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Ciência e Agrotecnologia

Print version ISSN 1413-7054

Ciênc. agrotec. vol.36 no.5 Lavras Sept./Oct. 2012 



Biological control of mycotoxin-producing molds


Controle biológico de fungos de armazenamento produtores de micotoxinas



Flávio Henrique Vasconcelos de MedeirosI; Samuel Julio MartinsII; Tiago Domingues ZucchiIII; Itamar Soares de MeloIII; Luis Roberto BatistaIV; José da Cruz MachadoV

IUniversidade Federal de Lavras/UFLA - Departamento de Fitopatologia/DFP - Cx. P. 3037 - 37200-000 - Lavras - MG - Brasil -
IIUniversidade Federal de Lavras/UFLA - Lavras - MG - Brasil
IIIEmpresa Brasileira de Pesquisa Agropecuária/EMBRAPA - Meio Ambiente - Jaguariúna - SP - Brasil
IVUniversidade Federal de Lavras/UFLA - Departamento de Ciência dos Alimentos/DCA - Lavras - MG - Brasil
VUniversidade Federal de Lavras/UFLA - Departamento de Fitopatologia/DFP - Lavras - MG - Brasil




Mycotoxins are produced by the secondary metabolism of many fungi and can be found in almost 25% of the world's agricultural commodities. These compounds are toxic to humans, animals, and plants and therefore, efforts should be made to avoid mycotoxin contamination in food and feed. Besides, up to 25% of all harvested fruits and vegetables are lost due to storage molds and/or mycotoxin contamination and many methods have been applied to mitigate these issues, but most of them rely on the use of fungicides. Although chemicals are often the first defensive line against mycotoxigenic fungi, the indiscriminate use of fungicides are awakening the public perception due to their noxious effects on the environment and human/animal health. Thus, there is an increasing public pressure for a safer and eco-friendly alternative to control these organisms. In this background, biological control using microbial antagonists such as bacteria, fungi and yeasts have been shown to be a feasible substitute to reduce the use of chemical compounds. Despite of the positive findings using the biocontrol agents only a few products have been registered and are commercially available to control mycotoxin-producing fungi. This review brings about the up-to-date biological control strategies to prevent or reduce harvested commodity damages caused by storage fungi and the contamination of food and feed by mycotoxins.

Index terms: Biocontrol, microbial antagonists, postharvest decay, food safety.


As micotoxinas são produzidas pelo metabolismo secundário de várias espécies de fungos e podem ser encontradas em quase 25% das commodities agrícolas. Esses compostos são tóxicos a humanos, animais e plantas e, portanto, esforços para evitar a contaminação de micotoxinas em alimentos e rações devem ser feitos. Além disso, até 25% das frutas e legumes em pós-colheita são perdidos em decorrência do ataque de fungos de armazenamento e/ou contaminações por micotoxinas. Vários métodos têm sido aplicados para mitigar os problemas de micotoxinas, mas a maioria deles se baseia no uso de fungicidas. Embora os produtos químicos sejam, muitas vezes, a primeira estratégia de defesa contra fungos micotoxigênicos, o uso indiscriminado de fungicidas vem despertando a percepção pública, em razão de seus efeitos nocivos sobre o meio ambiente e à saúde humana/animal. Assim, existe uma crescente pressão pública em busca de alternativas mais segura e não nocivas ao meio ambiente para controlar estes organismos. Nesse contexto, o controle biológico utilizando antagonistas microbianos, tais como bactérias, fungos e leveduras têm mostrado ser um substituto viável para reduzir a utilização de produtos químicos. Apesar dos resultados positivos, usando os agentes de controle biológico, poucos produtos apenas foram registrados e estão comercialmente disponíveis para controlar fungos produtores de micotoxinas. Esta revisão traz estratégias de controle biológico para evitar ou reduzir danos em commodities agrícolas causadas por fungos de armazenamento e a contaminação de alimentos e rações por micotoxinas.

Termos para indexação: Agentes de biocontrole, microrganismos antagonistas, perda em pós-colheita, segurança alimentar.




Postharvest diseases, caused by storage moulds, account for considerable levels of postharvest losses. Conservative estimates consider that about 20-25% of the harvested fruits and vegetables are lost due to postharvest diseases even in developed countries (SPADARO; GULLINO, 2004). In developing countries, postharvest losses are often more severe due to inadequate storage and transportation facilities (SHARMA; SINGH; SINGH, 2009), which often makes the environment more favorable to the storage fungal development. Furthermore, most of these fungi may produce dangerous metabolites, namely mycotoxins, often acutely toxic to humans, animals, and plants (LACKNER; MARTINEZ; HERTWECK, 2009; PROCTOR, et al., 2009; REVERBERI, et al., 2010). Some mycotoxins are present only in the fungus whereas others are excreted, in some cases, in foods and feeds (FILTENBORG; FRISVAD; THRANE, 1996). Mycotoxin contaminations can occur in the field, before or after the harvest, and during the transfer and product storage (CALDAS; SILVA; OLIVEIRA, 2002). Also, as these compounds are highly resistant to physical and chemical treatment, once mycotoxins are found in food, generally, persist during the processing and storage (SCOTT et al., 1992). Thus, to prevent or, at least minimize the production losses and to obtain stored food products of high quality for market place, strategies to control storage fungi as well as mycotoxin productions must be done.

Although synthetic fungicides are the primary means by which postharvest diseases is controlled (KORSTEN, 2006; DAL BELLO et al., 2008), currently the global trend is turned to safer and eco-friendly alternative approaches (JANISIEWICZ; KORSTEN, 2002; MARI; NERI; BERTOLINI, 2007; SHARMA et al., 2009). One of these possibilities is the use of antagonistic microorganisms to control mycotoxigenic fungi. This method (biological control) have been applied during the last decades (WELLER, 1988) and substantial progress in the management of these pathogens and their mycotoxins have also been achieved (JANISIEWICZ; KORSTEN, 2002; SPADARO; GULLINO 2004; KORSTEN, 2006; VELMOUROUGANE et al., 2011).



Many of the storage fungi may produce a plenty of natural products, often called secondary metabolites, which include pigments, toxins, plant growth regulators, antibiotics (CALVO et al., 2002; PROCTOR et al., 2009). Some of these fungal compounds have beneficial importance to mankind, such as the antibiotic penicillin - a secondary metabolite from Penicillium notatum which is still widely used nowadays, though many bacterial species are now resistant to it. On the other hand, others secondary metabolites, namely mycotoxins, are dangerous and often present noxious effect to eukaryotes, including humans, animals, and plants (LACKNER; MARTINEZ; HERTWECK, 2009; PROCTOR et al., 2009; REVERBERI et al., 2010).

Mycotoxin (from Greek ''mykes'', fungus, from Latin ''toxicum'', poison) is produced during the fungal growth and can be found in the hyphae and spores of these organisms (ZUCCHI; MELO, 2009; KÖPPEN et al., 2010). If ingested, mycotoxins may cause acute or chronic disease episodes, termed mycotoxicosis (MILICEVIC; SKRINJAR, BALTIC, 2010; KÖPPEN et al., 2010).

Foods are usually the preferred via for mycotoxin contamination and once consumed the exerted toxic effects are induced (KÖPPEN et al., 2010). Mycotoxin long-term exposure has also been related to several mycotoxicosis, such as carcinogenic, mutagenic, teratogenic, estrogenic, hemorrhagic, immunotoxic, nephrotoxic, hepatotoxic, dermotoxic neurotoxic and immunosuppressive (RICHARD, 2007; MILICEVIC; SKRINJAR, BALTIC, 2010).

Decontamination of food or feed are extremely difficult (RICHARD, 2007) and to avoid medical or veterinary problems usually the contaminated commodities or byproducts are destroyed.

Mycotoxins background

History facts of outbreaks, deaths, and losses involving the presence of mycotoxins date the Middle Ages. The oldest recognized mycotoxicosis of humans is the ergotism. This condition is the direct result of the consumption of products made with grains contaminated with ergotoxin - produced by the sclerotia of Claviceps purpurea (CAST, 2003). The ergotism can cause convulsion due to serotonergic stimulation of central nervous system or gangrenes of acral parts of the human body (HULVOVÁ et al., 2012). It reached epidemic proportions in central Europe, where thousands of people were mutilated and killed. Ergotism was also known as ignis sacer (sacred fire) or St. Anthony's fire, because at the time it was thought that a pilgrimage to the shrine of St. Anthony would bring relief from the intense burning sensation experienced (PERAICA et al., 1999; RICHARD, 2007).

Nevertheless, the magnitude of the fungal contamination problem began to be appreciated during World War II. At that time, it was noted that the consumption of moldy grain led to necroses of the skin, hemorrhage, liver and kidney failure, and death in numerous humans and animals (AGRIOS, 2005). For instance, during the wartime winter of 1940 in the USSR many people died after eating grain poorly stored and highly contaminated with mycotoxins (SCHUSTER; MARX; RATHAUPT, 1993). Nevertheless, although cause and effect of contaminated food ingestion could be correlated, there was no report addressing these symptoms to fungal secondary metabolites.

Consequently, the most famous episode involving mycotoxicosis was the ''turkey X disease" that occurred in England in 1960, in which more than 100,000 turkeys died without any apparent reason. Posteriorly, this disease was related to the peanuts contained in the turkey feed (ASAO et al., 1963) and its cause was attributed to a secondary metabolite produced by Aspergillus flavus, aflatoxin (PAPP et al., 2002). Indeed, it was only after this episode that the scientific community has begun to give importance to the hazardous properties of fungal metabolites. Furthermore, from all known mycotoxins, aflatoxin is still considered the worst carcinogen compound produced by microorganisms (SHENASI; AIDOO; CANDLISH, 2002).

What kind of mycotoxins can be found in the food commodities?

Currently, more than 500 different mycotoxins have been discovered and this number do not stop increasing. Many mycotoxins are classified as polyketides, i.e. bioactive secondary metabolites synthetized as fatty acids (HOPWOOD; SHERMAN, 1990). Among the most economically and toxicologically important mycotoxins that pose greatest potential risk to human and animal health as food and feed contaminants are: aflatoxins, trichothecenes, fumonisins, zearalenone, ochratoxin, patulin, and certain ergot alkaloids (CAST, 2003; BENNETT; KLICH, 2003; RICHARD, 2007; KÖPPEN et al., 2010). Economic losses due to decrease of productivity have been estimated around one billion dollar/year, and over US$ 500 million to mitigate the damage of only three mycotoxins: aflatoxins, fumonisins and trichothecenes (BHATNAGAR et al., 2006).

Mycotoxins are produced by a large number of fungal species and some are able to produce more than one mycotoxin (Table1). Also, some mycotoxins can be produced by more than one species (HUNSSEIN; BRASEL, 2001).



Since the discovery of aflatoxins, the scientific community has been attempting to limit mycotoxin contamination in foods and feeds (REVERBERI, et al., 2010). Regulations relating to mycotoxins have been established in many countries to protect the consumer from the harmful effects of these compounds (MILIÆEVIÆ; SKRINJAR; BALTIC, 2010). Virtually all countries with fully developed market economies have established regulations for mycotoxins whilst many developing countries, where subsistence farming is significant, the maximum limits of mycotoxins were not regulated yet (Figure 1; CAST, 2003).

During a long time, mycotoxins concentrations were not regulated in Brazil. However, due to a pressure increase from foreign consumers for food free of mycotoxins, Brazilian government has regulated the maximum limits for aflatoxin in food and feeds (Table 2).

Although aflatoxin is still the only regulated mycotoxin in Brazil: 20 µ for total aflatoxin in feed and 30 µ for aflatoxin B1+G1 in food; (CALDAS; SILVA; OLIVEIRA, 2002), other country's regulations have presented a lower tolerance for this mycotoxin. For instance, values for total aflatoxins found in food vary from 1 µ (Bosnian) to 10 µ (France) (CREPPY, 2002). Also, some regulatory policies are greatly developed as shown by countries which regulate more than one mycotoxin (Table 2). Furthermore, according to Fao, 2003 data, on a worldwide basis, at least 99 countries regulated mycotoxins for food and/or feed in 2003 representing an increase of approximately 30 percent compared to 1995. The total population in these countries represents approximately 87% of the inhabitants of the world. This number was 77% in 1995. The increase in 2003 is due a slight increase in coverage in Latin America and Europe, and more significant increases in Africa and Asia/Oceania. Nevertheless, currently still 13% of the inhabitants of the world live in a region where no known mycotoxin regulation is in force. Thus, it is important the use of safe methods of control of mycotoxin-producing fungi to allow the marketing of healthy products without risk to human and animal health (FOOD AND AGRICULTURE ORGANIZATION - FAO, 2003).



Currently, over 25% of the world's agricultural commodities are estimates to be contaminated with mycotoxins to a certain degree (STEPIEN et al. 2007 cited by KÖPPEN et al., 2010). This serious issue has been focus of several strategies to mitigate the concentration of mycotoxins in food. The main strategy includes the use of fungicides (EDWARDS, et al., 2001) which is also considered the primary means by which postharvest diseases are controlled (SPADARO; GULLINO, 2004; KORSTEN, 2006; DAL BELLO et al., 2008). Besides, currently many reasons - public perception that pesticides are harmful to human health and the environment (JANISIEWICZ; KORSTEN, 2002), limited efficacy for the development of pathogen resistance (LIMA et al., 2006; BRODERS et al., 2007), and the public demand for produce food free of synthetic pesticides (SIPICZKI, 2006) - have been requesting to replace the synthetic chemicals use to a safer and cleaner alternative approach. In this background, biological control using antagonistic microorganisms has been an emergent alternative to efficiently manage storage fungi and mycotoxins production and hence, reducing the use of chemical compounds (JANISIEWICZ; KORSTEN, 2002; SPADARO; GULLINO 2004; KORSTEN, 2006; VELMOUROUGANE et al., 2011).

Although many useful biocontrol agents were first identified through in vitro inhibition tests (i.e., evaluating inhibition of a target pathogen on an agar medium), several researchers have reported no correlation between in vitro inhibition tests and field performance of biocontrol agents (FRAVEL, 2005). This difference is usually explained by various environmental conditions which may affect the antagonist performance (COTTY; MELLON, 2006) or laboratory conditions may artificially favour the antagonist (WELLER, 1988). The trend currently seems to drift through screening procedures that simulate conditions under which the agent will be used (ABRAHAM; LAING; BOWER, 2010; ZHANG et al., 2010; MANSO; NUNES, 2011).

Recently, the number of the biocontrol products available at the market is incresing. Some examples of few products commercially available may be found at the the table 3.

Despite of the increasing of this number, these products still represent only about 1% of agricultural chemical sales (FRAVEL, 2005). In near future is expect to find new registrations of biofungicides to control storage mould and mycotoxins.

Sources of antagonists

There are a variety of microrganisms which may be used as biocontrol agents against mycotoxigenic fungi that include different species of yeasts, fungi, and bacteria. Due to the positive findings regarding the use of these microbial antagonists, biocontrol agents have been gaining popularity worldwide (BONATERRA et al., 2003; KORSTEN, 2006; SARAVANAKUMAR et al., 2009; DE CAL et al., 2009; VELMOUROUGANE et al., 2011, SAGAHÓN et al., 2011).

According to Wilson and Wisniewski (1994) cited by Spadaro and Gullino (2004), the major characteristics of an ideal antagonist are: genetic stability, efficacy at low concentrations and against a wide range of pathogens on various fruit products, simple nutritional requirements, survival in adverse environmental conditions, growth on cheap substrates in fermenters, lack of pathogenicity for the host plant and no production of metabolites potentially toxic to humans, resistance to the most frequently used pesticides and compatibility with other chemical and physical treatments.

Based on these traits, yeasts seems to be an excellent candidate for biocontrol agents and therefore, researches have been focused on their isolation, selection and potential use for controlling phytopathogenic fungi (SIPICZKI, 2006; ABRAHAM; LAING; BOWER, 2010; LAHLALI, 2011; MANSO; NUNES, 2011). Moreover, yeasts inherent characteristics such as fast growth, fruit surface colonization and deprive nutrients from pathogens (through competition) have placed these organisms as one of the most suitable biocontrol agents (RICHARD; PRUSKY, 2002).

Information on the mechanism(s) of action by which antagonists suppress postharvest disease is still incomplete mainly due to the difficulties faced during the study of the complex interactions between host, pathogen, antagonist and other microorganisms present (SPADARO; GULLINO, 2004). However, several possible biocontrol mechanisms have been suggested including production of antibiotics, lytic enzymes, direct parasitism, induction of resistance in the host tissue, competition for nutrients and space. Yet competition for nutrients and space is most widely accepted mode action of the antagonists (SHARMA; SING; SING, 2009).

Where to look for antagonists?

Virtually any place is a potential reservoir for new biocontrol antagonists. However, the prefered niche for survey and screening of these organisms is usually healthy commodities in the storage, orchard, and untreated fields (BAKER; COOK, 1974). If these places have had a history of mycotoxigenic fungi contamination the success of selection may be enhanced due to a natural selection of organisms which could compete with the pathogen. For instance, yeasts were isolated from aflatoxin contaminated areas and positive antagonistic effect in decreasing the levels of norsolorinic acids (an aflatoxin precursor) was observed in vitro (HUA; BAKER; FLORES-ESPIRITU, 1999). In general, the grain commodities phylloplane is the preferred location for antagonists screening as it is considered a natural source of occurrence (JANISIEWICZ; KORSTEN, 2002). Many other examples can be found in the literature and probably the ultimate success for biocontrol programs depends on the methodology applyied in this search (FRAVEL, 2005). Selective isolation requirements should be taken into account to isolate different groups of antagonists and therefore, several methodologies have been proposed (BAKER; COOK 1974; SCHISLER; SLININGER 1997).

The antagonists may also come from other closely related or unrelated sources like the soil that has also been an abundant and diverse source of antagonists (MOTOMURA et al., 1996; JUNG-IL; HONG; KANG, 2000; JANISIEWICZ; KORSTEN, 2002; SAGAHÓN et al., 2011), from collections of microorganisms (LAITILA et al., 2007) or microorganisms that are involved in the production of fermented foods (PUSEY, 1991). These others sources may also yield effective antagonists (JANISIEWICZ; KORSTEN, 2002).

Furthermore, biocontrol agent mode of action, mainly antibiotics, have driven researches for surveying the bacterial diversity in a huge variety of environmental niches in which the extreme environment conditions (high pressure, salinity, temperature or aridity and low tempertatures) have recently increased in importance. Hypothetically, in these extreme conditions the organism may evolve to unique biosynthetic pathways which may lead to exclusives traits. This hypothesis have been corroborate in the vast literature regarding to description of new species from these areas (ZUCCHI et al., 2012a,b) or novel biocompounds produced by these organisms (GOODFELLOW et al., 2012).



Mould and mycotoxin contamination may occur at any stage in the food and feed production chain: before harvest, at harvesting, or in storage (KÖPPEN et al., 2010). Therefore, after promising antagonists are selected it is necessary to search for strategies of delivery which applies it effectively for controlling or suppressing the pathogen and consequently their mycotoxin production. Basically, microbial antagonists may be delivery through two main ways: at preharvest or post-harvest stage (CAST 2003; SHARMA; SINGH; SINGH, 2009).

Preharvest delivery

The preharvest delivery strategy aims to prevent the development of fungi already in the field and hence their mycotoxin production. A current successful example is the use of the competitive nontoxigenic strains of Aspergillus flavus. This strategy is based on the competition between the toxigenic and nontoxigenic strains to exclude naturally the toxigenic strains in the same niche and compete for crop substrates (YIN et al., 2008). Some field experiments in different crops have demonstrated significant reductions in the aflatoxin contamination, values which correspond to 70-90% (DORNER, 2004; DORNER, 2008; DORNER, 2009). Two products have been registered as biopesticides to control aflatoxin. One is called AF-36 based on the nontoxigenic strain A. flavus AF36 for control of aflatoxin in cottonseed. The second one is the Afla-Guard based on the nontoxigenic strain A. flavus NRRL21882 for aflatoxin control on corn (field, sweet, and popcorn) and peanuts (ISAKEIT, 2012).

Postharvest delivery

These second approach of delivery lies in two ways: 1) suppressing the pathogens, in this time after harvest and 2) through the mycotoxin decontamination by the application of microorganism antagonists.

Pathogens may be suppressed by microbial cultures which can be applied either as postharvest sprays or as dips in an antagonist's solution (IRTWANGE, 2006). The dip treatment containing a yeast suspension (Saccharomyces cerevisiae) was used in coffee postharvest, during its processing, and resulted in a significant reduction of total mould incidence (Aspergillus niger, Aspergillus ochraceus) and ochratoxin A contamination without affecting the cup quality (VELMOUROUGANE et al., 2011). Similarly, a significant reduction on the production and accumulation of aflatoxins by A. parasiticus in peanuts was observed after the grains were treated with a Streptomyces suspension (ZUCCHI et al., 2008).

Studies have demonstrated that mycotoxin decontamination can be reached using some yeasts, bacteria or fungal enzymes which degrade mycotoxins into non-toxic compounds and therefore, reduce the harmful effects of mycotoxins (EUROPEAN FOOD SAFETY AUTHORITY-EFSA, 2009). For instance, the yeast Trichosporon mycotoxinivorans can detoxify the zearalenone (VEKIRU et al., 2010) and ochratoxin. The latter is detoxified by the cleavage of the phenylalanine moiety to form the derivate ochratoxin, a virtually nontoxic metabolite compared to the parent compound (SCHATZMAYR et al., 2006). Due to the fact that T. mycotoxinivorans can be fermented, concentrated, freeze-dried, and stabilized without losing its deactivating capacity, its utilization in postharvest delivery as a feed additive for ochratoxin and/or zearalenone detoxification seems to be feasible alternative (CHAYTOR, et al., 2011).

Furthermore, an interesting trait for controlling mycotoxins in postharvest conditions, which may also be exploited, is the capacity of some compounds-producing actinomycetes that block the mycotoxin biosynthetic pathway. This recent new research line has demonstrated promising results to control aflatoxin contamination (SAKUDA et al., 1996). Streptomyces is the preferred chosen actinomycete and some compounds (aflastatin A and B; Blasticidin A and dioctatin A) have prevented the aflatoxin production without inhibition the fungus growth (SAKUDA et al, 1999; SAKUDA et al., 2000a, b; YOSHINARI et al., 2007). Since these compounds have not interfered in the fungal development, the treated fungus may confer an extra protection by niche competition against further infections.



Although the vast progress achieved on the biological control of postharvest diseases during the last decades, difficulties can be arised in order to obtain antagonistic strains which alone show a broad spectrum of activity against a variety of mycotoxigenic pathogens. Because of that, instead of using only one isolate the trend commonly used nowadays is applying the microbial agent in a consortium with another approach. This strategy can greatly enhance the biocontrol efficaciness and some of these approaches are discussed below.

Biological control and the good agricultural practices

The first and logical step to manage phytopathogen contamination is a good agricultural practice in the field and at the storage. Some of these practices rely on the careful selection of crop material to sow as well as the time to harvest (WILSON et al., 2006; BRANDINO et al., 2009). In general, late crops are most likely to develop mycotoxin contamination issues. Cereals, coffee beans, fruits and seeds should be dried immediately after the harvest. Moreover, attention must be taken on the temperature and moisture at storage conditions (CAST, 2003). For other commodities, i.e. maize grains, the selection of hybrids, plant density, time of planting, and insect control may have an influence on toxin contamination (MAGAN; ALDRED, 2007). Some factors affecting fungi and mycotoxin occurrence in the food chain are given bellow:

- Biological factors: susceptible crop and compatible toxigenic fungus;

- Environmental factors: temperature, moisture, mechanical injury and insect/bird damage;

- Harvesting: crop maturity, temperature, moisture and contaminant detection;

- Storage: temperature, moisture and contaminant detection;

- Distribuition: contaminant detection and diversion.

Antagonist mixtures

An effective biological control based on a mixture of several complementary and non-competitive antagonists usually present more chances to success than a control based on only one single microorganism (SPADARO; GULLINO, 2004). Sharma et al. (2009) pointed out several advantages for using mixtures of microbial antagonists, such as:

- Widening the spectrum of phytopathogens targets;

- Decreasing the efficacy loss due to adverse environmental conditions;

- Exploring more than one mechanism of control;

- Combination of different biocontrol traits without the transfer of exogenous genes through genetic transformation.

For instance, a broader spectrum of pathogens on apple was controlled when microbial antagonists were applied in mixtures instead of use individual microbial strains (CALVO et al., 2003; CONWAY et al., 2005). Similarly, a decrease in the aflatoxin concentration from 75 to 99.9% was observed in peanut fields using a misture of nontoxigenic mutants of A. flavus and A. parasiticus (DORNER et al., 1998). Both examples highlight the high degree of control which may be achieved using mixtures of biocontrol agents even in field conditions.

Biological agent additives

Many additives can enhance the biological control activity of antagonists and salts usually are the most related ones. Thus, the combination of 2% sodium bicarbonate with the yeast antagonist Candida oleophila enhanced significantly its biocontrol performance (curative and protective effect) against fungi rot diseases caused by Botrytis, Penicillium, Monilinia and Rhizopus in apple and peach (DROBY et al., 2003). Similarly, a sugar analogue (2-deoxy-dscp-glucose) has also demonstrated the capacity to increase efficacy. The bioagent Candida saitoana supplemented with 0.2% 2-deoxy-D-glucose was more effective in controlling decay of apple, orange, and lemon caused by Botrytis cinerea, Penicillium expansum, and P. digitatum than either C. saitoana or the application of a 0.2% solution of 2-deoxy-D-glucose alone (EL GHAOUTH et al., 2000).

Other additives such as ethanol, silicon, nisin and chitosan, have been reported to enhance the quality and control efficacy of different biocontrol agents (JANISIEWICZ; CONWAY, 2010).

Integration of biological control with other methods

Some examples of integration of the biological control with others postharvest methods have been proposed. Thus, modified storage conditions, physical and chemical treatments have been used in combination with biocontrol agents and their additive or synergic effect have increased the level of disease control (MARI; NERI; BERTOLINI, 2007; JANISIEWICZ; CONWAY, 2010). Integrating the antagonistic Cryptococcus laurentii with 104 ppm of thiabendazole improved the control of grey mould caused by Botrytis cinerea on apples (LIMA et al., 2006). Similarly, the application of the same antagonist in combination with 25 ppm imazalil or 50 ppm kresoxim-methyl resulted in less decay caused by Alternaria alternata and Monilinia fructicola (compared with separate applications) on jujube fruits stored in a controlled atmosphere (QIN; TIAN, 2004).

Besides, to enhance the bioefficacy of microbial antagonists the attractive approache which may be used in a large scale in the future is the improvement of genetic traits involved with the ability of the antagonist to inhibit the establishment and the development of the pathogen as well as the mycotoxin production. Some techniques to manipulate the antagonists have already been described using conventional mutagenesis (ionizing radiations, mutagenic chemicals, fungicide or antibiotic exposure) or sexual recombination, through protoplast fusion or genetic transformation (SPADARO; GULLINO, 2004).



In this paper, we reviewed the major trends on biological control which has been considerated an effective approach to reduce the postharvest losses caused by store fungi and mycotoxin contamination. Probably, the most positive trait of this strategy is the reduction of pesticides use which brings relevant prospects to environmental and human health (JANISIEWICZ; KORSTEN 2002). In addition, unlike chemical pesticides the biocontrol agents usually offer disease management alternatives using more than one mechanism of action (FRAVEL, 2005). This characteristic confers several advantages on the pest control mainly due to a lower probabity to select resistant phytopathogenic strains.

Generally, studies related on the use of microorganisms as biocontrol agents focus only on efficacy, ignoring the lack of toxic residue and the effect on the food quality (ZHANG et al., 2010). Yeast used as biological microrganisms in coffee crop have been reported to suppress mold incidence and mycotoxin contamination apart from improving the coffee cup quality and aroma (VELMOUROUGANE et al., 2011). Other secondary benefits, such as enhancement of fruit firmness and longer shelf-life, have also been correlated with biocontrol agents (VIOLANTE et al., 2009).

However, it is unrealistic to imagine that biological control alone will solve all problems of storage fungi and mycotoxin contamination. Nevertheless, the use of antagonist mixtures or combine them with other methods can easily overcome many difficulties found during the crop development. Therefore, it is increasingly clear the trend and necessity of inserting the biocontrol agents in a integrated pest management. Indeed, many efforts have been made to develop a whole biological control programs (ESHEL et al., 2009; JANISIEWICZ; CONWAY, 2010). Finally, the benefits of antagonists utilization outweigh their capacity to reduce the storage fungi inoculums or mycotoxin contamination. Since they are virtually non-toxic to non-target organisms, biocontrol agents have become largely accepted by 'eco-friendly' consumers. This new economical niche is fiercely influencing the farmers to include the biological control as an alternative for chemical pesticides. Because of that, it can be expected that the participation of biocontrol products on the agricultural chemical sales will increase in a near future.



The authors are in debt to FAPESP (Fundação de Amparo à Pesquisa do Estado de São Paulo) for providing fellowships and research funds to TDZ (grants 11/50243-1 and 11/14333-6) and to CNPq for providing assistantships to the first and fifth authors.



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(Received in july 30, 2012 and approved in august 28, 2012)

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