Main Article Content
Abstract
This study aimed to identify prevalent pathogens of a caused moldy core of postharvest apple fruits and the efficiency of essential oils (EO) of clove (Syzygium aromaticum), eucalyptus (Eucalyptus globulus), sage (Salvia officinalis), and thyme (Thymus vulgaris), and Trichoderma harzianum filtrate to inhibit pathogens growth of Alternaria alternata, Botrytis cinerea, and Penicillium griseofulvum. The examined pathogens are recognized dependent on morphological and also molecular identification. In vivo, clove EO and T. harzianum filtrate were strongly restricted decay area on fruits with 82.36% and 81.69%, respectively when applied as direct inhibition. Growth of all examined pathogens was entirely stopped on fruits treated with both clove and thyme oils at 10%. The results also illustrated that T. harzianum filtrate and EOs exhibited considerable growth inhibition of B. cinerea and ranged between 86.53% and 100%. The lowest inhibitory potential of EOs 47.95% and 75.9% were observed with P. griseofulvum. T. harzianum filtrate was the most effective biocontrol that inhibited fruit decay by 64.5% followed by 45.9%, 38.6%, 37.5%, and 35.9% when utilized EOs of thyme, sage, eucalyptus, and clove, respectively. The growth of both pathogens A. alternata and B. cinerea depressed with up to 90% using T. harzianum filtrate followed by EOs of eucalyptus and thyme. Whereas fruits inoculated with P. griseofulvum were not frustrated when applied to each EOs or T. harzianum. Their systemic induction was restricted between 3.16% and 23.82%.
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References
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References
Abo-El-Seoud, M.A., Sarhan, M. M., Omar, A. E., & Helal, I. (2005). Biocide’s formulation of essential oils has antimicrobial activity. Archives of Phytopathology and Plant Protection, 38(3), 175-184.
https://doi.org/10.1080/03235400500094340
Adams, R. P. (2007). Identification of Essential Oils Components by Gas Chromatography/Quadruple Mass Spectroscopy, 4th edition. Allured Publishing Corporation, Carol Stream, Illinois, USA. 804pp.
Andrew, M., Peever, T. L., & Pryor, B. M. (2009). An expanded multilocus phylogeny does not resolve morphological species within the small-spored Alternaria species complex. Mycologia, 101, 95-109.
https://doi.org/10.3852/08-135
Anjum, T. & Akhtar, N. (2012). Antifungal activity of essential oils extracted from clove, cumin, and cinnamon against blue mold disease on citrus fruit. International Conference on Applied Life Sciences (ICALS2012) Turkey, September 10-12, 321-326.
https://www.intechopen.com/chapters/39915
Banani, H., Marcet-Houben, M., Ballester, A., Abbruscato, P., González-Candelas, L., Gabaldón, T., & Spadaro, D. (2016). Genome sequencing and secondary metabolism of the postharvest pathogen Penicillium griseofulvum. BMC Genomics, 17, 19.
https://doi.org/10.1186/s12864-015-2347-x
Barnett, H.L., & Hunter, B.B. (1998). Illustrated Genera of Imperfect Fungi. 4th edn, APS Press, Minncapolis, Minesota, St. Paul, 218pp.
Behiry, S., Nasser, R., Abd El-Kareem, M., Ali, H., & Salem, M. (2020). Mass spectroscopic analysis. MNDO quantum chemical studies and antifungal activity of essential and recovered oil constituents of lemon-scented game against three common molds. Processes, 8(3), 275.
https://doi.org/10.3390/pr8030275
Calvo, G., & Sozzi, G. O. (2004). Improvement of postharvest storage quality of “Red Clapp’s” pears by treatment with 1-methylcyclopropene at low temperature. Journal Horticulture Science Biotechnology, 79, 930-934.
https://doi.org/10.1080/14620316.2004.11511868
Campos, M. R., Ruiz, J., Chel-Guerrero, L., & Ancna, D. (2015). Coccoloba uvifera L. (Polygonaceae) fruit: Phytochemical screening and potential antioxidant activity. Journal of Chemistry, 1, 4-9.
https://doi.org/10.1155/2015/534954
Choudhury, D., Dobhal, P., Srivastava, S., Soumen, S., & Kundu, S. (2018). Role of botanical plant extracts to control plant pathogens, a review. Indian Journal of Agricultural Research, 52(4), 341-346
https://doi.org/10.18805/IJARe.A-5005
Coley-Smith, J. R., Verhoeff, K., & Jarvis, W.R. (1980). The Biology of Botrytis. Academic Press, London, 318pp.
Eid, A. M. (2013). Biological control of post-harvest diseases on apple by using plant essential oils and Trichoderma culture filtrates” Ph. D. Thesis. Agrobiology and Agrochemistry, University of Naples “Federico Ii” Italy. 170 pp.
Elad, Y., Williamson, B., Tudzynski, P., & Delen, N. (2007). Botrytis: Biology, Pathology, and Control, Springer Science, Dordrecht, 393pp.
Ellis, M. B. (1970). More Dematious Hypomycetes. Commonwealth Mycol. England, 507pp.
Fayyadh, M. A., & Yousif, E. Q. (2019). Biological control of tomato leaf spot disease caused by Alternaria alternata using Chaetomium globosum and some other saprophytic fungi. IOP Conf. Ser.: Earth Environment Science 388 012017.
Gao, L. L., Zhang, Q., Sun, X. Y., Jiang, L., Zhang, R., Sun, G. Y., Zha, Y. L., & Biggs, A. R. (2013). Etiology of moldy core, core browning, and core rot of Fuji apple in China. Plant Diseases, 97, 510-516.
https://doi.org/10.1094/PDIS-01-12-0024-RE
Goes, L. B., Lima da Costa, A. B., Freire, L. L. C., & Oliveria, N. T. (2002). Randomly Amplified Polymorphic DNA of Trichoderma isolates and antagonism against Rhizoctonia solani. Brazilian Archives of Biology and Technology, 45(2), 1-13.
https://doi.org/10.1590/S1516-89132002000200005
Hadizadeh, I., Peivastegan, B., & Kolahi, M. (2009). Antifungal activity of Nettle (Urticadioica L.), Colocynth (Citrullus colocynthis L. Schrad), Oleander (Nerium oleander L.) and Konar (Ziziphusspina christi L.) extracts on plants pathogenic fungi. Pakistan Journal of Biological Sciences, 12, 58-63.
https://doi.org/10.3923/pjbs.2009.58.63
Harman, G. E. (2006). Overview of mechanisms and uses of Trichoderma spp. Phytopathology, 96, 190-194. https://doi.org/10.1094/PHYTO-96-0190
Harman, G., Howell, C., Viterbo, A., Chet, I., & Lorito, M. (2004). Trichoderma species - opportunistic, a virulent plant symbionts. Nature Reviews Microbiology, 2, 43-56.
https://doi.org/10.1038/nrmicro797
Jhalegar, M.J., Sharma, R.R., & Singh, D. (2014). In vitro and in vivo activity of essential oils against major postharvest pathogens of Kinnow (Citrus nobilis × C. deliciosa) mandarin. Journal of Food Scientists & Technologists. 52 (4), 2229-2237.
https://doi.org/10.1007/s13197-014-1281-2
Kishore, G. K., Pande, S., & Harish, S. (2007). Evaluation of essential oils and their components for broad-spectrum antifungal activity and control of late leaf spot and crown rot diseases in peanut. Plant Disease, 91, 375-379.
https://doi.org/10.1094/PDIS-91-4-0375
Lopez-Reyes, J., Spadaro. D., Gullino. M., & Garibaldi, A. (2010). Efficacy of plant essential oils on postharvest control of rot caused by fungi on four cultivars of apples in vivo. Flavour and Fragrance Journal, 25, 171-177.
https://doi.org/10.1002/ffj.1989
Lorito, M., Di Pietro, A., Hayes, C. K., Woo, S. L., & Harman, G. E. (1993). Antifungal, synergistic interaction between chitinolytic enzymes from Trichoderma harzianum and Enterobacter cloacae. Phytopathology, 83, 721-728.
https://doi.org/10.1094/Phyto-83-721
Lorito, M., Peterbauer, C., Hayes, C. K., Woo, S. L., & Harman, G. E. (1994). Synergistic interaction between fungal cell wall degrading enzymes and different antifungal compounds enhances inhibition of spore germination. Microbiology, 140(3), 623-629. https://doi.org/10.1099/00221287-140-3-623
Made, B. Y.; Fayyadh, M. F., & Al-Luaibi, S. S. (2019). Evaluation of biofungicide formulation of Trichoderma longibrachiatum in controlling of tomato seedling damping-off caused by Rhizoctonia solani. Basrah Journal of Agricultural Science, 32(2), 135-149.
https://doi.org/10.37077/25200860.2019.204
Mc Leod, A. (2014). Moldy core and core rot. Pp, 40-41 In Sutton, T. B., Aldwinkle, H. S., Agnello, A. M., & Walgenbach, J. F. (Eds.). Compendium of Apple and Pear Diseases and Pest, 2nd ed. eds. American Phytopathological Society, St Paul, MN. 224pp.
Mohamed, A., Behiry, S., Ali, H., El-Hefiny, M., Salem, M. & Ashmawy, N. (2020). Phytochemical compounds of branches from P. halepseis oily liquid extract and S. terebinthifolius essential oils and their potential antifungal activity. Prosses, 8(3), 330.
https://doi.org/10.3390/pr8030330
Morgan, D. J. (1971). Numerical taxonomic studies of the genus Botrytis. Transactions of British Mycological Society, 56, 319-325.
https://doi.org/10.1016/S0007-1536(71)80125-0
Notte, A., Plaza, V., Marambio-Alvarado, V., Olivares-Urbina, l., Poblete-Morales, M., Silva-Moreno, E., & Castillo, A. (2021). Molecular identification and characterization of Botrytis cinerea associated with the endemic flora of semi-desert climate in Chile. Current Research in Microbial Sciences, 2, 1-11.
https://doi.org/10.1016/j.crmicr.2021.100049
Ntasiou, P., Myresiotis, C., Konstantinou, S., Papadopoulou-Mourkidou, E., & Karaoglanidis, G. S. (2015). Identification, characterization, and mycotoxigenic ability of Alternaria spp. causing core rot of apple fruit in Greece. International Journal of Food Microbiology, 197, 22-29.
https://doi.org/10.1016/j.ijfoodmicro.2014.12.008
Okla, M. K., Alamri, S. A., Salem, M. Z., Ali, H. M., Behiry, S. I., Nassser, R. A., & Soufan, W. (2019). Yield, phytochemical constituents, and antibacterial activity of essential oils from the leaves, twigs, branches, branch wood, and branch bark of sour orange (Citrus aurantium L.). Processes, 7(6), 363.
https://doi.org/10.3390/pr7060363
Parveen, S., Wani, A.H., Bhat, M. Y., & Koka, J. A. (2016). Biological control of postharvest fungal rots of rosaceous fruits using microbial antagonists and plant extracts a review. Czech Mycology, 68(1), 41–66.
https://doi.org/10.33585/CMY.68102
Peralta-Ruiz, Y., Grande-Tovar, C. D., Navia Porras, D. P., Sinning-Mangonez, A., Delgado-Ospina, J., González-Locarno, M., Maza Pautt, Y., & Chaves-López, C. (2021). Packham’s triumph pears (Pyrus communis L.) post-harvest treatment during cold storage based on chitosan and rue essential oil. Molecules, 26, 725.
https://doi.org/10.3390/molecules26030725
Povi, L.-E., Batomayena, B., Hode, T. A., Kwashie, E. G., Kodjo, A., & Messanvi, G. (2015). Phytochemical screening, antioxidant and hypoglycemic activity of Coccoloba uvifera leaves and Waltheria indica roots extracts. International Journal of Pharmacy and Pharmaceutical Sciences, 7(5), 279-283.
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