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Review

Endophytic Fungi Volatile Organic Compounds as Crucial Biocontrol Agents Used for Controlling Fruit and Vegetable Postharvest Diseases

by
Lijun Ling
1,2,3,*,
Lijun Feng
1,2,
Yao Li
1,2,
Rui Yue
1,2,
Yuanyuan Wang
1,2 and
Yongpeng Zhou
1,2
1
College of Life Science, Northwest Normal University, Lanzhou 730070, China
2
Bioactive Products Engineering Research Center for Gansu Distinctive Plants, Northwest Normal University, Lanzhou 730070, China
3
New Rural Development Research Institute, Northwest Normal University, Lanzhou 730070, China
*
Author to whom correspondence should be addressed.
J. Fungi 2024, 10(5), 332; https://doi.org/10.3390/jof10050332
Submission received: 28 March 2024 / Revised: 25 April 2024 / Accepted: 30 April 2024 / Published: 4 May 2024
(This article belongs to the Special Issue Control of Postharvest Fungal Diseases)
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Abstract

:
Fruits and vegetables are an important part of the human diet, but during transportation and storage, microbial pathogens attack and spoil fruits and vegetables, causing huge economic losses to agriculture. Traditionally used chemical fungicides leave chemical residues, leading to environmental pollution and health risks. With the emphasis on food safety, biocontrol agents are attracting more and more attention due to their environmental friendliness. Endophytic fungi are present in plant tissues and do not cause host disease. The volatile organic compounds (VOCs) they produce are used to control postharvest diseases due to their significant antifungal activity, as well as their volatility, safety and environmental protection characteristics. This review provides the concept and characterization of endophytic fungal VOCs, concludes the types of endophytic fungi that release antifungal VOCs and their biological control mechanisms, as well as focuses on the practical applications and the challenges of applying VOCs as fumigants. Endophytic fungal VOCs can be used as emerging biocontrol resources to control postharvest diseases that affect fruits and vegetables.

1. Introduction

Fruits and vegetables are a crucial part of the human diet. They provide fiber, organic acids, vitamins, minerals, amino acids, and certain trace elements required by the body. Thus, they are rich in nutritional value and beneficial to human health [1,2]. However, it is important to note that fruits and vegetables can develop postharvest rot during various stages such as sorting, packaging, storage, transport, and marketing [3]. This is due to their susceptibility to mechanical damage, which can lead to the deposition of microbial pathogens on their surface. Under the right environmental conditions, these pathogens can directly invade fruits and vegetables through wounds, leading to postharvest rot [4]. Additionally, natural openings such as lenticels act as penetration sites [5]. Microbe-induced fruit and vegetable spoilage is a global problem. Fungal genera of Alternaria, Aspergillus, Botrytis, Fusarium, Geotrichum, Gloeosporium, Monilinia, Penicillium, Mucor and Rhizopus are the main causative pathogens of postharvest diseases of fruits and vegetables [6]. In addition to fruit and vegetable rot, these pathogenic fungi also produce other harmful metabolites, such as aflatoxin from Aspergillus flavus and ochratoxin A from Aspergillus ochraceus, some of which are also carcinogenic [7,8]. Thus, they pose huge safety risks to animals and humans [9]. According to the Food and Agriculture Organization of the United Nations (FAO), fruit and vegetable loss accounts for at least 40% of the total food loss produced annually worldwide [10]. Postharvest storage of fruits and vegetables is a major challenge.
Traditionally, chemical fungicides have been used as the main means of controlling or preventing the spoilage of postharvest fruits and vegetables. They include hydrogen peroxide, chlorine, trisodium phosphate, organic acids, and electrolytic water [11]. In addition, pesticides such as sterol biosynthesis inhibitors and imidazoline are registered for the control of postharvest diseases [12]. These chemical fungicides can kill microorganisms to some extent and prolong the shelf life of fresh produce. However, as people’s quality of life is improving, they are increasingly paying attention to the safety of agricultural products, which has gradually led to the withdrawal of chemical fungicides. Chlorine releases chlorine gas and produces carcinogenic by-products (trihalomethanes and haloacetic acids); hydrogen peroxide causes discoloration; and organic acids can damage human tissue and corrode equipment [13,14,15]. Chemical fungicides can also cause drug resistance in pathogenic microorganisms when used for a long period. For example, most citrus postharvest pathogens have developed substantial resistance to the commonly used fungicides thiamethoxam and imidazoline [16]. In addition, chemical fungicides can remain in the air, soil, plants, and other non-target organisms, affect water and soil quality, and cause considerable harm to plants, animals, and the environment [17]. Long-term direct or indirect pesticide exposure is a serious threat to human health, and the use of chemical fungicides needs to be reduced. Postharvest fungicide use is banned in some European countries or limited to a few registered chemicals [18].
Therefore, green environmental protection fungicides are becoming increasingly popular, and new safe fungicides are continually being sought to substitute chemical fungicides to reduce the occurrence of postharvest diseases in fruits and vegetables. In recent years, biological control has been a very promising direction for research and development. Biological control can effectively inhibit the attack of pathogens and has become a new trend in postharvest fruit and vegetable preservation [19,20]. As biological control agents, antagonistic microorganisms can use their structures and secondary metabolites to inhibit or kill pathogenic microorganisms, thereby significantly reducing the use of chemical fungicides [21]. Volatile organic compounds (VOCs) are released by microbes during their growth and reproduction and have been extensively studied for their apparent antifungal activity [22]. Ling et al. [23] found that VOCs from endophytic bacteria (such as Bacillus spp. and Pseudomonas spp.) have antifungal potential against numerous plant diseases. Compared with chemical fungicides, microbial VOCs have small molecular weights, are volatiles and quickly proliferate, and therefore do not easily remain on fruit and vegetable surfaces, which is beneficial for human health and environmental protection [24]. Second, VOCs are relatively safe, and their dosage is small enough to inhibit pathogenic fungi and are mostly harmless. 2,3-butanedione at 5 μL per plate effectively inhibited the mycelial growth, spore germination, and sporulation ability of wolfberry pathogenic fungi Mucor circinelloides LB1, F. arcuatisporum LB5, Alternaria iridiaustralis LB7, and Colletotrichum fioriniae LB8 [25]. Pathogen resistance is unlikely to emerge because microbial VOCs have a variety of resistance mechanisms against pathogenic fungi, such as via the inhibition of mycelial growth, spore germination, and the disruption of cell walls and cell membranes [26]. In addition, T. asperellum HbGT6-07 VOCs effectively reduced the colonial diameter, growth rate, and sclerotia production of two fungal pathogens: Botrytis cinerea (B05.10) and Sclerotinia sclerotiorum (A367) [27]. Consequently, microbial VOCs are promising biocontrol agents in terms of postharvest disease applications.
Endophytic fungi have received remarkable attention as microorganisms that can colonize the internal tissues of host plants without causing disease [28]. They colonize a wide range of plants and can be isolated from all plant organs, including roots, stems, leaves, flowers, fruits, and seeds [29]. Currently, some fungi with antagonistic effects, such as Trichoderma spp., are used in a large number of applications for controlling fruit and vegetable postharvest diseases, but the application regarding endophytes is very limited [30]. On the other hand, endophytic fungi are considered to have superior properties to non-endophytic fungi due to their better colonization ability and resistance to many biotic and abiotic stresses [31]. Endophytic fungi and their host plants have a mutually beneficial and symbiotic relationship. These fungi produce nutrients (polysaccharides, lipids, minerals and vitamins) and phytohormones, thereby promoting plant growth [32,33,34,35]. Second, they can improve plant resistance to stress, promote nutrient absorption by plants, and resist infection by pathogenic fungi [31]. Two endophytic fungi (Penicillium citrinum LWL4 and Aspergillus terreus LWL5) not only promote the growth of sunflower (Helianthus annuus L.) but also stimulate plant defense responses through the production of gibberellins, organic acids, and siderophore [36]. Endophytic fungal Diaporthe sp. CEL3 emits a characteristic scent (a fruity, sweet camphor odor) and inhibits the growth of 10 fungal pathogens from wide taxonomic groups like ascomycetes, basidiomycetes, and oomycetes [37]. Primary VOCs were generated by the endophytic fungus Diaporthe apiculatum strain FPYF 3052 and can suppress the growth of phytopathogenic fungi (Alternaria alternata, Botryosphaeria dothidea, B. cinerea, Cercospora asparagi, Colletotrichum gloeosporioides, F. graminearum, Sphaeropsis sapinea, and Valsa sordida), having inhibitory activities in the range of 23.8–66.7% within 24 h. Among the primary VOCs, commercial (−)-4-terpineol stood out as the terpenoid with the strongest inhibitory activity against these phytopathogenic fungi, with up to 100% inhibition [38]. Endophytic fungi can produce various VOCs with various biological activities, such as host plant growth promotion and antifungal, antioxidative, and antitumor activities, which are widely used in agriculture and industry [39]. Among them, VOCs released by endophytic fungi have strong fungicidal activity. This fungicidal activity is the main mechanism of antagonizing microbial pathogens after harvesting vegetables and has attracted significant research attention [40,41]. Naik [42] discusses the production of VOCs by endophytic fungi in fuel production and their potential applications in biological control. Studies conducted by Kaddes [41] have highlighted the importance of VOCs as antimicrobial agents. At present, research on the biocontrol mechanisms and practical applications of VOCs produced by endophytic fungi has not been sufficiently in-depth and has not been comprehensively reported yet.
In addition, Endophytic fungi release a wide variety of VOCs, which are still being explored in the study of mechanisms of resistance to pathogenic fungi. Therefore, special attention needs to be paid to the important role played by endophytic fungal VOCs in the control of fruit and vegetable postharvest diseases and to discuss the prospects and modalities of their application. Firstly, we here review the biological properties of endophytic fungal VOCs and their diversity, as well as types of endophytic fungi that release antifungal VOCs. Secondly, it also focuses on the mechanisms of endophytic fungal VOCs against pathogenic fungi, as well as practical applications of VOCs and future challenges and obstacles. Endophytic fungal VOCs play an important role in the postharvest disease control of fruits and vegetables as emerging biocontrol resources.

2. Endophytic Fungal Volatile Organic Compounds (VOCs)

Endophytic fungi colonize plant tissues and spend all or part of their life cycle in the host without inducing any noticeable symptoms of infection. They are widespread in nature and influence various biological activities in plants [43]. When endophytic fungi absorb various nutrients through catabolism and anabolism during the metabolic process, various fungal VOCs are finally produced [44]. VOCs are hydrophobic organic molecular compounds that evaporate into the gaseous phase at normal temperatures and pressures. They have a low molecular weight (<300 Da) and high vapor pressure (≥0.01 kPa at 20 °C). They are efficiently transported through air or soil when released [45]. VOCs can hence spread over a long distance at a high speed [45]. They are widely distributed in air, soil, water, animals, plants, etc., and can be used in ecosystems comprising various life forms such as microbes, plants, and insects. Thus, VOCs are crucial signaling molecules mediating the scientific niche [46,47].
Current studies on microbial VOCs usually use gas chromatography (GC) coupled with mass spectrometry (GC-MS) for VOC separation and identification [48]. For example, the use of SPME-GC/MS identified D. apiculatum strain FPYF 3052 as producing 15 volatile organic compounds (VOCs) mainly categorized as terpenes, benzene and benzene derivatives, alcohols, and hydrocarbons [38]. According to statistics, more than 250 different VOCs have been identified in fungi, mainly acids, alcohols, aldehydes, aromatics, esters, heterocycles, ketones, terpenes, and thiols [44]. These VOCs can be categorized into five types: terpenoids, fatty acid derivatives, benzene compounds, acetone, and amino acid derivatives. VOCs originate from different anabolic pathways, mainly the manganate/phenylalanine, mevalonate (MVA), methylerythritol phosphate (MEP), and lipoxygenase (LOX) pathways, which involve different enzymatic reactions to produce different VOC types [41]. According to incomplete statistics, more than 500 VOC-producing microbes have been identified and the VOCs of each strain vary with environmental variables, such as temperature [49]. In the future, more unique new VOCs will be discovered, and so, this emerging field of fungal endogenous VOCs is promising.

3. Endophytic Fungal Species Releasing VOCs of Antifungal Activity

In 2001, researchers isolated the endophytic fungus Muscodor albus from cinnamon trees, which produce five classes of VOCs (alcohols, esters, ketones, acids, and lipids) that are effective in inhibiting or killing multiple pathogenic microorganisms (Aspergillus fumigatus, Candida albicans, and F. solani, among others); esters are the most effective inhibitory compound class [50]. Researchers from various fields are keen on studying the fungal inhibitory activity of endophytic fungal VOCs. As summarized in Table 1, recent reports have indicated that endogenous fungal VOCs may be used as protectants against pathogens damaging stored fruits and vegetables. VOCs are safe and harmless to the human body within certain limits. For example, 2,3-butanedione, which is used as an edible additive, exhibited no hazards [51]. It was found that the concentration of volatile 6-pentyl-α-pyrone (6PP) of T. atroviride IC-11 was around 190 μg/mL, which had no adverse effect on human cells. Moreover, T. atroviride IC-11 VOCs were not cytotoxic to intestinal human colon carcinoma cells (Caco-2) [52]. Thus, owing to their advantages of rapid diffusion, safety, and effectiveness in biological control, endophytic fungal VOCs can be used as biological control agents.
The release of VOCs with antifungal activity produced by endophytic fungi is increasingly being reported. The main endophytic fungi that currently produce VOCs with antifungal activity are Muscodor, Trichoderma spp. and yeasts. The VOCs of Muscodor are a double-edged sword as they have been summarized as having major antifungal activity in Kaddes et al. [41] and Naik [42] as well as inhibitory effects on the growth of some plants (Artemisia annua seedlings) [72]. Trichoderma spp. are a particularly abundant source that can sustainably resist the growth of various phytopathogens [41,72]. Second, the release of antifungal active VOCs by yeasts, a generally abundant endophytic fungal species, has also received considerable research attention [55]. Therefore, this section focuses on Trichoderma spp. and yeasts. Therefore, Figure 1 summarizes the chemical classes of VOCs released by various endogenous fungi and their application methods.

3.1. Trichoderma spp.

Trichoderma spp. is a filamentous fungus exhibiting rapid mycelial growth and strong environmental adaptability. It serves as an antagonist of various phytopathogens and can be effectively used as a biocontrol agent [73,74,75]. Trichoderma spp. is among the most common fungi. It can settle asymptomatically in plant tissues, compete with harmful fungi for space and nutrition, improve the growth and defense functions of host plants [76], and play a crucial role in the prevention of pathogenic fungi by releasing antifungal active VOCs [41].
The endophytic fungus T. koningiopsis YIM PH30002 was isolated from the roots of a 2-year-old healthy sanqi (Panax notoginseng) plant. This fungus produced at least 10 VOCs, which were identified through the use of GC-MS as alkanes, monoterpenes, aromatic hydrocarbons, heterocycles, and aldehydes. These compounds could inhibit the root rot phytopathogenic fungi Phoma herbar, F. flocciferum, Scytalidium lignicola, and Epicoccum nigrum [67]. T. koningiopsis YIM PH30002 VOCs were expected to act as biological control agents for Panax ginseng root rot. Phenethyl alcohol, a VOC with antibacterial activity, could suppress postharvest rot caused by F. incarnatum. Phenylethyl alcohol produced by T. asperellum T76-14 can cause abnormal changes in the mycelium of the muskmelon pathogen F. incarnatum, leading to a 62.5% inhibition rate [77]. T. spirale T76-1 volatiles alcohol and pyran exhibited antifungal activity against Corynespora cassiicola and Curvularia aeria, with 41.29% and 42.35% inhibition rates [78]. Additionally, different strains of the same genus of the same plant differ in producing VOCs that exhibit different inhibitory effects. The isolation of seven T. virens strains from crop roots that release VOCs effectively inhibited the growth of the pathogenic fungus Rhizoctonia solani. However, VOCs from the seven strains exhibited different antifungal activities against R. solani strains. Among them, T. V3 and T. V4 displayed >50% inhibition at 5 days (52.8% and 59.4%), while inhibition caused by the remaining strains was below 50% [65].

3.2. Yeasts

Yeasts, unicellular fungi, rapidly colonize the surface of fruits and vegetables due to their high sugar content. They may produce extracellular polysaccharides to protect against pathogenic fungi and are resistant to long-term colonization under unfavorable conditions [79]. Yeasts interact with fruit and vegetable pathogens primarily through their antifungal activity, fungal parasitism, lytic enzyme production, induction of resistance, competition for scarce nutrients and space, and oxidative stress [80]. In addition, a growing body of research has found that endophytic yeasts can colonize plant tissues without harming the plant and can release various active VOCs that inhibit the growth and reproduction of fungal pathogens [55].
Wickerhamomyces anomalus (BS91), Metschnikowia pulcherrima (MPR3), Aureobasidium pullulans (PI1), and Saccharomyces cerevisiae (BCA61) strains release antifungal active VOCs, mainly ethanol and ethyl acetate. Furthermore, by incubating for 5 days at 25 °C, the yeast strains exhibited substantial oxygen consumption and carbon dioxide production. This acted synergistically with VOCs to exert antagonistic effects, thereby prolonging fruit and vegetable freshness [81]. The endophytic yeast Geotrichum candidum PF005, isolated from rice and wheat grains by Mitra et al. [58], releases the main VOC of ethyl isovalerate, which has significant antifungal activity and can reduce the formation of plant pathogens Curvularia oryzae and Rhizoctonia solani fungi nuclei, inhibit aerial mycelial development, and affect chitin distribution as well as mycelial and spore morphology. Alcohol acetyltransferases (AATs) catalyze ester formation between various alcohols and acetyl-CoA. The structure and function of AATs were investigated. They were found to be critical for the synthesis of antifungal volatile acetate by the endophytic fungi G. candidum PF005 [82]. The yeast Hanseniaspora uvarum 793 isolated from fig was used in in vivo experiments on strawberries and cherries because of its excellent biocontrol properties. VOCs released by H. uvarum 793 reduced the growth of B. cinerea at different temperatures (25 °C and 7 °C) [60]. The production of antifungal VOCs by yeast is a promising technology for extending the shelf life of fruits and reducing food waste and losses in the supply chain

4. Control Mechanism of Endophytic Fungal VOCs on Postharvest Fruit and Vegetable Diseases

Many microorganisms colonize fruit and vegetable surfaces before or after harvest. However, they generally cannot cause fruit and vegetable rot [83]. When fruits and vegetables are in an environment prone to invasion by pathogenic fungi, pathogenic fungi become extremely active, especially in the postharvest ripening period of fruits and vegetables [4]. Under suitable environmental conditions, these pathogenic microorganisms germinate, grow, multiply, and colonize rapidly, resulting in the postharvest rot of fruits and vegetables. Therefore, whether fungal VOCs can inhibit spore germination and hyphal growth is of great significance for fungal inhibition research [84]. Two strains of Aureobasidium pullulans (L1 and L8) produced VOCs that were efficient in preventing conidial growth of P. expansum, P. digitatum, and P. italicum. In vivo investigations revealed that 2-phenethyl alcohol, the primary component of L1 and L8 VOCs, could dramatically suppress lesions and reduce lesion diameter by >88% in B. cinerea-inoculated apples [53]. The endophytic fungi T. asperellum 6S-2 was isolated from apple tree roots, and 6-pentyl-2H-pyran-2-one (6-PP) was the main component of its volatile substance, accounting for 36.45% of its volatile substance. 6-PP could inhibit Fusarium proliferatum f. sp. malus domestica MR5, which causes apple replant disease, resulting in twisting, shrinking, swelling, and rupture [70]. VOCs of the endophytic fungi Phaeosphaeria nodorum could inhibit the mycelial growth of Monilinia fructicola, resulting in the narrowing of mycelial width [62].
Cell walls and membranes are crucial and essential tissue structures for microbes, with the function of protecting the cell and participating in the transport of substances. Cell wall and membrane integrity are critical for the survival of pathogenic fungi [85]. Endophytic fungal VOCs can damage the cell walls and membranes of pathogenic microorganisms, leading to changes in microbial morphology and leakage of contents and affecting microbial physiological function. A mixture of six endophytic fungal VOCs and alcohol synergistically alters the cell membrane permeability of the plant pathogen F. oxysporum. This causes a disruption in mycelial morphology as well as the inhibition of respiration and, eventually, the growth of the pathogen [86]. The VOCs of the endogenous fungus Diaporthe sp. CEL3 treat the pathogenic microorganism Monilinia fructicola and Pythium ultimum, causing the intracellular discharge of compounds of pathogenic microorganism, and with the extension of the processing time, the protein discharges also increase [37]. Some endophytic fungal VOCs can also kill pathogenic microorganisms by damaging their DNA. Single knockout testing revealed that the DNA repair, DNA metabolic activities, and stress response pathways of enzyme-deficient Escherichia coli are hypersensitive to Muscodor albus volatiles. VOCs prevent Escherichia coli from repairing damaged DNA, thereby preventing DNA replication or transcription. Second, VOCs can change Escherichia coli cell morphology, interfere with their selective permeability barrier, and make their cell membranes more permeable [87].
Endophytic fungal VOCs may act as signaling molecules that induce resistance in the plants that they colonize. They enhance the plant defense system to resist pathogens and promote plant growth. VOCs released by T. asperloides PSU-P1 increased the gene expression of the cell wall-degrading enzymes chitinase (CHI) and β-1,3-glucanase (GLU), as well as defense-related enzyme (peroxidase (POD)) activity in Arabidopsis thaliana, which is associated with increased oxidative stress in postharvest fruits and vegetables [88]. Similarly, 3-methyl-1-butanol, 1-decene, and 2-heptylfuran can improve the total chlorophyll content and fresh weight of Arabidopsis thaliana plants and promote their development [89]. The fungi T. asperellum T1 releases VOCs that increase the activity of cell wall-degrading enzymes, namely chitinase and β-1,3-glucanase, in lettuce. The pathogenic fungi cell wall undergoes morphological alterations owing to the accumulation of cell wall-degrading enzymes, thereby preventing the growth of the lettuce leaf spot-causing pathogens, Corynespora cassiicola and Curvularia aeria. Likewise, VOCs of T. asperellum T1 promote lettuce growth by increasing, for instance, the number of leaves and roots, plant biomass, and total chlorophyll content [71].
An in-depth understanding of the specific physiological mechanism of the antifungal activity of endophytic fungal VOCs will help to comprehend the role and efficacy of fungal volatiles and their application in biocide research. Nowadays, the action mechanisms of fungal VOCs on pathogens of postharvest fruits and vegetables mainly include the inhibition of spore germination and mycelial growth of microbial pathogens (Figure 2); destruction of cell walls and membranes and change in the cell morphology of pathogens, which causes structural deformation, leakage of contents, and DNA damage and results in the impairment of physiological functions of pathogens (Figure 2); and the induction of resistance in fruits and vegetables by enhancing defense enzyme (peroxidase (POD)) activities, thus resisting postharvest diseases and promoting plant growth (Figure 3). Of course, fungal VOCs may act against pathogens through one or multiple mechanisms. Sarocladium brachiariae HND5 VOCs, for example, exhibit many fungi inhibitory mechanisms against detrimental microorganisms. It can destroy the cell wall and membrane of pathogenic fungi, leading to cell death. It can also trigger the production of plant chitinase and the accumulation of reactive oxygen species (ROS) in the pathogenic mycelium [63]. However, because of the diversity of fungi and their VOCs, the mechanisms of action are still poorly studied and need to be further explored. Some representative studies are summarized in Table 2.

5. Application of Endophytic Fungal VOCs as Postharvest Fruit and Vegetable Fumigants

As biological control mechanisms, endophytic fungal VOCs can be used to control the growth of plant diseases, thereby replacing chemical fungicides and addressing the issue of easy-lingering chemical fungicides in the environment and contaminating human health and the environment. Owing to their fast dispersion time, high efficiency, and other beneficial qualities, VOCs can be widely employed in agriculture. However, VOCs might be influenced by various circumstances during the application process. The production rate of VOCs is easily influenced by temperature, time, and culture substrate, as well as microbe-specific environmental conditions and even interactions with other species [86]. Whenever a fungus is cultivated in vitro, previously undiscovered VOCs are established, and VOCs vary with the age of the fungus and intraspecific and interspecific interactions [90]. The relative abundance of VOCs in Xylaria sp. PB3f3 varied with culture time and strain age. From the total VOCs, 25, 20, and 22 compounds were, respectively, produced at days 10, 20, and 30 of fungal growth [91]. Secondly, the different times and concentrations that VOCs access pathogen-infected fruits and vegetables lead to different inhibition effects. The endophytic fungus Aureobasidium pullulans L1, for example, exhibited good inhibitory activity against Colletotrichum acutatum and P. expansum for 12 h after apples were inoculated with the pathogenic fungus; introduced just 6 h after inoculation, it displayed the strongest inhibitory action against B. cinerea [92]. Candida quercitrusa Cq-1 VOCs effectively inhibited the growth of Phytophthora infestans mycelium, and the inhibition rate showed a linear relationship with the concentration of the fungi solution in the lower range. When the concentration of C. quercitrusa Cq-1 was 103 CFU/mL, Phytophthora infestans mycelium barely grew, and the maximum inhibition was about 96.79% [54]. The optimal growth cycles of endophytic fungi are different, resulting in different concentrations of VOCs released during their growth and metabolism. Therefore, the use of optimum fumigation time and concentration will be effective in improving the inhibitory activity of endophytic fungal VOCs.
Fungi are diversified in terms of their generation of VOCs, comprising acids, alcohols, aldehydes, aromatics, esters, heterocycles, ketones, terpenes, thiols, and various other chemicals [44]. These compounds frequently mix to form complex combinations with inhibitory effects against one or more pathogenic fungi. VOCs from Daldinia cf. concentrica, for example, can effectively inhibit both mold growth on wheat seeds and Aspergillus niger infection in peanuts [56]. The volatile eucalyptol of the endophytic fungus Nodulisporium spp. CMU-UPE34 can control citrus fruit postharvest blight by inhibiting P. digitatum and P. expansum [93]. Microbial strains are susceptible to interference from various environmental factors. They are not susceptible to normal growth and metabolic activities, or even survival, under extreme acid–base conditions, too-high or too-low temperatures, extreme water scarcity, and UV radiation [94], which decreases the ability of microbes to produce VOCs and unstable effects. Consequently, additional studies need to be conducted on the biocontrol mechanism of VOCs, the screening of VOCs with broad-spectrum inhibitory activity and a high control effect, and environmentally resistant cultivars. Although VOCs do not easily stay on the fruit and vegetable surfaces, a limited percentage of fungal VOCs are detrimental. VOCs interfere with seed germination, seedling respiration, and root growth in Amaranthus hypochondriacus, Panicum miliaceum, Trifolium pratense, and Medicago sativa plants [95]. Therefore, when using endophytic fungal VOCs as control agents, it is necessary to consider whether VOCs have toxic effects on plants, damage plant cells, and affect their growth, metabolism, and physiological functions. It is necessary to find safe biological control agents.
On the market, products that control the consequences of vegetable harvesting are still controlled by physical methods, such as low-temperature storage, and chemical methods, such as using fludioxonil [96,97]. Concerning the use of endophytes, as a new concept, some preparations such as CandifruitTM, ShemerTM, and Boni-protectTM have successfully prevented post-traumatic diseases [98]. Although products for endophytic fungal VOCs are not yet mature, research has been conducted on the subject of replacing chemical fungicides with endophytic fungal VOC fumigation to maintain the quality of postharvest fruits and vegetables. Because VOCs are easily volatilized in space, the problems of their airtightness and stability must be considered in the actual application process. Thus, in the laboratory, it is mainly taken as a flat plate to buckle and seal with a sealing film to prevent the volatilization of VOCs and avoid reducing their fungistatic activity [26]. In practical applications, depending on the type of fruits and vegetables and the storage conditions, fumigation can be used to achieve antagonistic effects against pathogenic fungi in a closed environment, such as entire storage rooms and individual transport containers [30]. In this case, endophytic fungi can be cultivated in a separate chamber, and the VOCs produced are released into the storage room via a pump without any direct contact with the fruits and vegetables, preventing infection of the fruits by the strain [40]. Instability caused by VOCs can be effectively reduced through closed environments. Secondly, VOCs produced by endophytic fungi can be incorporated into edible films and edible coatings and can also be used as ingredients in active packaging to effectively control microbial spoilage in fruits and vegetables and maintain fruit and vegetable quality [40]. Microencapsulation is a packaging technology that utilizes natural or synthetic polymer film-forming materials to encapsulate gases, liquids, or solids into particles with a particle size of 1–1000 μm [99]. Natural polymers, such as alginate, pectins, guar gums, and chitosan, are widely used as materials for the microencapsulation of many bioactive compounds [100]. Preparing trans-2-hexenal loaded polyurea microcapsules via an interfacial polymerization method effectively reduced the incidence of seed blight during wheat storage and prolonged the inhibition of pathogenic fungi [101]. By packaging VOCs in microcapsules, it is possible to effectively avoid the influence of environmental factors and to tackle the problem of VOC exposure and instability. In addition, sol-gel technology is used to encapsulate VOCs and can control the release rate of VOCs. Cross-linking during the sol-gel process can be controlled to produce a formulation with a constant release rate [102]. At present, VOC evaporation technology is still in the lab stage, and the development of economical, safe, and efficient technologies, such as microencapsulation and new packaging, will drive the industrialization and commercialization of VOCs.
In addition, the commercialization of endogenous fungal VOCs must take into account the originality of new technologies, as well as consistency and reliability under different production lines. Developing the product needs to relate to the business environment to solve its limitations and consider public acceptance. For large-scale production applications, the health assessment of the registration process needs to be fully clarified. Endophytic fungal VOCs still face great obstacles and challenges in terms of their future practical applications. (1) There is a wide variety of VOCs, some of which are even trace amounts, which are difficult to detect and characterize. (2) VOCs exert antifungal activity in the form of mixtures, and most of the current studies utilize single compounds in their pure form; therefore, it is necessary to study the antifungal activity of mixtures and explore whether there are synergistic or antagonistic effects between VOCs. (3) VOCs are highly unstable due to their volatility and can only be used in a closed environment. Therefore, the specific application model of VOC commercialization will become a complex issue and challenge in the future. (4) The mechanism of endophytic fungi VOCs to prevent and control postharvest diseases in fruits and vegetables is not comprehensive enough, and whether it affects the taste and nutrition of fruits and vegetables requires further research. (5) The safety of some VOCs is still a concern because workers who use endophytic fungi for fumigation with volatile organic compounds will inevitably inhale or be exposed to these volatile organic compounds during transportation and storage. (6) Most of the current antifungal applications of VOCs are still concentrated in the laboratory stage, and the gap between the application conditions in the laboratory and the factory is so large that it is a great challenge to realize the transition from the laboratory to the factory. The introduction of natural products into practice is complex, and aspects such as barriers to registration, difficulties in large-scale production, and industrial acceptance must be considered.

6. Conclusions

Endophytic fungi are isolated from plant tissues, and the use of the VOCs they produce to control postharvest diseases has received widespread attention. Currently, fungal species that release endophytic VOCs mainly include Trichoderma spp. and yeasts. Its mechanism of action is achieved via the disruption of the cellular and molecular structure of pathogenic fungi and enhancing the resistance of fruits and vegetables. The use of VOCs still faces many environmental factors and challenges in practical applications, and technical difficulties must be overcome to achieve commercialization. The application of endophytic fungi VOCs can effectively replace the harmful dependence on chemical fungicides and achieve guaranteed food safety in fruits and vegetables.

Author Contributions

Conceptualization, L.L. and L.F.; methodology, L.F.; software, Y.L. and Y.W.; validation, L.F., R.Y. and Y.Z.; formal analysis, Y.W.; investigation, Y.L. and R.Y; resources, L.L.; data curation, L.F.; writing—original draft preparation, L.F.; writing—review and editing, L.L.; visualization, Y.L.; supervision, Y.W. and Y.Z.; project administration, L.L. and L.F; funding acquisition, L.L. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the Key Research and Development Project of Gansu Province (22YF7NA120), Science and Technology Program of Gansu Province (22CX8GA136).

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We want to express our gratitude for the drawing materials provided by BioRender.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Chemical classification of endophytic fungal VOCs and their application methods. Numbers 1 and 2 represent the specific application of the other endophytic fungi flat button method in the first or second way. Created with BioRender.com.
Figure 1. Chemical classification of endophytic fungal VOCs and their application methods. Numbers 1 and 2 represent the specific application of the other endophytic fungi flat button method in the first or second way. Created with BioRender.com.
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Figure 2. Mechanisms of the effects of endophytic fungal VOCs on postharvest diseases. Created with BioRender.com.
Figure 2. Mechanisms of the effects of endophytic fungal VOCs on postharvest diseases. Created with BioRender.com.
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Figure 3. Endophytic fungal VOCs improve defense and promote the growth of fruits and vegetables. Created with BioRender.com.
Figure 3. Endophytic fungal VOCs improve defense and promote the growth of fruits and vegetables. Created with BioRender.com.
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Table 1. VOCs from endophytic fungi: main chemical components and effect against phytopathogenic fungi.
Table 1. VOCs from endophytic fungi: main chemical components and effect against phytopathogenic fungi.
Endophytic FungiEndophytic Fungal Host PlantsMain VOCsPathogenPathogen HostsReferences
Aureobasidium pullulans (L1 and L8)‘Redhaven’ peaches (Prunus persica (L.) Batsch)2-phenethyl alcohol
1-butanol-3-methyl
1-butanol-2-methyl
1-propanol-2-methyl		Botrytis cinerea
Colletotrichum acutatum
Penicillium expansum
Penicillium digitatum
Penicillium italicum		‘Golden Delicious’ apples (Malus domestica L. Borkh)
‘Navel’ oranges (Citrus sinensis L. Osbeck)		[53]
Candida
quercitrusa strain Cq-1		Litchi (Litchi chinensis Sonn.)2-PhenylethanolPhytophthora infestansPotato (Solanum tuberosum L.)[54]
Candida nivariensis DMKU-CE18Leaves of rice (Oryza sativa L.), sugarcane (Saccharum officenarum L.) and corn (Zea mays L.)1-pentanolAspergillus flavus A39Corn grains (Zea mays L.)[55]
Daldinia cf. concentricaOlive tree (Olea europaea L.)Alcohols
Dienes
Ketones
Aldehydes
Sesquiterpenes		Molds
Aspergillus niger		Wheat grains (Triticum aestivum L.)
Peanuts (Arachis hypogaea L.)		[56]
Fusarium solani-F4-1007Argel (Solenostemma arghel)3,4-dihydro-2H-1,5-(3″-t-butyl) benzodioxepine
4-(2-hydroxyethyl) phenol
phenylethyl alcohol		Cochliobolus spicifer-CSN-20Okra (Abelmoschus esculentus)[57]
Geotrichum candidum PF005Eggplant (Solanum melongena)Ethyl isovalerateRhizoctonia solani
Curvularia oryzae		Rice (Oryza sativa L.)
Wheat (Triticum aestivum L.)		[58]
Hypoxylon anthochroum strains Blaeg1, Gseg1, Haeg2 and Smeg4Burseraceae (Bursera lancifolia)
Fabaceae (Gliricidia sepium)
Celastraceae (Hippocratea acapulcensis)
Euphorbiaceae (Sapium macrocarpum)		Sesquiterpenes
Monoterpenes(eucalyptol)		Fusarium oxysporumCherry tomatoes (Solanum lycopersicum var. cerasiforme)[59]
Hanseniaspora uvarum 793Figs (Ficus carica L.)Acids (acetic acid and octanoic acid)
Esters (ethyl propionate, n-Propyl acetate, Isobutyl acetate, 2-methylbutyl acetate, furfuryl acetate, phenylmethyl acetate, 2-phenylethyl acetate)		Botrytis cinereaStrawberries (Fragaria × ananassa Duch.)
Cherries (Prunus pseudocerasus Lindl.)		[60]
Nodulisporium spp. CF016Lauraceae trees (Lauraceae Juss.)1-methyl-1,4-cyclo-hexadiene
β-selinene
α-selinene		Botrytis cinerea
Penicillium expansum		Apple (Malus pumila Mill.)[61]
Phaeosphaeria nodorumPlum (Prunus domestica) Ethyl acetate
3-methyl-1-butanol
Acetic acid
2-propyn-1-ol
2-propenenitrile		Monilinia fructicolaPlum (Prunus domestica)[62]
Sarocladium brachiariae HND5The coastal grass2-methoxy-4-vinylphenol
3,4-dimethoxystyrol
Caryophyllene		Fusarium oxysporum f. sp. cubense (FOC)Banana (Musa nana Lour.)[63]
Saccharomyces cerevisiae NJ-1Fig (Ficus carica L.)3-methyl-1-butanolAspergillus flavusWalnuts (Juglans regia L.)[64]
Trichoderma virensCropsSesquiterpenes (aromanderen, element, cadinene, and 2-Octanone)
Monoterpene (limonene and bisnorhopane)
Fatty acids (oleic acid, and monopalmtin)
Caryophyllene
Thojupsene		Rhizoctonia solaniPlants[65]
Trichoderma longibrachiatum T (SP)-20Groundnut (Arachis hypogaea L.)Isolongifolan-7-ol
Trans-sesquisabinene hydrate		Sclerotium rolfsiiGroundnut (Arachis hypogaea L.)[66]
Trichoderma koningiopsis YIM PH300022-year-old healthy Sanqi (Panax notoginseng)Alkanes
Monoterpenes
Aromatic hydrocarbons
Heterocyclic
Aldehydes		Phoma herbarum
Fusarium flocciferum
Scytalidium lignicola
Epicoccum nigrum		Sanqi (Panax notoginseng)[67]
Trichoderma afroharzianum strain MFLUCC19-0090
Trichoderma afroharzianum strain MFLUCC19-0091		Schefflera leucantha leavesPhenylethyl alcoholFusarium oxysporum
Fusarium proliferatum		Chili (Capsicum annuum L.)[68]
Trichoderma longibrachiatum EF5Rice (Oryza sativa L.)Longifolene
Caryophyllene
Butanol 2-methyl
Cedrene
Cuprenene		Sclerotium rolfsii
Macrophomina phaseolina		Plants[69]
Trichoderma asperellum 6S-2Roots of healthy apple (Malus pumila Mill.) trees6-pentyl-2H-pyran-2-oneFusarium proliferatum f. sp malus domestica MR5Apple (Malus pumila Mill.)[70]
Trichoderma atroviride IC-11 Rhizosphere of citrus(Citrus reticulata Blanco) tree6-pentyl-α-pyrone Botrytis cinereaBlueberry (Vaccinium spp.) [52]
Trichoderma asperellum T1Lettuce (Lactuca sativa)Thyl-1-hexanol
1-nonanol
6-pentyl-2H-pyran-2-one		Corynespora cassiicola
Curvularia aeria		Lettuce (Lactuca sativa)[71]
Table 2. The mechanisms of endophytic fungal VOCs in the control of postharvest diseases.
Table 2. The mechanisms of endophytic fungal VOCs in the control of postharvest diseases.
Main VOCs Endophytic FungiPathogenEndophytic Fungal Usage and Dosage MechanismsReferences
2-PhenylethanolCandida
quercitrusa strain Cq-1		Phytophthora infestans20 µL cell concentration of 1 × 103 CFU/mL Inhibition of pathogen fungal mycelial development, blockage of the oxidative phosphorylation pathway[54]
Ethyl isovalerateGeotrichum candidum PF005Curvularia oryzae
Rhizoctonia solani		200 μL, OD600 = 5Alteration of pathogen fungal mycelial morphology, influence on mycelial chitin distribution, and generation of oxidative stress[58]
Ethyl acetate
3-methyl-1-butanol
Acetic acid
2-propyn-1-ol
2-propenenitrile		Phaeosphaeria nodorumMonilinia fructicola5-mm-diameter plug of endophytic fungiReduced width of the pathogen fungal mycelial, causing disintegration of the mycelial content.[62]
2-methoxy-4-vinylphenol
3,4-dimethoxystyrol
Caryophyllene		Sarocladium brachiariae HND5Fusarium oxysporum f. sp.Plug of endophytic fungiInduction of pathogenic fungal reactive oxygen species and chitinase gene accumulation and expression[63]
3-methyl-1-butanolSaccharomyces cerevisiae NJ-1Aspergillus flavus20 µL cell concentration of 1 × 107 CFU/mLDisruption of pathogen fungal cell membrane[64]
6-pentyl-2H-pyran-2-oneTrichoderma asperellum 6S-2Fusarium proliferatum f. sp malus domestica MR5Plug of endophytic fungiDestroys hyphae morphology and spore shape[70]
Thyl-1-hexanol
1-nonanol
6-pentyl-2H-pyran-2-one		Trichoderma asperellum T1Corynespora cassiicola
Curvularia aeria		5-mm-diameter plug of endophytic fungiEnhanced accumulation of cell wall degrading enzymes in lettuce[71]
2-methyl-1-butanol
2-pentylfuran
Acetic acid
6-pentyl-2H-pyran-2-one		Trichoderma asperelloides PSU-P1Colletotrichum sp.
Corynespora cassiicola
Curvularia lunata
Ganoderma sp.
Macrophomina phaseolina
Neopestalotiopsis clavispora
Penicillium oxalicum
Sclerotium rolfsii
Stagonosporosis cucurbitacearm		5-mm-diameter plug of endophytic fungiAntagonism of fungal pathogens, activation of plant defense responses, and promotion of plant growth[88]
Longifolene
Caryophyllene
Butanol 2-methyl
Cedrene
Cuprenene		Trichoderma longibrachiatum EF5Sclerotium rolfsii8-mm-diameter plug of endophytic fungiAlteration of mycelial structure[69]
Sesquiterpenes (aromanderen, element, cadinene, and 2-Octanone)
Monoterpene (limonene and bisnorhopane)
Fatty acids (oleic acid, and monopalmtin)
Caryophyllene
Thojupsene		Trichoderma virensRhizoctoniasolani5-mm-diameter plug of endophytic fungiDestruction of pathogenic fungal hyphae morphology[65]
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Ling, L.; Feng, L.; Li, Y.; Yue, R.; Wang, Y.; Zhou, Y. Endophytic Fungi Volatile Organic Compounds as Crucial Biocontrol Agents Used for Controlling Fruit and Vegetable Postharvest Diseases. J. Fungi 2024, 10, 332. https://doi.org/10.3390/jof10050332

AMA Style

Ling L, Feng L, Li Y, Yue R, Wang Y, Zhou Y. Endophytic Fungi Volatile Organic Compounds as Crucial Biocontrol Agents Used for Controlling Fruit and Vegetable Postharvest Diseases. Journal of Fungi. 2024; 10(5):332. https://doi.org/10.3390/jof10050332

Chicago/Turabian Style

Ling, Lijun, Lijun Feng, Yao Li, Rui Yue, Yuanyuan Wang, and Yongpeng Zhou. 2024. "Endophytic Fungi Volatile Organic Compounds as Crucial Biocontrol Agents Used for Controlling Fruit and Vegetable Postharvest Diseases" Journal of Fungi 10, no. 5: 332. https://doi.org/10.3390/jof10050332

APA Style

Ling, L., Feng, L., Li, Y., Yue, R., Wang, Y., & Zhou, Y. (2024). Endophytic Fungi Volatile Organic Compounds as Crucial Biocontrol Agents Used for Controlling Fruit and Vegetable Postharvest Diseases. Journal of Fungi, 10(5), 332. https://doi.org/10.3390/jof10050332

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