Open access peer-reviewed chapter

Alternative Eco-Friendly Methods in the Control of Post-Harvest Decay of Tropical and Subtropical Fruits

Written By

Ramsés González-Estrada, Francisco Blancas-Benítez, Rita M. Velázquez-Estrada, Beatriz Montaño-Leyva, Anelsy Ramos-Guerrero, Lizet Aguirre-Güitrón, Cristina Moreno-Hernández, Leonardo Coronado-Partida, Juan A. Herrera-González, Carlos A. Rodríguez-Guzmán, José A. Del Ángel-Cruz, Edson Rayón-Díaz, Hector J. Cortés-Rivera, Miguel A. Santoyo-González and Porfirio Gutierrez-Martinez

Submitted: 12 December 2018 Reviewed: 06 March 2019 Published: 11 April 2019

DOI: 10.5772/intechopen.85682

From the Edited Volume

Modern Fruit Industry

Edited by Ibrahim Kahramanoglu, Nesibe Ebru Kafkas, Ayzin Küden and Songül Çömlekçioğlu

Chapter metrics overview

1,810 Chapter Downloads

View Full Metrics

Abstract

The effectiveness on several fruits by the application of alternative methods against fungi is summarized in the present chapter. Several investigations have reported the efficacy of these technologies for controlling fungal infections. Currently, high post-harvest loses have been reported due to several factors such as inefficient management, lack of training for farmers, and problems with appropriate conditions for storage of fruits and vegetables. Even now, in many countries, post-harvest disease control is led by the application of chemical fungicides. However, in this time, awareness about fungi resistance, environmental, and health issues has led to the research of eco-friendly and effective alternatives for disease management. The pathogen establishment on fruits can be affected by the application of GRAS compounds like chitosan, essential oils, salts, among others; besides, their efficacy can be enhanced by their combination with other technologies like ultrasound. Thus, the applications of these alternatives are suitable approaches for post-harvest management of fruits.

Keywords

  • alternative systems
  • antifungal activity
  • postharvest fungi
  • tropical and subtropical fruits

1. Introduction

The consumption of fresh fruits and vegetables is essential for a healthy diet [1]. However, their production can be affected by microbial pathogens (mostly fungus) during the production chain [2]. In order to reduce the presence of pathogens, several post-harvest technologies have been applied [2]. One of them is the application of chemical fungicides; however, this practice is not accepted due to environmental and health issues [3]. Other alternatives are the use of eco-friendly substances such as generally recognized as safe (GRAS) compounds and emergent technologies like ultrasound and fogging. Currently, consumers demand fresh products free of chemical residues; therefore, it is necessary to develop technologies eco-friendly, effective to protect against pathogens infection, and that these technologies can maintain the fruit quality. Alternative systems such as edible coatings, essential oils, salts, natural compounds (plant extracts), among others to chemical use are suitable approaches for post-harvest disease management. These alternatives can be applied in combination with other control systems like emerging technologies (ultrasound) in order to improve their efficacy. The aim of this chapter is to make a compilation of several studies conducted on fruits for controlling important pathogens in several crops.

Advertisement

2. Fruit industry: importance in the world

Fruits and vegetables are essential sources for the micronutrients needed for healthier diets [4]. The potential of vegetables is to generate positive economic and nutritional impacts. The estimated farm gate value of annual global fruit and vegetable production, at nearly $1 trillion per year, exceeds the farm gate value of all food grains combined (US$ 837 billion). On the other hand, it is likely that the production of fruit and vegetable crops will not increase as rapidly as would be expected. Environmental changes can affect many different aspects of agricultural production. With greater climatic variability, temperature patterns and precipitation are some of the problems faced by fruit producers [5]. Technological advances have focused their efforts on the development of new varieties, crop management techniques, and innovations in postharvest handling and processing. Even in high-income countries such as the US, there is evidence that public funding for research in the agricultural area is less than expected, given its economic value and its contribution to human health [6].

Advertisement

3. Post-harvest losses: tropical and subtropical fruit

It is reported that about one-third of the production of food intended for human consumption is lost or wasted worldwide, which is roughly equivalent to 1.3 billion tons per year. This means that huge amounts of resources directed to food production are used in vain, and that greenhouse gas emissions caused by food production that is lost or wasted are also unnecessary [7]. A very significant part of the food that deteriorates or that is lost at post-harvest stage are fruits and vegetables. These losses occur throughout the management system of fruits during the harvest, transfer to the packinghouse, in the packing, during the storage, transportation and distribution to marketing centers. The causes of the losses in post-harvest are due to economic limitations, the lack of post-harvest technology as well as the lack of trained personnel about the knowledge in technology, management, physiology, and post-harvest pathology of horticultural products. This problem occurs mainly in developing countries, reaching up to 30 or 40% of post-harvest losses [8].

The fruits during their growth in the field are exposed to the attack of pathogenic fungi; they can be established as a latent infection in the fruit; and when the fruit begins its maturation process, the fungi can be activated and continue with their development, leading the deterioration of fruit. To control these pathogens, synthetic fungicides have been applied in a traditional manner; however, due to pollution and the environment issues, damage to the health of people and in general to living beings, as well as generating resistant strains of fungi, it is necessary to find alternatives to pathogen control [9, 10]. Currently, the research of alternative systems to the use of fungicides to control the losses caused by fungi, applying products of biological origin as well as organic and inorganic salts, among others, in order to control fungi infections, without contaminating the environment and without harming living beings has increased [11, 12]. Reducing the losses of post-harvest could solve the problem of hunger in many countries of the world, where not only it is producing more food but rather it is to conserve the food that is currently produced.

Advertisement

4. Chemical methods: applications for post-harvest disease management

Most of the post-harvest losses are attributed to the attack of a large amount of fungus in tropical and subtropical fruits. Chemical control of post-harvest diseases is widely used to maintain fruit quality [13]. There are a wide variety of fungicides for chemical control, and the vast majority is destined or directed to the pre-harvest applications, leaving aside the use in post-harvest stage [14, 15]. To make efficient the use of chemical fungicides, it is necessary to know both the pathogen and the fungicide. From the pathogen, it is necessary to know the genus and the species as well as their concentration found at pre- and post-harvest stages. On the part of the fungicide, it is necessary to know the mode and site of action, as well as the maximum residual limit (MRL) (Table 1) permitted on fruits and specific regulations where the fruit will be exported [16]. In Table 1, some fungicides used for post-harvest disease of tropical and subtropical fruit diseases are listed. The site and mode of action are summarized in the table, as well as the MRL that are allowed in the US [17] and the EU [18]. An important consequence for the inadequate use and irrational applications of chemical treatments is microbial resistance, and in this sense, it is recommended to alternate formulations to avoid this problem. Besides, post-harvest chemical control should be regionalized to the specific conditions and environment of each crop [19]. It is important to mention that agrochemical companies suggest the doses and formulations to use in a specific crop. At this point, public research centers have an important contribution, not only to verify the efficiency of fungicides but also to establish strategies for the efficient use of post-harvest chemical control [15]. Considering the new consumer tendencies, about secure products free of chemical residues, it is necessary to consider the rational use of chemical fungicides without exceeding the MRL [20, 21, 22].

Common nameMRL (ppm)Chemical groupMode actionTarget site
EU [17]US [16]
AvocadoMangoPapayaAvocadoMangoPapaya
Cyprodinil1.21.21.2111Anilino-pyrimidinesAmino acids and protein synthesisMethionine biosynthesis (proposed)
Carbendazim323BenzimidazolesCytoskeleton and motor proteinsß-tubulin assembly in mitosis
Thiabendazole101053310
Pyraclostrobin0.60.60.60.050.2Methoxy-carbamatesRespirationComplex III: cytochrome bc1 (ubiquinol oxidase) at Qo site
Trifloxystrobin0.70.70.7Oximino-acetates
Fludioxonil555555PhenylpyrrolesSignal transductionMAP/Histidine-Kinase in osmotic signal transduction
Iprodione101010Dicarboximides
Prochloraz521ImidazolesSterol biosynthesis in membranesC14-demethylase in sterol biosynthesis
Difenoconazole0.10.60.60.070.2Triazoles

Table 1.

Common name, chemical group, mode and target site as well as its MRL in some fruits for consumption [23].

Therefore, the worldwide trend for both consumers and researchers is the reduction of the use of chemical fungicides and the research for biological, organic, and environmentally friendly alternatives. All this is under certification systems to guarantee the implementation, improvement, integration, and harmonization of all mechanisms to ensure a production of healthy and good quality fruit, with high traceability (GLOBALG.AP) [23, 24].

Advertisement

5. Alternative methods in the control of post-harvest decay of tropical and subtropical fruit

5.1 Chitosan

The excessive use of agrochemicals in tropical and in subtropical fruit has leaded the search for new natural products, eco-friendly, and nontoxic to humans. In several investigations, chitosan has proved their efficacy for controlling several post-harvest diseases. Several mechanisms of action have been proposed for chitosan:

  1. Pathogens: the interaction of the biopolymer with the microorganism causes changes on cell permeability affecting biochemical processes like homeostasis, fungal respiration as well as nutrient uptake and the synthesis of proteins causing severe damage on fungal cells [12].

  2. Plants: induction of defense systems, by the production of important enzymes (phenylalanine ammonium lyase, polyphenol oxidase, among others) and plant immunity, favoring the adaptation of plants to biotic and abiotic stresses [25].

  3. Fruits: the capability of chitosan to form mechanical barrier (coating) on fruits offers several advantages of coated fruits like a reduction on respiration rate, avoid water losses maintaining fruit firmness, maintenance of color, among others. Thus the shelf-life of fruits can be extended [36].

The induction of defense systems has been reported by the application of chitosan at post-harvest stage, preventing the development and dispersion of important pathogens such as Colletotrichum gloeosporioides, Alternaria alternata, Rhizopus stolonifer, and Fusarium oxysporum [26, 27, 28]. Enzymatic activity is also affected by the curative application of chitosan, and it increases the activity of polyphenol oxidase (PPO), peroxidase (POD), and phenylalanine amino-lyase (PAL) that induce the expression genes of β-1,3-glucanase and chitinase, involved in the defense against pathogens [29, 30]. The physiological mechanisms of the fruit are positively affected by the application of chitosan at post-harvest management under biotic and abiotic stress, that is why the post-harvest shelf-life and quality (firmness, appearance, color) of fruit can be maintained during the storage time, besides the respiration rate and ethylene production of fruits decrease [31]. Some studies reported an enhanced content of total soluble solids, ascorbic acid, the nutritional value, and acceptability [30, 32, 33]. Chitosan is compatible with other substances like organic salts, gums, or essential oils, and this alternative can improve their efficacy against pathogens due to a synergistic effect [34, 35]. Even when important information has been generated on the use of chitosan in post-harvest tropical and subtropical fruits, it is still necessary to generate information on the regulation (activation and suppression) of genes that participate in both systems of acquired resistance and those that control the processes physiological, enzymatic, and physicochemical factors of maturation in post-harvest.

5.2 Essential oils

The use of GRAS substances like essential oils (EOs) has increased in the last years, due to the research of alternatives to chemical treatments for disease control [36]. Several investigations have reported the efficacy of essential oils in vitro and vivo tests [37, 38, 39, 40]. The application of EOs in fruits has advantages such as: high effectiveness against several pathogens and low toxicity (nontarget microorganism and humans) [36]. EOs can be applied on fruits directly (vapor phase) or incorporated as active microbial agents in different matrices (films, coatings, among others) at pre-harvest or post-harvest stages. In a recent investigation, cinnamon essential oil was added into biodegradable polyester nets for controlling A. alternata [41]. The results are promising due to their efficacy in vitro tests by stopping the development of fungus on mycelial growth (72% of inhibition) and the total control of germination. The presence of essential oil did not alter the biodegradability of nets as well as their efficiency to maintain fruit quality and the disease control on infected fruits by reducing the disease incidence. Incorporation of EOs into edible films for active packaging has demonstrated high efficacy against important post-harvest pathogens. Recently, soy protein isolate was used as a carrier for limonene with good results against P. italicum (isolated from infected limes) [42]. The liberation and efficacy (in vitro tests) of the active agents were evaluated simulating the storage conditions of limes (13 and 28°C). The mycelial growth and germination process were successfully inhibited by the incorporation of limonene into the protein matrix. The results in vitro were confirmed in infected limes with P. italicum by reducing the severity and blue mold incidence with the application of soy protein isolate with limonene added [43]. In another study, films based on chitosan, oleic acid/beeswax, and lemon essential oils were tested on tomatoes for preserving their quality. According to their results, the applications of these films improve the fruit quality by reducing water losses and the maintenance of appearance of fruit [44]. In a recent study, anthracnose and stem-end rot in the green-skinned on avocado fruits was successfully controlled by the application of thyme oil in combination with a prochloraz solution; besides, this treatment improved fruit quality (firmness) during the storage time [20]. Essential oils of copaiba and eucalyptus were tested against Alternaria alternata and Colletotrichum musae under in vitro, and the results showed good efficacy at low concentrations of the treatments (0.0–1.0%) [45].

The efficacy of black caraway (Carum carvi) and anise (Pimpinella anisum) essential oils was tested against Penicillium digitatum in vitro as well as in vivo (on oranges) evaluations. The results showed that treatments were capable to control fungi development in vivo and in vitro tests; besides, the quality of oranges was preserved by the application of the treatment of 600 μL/L [46]. In a study, lemongrass oil was tested against Colletotrichum coccodes, Botrytis cinerea, Cladosporium herbarum, Rhizopus stolonifer, and Aspergillus niger in vitro. According to their results, fungal development, sporulation process as well as spore germination of fungi was affected in different levels (depending on the concentration of treatment) when they were exposed to the treatments by stopping their development [47].

Thus, utilization of EOs for controlling diseases can be alternatives to chemical treatments.

5.3 Plant extracts

Currently, the study of fruits and vegetables at post-harvest stage has focused on the development of alternative control for conservation with better efficiency, sustainability, and lower cost than conventional methods. In this sense, some extracts from plants have proven to be a viable alternative for the extraction of substances with antimicrobial activity with high efficiency and low toxicity [48]. In a study, aqueous and ethanolic extracts from garlic (Allium sativum) were evaluated on citrus fruits (Citrus sinensis, Jaffa, and Valencia) with good results (Table 2), and it is suggested that the highest antifungal activity of the extract can be produced by the presence of allicin in the soluble fractions of extracts from garlic [49]. In the same way, extracts of garlic, ginger, and celery have been shown to have different effects on the control of the incidence of Penicillium sp. in fruits of the species Citrus reticulata Blanco [50]. In a similar study, soybean extracts were evaluated as protection method on oranges infected with P. digitatum, and green mold was significantly reduced (88–100%) due to the presence of β-conglycinin in the soy protein fraction [51]. In recent years, extracts of some angiosperm species have been studied as natural fungicides, such as Orobanche crenata and Sanguisorba minor, which have shown high efficiency in the control of the diseases produced by Monilinia laxa in stone fruits such as apricot, cherry, and nectarine [52, 53, 54]. For the case O. crenata extracts, the antifungal activity is attributed for the presence of the phenolic compound verbacoside, and for S. minor extracts, the efficacy is related to the presence of a combination of phenolic compounds like caffeic acid, quercetin, luteolin, and kaempferol [52, 53, 54].

FruitDiseasePathogenExtract sourceDisease inhibition (%)References
OrangeBlue moldP. italicumGarlic92[47]
Green moldP. digitatumGarlic90[47]
Soybean100[49]
Citrus rotPenicillium sp.Garlic80.2[48]
Celery5.3
Ginger16.3
CherryBrown rotM. laxaO. crenata76[51]
S. minor89
NectarineBrown rotM. laxaO. crenata75[53]
S. minor100

Table 2.

Disease control of plant extracts.

An important approach in fruits is quality. In this sense, the application of some plant extracts can help preserve the fruit quality and improve their shelf life. In a recent investigation, the application of guava extracts (from leaves) and lemon on banana fruits (Musa sapientum L.) at post-harvest stage considerably improved the shelf life of the fruits (up to 8 days) compared to untreated fruits (only 4 days), having a positive effect on the conservation of the physicochemical characteristics of fruit during the storage time [55]. Utilization of plant extracts for disease management in both pre- and post-harvest stages can be another alternative to the use of chemical treatments, due to their effectiveness and eco-friendly characteristics.

5.4 Acetic acid, peracetic acid, and hydrogen peroxide

The use of sanitizing agents such as acetic acid (C2H4O2), peracetic acid (C2H4O3), and hydrogen peroxide (H2O2) on the processing and marketing industries of fruits and vegetables have been considered a useful tool to the control of different kinds of pathogens [56]. The FDA has approved the use of these compounds because their decomposition products are water, oxygen, and acetic acid, and these are not toxic compounds and are friendly with the environment [57, 58]. For these reasons, they are classified as GRAS [56]. The acetic acid, peracetic acid, and hydrogen peroxide are recognized as antimicrobial and antifungal agents, because they have high spectrum of attack on bacteria, fungi, spores, and viruses. In vivo studies realized on fresh and fresh-cut horticultural products confirm their antimicrobial capacity with the reduction of human pathogens such as Staphylococcus aureus, Escherichia coli, Streptococcus mutant, Salmonella Thompson, and Listeria monocytogenes [59, 60]. The application of acetic acid, peracetic acid, and hydrogen peroxide also decreases the microbial pollution of aerobic mesophiles, molds, and yeast, obtaining with these innocuous and acceptable products to the consumers [61]. In fruits like guavas, peaches, and tomatoes, the antifungal effect of these sanitizers has been confirmed with the inhibition of phytopathogens such as Rhizopus stolonifer, Monilinia fructicola, Alternaria alternata, Botrytis cinerea, Fusarium solani, and Rhizoctonia solani [62, 63, 64, 65]. The inactivation capacity of these compounds on pathogens is based on their high oxidizing power, producing reactive oxygen species (ROS) that generate instability in biomolecules such as DNA, lipids, and proteins, which are vital for the correct cellular functioning of pathogens [56]. Usually, the application of these sanitizers at post-harvest stage in fruits and vegetables is by spraying, dipping, and fumigation. Several authors have investigated the pathogen inhibitory effect of each application system, with the finality to know which application system has better efficiency. The inhibition of A. alternata and B. cinerea in tomato fruits treated with acetic acid by immersion (50 ml/L by 3 min) and fumigation (50 μl/L by 30 min) was evaluated [64]. The results of this investigation showed the efficacy of both application systems. The growth inhibition of the pathogens tested ranged from 90 to 100% by immersion and fumigation, respectively. In strawberry fruits infected with B. cinerea and treated with peracetic acid, where the lower incidence of gray mold disease was obtained with the fumigation system (66%) compared to immersion method (80%) [66]. These results confirm that the capacity of inhibition of these GRAS substances against phytopathogens depends not only on the concentration used but also on the exposure time, the microorganism tested, and the application method [67]. The individual application of acetic acid, peracetic acid, and hydrogen peroxide has controlled microbial contamination in an acceptable way, but different reports have been showed that their combination with other compounds and technologies increases microbial control. Some of the technologies used include ultrasonic, organics salts, essential oils, ultraviolet light, hot water, and steam [63, 68, 69, 70, 71, 72, 73]. Maintaining not only the safety but also the quality on post-harvest products is a constant challenge for the horticulture industry. The application of acetic acid, peracetic acid, and hydrogen peroxide can also improve the quality of the products, according to different in vivo studies carried out. In peppers, fruits treated with the solution of hydrogen peroxide and applied by dipping (15 mM by 30 min) increased their shelf life and the fruits maintained their appearance after 2 weeks stored at 20°C compared to control fruits [74]. In according to their results, fruits and vegetables such as tomatoes [75], grapes [76], nectarines [63], apples [68], and cherries [77] have been maintained the quality. Thus, the application of these sanitizers in post-harvest is a practical strategy to maintain the safe and quality of the post-harvest products.

5.5 Salts: organic and inorganic

Nowadays, there is a tendency to reduce the use of synthetic fungicides in agriculture. In this sense, organic and inorganic salts are chemical substances that are food additives generally recognized as safe (GRAS). They are widely used in the food industry due to the low toxicity and environmental impact, besides they can be combined with other control systems to control phytopathogens in post-harvest stage in different fruits and vegetables [78, 79]. It has been shown that salts such as calcium propionate completely inhibit the mycelial growth of B. cinerea at a concentration of 5% (w/v) [78]. This may be due to the fact that it changes the plasma membrane, thus inhibiting essential metabolic functions. Some authors have described that high concentrations of sodium benzoate inhibited the growth of A. Alternata [80], and this is attributed to the fact that weak acids within the cell create a dissociation, causing that protons and anions accumulate and cannot cross the plasma membrane again [81]. Bicarbonate salts, also were effective to inhibit the growth of various pathogens, the efficiency of this salt is attributed to the fact that it creates cellular ionic imbalances affecting the synthesis of polyamines and DNA during cell division [82, 83]. With the accessibility of these compounds and their effectiveness, it is possible that they can be adopted to reduce the use of traditional fungal agents. In a study, potassium sorbate was applied at low concentrations (1%) on infected tomato fruits, and significant reduction of disease incidence was obtained against Rhizoctonia solani, Colletotrichum coccodes, Botrytis cinerea, and Alternaria solani [84]. In another study, gray mold caused by Botrytis cinerea was totally controlled by the application of potassium sorbate at 1% [85]. The effectiveness of potassium sorbate is related to its undissociated form (sorbic acid), which has the ability to penetrate the cell membranes, causing an internal imbalance affecting enzymes related to the growth of microorganisms [86]. In a study on citrus, potassium sorbate at 3% solutions was applied in combination with heat treatment (62°C, 60 s) to evaluate their effectiveness in reducing the disease incidence caused by Penicillium strains. The results showed that the treatments can reduce the disease incidence on “Clemenules” (20%), “Nadorcott” mandarins (25%), “Fino” lemon (50%), tangerine “Ortanique” (80%), and “Valencia” oranges (95%) stored 20°C for 7 days. Besides, when infected and treated fruits were stored at 5°C during 60 days, on “Valencia” oranges, the green mold (Penicillium digitatum) was reduced up to 95% and blue mold (Penicillium italicum) up to 80% [87]. Green mold caused by P. digitatum was reduced up to 80% on infected oranges by the application of sodium benzoate (3%) in combination with hot water (53°C) during 60 s, and fruits were stored at 20°C for 7 days [88]. The effectiveness of sodium benzoate is related to its undissociated form of benzoic acid, which can enter the cell membrane, and its neutralization within the cell leads to acidification of the intracellular space, thus affecting the growth of fungus [89]. On the other hand, another alternative to avoid pathogen development is the use of silicates, and the most used in the fruit industry is: potassium, calcium, and sodium. It has been reported that the action of these organic salts causes, among other effects, inhibition of mycelial growth and alteration of the morphology of the hyphae, and in addition, the germination of conidia is inhibited and causes alterations in their external morphology. The application of sodium silicate induces alterations in the cell wall and in the morphology of the hyphae on pathogenic fungi. It is important to mention that the application of silicate as post-harvest treatment presents results similar to those reported with chitosan and tebuconazole [90]. The investigations of the use of inorganic salts in post-harvest stage are not very frequent, even there are not yet many studies that determine the effect that this may have if applied to different types of crops. These salts have been applied on orange [91], melon [92], avocado [93], and papaya [94], with good results due to the treatments, which form a barrier against pathogens on surface fruit. In addition, the application of silicates can improve some quality attributes of fruits like the maintenance of weight and reducing the respiration rate due to the capacity of the silicates to deposit between the cell wall and the cell membrane, thus decreasing the permeability, besides the stomata are covered, maintaining the humidity of the fruit and reducing its respiration [95, 96]. With the accessibility of these compounds and their effectiveness, it is possible that they can be adopted to reduce the use and applications of traditional fungal agents.

5.6 Jasmonic and salicylic acid

Resistance induced to disease in plants by biotic and abiotic elicitors is a very effective method for restricting the spread of fungal infection [97]. In general, pathogen resistance processes in plants are based on their own defense mechanisms, such as pre-existing antimicrobial compounds and inducible defense mechanisms. Resistance to diseases induced in plants and fruits by biotic or abiotic treatments is a very attractive strategy to control diseases [98]. The signal molecules salicylic acid (SA), jasmonic acid (JA), and methyl jasmonate (MeJA) are endogenous plant growth substances that play key roles in development and responses to environmental stresses. These signal molecules are involved in some signal transduction systems in plants and fruits, which induce particular enzymes catalyzing biosynthetic reactions to form defense compounds such as polyphenols, alkaloids, or pathogenesis-related (PR) proteins. This can result in induction of defense responses and provide protection for plants and fruits from pathogen attack [99]. Salicylic acid activates induction of acquired systemic resistance (SAR) response in plants, proving that in the plant-microorganism interaction, the enzyme phenylalanine ammonia lyase (PAL) is induced, which is the key in the biosynthesis of phenolic compounds [100]. Peroxide has an antibiotic activity against pathogens; it could intervene in the signaling cascade for the expression of defense genes. SA regulates activities of enzymes, peroxidase (POD), and polyphenoloxidase (PPO), that are related to induced defense of plants and fruits against biotic and abiotic stress [101]. Jasmonic acid (JA) and methyl jasmonate (MeJA) have been found to occur naturally in a wide range of higher plants. MeJA is an occurring plant growth regulator that modulates many physiological processes including responses to environmental stresses [99]. Studies indicate that acquired systemic resistance depends on signaling mediated by MeJA and is associated with some signal transduction systems, which induce particular enzymes that catalyze biosynthetic reactions to form defense compounds such as polyphenols, alkaloids, reactive oxygen species (ROS), or PR proteins [102]. The exogenous application of MeJA induces and increases the activity of defense enzymes such as β-1,3-glucanase (β-Gluc), chitinase, polyphenoloxidase (PPO), and phenylalanine ammonia lyase (PAL), which are enzymes associated with resistance to diseases [103]. Application of MeJA effectively suppressed gray mold rot caused by Botrytis cinerea in strawberry [104] and decreased fruit decay on papaya fruit infected by C. gloeosporioides and Alternaria alternata [105]. For grape fruits inoculated with Botrytis cinerea, the application of MJ (0.01 mM) increased the enzymatic activity of PAL and PPO [106], and the same behavior was reported on Hass avocado fruits with an increase in the activity of the resistance enzymes, chitinase, β-1,3-glucanase and PAL [11]. The application of MeJA (10 mM) in cranberry fruit inoculated with Penicillium citrinum maintained greater POD and PAL activity [107]. There are several studies on the application of SA in fruits for the induction of defense mechanisms against pathogens. Resistance of the tomato fruit against Botrytis cinerea using SA as a resistance inducer, a significant increase in the expression level of the PR1 gene was observed in the fruit and a lower expression in the PR2 and PR3 genes [108]. The post-harvest application of SA (2 mg/mL) showed a decrease in the severity of anthracnose in mango cv. Kensington Pride [109]. Thus, the use of inducers offers several advantages for post-harvest disease control; besides, they can combine it with other methods to enhance their efficacy.

5.7 Coatings and edible film from natural sources

Edible coatings on fruits and films made from natural sources are a novelty method and an alternative to the use of post-harvest chemical treatments, particularly in highly perishable fruits [110]. The coatings act as a barrier during processing, handling and storage, delaying the deterioration of food, improving its quality, and extending their shelf life. The functional properties of edible coatings and films depend on their application and the characteristics of the fruit in which they are going to be used. The nature of the compound that is used to produce the coating strongly influences its efficiency, thus it must take into account both its physical and chemical properties, as well as its mechanical and permeable properties. Based on this, if the edible coatings are used properly, they may be able to delay the ripening of the fruit, slow the decomposition of the chlorophyll, reduce the weight loss, retain the ascorbic acid, improve the appearance of the fruit, and especially prolong the shelf life [111, 112, 113]. To date, the functional properties of different compounds for the production of edible coatings have been studied. Compounds from natural sources such as Aloe vera and waxes have shown promising properties to be applied in the preservation of tropical fruits, and therefore coatings based on these compounds can represent an innovation in the commercial application and exploitation of these resources. Aloe vera gel is one of the natural compounds, which has gained a great interest. Because of its nature mainly constituted by polysaccharides, it is capable to form a uniform layer on the surface of the fruit and be easily applied [114]. Aloe vera coating can improve the post-harvest qualitative and quantitative traits, thus it can be an alternative for chemicals preservative in the commercial storage of tropical and subtropical fruits.

Aloe vera-based coatings have been successfully tested in mango fruit ripening (Mangifera indica L. cv. Kensington Pride) [111]. Aloe vera coating reduced aroma volatile biosynthesis in the fruit pulp. Likewise, it was found that coatings delayed ripening of the fruit compared to control. They state that this effect was characterized by the suppression respiration and/or delayed climacteric peak, late fruit color development, and a greater firmness in the coated fruit compared to the uncoated ones. Similarly, the effect of edible coatings based on Aloe vera to extend the shelf life of the guava (Psidium guajava) has been demonstrated. Achipiz et al. [112] found that a coating with a concentration of 4% potato starch and 20% A. vera showed a favorable effect by reducing the weight loss and the respiratory rate of the fruit and increasing the firmness and retention of the vitamin C content after 10 days of storage. In another study, the effect of the Aloe vera gel coating on the store ability of peach fruits was evaluated [115].

The Carnauba wax stems from the leaves of the Brazilian palm Copernicia cerifera. It is produced as a protection method to prevent dehydration and damage. The Carnauba wax as an edible coating is being extensively studied because it has been demonstrated to reduce water loss, improve appearance, and prolong shelf life in a wide variety of fruits. An edible coating based on cassava starch and carnauba wax adding organic acids and calcium chloride was evaluated in mangoes cv Tommy Atkins minimally processed [113]. According to the results, the attributes of sensory, physical, and chemical quality were maintained, and the useful life of fruit was possible to prolong up to 24 days under refrigeration conditions (5 ± 1°C and 90 ± 2% RH).

Saucedo-Pompa et al. [116] developed an edible coating based on candelilla wax to improve avocado quality. Furthermore, they studied the effect of the ellagic acid addition in the shelf life of the fruit. The results showing the application of edible films based on candelilla wax improved the quality of the avocado fruits and extended its shelf life compared to the control fruits. Also, the addition of ellagic acid to the edible film showed an important effect, since it reduced the damage caused by the fungus C. gloeosporioides (the main phytopathogenic fungus for avocados) and significantly improved the quality and shelf life of avocado. Another coating based on mesquite gum-candelilla wax was evaluated in Persian limes [117]. The results showed that coatings decreased the weight loss of the fruit. In addition, by adding mineral oil (33%) to the emulsion, they observed that water vapor permeability was significantly improved, as well as its appearance.

5.8 Ultrasound

Ultrasonic is an economically and environmentally viable alternative for the processing of fruit and vegetable post-harvest [118]. Low intensity ultrasound has been used for quality control of fresh fruit and vegetables in pre- and post-harvest processes [119]. Harvesting time and storage period can be indirectly assessed by ultrasound measurements that are linked physicochemical measurements such as firmness, mealiness, dry weight percentage, oil contents, total soluble solids, and acidity [119]. On the other hand, decontamination of fresh product by ultrasound is relatively recent. The inactivation of microorganism caused by cavitation phenomenon has promoted high intensity ultrasound as method to decontaminate fruits and vegetables. The efficiency of the ultrasound process is affected by several factors such as power level, treatment time, and temperature [120]. Additionally, ultrasound can be applied directly to the medium (water) or in combination with some compounds (organic salts, organic acids, chitosan, among others) to achieve better results. Concerning individual ultrasound application, ultrasound at low frequencies (20 and 40 kHz) has demonstrated to decrease the microbial load of mesophilic aerobes in lettuce (0.9 log CFU/g) and strawberry (1.49 log CFU/g) [121, 122]. At the present time, ultrasound is being implemented in combination with various aqueous sanitizers in order to improve microbial safety and maintain food quality on organic fresh produce. In vitro assay, the addition of low weight chitosan (1000 ppm) enhanced the inactivation of Saccharomyces cerevisiae by ultrasound (20 kHz) at 45°C in Sabouraud broth (pH 5.6). After 30 min of exposure to chitosan, approximately 1-log cycle reduction of the yeast was obtained leading to a final reduction of more than three log cycles after 30 min of the ultrasonic treatment [123]. In the case of in vivo assays, the effectiveness of ultrasound (40 kHz, 5 min) alone and organic acids (0.3, 0.5, 0.7, 1.0, and 2.0% of malic acid, lactic acid, and citric acid) alone and their combination on reducing Escherichia coli O157:H7, Salmonella Typhimurium, and Listeria monocytogenes in fresh lettuce was compared. For all three pathogens, the combined treatment of ultrasound and organic acids resulted in additional 0.8–1.0 log reduction compared to individual treatments, without causing significant quality change (color and texture) on lettuce during 7 day storage. The maximum reductions of E. coli O157:H7, S. Typhimurium, and L. monocytogenes were 2.75, 3.18, and 2.87 log CFU/g observed after combined treatment with ultrasound and 2% organic acid for 5 min, respectively (Sagong et al., 2011). In peach fruit, the effect of ultrasound (40 kHz, 10 min) and salicylic acid (0.05 mM) either separately, or combined on blue mold caused by Penicillium expansum was investigated. The results showed that the application of salicylic acid alone could reduce blue mold, while the use of ultrasound had no effect. Results also revealed that salicylic acid combined with ultrasound treatment was more effective in inhibiting fungal decay during storage than the salicylic acid treatment alone. The combined treatment increased the activities of defense enzymes such as chitinase, β-1,3-glucanase, phenylalanine ammonia lyase, polyphenol oxidase, and peroxidase, which were associated with higher disease resistance induced by the combined treatment. Furthermore, the combined treatment did not impair the quality parameters of peach fruit after 6 days of storage at 20°C [124]. The incorporation of ultrasound alone or in combination with other agents in decontamination process could be a useful preservation technique for post-harvest fruits and vegetables. Combination of ultrasound and sanitizers could increase pathogen reduction without affecting the product quality, while concentration of sanitizers could be reduced as well as treatment time required, saving time and money and avoiding significant risks to consumers.

5.9 Fogging

In order to prolong the shelf life of fruits and vegetables in post-harvest periods, various technologies have been developed that maintain their integrity as well as their nutritional properties. One of the technologies little explored at present is the use of ultrasonic nebulization (Fogging) as a method of distribution of compounds that serve to prevent or control pathogenic diseases in the post-harvest period. Fogging has been used successfully for the spraying of disinfectants such as chlorine dioxide, sodium hypochlorite, hydrogen peroxide, acetic acid, and ethanol, achieving the control of epiphytic microorganisms on the surface of the strawberry (fungi and bacteria), thus reducing the decay index by up to 83.2%, demonstrating that nebulization is an effective method for the reduction of diseases in the post-harvest stage [125]. Regarding fruit quality, in a study with strawberry, peracetic acid was applied as a disinfectant by ultrasonic nebulization, and the results showed that the anthocyanin and phenolic compound contents were preserved even when the fruits were exposed to low concentrations of peracetic acid [126]. In the post-harvest and fruit storage period, it is necessary to minimize chemical products as environmental precautions and avoid adapting pathogens to various fungicides, causing high losses of between 30 and 50% in vegetables and fruits [125, 127]. The use of ultrasonic nebulization offers advantages such as the reduction of the amount of disinfectant and a better distribution of the treatment on the fruits, and in a study of figs, the inhibition of gray mold disease (B. cinerea) 80% of control was achieved with only the application of chlorine dioxide (1000 μL/L) [127]. Ultrasonic nebulization as a conservation method in the post-harvest period gives high benefits in different ways, by reducing the quantity of substances applied, the exposure time as well as a better distribution of the treatments, its application in fruits and vegetables has not been explored, thus the development of this technology can offer an alternative to the use of chemical fungicides for the control of diseases.

Advertisement

6. Conclusions

Considering the new tendencies in fruit industry and marketing, the use of alternative methods represents a suitable approach for several agriculture commodities not only for controlling post-harvest diseases but also for maintaining fruit quality.

References

  1. 1. Rodriguez-Casado A. The health potential of fruits and vegetables phytochemicals: Notable examples. Critical Reviews in Food Science and Nutrition. 2016;56(7):1097-1107
  2. 2. Singh D, Sharma RR. Postharvest diseases of fruits and vegetables and their management. In: Postharvest Disinfection of Fruits and Vegetables. Academic Press: Elsevier; 2018. pp. 1-52. DOI: https://doi.org/10.1016/B978-0-12- 812698-1.00001-7
  3. 3. Sharma RR, Singh D, Singh R. Biological control of postharvest diseases of fruits and vegetables by microbial antagonists: A review. Biological Control. 2009;50(3):205-221
  4. 4. WHO FAO. Promoting fruit and vegetable consumption around the world. 2012. Available from: https://www.who.int/dietphysicalacti vity/fruit/en/. [Review date: January 2019]
  5. 5. Lin BB. Resilience in agriculture through crop diversification: Adaptive management for environmental change. Bioscience. 2011;61(3):183-193
  6. 6. Alston JM, Pardey PG. Public funding for research into specialty crops. HortScience. 2008;43(5):1461-1470
  7. 7. FAO. Tropical fruits, 2017. Available from: http://www.fao.org/3/y5143e/y5143e 1a.htm. [Review date: January 2019]
  8. 8. Mohamed Z, AbdLatif I, Mahir Abdullah A. 1-Economic importance of tropical and subtropical fruits. In: Elhadi M. Yahia, editors. Woodhead Publishing Series in Food Science, Technology and Nutrition; 2011. pp. 1-20 . DOI: https://doi.org/10.1533/9780857093622.1
  9. 9. Singh D, Thakur AK. Effect of fungicides on spoilage caused by mycoflora in kinnow (Citrus reticulata Blanco.) fruits during storage. Journal of Mycology and Plant Pathology. 2005;35:125-127
  10. 10. Spalding DH. Resistance of mango pathogens to fungicides used to control postharvest diseases. Plant Disease. 1982;66(12):1185-1186
  11. 11. Spadaro D, Droby S. Development of biocontrol products for postharvest diseases of fruit: The importance of elucidating the mechanisms of action of yeast antagonists. Trends in Food Science & Technology. 2016;47:39-49
  12. 12. Gutierrez-Martinez P, Ledezma-Morales A, del Carmen Romero-Islas L, Ramos-Guerrero A, Romero-Islas J, Rodríguez-Pereida C, et al. Antifungal activity of chitosan against postharvest fungi of tropical and subtropical fruits. In: Chitin-Chitosan-Myriad Functionalities in Science and Technology. IntechOpen; 2018. DOI: 10.5772/intechopen.76095
  13. 13. May-De Mio LL, Luo Y, Michailides TJ. Sensitivity of monilinia fructicola from Brazil to tebuconazole, azoxystrobin, and thiophanate-methyl and implications for disease management. Plant Disease. 2011;97(7):821-827
  14. 14. Brent KJ, Hollomon DW. Fungicide Resistance in Crop Pathogens: How Can it be Managed? 2nd ed. Fungicide Resistance Action Committee: Brussels, Belgium; 2007. 60 p
  15. 15. Brent KJ, Hollomon DW. Fungicide Resistance: The Assessment of Risk. 2nd ed. Brussels, Belgium: The Fungicide Resistance Action Committee; 2007. 28 p
  16. 16. Feng G, Zhang X, Zhang Z, Ye H, Liu Y. Fungicidal activities of camptothecin semisynthetic derivatives against Colletotrichum gloeosporioides in vitro and in mango fruit. Postharvest Biology and Technology. 2019;147(2018):139-147
  17. 17. Electronic Code of Federal Regulations. Title 40 (Protection of Environment), Chapter I, Subchapter E, Part 180 (tolerances and exemptions for pesticide chemical residues in food). 2018. Available from: https://www.law.cornell.edu/cfr/text/40/part-180. [Review date: February 2019]
  18. 18. EU legislation on MRLs. European Commission, Foodfarming-fisheries, Food Safety, Plants, Pesticides, Pesticides Database. 2019. Available from: http://ec.europa.eu/food/plant/pesticides/eu-pesticidesdatabase/ public/?event=homepage&langu age=EN. [Review date: January 2019]
  19. 19. Abi Tarabay P, Chahine-Tsouvalakis H, Tohmé Tawk S, Nemer N, Habib W. Reduction of food losses in Lebanese apple through good harvesting and postharvest practices. Annals of Agricultural Sciences. 2018;63(2):207-213
  20. 20. Obianom C, Sivakumar D. Differential response to combined prochloraz and thyme oil drench treatment in avocados against the control of anthracnose and stem-end rot. Phytoparasitica. 2018;46(3):273-281
  21. 21. Romanazzi G, Sanzani SM, Bi Y, Tian S, Martínez PG, Alkan N. Induced resistance to control postharvest decay of fruit and vegetables. Postharvest Biology and Technology. 2016;122:82-94
  22. 22. Cavalcante RD, Lima WG, Martins RB. Thiophanate-methyl sensitivity and fitness in Lasiodiplodia theobromae populations from papaya in Brazil. European Journal of Plant Pathology. 2014;140(10):251-259
  23. 23. Sellamuthu PS, Sivakumar D, Soundy P. Antifungal activity and chemical composition of thyme, peppermint and citronella oils in vapor phase against avocado and peach postharvest pathogens. Journal of Food Safety. 2013;33(1):86-93
  24. 24. GLOBALG.A.P. The Worldwide Standard for Good Agricultural Practices. 2018. Available from: https://www.globalgap.org/es/. [Review date: January 2019]
  25. 25. Katiyar D, Hemantaranjan A, Singh B. Chitosan as a promising natural compound to enhance potential physiological responses in plant: A review. Indian Journal of Plant Physiology. 2015;20(1):1-9
  26. 26. El Hadrami A, Adam LR, El Hadrami I, Daayf F. Chitosan in plant protection. Marine Drugs. 2010;8(4):968-987
  27. 27. Gutiérrez-Martínez P, Ramos-Guerrero A, Rodríguez-Pereida C, Coronado-Partida L, Angulo-Parra J, González-Estrada R. Chitosan for Postharvest Disinfection of Fruits and Vegetables. In: Postharvest Disinfection of Fruits and Vegetables. 1st edit. Academic Press: Elsevier; 2018. pp. 231-241. DOI: https://doi.org/10.1016/B978-0- 12-812698-1.00012-1
  28. 28. Gutierrez-Martinez P, Ramos-Guerrero A, Cabanillas-Beltran H, Romero-Islas J, Cruz-Hernandez A. Chitosan as alternative treatment to control postharvest losses of tropical and subtropical fruits. In: Méndez-Vilas A, editor. Science within Food: Up-to-date Advances on Research and Educational Ideas. 2015. pp. 42-47. Available from: http://www.formatex.info/foodscience1/book/42-47.pdf
  29. 29. Gutiérrez-Martínez P, Bautista-Baños S, Berúmen-Varela G, Ramos-Guerrero A, Hernández-Ibañez AM. In vitro response of Colletotrichum to chitosan. Effect on incidence and quality on tropical fruit. Enzymatic expression in mango. Acta Agronomica Journal. 2017;66(2):282-289
  30. 30. Khaliq G, Mohamed MTM, Ding P, Ghazali HM, Ali A. Storage behaviour and quality responses of mango (Mangifera indica L.) fruit treated with chitosan and gum arabic coatings during cold storage conditions. International Food Research Journal. 2016;23(December):S141-S148
  31. 31. Sharif R, Mujtaba M, Ur Rahman M, Shalmani A, Ahmad H, Anwar T, et al. The multifunctional role of chitosan in horticultural crops: A review. Molecules. 2018;23(4):872
  32. 32. Devi EP, Kumari B. A review on prospects of pre-harvest application of bioagents in managing post-harvest diseases of horticultural crops. International Journal of Agriculture Environment & Biotechnology. 2015;8(December):933-941
  33. 33. Xoca-Orozco L-Á, Cuellar-Torres EA, González-Morales S, Gutiérrez-Martínez P, López-García U, Herrera-Estrella L, et al. Transcriptomic analysis of avocado hass (Persea americana Mill) in the interaction system fruit-chitosan-colletotrichum. Frontiers in Plant Science. 2017;8:1-13
  34. 34. Chávez-Magdaleno ME, González-Estrada RR, Ramos-Guerrero A, Plascencia-Jatomea M, Gutiérrez-Martínez P. Effect of pepper tree (Schinus molle) essential oil-loaded chitosan bio-nanocomposites on postharvest control of Colletotrichum gloeosporioides and quality evaluations in avocado (Persea americana) cv. Hass. Food Science and Biotechnology. 2018;27(6):1871-1875
  35. 35. Zeray S, Samukelo L. Evaluating the efficacy of moringa leaf extract , chitosan and carboxymethyl cellulose as edible coatings for enhancing quality and extending postharvest life of avocado (Persea americana Mill.) fruit. Food Packaging and Shelf Life. 2017;11:40-48
  36. 36. Pavela R, Benelli G. Essential oils as ecofriendly biopesticides? Challenges and constraints. Trends in Plant Science. 2016;21(12):1000-1007
  37. 37. Boubaker H, Karim H, El Hamdaoui A, Msanda F, Leach D, Bombarda I, et al. Chemical characterization and antifungal activities of four Thymus species essential oils against postharvest fungal pathogens of citrus. Industrial Crops and Products. 2016;86:95-101
  38. 38. Elshafie HS, Mancini E, Camele I, De Martino L, De Feo V. In vivo antifungal activity of two essential oils from Mediterranean plants against postharvest brown rot disease of peach fruit. Industrial Crops and Products. 2015;66:11-15
  39. 39. Prakash B, Kedia A, Mishra PK, Dubey NK. Plant essential oils as food preservatives to control moulds, mycotoxin contamination and oxidative deterioration of agri-food commodities—Potentials and challenges. Food Control. 2015;47:381-391
  40. 40. Guerra ICD, de Oliveira PDL, de Souza Pontes AL, Lúcio ASSC, Tavares JF, Barbosa-Filho JM, et al. Coatings comprising chitosan and Mentha piperita L. or Mentha× villosa Huds essential oils to prevent common postharvest mold infections and maintain the quality of cherry tomato fruit. Int J Food Microbiol. 2015;214:168-178
  41. 41. Black-Solis J, Ventura-Aguilar RI, Correa-Pacheco Z, Corona-Rangel ML, Bautista-Baños S. Preharvest use of biodegradable polyester nets added with cinnamon essential oil and the effect on the storage life of tomatoes and the development of Alternaria alternata. Sci Hortic (Amsterdam). 2019;245:65-73
  42. 42. González-Estrada RR, Calderón-Santoyo M, Ragazzo-Sánchez JA, Peyron S, Chalier P. Antimicrobial soy protein isolate-based films: Physical characterisation, active agent retention and antifungal properties against Penicillium italicum. International Journal of Food Science and Technology. 2018;53(4):921-929
  43. 43. González-Estrada RR, Chalier P, Ragazzo-Sánchez JA, Konuk D, Calderón-Santoyo M. Antimicrobial soy protein based coatings: Application to Persian lime (Citrus latifolia Tanaka) for protection and preservation. Postharvest Biology and Technology. 2017;132(June):138-144
  44. 44. Ramos-García ML, Bautista-Baños S, González-Soto R. Propiedades Físicas de Películas de Quitosano Adicionadas con Aceite Esencial de Limón y su Impacto en la Vida. Revista Mexicana de Ingeniería Química. 2018;17(1):1-11
  45. 45. da Nóbrega LP, da Silva França KR, Lima TS, de Figueredo Alves FM, Ugulino ALN, da Silva AM, et al. In vitro fungitoxic potential of copaiba and eucalyptus essential oils on phytopathogens. Journal of Experimental Agriculture International. 2019;29(3):1-10
  46. 46. Aminifard MH, Bayat H. Antifungal activity of black caraway and anise essential oils against Penicillium digitatum on blood orange fruits, International Journal of Fruit Science. 2018;18(3):307-319
  47. 47. Tzortzakis NG, Economakis CD. Antifungal activity of lemongrass (Cympopogon citratus L.) essential oil against key postharvest pathogens. Innovative Food Science and Emerging Technologies. 2007;8(2):253-258
  48. 48. Chen J, Shen Y, Chen C, Wan C. Inhibition of key citrus postharvest fungal strains by plant extracts in vitro and in vivo: A review. Plants. 2019;8(2):26
  49. 49. Obagwu J, Korsten L. Control of citrus green and blue molds with garlic extracts. European Journal of Plant Pathology. 2003;109(3):221-225
  50. 50. Gong M, Guan Q , Xu S. Inhibitory effects of crude extracts from several plants on postharvest pathogens of citrus. AIP Conference Proceedings. 2018;1956:200431-200434. Available from: https://aip.scitation.org/doi/abs/10.10 63/1.5034295. DOI: https://doi.org/10.1063/1.5034295
  51. 51. Osman A, Abbas E, Mahgoub S, Sitohy M. Inhibition of Penicillium digitatum in vitro and in postharvest orange fruit by a soy protein fraction containing mainly β-conglycinin. Journal of General Plant Pathology. 2016;82(6):293-301
  52. 52. Gatto MA, Sanzani SM, Tardia P, Linsalata V, Pieralice M, Sergio L, et al. Antifungal activity of total and fractionated phenolic extracts from two wild edible herbs. Natural Science. 2013;05(08):895-902
  53. 53. Gatto MA, Sergio L, Ippolito A, Di Venere D. Phenolic extracts from wild edible plants to control postharvest diseases of sweet cherry fruit. Postharvest Biology and Technology. 2016;120(July):180-187
  54. 54. Gatto MA, Ippolito A, Sergio L, Di Venere D. Extracts from wild edible herbs for controlling postharvest rots of fruit and vegetables. Acta Horticulturae. 2016;1144:349-354
  55. 55. Tabassum P, Ahmed S, Uddin K, Siddiqua M, Sultana S. Effect of guava leaf and lemon extracts on postharvest quality and shelf life of banana cv. Sabri (Musa sapientum L.). Journal of the Bangladesh Agricultural University. 2018;16(3):337-342
  56. 56. Feliziani E, Lichter A, Smilanick JL, Ippolito A. Disinfecting agents for controlling fruit and vegetable diseases after harvest. Postharvest Biology and Technology. 2016;122:53-69
  57. 57. FDA. Code of Federal Regulations. 21 CFR Part 173, Section 173.370: Peroxyacids. 2018. Available from: https://www.accessdata.fda.gov/scrip ts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?fr =173.370. [Review date: January 2019]
  58. 58. FDA. Code of Federal Regulations. 21CFR 173.356. Section 173.356 Hydrogen peroxide. 2018. Available from: https://www.accessdata.fda.gov/scrip ts/cdrh/cfdocs/cfcfr/CFRSearch.cfm? fr=173.356. [Review date: January 2019]
  59. 59. Amrutha B, Sundar K, Shetty PH. Effect of organic acids on biofilm formation and quorum signaling of pathogens from fresh fruits and vegetables. Microbial Pathogenesis. 2017;111:156-162
  60. 60. Rosli NMI, Tang JYH. Effect of different conditions of citric acid and acetic acid decontamination against Esherichia coli in lettuce. Journal of Agrobiotechnology. 2018;9(1S):54-61
  61. 61. Crowe KM, Bushway AA, Bushway RJ. Bushway RJ. Effects of alternative postharvest treatments on the microbiological quality of lowbush blueberries. Small Fruits Review. 2005;4(3):29-39
  62. 62. Massalimov I. The efficancy of micron and nanoscale sulfur the schutte fungi. International Journal of Science. 2013;2(2013-03):25-30
  63. 63. Sisquella M, Casals C, Vinas I, Teixidó N, Usall J. Combination of peracetic acid and hot water treatment to control postharvest brown rot on peaches and nectarines. Postharvest Biology and Technology. 2013;83:1-8
  64. 64. Alawlaqi MM, Alharbi AA. Impact of acetic acid on controlling tomato fruit decay. Life Science Journal. 2014;11:114-119
  65. 65. Abd-El-Kareem F, Abd-El-Latif FM. No title. Journal of Applied Sciences Research. 2014;10(1):32-36
  66. 66. Abd-AllA MA, Abd-El-Kader MM, Abd-El-Kareem F, El-Mohamedy RSR. Evaluation of lemongrass, thyme and peracetic acid against gray mold of strawberry fruits. Journal of Agricultural Technology. 2011;7(6):1775-1787
  67. 67. Alasri A, Roques C, Michel G, Cabassud C, Aptel P. Bactericidal properties of peracetic acid and hydrogen peroxide, alone and in combination, and chlorine and formaldehyde against bacterial water strains. Canadian Journal of Microbiology. 1992;38(7):635-642
  68. 68. Radi M, Jouybari HA, Mesbahi G, Farahnaky A, Amiri S. Effect of hot acetic acid solutions on postharvest decay caused by Penicillium expansum on Red Delicious apples. Scientia Horticulturae. 2010;126(4):421-425
  69. 69. de São José JFB, Vanetti MCD. Application of ultrasound and chemical sanitizers to watercress, parsley and strawberry: Microbiological and physicochemical quality. LWT—Food Science and Technology. 2015;63(2):946-952
  70. 70. Cerioni L, Sepulveda M, Rubio-Ames Z, Volentini SI, Rodríguez-Montelongo L, Smilanick JL, et al. Control of lemon postharvest diseases by low-toxicity salts combined with hydrogen peroxide and heat. Postharvest Biology and Technology. 2013;83:17-21
  71. 71. Ismail OM, El-Moniem E, Abd-Allah ASE, Rl-Naggar MAA. Influence of some post-harvest treatments on guava fruits. Agriculture and Biology Journal of North America. 2010;1(6):1309-1318
  72. 72. Eshel D, Regev R, Orenstein J, Droby S, Gan-Mor S. Combining physical, chemical and biological methods for synergistic control of postharvest diseases: A case study of Black Root Rot of carrot. Postharvest Biology and Technology. 2009;54(1):48-52
  73. 73. Guan W, Fan X, Yan R. Effect of combination of ultraviolet light and hydrogen peroxide on inactivation of Escherichia coli O157: H7, native microbial loads, and quality of button mushrooms. Food Control. 2013;34(2):554-559
  74. 74. Bayoumi YA. Improvement of postharvest keeping quality of white pepper fruits (Capsicum annuum, L.) by hydrogen peroxide treatment under storage conditions. Acta Biologica Szegediensis. 2008;52(1):7-15
  75. 75. Islam MZ, Mele MA, Hussein KA, Kang H-M. Acidic electrolyzed water, hydrogen peroxide, ozone water and sodium hypochlorite influence quality, shelf life and antimicrobial efficacy of cherry tomatoes. Research Journal of BioTechnology. 2018;13:4
  76. 76. Venditti T, Ladu G, Cubaiu L, Myronycheva O, D’hallewin G. Repeated treatments with acetic acid vapors during storage preserve table grapes fruit quality. Postharvest Biology and Technology. 2017;125:91-98
  77. 77. Chu C-L, Liu W-T, Zhou T. Fumigation of sweet cherries with thymol and acetic acid to reduce postharvest brown rot and blue mold rot. Fruits. 2001;56(2):123-130
  78. 78. Droby S, Wisniewski M, El A, Wilson C. Influence of food additi v es on the control of postharvest rots of apple and peach and efficacy of the yeast-based biocontrol product aspire. Postharvest Biology and Technology. 2003;27:127-135
  79. 79. Deliopoulos T, Kettlewell PS, Hare MC. Fungal disease suppression by inorganic salts: A review. Crop Protection. 2010;29(10):1059-1075
  80. 80. Montesinos-herrero C, Moscoso-ramírez PA, Palou L. Postharvest Biology and Technology Evaluation of sodium benzoate and other food additives for the control of citrus postharvest green and blue molds. Postharvest Biology and Technology. 2016;115:72-80
  81. 81. Palou L, Ali A, Fallik E, Romanazzi G. GRAS , plant- and animal-derived compounds as alternatives to conventional fungicides for the control of postharvest diseases of fresh horticultural produce. Postharvest Biology and Technology. 2016;122:41-52
  82. 82. Minocha R, Minocha SC, Long SL, Shortle WC, Effects WC. Effects of aluminum on DNA synthesis, cellular polyamines, polyamine biosynthetic enzymes and inorganic ions in cell suspension cultures of a woody plant, Catkaranthus roseus. Physiologia Plantarum. 1992;85:417-424
  83. 83. Vilaplana R, Alba P, Valencia-chamorro S. Sodium bicarbonate salts for the control of postharvest black rot disease in yellow pitahaya (Selenicereus megalanthus). Crop protection. 2018;114(March):90-96
  84. 84. Jabnoun-Khiareddine H, Abdallah R, El-Mohamedy R, Abdel-Kareem F, Gueddes-Chahed M, Hajlaoui A, et al. Comparative efficacy of potassium salts against soil-borne and air-borne fungi and their ability to suppress tomato wilt and fruit rots. Journal of Microbial & Biochemical Technology. 2016;08(02):45-55
  85. 85. Youssef K, Roberto SR. Applications of salt solutions before and after harvest affect the quality and incidence of postharvest gray mold of ‘Italia’table grapes. Postharvest Biology and Technology. 2014;87:95-102
  86. 86. York GK, Vaughn RH. Mechanisms in the inhibition of microorganisms by sorbic acid. Journal of Bacteriology. 1964;88(2):411-417
  87. 87. Montesinos-Herrero C, del Río MÁ, Pastor C, Brunetti O, Palou L. Evaluation of brief potassium sorbate dips to control postharvest penicillium decay on major citrus species and cultivars. Postharvest Biology and Technology. 2009;52(1):117-125
  88. 88. Palou L, Moscoso-Ramírez PA, Montesinos-Herrero C. Assessment of optimal postharvest treatment conditions to control green mold of oranges with sodium benzoate. Acta Horticulturae. 2018;1194:221-225
  89. 89. Krebs H, Wiggins D, Stubbs M, Sols A, Bedoya F. Studies on the mechanism of the antifungal action of benzoate. The Biochemical Journal. 1983;214(3):657-663
  90. 90. Li YC, Bi Y, Ge YH, Sun XJ, Wang Y. Antifungal activity of sodium silicate on Fusarium sulphureum and its effect on dry rot of potato tubers. Journal of Food Science. 2009;74(5):213-218
  91. 91. Mshraky A, Ahmed FK, El-hadidy GAM. Influence of pre and post applications of potassium silicate on resistance of chilling injury of olinda valencia orange fruits during cold storage at low temperatures. Middle East Journal of Agriculture Research. 2016;5(04):442-453
  92. 92. Bi Y, Tian SP, Guo YR, Ge YH, Qin GZ. Sodium silicate reduces postharvest decay on hami melons: Induced resistance and fungistatic effects. Plant Disease. 2006;90(3):279-283
  93. 93. Coskun D, Deshmukh R, Sonah H, Menzies JG, Reynolds O, Ma JF, et al. The controversies of silicon’s role in plant biology. The New Phytologist. 2018;221:67-85
  94. 94. Bandara WMKI, Perera ODAN, Weerahewa HLD. Enhancing disease resistance and improving quality of papaya (Carica papaya L.) by postharvest application of silicon. International Journal of Agriculture, Forestry and Plantation. 2015;1:24-27
  95. 95. Tesfay SZ, Bertling I, Bower JP. Postharvest biology and technology effects of postharvest potassium silicate application on phenolics and other anti-oxidant systems aligned to avocado fruit quality. Postharvest Biol Technol. 2011;60(2):92-99
  96. 96. Moscoso-Ramírez PA, Palou L. Potassium silicate: A new organic tool for the control of citrus postharvest green mold. ISHS Acta Horticulturae. 2016;1144:287-292
  97. 97. Soylu S, Baysal Ö, Soylu EM. Induction of disease resistance by the plant activator, acibenzolar-S-methyl (ASM), against bacterial canker (Clavibacter michiganensis subsp. michiganensis) in tomato seedlings. Plant Science. 2003;165(5):1069-1075
  98. 98. Qin GZ, Tian SP, Xu Y, Wan YK. Enhancement of biocontrol efficacy of antagonistic yeasts by salicylic acid in sweet cherry fruit. Physiological and Molecular Plant Pathology. 2003;62(3):147-154
  99. 99. Creelman RA, Mullet JE. Biosynthesis and action of jasmonates in plants. Annual Review of Plant Physiology and Plant Molecular Biology. 1997;48(1):355-381
  100. 100. Potlakayala SD, Reed DW, Covello PS, Fobert PR. Systemic acquired resistance in canola is linked with pathogenesis-related gene expression and requires salicylic acid. Phytopathology. 2007;97(7):794-802
  101. 101. Idrees M, Naeem M, Aftab T, Khan MMA. Salicylic acid mitigates salinity stress by improving antioxidant defence system and enhances vincristine and vinblastine alkaloids production in periwinkle [Catharanthus roseus (L.) G. Don]. Acta Physiologiae Plantarum. 2011;33(3):987-999
  102. 102. Wasternack C, Parthier B. Jasmonate-signalled plant gene expression. Trends in Plant Science. 1997;2(8):302-307
  103. 103. Haggag WM, Mahmoud YS, Farag EM. Signaling necessities and function of polyamines/jasmonate-dependent induced resistance in sugar beet against beet mosaic virus (BtMV) infection. New York Science Journal. 2010;3(8):95-103
  104. 104. Moline HE, Buta JG, Saftner RA, Maas JL. Comparison of three volatile natural products for the reduction of postharvest decay in strawberries. Advances in Strawberry Research. 1997. Available from: http://agris.fao.org/agrissearch/search.do?recordID=US201302953441
  105. 105. Gonzalez-Aguilar GA, Buta JG, Wang CY. Methyl jasmonate and modified atmosphere packaging (MAP) reduce decay and maintain postharvest quality of papaya ‘Sunrise.’. Postharvest Biology and Technology. 2003;28(3):361-370
  106. 106. Jiang L, Jin P, Wang L, Yu X, Wang H, Zheng Y. Methyl jasmonate primes defense responses against Botrytis cinerea and reduces disease development in harvested table grapes. Sci Hortic (Amsterdam). 2015;192:218-223
  107. 107. Wang K, Jin P, Han L, Shang H, Tang S, Rui H, et al. Methyl jasmonate induces resistance against Penicillium citrinum in Chinese bayberry by priming of defense responses. Postharvest Biology and Technology. 2014;98:90-97
  108. 108. Wang AY, Lou BG, Xu T, Lin C. Defense responses in tomato fruit induced by oligandrin against Botrytis cinerea. African J Biotechnol. 2011;10(22):4596-4601
  109. 109. Joyce DC, Wearing H, Coates L, Terry L. Effects of phosphonate and salicylic acid treatments on anthracnose disease development and ripening of’Kensington Pride’mango fruit. Australian Journal of Experimental Agriculture. 2001;41(6):805-813
  110. 110. Michailides TJ, Manganaris GA. Harvesting and handling effects on postharvest decay. Stewart Postharvest Review. 2009;5(2):1-7
  111. 111. Dang KTH, Singh Z, Swinny EE. Edible coatings influence fruit ripening, quality, and aroma biosynthesis in mango fruit. Journal of Agricultural and Food Chemistry. 2008;56(4):1361-1370
  112. 112. Achipiz SM, Castillo AE, Mosquera SA, Hoyos JL, Navia DP. Efecto de Recubrimiento a Base de Almidón Sobre la maduracion de la Guayaba (Psidium guajava). Biotecnología en el Sector Agropecuario y Agroindustrial. 2013;2(2):92-101
  113. 113. Dussán-Sarria S, Torres-León C, Hleap-Zapata JI. Efecto de un recubrimiento comestible y de diferentes empaques durante el almacenamiento refrigerado de mango Tommy Atkins mínimamente procesado. Información Tecnológica. 2014;25(4):123-130
  114. 114. Suriati L, Mangku IGP, Rudianta IN. The characteristics of Aloe vera gel as an edible coating. IOP Conference Series: Earth and Environmental Science. 2018;207:012051
  115. 115. Hazrati S, Beyraghdar Kashkooli A, Habibzadeh F, Tahmasebi-Sarvestani Z, Sadeghi AR. Beurteilung von Aloe-vera-Gel als alternative essbare Beschichtung für Pfirsichfrüchte während der kalten Lagerphase. Gesunde Pflanz. 2017;69(3):131-137
  116. 116. Saucedo-Pompa S, Rojas-Molina R, Aguilera-Carbó AF, Saenz-Galindo A, de La Garza H, Jasso-Cantú D, et al. Edible film based on candelilla wax to improve the shelf life and quality of avocado. Food Research International. 2009;42(4):511-515
  117. 117. Bosquez-Molina E, Guerrero-Legarreta I, Vernon-Carter EJ. Moisture barrier properties and morphology of mesquite gum-candelilla wax based edible emulsion coatings. Food Research International. 2003;36(9-10):885-893
  118. 118. López-Malo A, Palou E, Jiménez-Fernández M, Alzamora SM, Guerrero S. Multifactorial fungal inactivation combining thermosonication and antimicrobials. Journal of Food Engineering. 2005;67(1-2):87-93
  119. 119. Mizrach A. Ultrasonic technology for quality evaluation of fresh fruit and vegetables in pre- and postharvest processes. Postharvest Biology and Technology. 2008;48(3):315-330
  120. 120. Pinheiro J, Alegria C, Abreu M, Gonçalves EM, Silva CLM. Influence of postharvest ultrasounds treatments on tomato (Solanum lycopersicum, cv. Zinac) quality and microbial load during storage. Ultrasonics Sonochemistry. 2015;27:552-559
  121. 121. Ajlouni S, Sibrani H, Premier R, Tomkins BM. Food microbiology and safety ultrasonication and fresh produce (Cos lettuce) preservation. Journal of Food Science. 2006;71(2):M62-M68
  122. 122. Cao S, Hu Z, Pang B, Wang H, Xie H, Wu F. Effect of ultrasound treatment on fruit decay and quality maintenance in strawberry after harvest. Food Control. 2010;21(4):529-532
  123. 123. Guerrero S, Tognon M, Alzamora SM. Response of Saccharomyces cerevisiae to the combined action of ultrasound and low weight chitosan. Food Control. 2005;16(2):131-139
  124. 124. Yang Z, Cao S, Cai Y, Zheng Y. Combination of salicylic acid and ultrasound to control postharvest blue mold caused by Penicillium expansum in peach fruit. Innovative Food Science and Emerging Technologies. 2011;12(3):310-314
  125. 125. Vardar C, Ilhan K, Karabulut OA. The application of various disinfectants by fogging for decreasing postharvest diseases of strawberry. Postharvest Biology and Technology. 2012;66:30-34
  126. 126. Van De Velde F, Grace MH, Élida M, Ann M. Impact of a new postharvest disinfection method based on peracetic acid fogging on the phenolic profile of strawberries. Postharvest Biology and Technology. 2016;117:197-205
  127. 127. Karabulut OA, Ilhan K, Arslan U. Vardar C, Evaluation of the use of chlorine dioxide by fogging for decreasing postharvest decay of fig. Postharvest Biology and Technology. 2009;52:313-315

Written By

Ramsés González-Estrada, Francisco Blancas-Benítez, Rita M. Velázquez-Estrada, Beatriz Montaño-Leyva, Anelsy Ramos-Guerrero, Lizet Aguirre-Güitrón, Cristina Moreno-Hernández, Leonardo Coronado-Partida, Juan A. Herrera-González, Carlos A. Rodríguez-Guzmán, José A. Del Ángel-Cruz, Edson Rayón-Díaz, Hector J. Cortés-Rivera, Miguel A. Santoyo-González and Porfirio Gutierrez-Martinez

Submitted: 12 December 2018 Reviewed: 06 March 2019 Published: 11 April 2019