Significance of Mycotoxins to Food Safety and Human Health1,2

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.

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.


2016 ◽  
Vol 2 (1) ◽  
Author(s):  
V. Koteswara Rao ◽  
B. Aruna ◽  
Md. Rafiyuddin ◽  
K. Narasimha Rao ◽  
S. Girisham ◽  
...  

1972 ◽  
Vol 18 (5) ◽  
pp. 631-636 ◽  
Author(s):  
Alex Ciegler

Various strains of species belonging to the Aspergillus ochraceus group (A. ochraceus, A. sclerotiorum, A. alliaceus, A. ostianus, A. melleus, and A. sulphureus) can produce two mycotoxins, ochratoxin A and penicillic acid, on liquid media and in cereal grains. The quantity of each toxin produced is influenced by temperature; low temperature (10 and 20C) favor penicillic acid synthesis and higher (28C), ochratoxin A production. Generally penicillic acid is produced in yields about one to three magnitudes greater than ochratoxin A. A simple fluorodensitometric method for concomitant quantitative analysis of the two toxins has been developed based on conversion of penicillic acid and ochratoxin A to fluorescent derivatives by treatment with ammonia fumes.


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.


2001 ◽  
Vol 64 (5) ◽  
pp. 741-743 ◽  
Author(s):  
DANTE J. BUENO ◽  
JULIO O. SILVA ◽  
GUILLERMO OLIVER

This article reports on the identification of mycoflora of 21 dry pet foods (12 belonging to dogs and 9 to cats) that corresponded to 8 commercial brands made in Argentina and imported. The isolation frequency and relative density of the prevalent fungal genera are compared too. Ten genera and fungi classified as Mycelia sterilia were identified. The predominant genera were Aspergillus (62%), Rhizopus (48%), and Mucor (38%). The most prevalent among Aspergillus was Aspergillus flavus followed by Aspergillus niger and Aspergillus terreus. The predominant Mucor was Mucor racemosus followed by Mucor plumbeus and Mucor globosus. The moisture content of these foods ranged from 5.6 to 10.0% and from 7.2 to 9.9% for dog and cat foods, respectively. A greater moisture content in food for the senior category (9.5 ± 0.2) was observed only in comparison to adult and kitten/puppy. If the moisture content can be maintained at these levels, mold growth would be prevented or at least it would remain at an insignificant level. Some genera and species isolated and identified from the foods analyzed are potentially producing toxins, which are known as mycotoxins. This involves a risk for animal health.


2021 ◽  
Author(s):  
Deepshikha Shahdeo ◽  
Azmat Ali Khan ◽  
Amer M Alanazi ◽  
Yun Suk Huh ◽  
Shruti Shukla ◽  
...  

Abstract Ochratoxin A (OTA) is one of the predominant mycotoxins that contaminate a wide range of food commodities. In the present study, a 36-mer aptamer was used as a molecular recognition element coupled with gold nanoparticles (AuNPs) for colorimetric detection of OTA in a microfluidic paper-based analytical device (µPADs). The µPADs consisted of three zones: control, detection, and sample, interconnected by channels. The biophysical characterizations of aptamer conjugated AuNPs were done by UV-vis spectroscopy (UV-vis), dynamic Light Scattering (DLS), and transmission electron microscopy (TEM). The developed colorimetric assay for OTA showed a limit of detection of 242, 545, and 95.69 ng/mL in water, corn, and groundnut, respectively. The HPLC detection method achieved acceptable coefficient in standard curves (r2 = 0.9995), better detection range, and recovery rates in spiked corn and groundnut samples as 43.61 ± 2.18% to 87.10 ± 1.82% and 42.01 ± 1.31% to 86.03 ± 2.64% after multiple sample extractions and cleanup steps. However, the developed µPADs analytical device had the potent ability to rapidly detect OTA without any extraction pre-requirement, derivatization, and cleanup steps, thus illustrating its feasibility in the animal health sector, agricultural, and food industries.


Author(s):  
V.I. Dorozhkin ◽  

The article presents materials on the toxicological and biological safety of livestock products: contaminants of various natures that contaminate raw materials and food products (microorganisms, viruses, mycotoxins, parasites, heavy metals, etc.) are presented. To ensure biological and toxicological safety of livestock products and public health, the implementation of legislation, as well as decisions of the President of the Russian Federation, it is proposed to provide the development of a national innovative system for protecting animal health from the negative effects of pathogens and toxicants, including: conducting research on the development of fundamental foundations for the protection of animal health from the negative impact of ecotoxicants and veterinary and sanitary welfare, improvement of regulatory and legislative documents on the organization of quality control and safety of raw materials and food products; restoration of the procedure for state registration of diagnostic test systems, disinfectants, insectoacaricides and rodenticides; creation of the State Veterinary Pharmacological and Biological «State Veterinary Pharmaceutical Commission». For the implementation of these measures, provide federal state budgetary funding.


1977 ◽  
Vol 40 (3) ◽  
pp. 187-190 ◽  
Author(s):  
G. S. TORREY ◽  
E. H. MARTH

Penicillia (49% of 155 isolates) and aspergilli (38%) were the predominant molds isolated from food stored in private homes. Samples were taken from refrigerated and non-refrigerated food, and from refrigerator surfaces. Aflatoxin (9 isolates), kojic acid (3), ochratoxin A (3), penicillic acid (1), and patulin (1) were detected when culture extracts of isolates were screened for the presence of toxic mold metabolites.


Toxins ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 700 ◽  
Author(s):  
Randa Zeidan ◽  
Zahoor Ul-Hassan ◽  
Roda Al-Thani ◽  
Quirico Migheli ◽  
Samir Jaoua

Mycotoxins are secondary metabolites produced by certain filamentous fungi, causing human and animal health issues upon the ingestion of contaminated food and feed. Among the safest approaches to the control of mycotoxigenic fungi and mycotoxin detoxification is the application of microbial biocontrol agents. Burkholderia cepacia is known for producing metabolites active against a broad number of pathogenic fungi. In this study, the antifungal potential of a Qatari strain of Burkholderia cepacia (QBC03) was explored. QBC03 exhibited antifungal activity against a wide range of mycotoxigenic, as well as phytopathogenic, fungal genera and species. The QBC03 culture supernatant significantly inhibited the growth of Aspergillus carbonarius, Fusarium culmorum and Penicillium verrucosum in PDA medium, as well as A. carbonarius and P. verrucosum biomass in PDB medium. The QBC03 culture supernatant was found to dramatically reduce the synthesis of ochratoxin A (OTA) by A. carbonarius, in addition to inducing mycelia malformation. The antifungal activity of QBC03’s culture extract was retained following thermal treatment at 100 °C for 30 min. The findings of the present study advocate that QBC03 is a suitable biocontrol agent against toxigenic fungi, due to the inhibitory activity of its thermostable metabolites.


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