Decay mechanism of postharvest pathogens and their management using non-chemical and biological approaches
Keywords:
biocontrol, decay mechanism, pathogen,, plant extract, postharvestAbstract
Ripening is a physiological process that involves numerous biochemical changes including change in sugar composition and change in pH of the fruit and vegetable tissues. These changes attract a variety of pathogens causing decay, thereby leading to losses up to 25-50% in harvested crops. The infection by the postharvest pathogens may remain quiescent during fruit or vegetable growth due to unfavourable growth conditions for pathogen’s development to pathogenesis. Owing ripening and senescence the pathogen transform to necrotrophs, activation of the pathogen is primarily due to change in pH and cause typical decay symptoms. Some pathogens have developed a mechanism for altering the pH of host environment (tissue), thereby increasing virulence. The postharvest pathogens cause acidification by producing organic acids and alkalization by ammonification of host tissues. Management of postharvest tissue-decaying pathogens is usually performed by use of fungicides but due to raised environmental concerns and residual effects of fungicides on health alternative management strategies are required. This approach should be eco-friendly; the use of plant extract and biological agents are in limited use. Thus, it should be emphasized that management of postharvest food commodity (particularly those of direct consumption like fruit) pathogens can be achieved by altering the physiological environment and use of alternative management strategies to reduce the residual effect of inorganic fungicides and other chemicals. This review deals the both of the aspects and encourages the wide use of biorational and biological approaches for management of postharvest pathogens.
References
Albersheim, P. and Anderson, A.J. 1971. Proteins from plant cell walls inhibit polygalacturonases secreted by Plant Pathogens. Proceedings of the National Academy of Sciences, 68: 1815–1819.
Alkan, N., Fluhr, R, Sagi, M., Davydov, O. and Prusky, D. 2009. Ammonia secreted by Colletotrichum coccodes effects host NADPH oxidase activity enhancing cell death and pathogenicity in tomato fruits. Molecular Plant Microbe Interaction, 22: 256–263.
Alkan, N,, Fluhr, R., Sherman, A. and Prusky, D. 2008. Role of ammonia secretion and pH modulationon pathogenicity of Colletotrichum coccodes on tomato fruit. Molecular Plant Microbe Interaction, 21: 1058–1066.
Ansar, M., Ghatak, A., Ghatak, L.V., Srinivasaraghavan, A., Balodi, R. and Raj, C. 2017. Secondary metabolites in pathogen induced plant defense. In: Plant Secondary Metabolites: Their Roles in Stress Ecophysiology. Eds.: M.W. Siddiqui, and V. Bansal. ISBN: 9781771883566. Pp. 169–184.
Ark, P.A. and Thompson, J.P. 1959. Control of certain diseases of plants with antibiotics from garlic (Allium sativora). Plant Disease, 43: 276–282.
Arrebola, E., Jacobs, R. and Korsten, L. 2009. Iturin A is the principal inhibitor in the biocontrol activity of Bacillus amyloliquefaciens PPCB004 against postharvest fungal pathogens. Journal of Applied Microbiology, 108:386–395.
Bachmann, J. and Earles, R. 2000. Postharvest Handling of Fruits and Vegetables. NCAT.
Baker, K.F. 1987. Evaluating concepts of biological control of plant pathogens. Annual Review of Phytopathology, 25: 67–85. Basson, P.A. 1987. Poisoning of wildlife in southern Africa. Journal of South African Veterinary Association, 58: 219–228.
Baudoin, A. and Eckert, J.W. 1985. Development of resistance against Geotrichum candidum in lemon peel. Phytopathology, 75: 174–179.
Carvalho, D.D.C., Alves, E., Camargos, R.B., Oliveira, D.F., Scolforo, J.R.S., de Carvalho, D.A. and Batista, T.R.S. 2011. Plant extracts to control Alternaria alternata in Murcott tangor fruits. Revista Iberoamericana de Micología, 28: 173– 178.
Droby, S., Chalutz, E., Wilson, C.L. and Wisniewski, M.E. 1989. Characterization of the biological control activity of Debaryomyces hansenii in the control of Penicillium digitatum on grapefruit. Canadian Journal of Microbiology, 35: 794–800.
Drori, N.,Haimovich, H., Rollins, J., Dinoor, A., Okon, Y., Pines, O. and Prusky, D. 2003. External pH and nitrogen source affect secretion of pectatelyase by Colletotrichum gloeosporioides. Applied Environmental Microbiology, 69: 3258– 3262.
El-Mogy, M.M. and Alsanius, B.W. 2012. Cassia oil for controlling plant and human pathogens on fresh strawberries. Food Control, 28: 157–162.
Eshel, D., Miyara, I., Ailinng, T., Dinoor, A. and Prusky, D. 2002. pH regulates endoglucanase expression and virulence of Alternaria alternata in persimmon fruits. Molecular Plant Microbe Interaction, 15: 774–779.
Feng, W. and Zheng, X. 2007. Essential oils to control Alternaria alternata in vitro and in vivo. Food Control, 18: 1126–1130.
Germeier, C., Hedke, K. and Tiedemann, A.V. 1994. The use of pH-indicators in diagnostic media for acid producing plant pathogens. Plant Disease, 101: 498–507.
Ghatak, A., Ansar, M., Ghatak, L.V. and Balodi, R. 2015. Elucidation of relationship between Phytophthora leaf blight and fruit rot in tomato. Journal of Postharvest Technology, 03(02): 50–57.
Grainge, M. and Ahmed, S. 1988. Handbook of plants with pest control properties. Wilcy. New York. 470.
Gueldner, R.C., Reilly, C.C., Pusey, P.L., Costello, C.E. and Arrendale, R.F. 1988. Isolation and identification of iturins as antifungal peptides in biological control of peach brown rot with Bacillus sublilis. Journal of Agriculture Chemicals, 36: 366–370.
Hadas, Y., Goldberg, I., Pines, O. and Prusky, D. 2007. The relationship between expression of glucose oxidase, gluconic acid accumulation, acidification of host tissue and the pathogenicity of Penicillium expansum. Phytopathology, 97: 384– 390.
Janisiewicz, W.J. and Roitman, J. 1988. Biological control of blackmold and graymold on apple and pear with Pseudomonas cepacia. Plant Pathology, 78: 1697–1700.
Kerr, A. 1980. Biological control of crown gall through production of Agrocin 84. Plant Disease, 64: 30.
Kim, K.S., Min, J.Y. and Dickman, M.B. 2008. Oxalic acid is an elicitor of plant programmed cell death during Sclerotinia sclerotiorum disease development. Molecular Plant Microbe Interaction, 21: 605–612.
Lewis, J.A. and Papavizas, G.C. 1984. Chlamydospore formation by Trichoderma spp. in natural substrates. Canadian Journal of Microbiology, 30: 17.
Manteau, S., Abouna, S., Lambert, B. and Legendre, L. 2003. Differential regulation by ambient pH of putative virulence factors secretion by the phytopathogenic fungus Botrytis cinerea. Microbiological Ecology, 43: 359–366.
Maruzzella, J.C., Scrandis, D.A., Scrandis, J.B. and Grabon, G. 1960. Action of odoriterous organic chemicals and essential oils on wood destroying fungi. Plant Disease, 44: 789–792.
Matos, O.C. and Barreiro, M.G. 2004. Safety use of bioactive products of plant origin for the control of post harvested fungal diseases of “Rocha” pear. IV Simposium Ibérico de Maturação e pós-colheita: Frutos Hortícolas. Livro de Actas, Pp. 525–529.
Mendgen, K. and Hahn, M. 2001. Plant infection and the establishment of fungal biotrophy. Trends in Plant Science, 6: 496– 498.
Perfect, S.E., Hughes, B.H., Connell, R.J. and Green, J.R. 1999. Colletotrichum: a model genus for studies on pathology and fungal plant interactions. Fungal Genetic Biology, 27: 186–198.
Pezet, R., Viret, O., Perret, C. and Tabacchi, R. 2003. Latency of Botrytis cinerea and biochemical studies during growth and ripening of two grape berry cultivars, respectively susceptible and resistant to grey mould. Journal of Phytopathology, 151: 208–214.
Prasad, K. and Stadelbacker, G.J. 1973. Control of postharvest decay of fresh raspberries by acetaldehyde vapor. Plant Disease, 57: 795-797.
Prusky, D. 1996. Pathogen quiescence in postharvest diseases. Annual Review of Phytopathology, 34: 413–434.
Prusky, D. and Lichter, A. 2007. Activation of quiescent infections by postharvest pathogens during transition from the biotrophic to the necrotrophic stage. Microbiology, 268: 1–8.
Prusky, D. and Yakoby, N. 2003. Pathogenic fungi: leading or led by ambient pH? Molecular Plant Pathology, 4: 509–516.
Prusky, D., McEvoy, J.L., Saftner, R., Conway, W.S. and Jones, R. 2004. The relationship between host acidification and virulence of Penicillium spp. on apple and citrus fruit. Phytopathology, 94: 44–51.
Pusey, P.L. and Wilson, C.L. 1984. Postharvest biological control of stone fruit brown rot by Bacillus subtilis. Plant Disease, 68: 753–756.
Pusey, P.L. 1989. Use of Bacillus subtilis and related organisms as biofungicides. Petrichem Science, 27: 133–140.
Regnier, T., du Plooy, W., Combrinck, S. and Botha, B. 2008. Fungitoxicity of Lippia scaberrima essential oil and selected terpenoid components on two mango postharvest spoilage pathogens. Postharvest Biology Technology, 48: 254– 258.
Rollins, J.A. and Dickman, M.B. 2001. pH signaling in Sclerotinia sclerotiorum: Identification of pacC/RIM1 homolog. Applied Environmental Microbiology, 67: 75–81.
Rosenthal, G.A. and Jarsen, D.H. 1979. Herbivores and their Interaction with Secondarv Plant Metabolites. Academic Press, New York, 71: 8.
Schaller, A. and Oecking, C. 1999. Modulation of plasma membrane H+ ATPase activity differentially activates wound and pathogen defense responses in tomato plants. Plant Cell, 11: 263–272.
Singh, V. and Deverall, B.J. 1984. Bacillus subtilis as a control agent against fungal pathogens of citrus fruit. Transactions of the British Mycological Society, 83: 487–490.
Skene, D.S. 1981. Wound healing in apple fruits: The anatomical response of orange pippin at different stages of development. Journal of Horticultural Science, 56: 145–153.
Sommer, N.F. and Fartlage, R.J. 1988. Resistance in infection in mature apple and pear fruits. 5th International Congress of Plant Pathology, 424 (Kyoto, Japan).
Stewart, J.K., Aharoni, Y., Hartsell, P.L. and Young, D.K. 1980. Symptoms or acetaldehyde injury of head lettuce. Horticultural Science, 15: 148–149.
Tian, J., Ban, X., Zeng, H., He, J., Huang, B. and Wang, Y. 2011. Chemical composition and antifungal activity of essential oil from Cicuta virosa L. var. latisecta Celak. International Journal of Food Microbiology, 145: 464–470.
Tian, S.P., Fan, Q., Xu, Y. and Jiang, A.L. 2002. Effects of calcium on biocontrol activity of yeast antagonists against the postharvest fungal pathogen Rhizopus stolonifer. Plant Pathology, 51: 352–358.
Troncoso, R., Espinoza, C., Sánchez-Estrada, A., Tiznado, M.E. and García, H.S. 2005. Analysis of the isothiocyanates present in cabbage leaves extract and their potential application to control Alternaria rot in bell peppers. Food Research International, 38: 701–708.
Tzortzakis, N.G. 2010. Ethanol, vinegar and Origanum vulgare oil vapour suppress the development of anthracnose rot in tomato fruit. International Journal of Food Microbiology, 142: 14–18.
Wilson, C.L. and Wisniewski, M.E. 1989. Biological control of postharvest diseases of fruits and vegetables: An emerging technology. Annual Review of Phytopathology, 27: 425–441.
Wilson, C.L. 1989. Managing the microflora of harvested fruits and vegetables to enhance resistance. Phytopathology, 79: 1387–1390.
Wisniewski, M.E., Wilson, C.L. and Hershberger, W. 1989. Characterization of inhibition of Rhizopus stolonifer germination and growth by Enterobacter cloacae. Canadian Journal of Botany, 67: 2317–2323.
Yakoby, N., Beno-Moualem, D., Keen, N.T., Dinoor, A., Pines, O. and Prusky, D. 2001. Colletotrichum gloeosporioides pelB is an important factor in avocado fruit infection. Molecular Plant Microbes Interaction, 14: 988–995.
Yakoby, N., Kobiler, I., Dinoor, A. and Prusky, D. 2000. pH regulation of pectatelyase secretion modulates the attack of Colletotrichum gloeosporioides on avocado fruits. Applied Environmental Microbiology, 66: 1026–1030.