Formation and Control of Mycotoxins in Food

1984 ◽  
Vol 47 (8) ◽  
pp. 637-646 ◽  
Author(s):  
LLOYD B. BULLERMAN ◽  
LISA L. SCHROEDER ◽  
KUN-YOUNG PARK

Mycotoxin production is favored by high humidity and high water activity (aw). To control mycotoxin formation on the basis of moisture, the moisture content must be maintained below a certain critical level for each commodity. Aflatoxin production is favored by temperatures of 25 to 30°C, whereas below 8 to 10°C, aflatoxin production can occur, but the amounts produced are less and the time required for production is longer. Cycling or changing temperature may or may not increase aflatoxin production, depending on the temperatures, mold species and substrates involved. Other mycotoxic molds respond to temperature differently than the aspergilli. Species of Penicillium, Fusarium and Cladosporium are capable of growing at temperatures below 5°C, and some even just below freezing. Penicillium spp. can produce patulin, penicillic acid and ochratoxin at temperatures from 0 to 31°C, whereas Aspergillus ochraceus does not produce ochratoxin or penicillic acid below 12°C. Penitrem production by Penicillium crustosum can occur at refrigeration temperature. Fusarium spp. can produce zearalenone and the trichothecenes at temperatures below 10°C and even below freezing. Maintaining storage temperatures of stored commodities at 5°C or lower will prevent the production of aflatoxins and ochratoxin by aspergilli but will not prevent the production of mycotoxins by Penicillium spp. and Fusarium spp. Mycotoxic molds may grow on a vast array of substrates, but some substrates support little or no mycotoxin production while supporting extensive mold growth. Most substrates that support aflatoxin production are plant products, such as peanuts, Brazil nuts, pecans, walnuts, almonds, filberts, pistachio nuts, cottonseed, copra, corn sorghum, millet and figs. Animal products are less likely substrates for aflatoxin production. The main source of aflatoxins in animal products are residues in milk and animal tissues as a result of consumption of toxic feed by the animal. Some herbs and spices have antifungal properties and do not support mycotoxin production. However, aside from this, most food substrates are susceptible to mold growth and mycotoxin production. Some substrates, such as cheese, cured meats and soybeans, might be less favorable for mycotoxin production, but may still support mycotoxin formation. Drought stress, insect damage and mechanical damage may increase the ability of Aspergillus flavus and other fungi to invade peanuts, cottonseed and grain. Some measure of control can be gained by minimizing drought stress through irrigation and minimizing insect and mechanical damage. Development of peanut varieties and corn hybrids that are resistant to preharvest invasion by A. flavus may also offer some measure control. Competing microorganisms tend to restrict fungal growth and mycotoxin production. Low oxygen concentration (<1%) and/or increased concentrations of other gases (i.e., >90% CO2) may depress mold growth and mycotoxin formation. Antimycotic agents can be used to control mold growth and mycotoxin production. Sorbic acid, potassium sorbate, propionic acid and propionates appear to be more effective antimycotics over a greater range of conditions than benzoates. Other substances, such as sodium diacetate and BHA, also have antifungal activity. Certain herbs and spices, particularly cinnamon, cloves and mustard, may contain enough antifungal activity to exert a protective effect at normal usage levels.

1982 ◽  
Vol 45 (6) ◽  
pp. 519-526 ◽  
Author(s):  
MARTIN D. NORTHOLT ◽  
LLOYD B. BULLERMAN

Environmental conditions influence mold growth and mycotoxin production. Such things as water activity (aw), temperature, pH and atmosphere can strongly affect and profoundly alter patterns of growth and mycotoxin production. Generally, maintenance of low temperatures will prevent aflatoxin production in stored products, whereas other toxins such as penicillic acid, patulin, zearolenone and T-2 toxin may be produced at low temperatures. Toxic Penicillium and Fusarium species are generally more capable of growth at low temperatures than are toxic species of Aspergillus. Temperature interacts with aw to influence mold growth and mycotoxin production. Aflatoxin B1 can be produced at conditions of aw and temperature which are close to the minimum aw and temperature for growth. On the other hand, patulin, penicillic acid and ochratoxin A are produced within a narrower range of aw and temperature, compared with those for growth. In fact, production of patulin and penicillic acid by Penicillium species appears to be confined to high aw values only. In optimal substrates, the minima of aw and temperature for growth and toxin production may be lower than in other substrates. It appears that pH and substrate composition have no great effect on growth of toxic molds, but may have a great influence on toxin production. Presence of CO2 and O2 influences mold growth and mycotoxin production. A 20% level of CO2 in air depresses aflatoxin production and markedly depresses mold growth. Decreasing the O2 concentration of air to 10% depresses aflatoxin production, but only at O2 levels of less than 1% are growth and aflatoxin production completely inhibited. With patulin- and sterigmatocystin-producing molds, concentrations of 40% CO2 depress growth and toxin production, but a level of 90% CO2 is needed to completely inhibit production of these toxins. Decreasing O2 concentration to 2% depresses production of patulin and sterigmatocystin but does not affect fungal growth. Only at levels down to 0.2% are growth and toxin production completely inhibited. Controlled atmospheres with increased CO2 (above 10%) and decreased O2 (2%) can be used to retard mold growth. Exclusion of O2 by vacuum packaging in materials with low O2 permeability will depress or even prevent aflatoxin production. Presence of other microorganisms may also restrict fungal growth and mycotoxin production. Aflatoxin production by Aspergillus flavus in mixed cultures with Aspergillus niger is less than in pure culture. Mixtures of fungi growing in grains and nuts in competition with A. flavus seem to prevent aflatoxin production. Other organisms including Rhizopus nigricans, Saccharomyces cerevisiae, Brevibacterium linens and some lactic acid bacteria have been shown to reduce growth and aflatoxin production by Aspergillus parasiticus. In general, mold growth and mycotoxin production can be prevented by employing various measures based on knowledge of the factors involved. Choice of the measures depends upon the type of product, storage period and available techniques.


1979 ◽  
Vol 42 (1) ◽  
pp. 65-86 ◽  
Author(s):  
L. B. BULLERMAN

Mycotoxins are toxic substances produced by molds, which cause disease in animals or man. Acute diseases caused by mycotoxins are called mycotoxicoses. History has recorded several human disease outbreaks and numerous animal poisonings thought to be mycotoxicoses. The outbreak of Turkey X disease in England in 1960 culminated in the discovery of aflatoxins and the realization that low levels of mold metabolites in foods and feed could cause disease in man and animals. This gave great impetus to the study of mycotoxins. Mycotoxin-producing molds are quite ubiquitous and frequently contaminate food and agricultural commodities. Fortunately, the mere presence of a toxic mold in food does not automatically mean the presence of mycotoxins. Mycotoxins currently receiving the most attention as potential hazards to human and animal health include aflatoxins, ochratoxin A, sterigmatocystin, patulin, penicillic acid, citrinin, zearalenone and the toxic trichothecenes. These compounds all cause some degree of acute toxicity when given in high amounts. In addition, aflatoxins, sterigmatocystin, patulin and penicillic acid are potential carcinogens. The significance of mycotoxins as causes of human diseases is difficult to determine because there is no direct evidence of such involvement in terms of controlled experiments with man. Human cases of ergotism and alimentary toxic aleukia are known to be of fungal origin. Recent reports have linked aflatoxins to acute poisonings of humans in Africa, southeast Asia and India. Epidemiological studies have correlated aflatoxin contamination of foodstuffs with high incidences of liver cancer and other liver disease in certain regions of the world. It has been suggested that ochratoxin A may be involved in a fatal kidney disease of humans known as Balkan Endemic Nephropathy. Ochratoxin A has been found in foodstuffs from the endemic areas of this disease. Mycotoxins may enter the food supply by direct contamination, resulting from mold growth on the food, or by indirect contamination through the use of contaminated ingredients in processed foods. Indirect exposure to mycotoxins can also result from consumption of animal products, such as milk, which contain mycotoxin residues. caused by feeding moldy feed to the food-producing animal. Commodities susceptible to direct contamination with mycotoxins include nuts, oilseeds, grains and to a limited extent, certain fruits. Residues of aflatoxin have been found in animal products such as fluid milk, nonfat dry milk, cottage cheese and imported cheeses. In feeding experiments with aflatoxins, the toxins were found in livers, kidneys and certain tissues of pigs and broiler chickens, and in eggs from laying hens fed aflatoxin. Residues of ochratoxin A have been found in livers, kidneys, muscle and adipose tissues of bacon pigs and poultry. Refrigerated foods, such as cheeses, cured meats and certain flour-based products, subject to mold growth during storage, have been shown to be contaminated with a variety of potential mycotoxin-producing molds. Experimental evidence indicates that certain mycotoxins could be produced on refrigerated foods under certain conditions. Aflatoxin production is favored by temperatures of 20 to 25 C; but has been reported to occur as low as 7 to 12 C. Toxins produced by Penicillium species can be produced at temperatures as low as 5 C; however, patulin and penicillic acid do not appear to be produced to any extent on substrates such as cheeses and cured meats. Aflatoxins and ochratoxins appear to be relatively stable in most foods, whereas patulin and penicillic acid are not stable in proteinaceous foods such as cheeses and meats. Stability data on other mycotoxins are lacking for most foods. In general, mycotoxins are most stable in grains, nuts and oilseeds. The current tolerance level for aflatoxins in foods is 20 ppb, which will probably be lowered to 15 ppb in the near future. Recently, an action level of 0.5 ppb for aflatoxin in milk and milk products was announced which is essentially a tolerance level for these products.


1989 ◽  
Vol 52 (5) ◽  
pp. 329-336 ◽  
Author(s):  
C. I. LEBRON ◽  
R. A. MOLINS ◽  
H. W. WALKER ◽  
A. A. KRAFT ◽  
H. M. STAHR

Mold growth and mycotoxin production were studied in high-moisture (20%) corn treated with tetrasodium pyrophosphate (TSPP); acid and alkaline sodium polyphosphate, glassy (SPG), also known as sodium hexametaphosphate; sodium tripolyphosphate (STPP); and tricalcium phosphate. Six mold cultures belonging to the genera Aspergillus, Fusarium, and Penicillium were tested in corn varieties highly resistant or highly susceptible to mold infection in the field, and in a mixture of five other varieties of corn. The acidic SPG, as well as TSPP and STPP totally prevented or reduced mold growth when added in powder form to corn at 1.0% or 2.0% (w/w), regardless of corn variety and high moisture content. Phosphates afforded protection in whole and damaged kernels. Similar results were obtained with 2.0% acidic SPG and TSPP when added in spray form. Whenever mold growth occurred, treatment of corn with 1.0% or 2.0% (w/w) TSPP and acidic or alkaline SPG inhibited (P<0.01) aflatoxin production by aspergilli.


1982 ◽  
Vol 45 (10) ◽  
pp. 953-963 ◽  
Author(s):  
LISA L. RAY ◽  
LLOYD B. BULLERMAN

Mold inhibitors such as sorbates, propionates and benzoates have been used commercially for some time. Recently these and other potential inhibitors have been studied from the standpoint of their effects on growth of potentially toxic molds and mycotoxin production. In addition, other substances such as the antifungal antibiotic natamycin (pimaricin) and plant-derived products such as components of the essential oils of certain herbs and spices have recently been studied for their antifungal properties and effects on mycotoxin production. Some of these inhibitors inhibit mycotoxin production by greater than 70%, while only inhibiting growth of the mold by 25% or less. Of the organic acids, sorbic, propionic and benzoic, sorbic and its sorbate salts seems to be most effective over the widest range of conditions in preventing mold growth and mycotoxin production. Potassium sorbate is effective against toxic molds at levels of 0.10 to 0.15%. The antibiotic natamycin is very effective in preventing mold growth and toxin production at very low (0.001 to 0.005%) concentrations. A number of herbs and spices possess antifungal activity. At a level of 2.0%, in YES agar, cloves, cinnamon, mustard, allspice, garlic and oregano all completely inhibit mycotoxin production by a number of mycotoxigenic molds. Cloves, cinnamon and mustard seem to be the most effective of those tested, with complete inhibition occurring with amounts of spice less than 1%. Essential oils of orange and lemon also have antifungal properties at levels of 0.2 % and higher. Certain insecticides and fumigants also inhibit mold growth and mycotoxin production. The organophosphates naled and dichlorvos are both effective inhibitors at relatively low concentrations (0.002 to 0.01%). Phenolic antioxidants, particularly BHA, also inhibit toxic molds in concentrations of 0.025% and above. Naturally occurring methylxanthines, such as caffeine and theophylline, inhibit growth and aflatoxin production by A. parasiticus in concentrations of 0.1% and above. Chlorine, a commonly used sanitizer, will inactivate spores of toxic Aspergillus and Penicillium species at levels of residual chlorine commonly achieved with most sanitation procedures. Even though considerable information is available on inhibitory effects of a number of substances on mold growth and mycotoxin production, more work is needed to further define the conditions under which commercial antifungal agents are most effective in preventing growth of toxic molds and mycotoxin production.


2017 ◽  
Vol 14 (1) ◽  
pp. 45
Author(s):  
Angela P. Cajiao
Keyword(s):  

El comercio del café es uno de los renglones económicos más importantes a nivel mundial, sin embargo, también es susceptible a contaminaciones desde su cosecha hasta su transformación. Para la realización de este estudio se recolectaron muestras de café cereza procedentes de diferentes municipios productores de Norte de Santander y posteriormente en el laboratorio se aislaron y caracterizaron fenotípicamente los siguientes agentes fúngicos del grano de café: Aspergillus  spp., Penicillium spp., Fusarium spp., Cladosporium  spp., Mucor spp. y  Rhizopus spp. con ayuda de claves taxonómicas. Los hongos que presentaron una alta incidencia fueron Aspergillus spp. y Fusarium spp. Entre las tres variables fisicoquímicas analizadas en el café cereza (pH, actividad de agua, % de humedad) se puede afirmar con certeza que la actividad de agua y el porcentaje de humedad influyen directamente en el número y tipo de aislamientos fúngicos obtenidos. 


Toxins ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 134
Author(s):  
Ana Isabel Galván ◽  
Alicia Rodríguez ◽  
Alberto Martín ◽  
Manuel Joaquín Serradilla ◽  
Ana Martínez-Dorado ◽  
...  

Dried fig is susceptible to infection by Aspergillus flavus, the major producer of the carcinogenic mycotoxins. This fruit may be contaminated by the fungus throughout the entire chain production, especially during natural sun-drying, post-harvest, industrial processing, storage, and fruit retailing. Correct management of such critical stages is necessary to prevent mould growth and mycotoxin accumulation, with temperature being one of the main factors associated with these problems. The effect of different temperatures (5, 16, 25, 30, and 37 °C) related to dried-fig processing on growth, one of the regulatory genes of aflatoxin pathway (aflR) and mycotoxin production by A. flavus, was assessed. Firstly, growth and aflatoxin production of 11 A. flavus strains were checked before selecting two strains (M30 and M144) for in-depth studies. Findings showed that there were enormous differences in aflatoxin amounts and related-gene expression between the two selected strains. Based on the results, mild temperatures, and changes in temperature during drying and storage of dried figs should be avoided. Drying should be conducted at temperatures >30 °C and close to 37 °C, while industry processing, storage, and retailing of dried figs are advisable to perform at refrigeration temperatures (<10 °C) to avoid mycotoxin production.


2011 ◽  
pp. 165-176 ◽  
Author(s):  
Suncica Kocic-Tanackov ◽  
Gordana Dimic ◽  
Ilija Tanackov ◽  
Danijela Tuco

The paper presents the influence of oregano extract (Origanum vulgare L.) on growth of Aspergillus versicolor, Emericella nidulans, Eurotium herbariorum, E. amstelodami, E. chevalieri and E. rubrum - producers of sterigmatocystin (STC) isolated from salads. Antifungal tests were performed by agar plates method. The composition of the active component of extract was determined by GC-MS method and the major components were: carvacrol (34.20%), triacetin (22.91%), carvone (18.05%), p-cymene (8.05%) and thymol (3.74%). The examined extract showed the ability to reduce mold growth at all applied concentrations. Minimum inhibitory concentrations (MIC) for E. nidulans, E. chevalieri and E. amstelodami were 2.5% (v/v) and over 2.5% (v/v) for A. versicolor. At 1.5% (v/v) concentration the extract completely inhibited the growth of E. rubrum, whereas higher dose of 2.5% (v/v) was fungicidal against E. herbariorum. Besides its sensory role in food products, the examined oregano extract also exhibits antifungal activities against producers of STC.


2008 ◽  
Vol 32 (5) ◽  
pp. 1380-1386 ◽  
Author(s):  
Edlayne Gonçalez ◽  
Tiago Noel de Souza ◽  
Maria Helena Rossi ◽  
Joana D'arc Felicio ◽  
Benedito Corrêa

As cascas de amendoim (Arachis hypogaea L.) são de grande importância para confecção de cama de frangos, de gado de leite e como fonte de fibras para ruminantes, portanto a elucidação dos mecanismos de contaminação por fungos toxigênicos e por micotoxinas em amendoim é imprescindível, especialmente para que medidas preventivas possam ser tomadas. Realizou-se, este trabalho, em Junqueirópolis, Estado de São Paulo, Brasil. Os principais fungos isolados nas cascas de amendoim foram Fusarium ssp. (78,75 %), Rhizopus ssp. (14,1 %) e A. flavus (11,75 %). No solo foram isolados Penicillium spp., Fusarium spp. e Aspergillus flavus, entre outros. Aflatoxinas foram detectadas em amostras de cascas de amendoim a partir do estágio de granação em concentrações que variaram de 5,42 μg/kg a 218,52 μg/kg. Ácido ciclopiazônico e fumonisinas B1 e B2 não foram detectadas. A presença de A. flavus e aflatoxinas nas amostras, revela a importância de um controle das cascas de amendoim antes de sua utilização. Boas práticas agrícolas são indicadas para região, uma vez que a contaminação das vagens ocorreu antes da colheita.


2007 ◽  
Vol 70 (5) ◽  
pp. 1206-1212 ◽  
Author(s):  
CLELIA ALTIERI ◽  
DANIELA CARDILLO ◽  
ANTONIO BEVILACQUA ◽  
MILENA SINIGAGLIA

The antifungal activity of three fatty acids (lauric, myristic, and palmitic acids) and their monoglycerides (monolaurin, monomyristic acid, and palmitin, respectively) against Aspergillus and Penicillium species in a model system was investigated. Data were modeled through a reparameterized Gompertz equation. The maximum colony diameter attained within the experimental time (30 days), the maximal radial growth rate, the lag time (i.e., the number of days before the beginning of radial fungal growth), and the minimum detection time (MDT; the number of days needed to attain 1 cm colony diameter) were evaluated. Fatty acids and their monoglycerides inhibited mold growth by increasing MDT and lag times. The effectiveness of the active compounds seemed to be strain and genus dependent. Palmitic acid was the most effective chemical against aspergilli, whereas penicilli were strongly inhibited by myristic acid. Aspergilli also were more susceptible to fatty acids than were penicilli, as indicated by the longer MDT.


Sign in / Sign up

Export Citation Format

Share Document