection in tomato fruit. Journal Phytopathological, 154, 236–244.
SAS Institute (2007). JMP statistics and graphics guide. Cary: SAS Institute.
Sayago, J. E., Ordoñez, R. M., Negrillo Kovacevich, L., Torres, S., & Isla, M. I. (2012). Antifungal activity of extracts of extremophile plants from the argentine puma to control citrus postharvest pathogens and green mold. Postharvest Biology and Technology, 67, 19–24.
Schreiber, K. (1968). Steroid alkaloids: the Solanum group. In R. H. F. Manske (Ed.), The alkaloids–chemistry and physiology (Vol. X, pp. 1–192). New York: Academic Press.
Smith, D. L., Garrison, M. C., Hollowell, J. E., Isleib, T. G., & Shew, B. B. (2008). Evaluation of application timing and efficacy of the fungicides fluazinam and boscalid for control of sclerotinia blight of peanut. Crop Protection, 27, 823–833.
Soylu, S., Yigitbas, H., Soylu, E. M., & Kurt, S. (2007). Antifungal effects of essential oils from oregano and fennel on Sclerotinia sclerotiorum. Journal of Applied Microbiology, 103, 1021–1030.
Subbarao, K. V., Hubbard, J. C., & Schulbach, K. F. (1997). Comparison of lettuce diseases and yield under subsurface drip and furrow irrigation. Phytopathology, 87, 877–883.
Tian, J., Ban, X., Zeng, H., Huang, B., He, J., & Wang, Y. (2011). In vitro and in vivo activity of essential oil from dill (Anethum graveolens) against fungal spoilage of cherry tomatoes. Food Control, 22, 1992–1999.
Toppino, L., Vale’, G., & Rotino, G. L. (2008). Inheritance of Fusarium wilt resistance introgressed from Solanum aethiopicum Gilo and Aculeatum groups into cultivated eggplant (S. melongena) and development of associated PCR-based markers. Molecular Breeding, 22, 237–250.
Trigui, M., Hsouna, A. B., Hammami, I., Culioli, G., Ksantini, M., Tounsi, S., & Jaoua, S. (2013). Efficacy of Lawsonia inermis leaves extract and its phenolic compounds against olive knot and crown gall diseases. Crop Protection, 45, 83–88.
Uppal, A. K., El Hadrami, A., Adam, L. R., Tenuta, M., & Daayf, F. (2008). Biological control of potato Verticillium wilt under controlled and field conditions using selected bacterial antagonists and plant extracts. Biological Control, 44, 90–100.
Walters, D. R. (2003). Polyamines and plant disease. Phytochemistry, 64, 97–107.
Wang, H., Wang, J., Peng, X., Zhou, P., Bai, N., Meng, J., & Deng, X. (2014). Control efficacy against rice sheath blight of Platycladus orientalis extract and its antifungal active compounds. European Journal of Plant Pathology, 140, 515–525.
Wu, S.-B., Meyer, R. S., Whitaker, B. D., Litt, A., & Kennelly, E. J. (2013). A new liquid chromatography-mass spectrometry-based strategy to integrate chemistry, morphology, and evolution of eggplant (Solanum) species. Journal of Chromatography A, 1314, 154–172.
Yun, J. E., Lee, H., Ko, H. J., Woo, E. R., & Lee, D. G. (2015). Fungicidal effect of isoquercitrin via inducing membrane disturbance. Biochimica et Biophysica Acta, 1848, 695–701.
Acknowledgements
This work was carried-out within the Project: “Valorizzazione di produzioni ortive campane di eccellenza con strumenti di genomica avanzata (GenHort)”, funded by Italian Ministry of Education, University and Research - MIUR through the EU program P.O.N. Research and Competitiveness 2007-2013 (PON_02_00395_3215002). The authors thank dr. Rocco Sileo from ALSIA (Basilicata Region), for providing Rotonda’s eggplant samples, and Prof. Adelia Emilia de Almeida of the Universidade Estadual Paulista, São Paulo, Brazil, for the purified solamargine and solasonine supply.
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Pane, C., Francese, G., Raimo, F. et al. Activity of foliar extracts of cultivated eggplants against sclerotinia lettuce drop disease and their phytochemical profiles. Eur J Plant Pathol 148, 687–697 (2017). https://doi.org/10.1007/s10658-016-1126-0
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DOI: https://doi.org/10.1007/s10658-016-1126-0