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Multi-Mycotoxins in Corn Products, Crackers, Other Grain Products, Pasta and Gluten-Free Products – April 1, 2018 to March 31, 2019

Food chemistry – Targeted surveys – Final report


Targeted surveys provide information on potential food hazards and enhance the Canadian Food Inspection Agency's (CFIA's) routine monitoring programs. These surveys provide evidence regarding the safety of the food supply, identify potential emerging hazards, and contribute new information and data to food categories where it may be limited or non-existent. They are often used by the Agency to focus surveillance on potential areas of higher risk. Surveys can also help to identify trends and provide information about how industry complies with Canadian regulations.

The main objectives of this targeted survey were to expand baseline data on the presence and levels of mycotoxins in corn products, crackers, other grain (non-staple) products, pasta and gluten-free products; and to compare these results to other data, where feasible. Mycotoxins are natural toxins released by moulds that infect agricultural crops before and after harvest. Their human health effects are varied; the health effects depend on the type and level of mycotoxin in the food. Canada does not have maximum levels for the mycotoxins in the products targeted in this survey, with the exception of ochratoxin A (OTA), for which Canada has proposed maximum levels in certain foods.

A total of 750 samples corn and pasta products, crackers, gluten-free and other grain products were analyzed for the presence of mycotoxins. Mycotoxins were detected in 388 samples (52%). A total of 17 different mycotoxins were detected in the product types sampled by this survey. Aflatoxin G2, 3-acetyldeoxynivalenol (3-Ac-DON), 15-acetyldeoxynivalenol (15-Ac-DON), neosolaniol (NEO), diacetoxyscirpenol (DAS), fusarenone-X (FUS-X), alpha-zeranol, and beta-zeranol were not detected in any of the samples. The mycotoxin detected most frequently was deoxynivalenol (DON) in a total of 306 samples (41%).

All mycotoxin results were assessed by Health Canada's Bureau of Chemical Safety (BCS). Health Canada's BCS concluded that the levels detected in this survey were not expected to pose a human health concern. No product recalls were warranted given the lack of a human health concern.

What are targeted surveys

Targeted surveys are used by the CFIA to focus its surveillance activities on areas of highest health risk. The information gained from these surveys provides support for the allocation and prioritization of the Agency's activities to areas of greater concern. Originally started as a project under the Food Safety Action Plan (FSAP), targeted surveys have been embedded in our regular surveillance activities since 2013. Targeted surveys are a valuable tool for generating information on certain hazards in foods, identifying and characterizing new and emerging hazards, informing trend analysis, prompting and refining health risk assessments, highlighting potential contamination issues, as well as assessing and promoting compliance with Canadian regulations.

Food safety is a shared responsibility. We work with federal, provincial, territorial and municipal governments and provide regulatory oversight of the food industry to promote safe handling of foods throughout the food production chain. The food industry and retail sectors in Canada are responsible for the food they produce and sell, while individual consumers are responsible for the safe handling of the food they have in their possession.

Why did we conduct this survey

Mycotoxins are natural toxins released by moulds that can grow on crops in the field or after harvestFootnote 1. These toxins are released by moulds which can grow on agricultural products, such as on cereals (for example, wheat, oats, and corn), legumes, nuts and fruit. The type of agricultural product, insect damage, and the climatic conditions (temperature, humidity) during growth, processing, and storage are some factors that can influence the types and levels of mycotoxins present in the foods available at the retail levelFootnote 2. The human health effects are varied; ranging from gastrointestinal distress to cancer, the health effects depend on the type and level of mycotoxin in the food.

Research has shown that of the hundreds of mycotoxins associated with food, a small fraction has the potential to adversely affect human health and pose a global health concernFootnote 2. The Codex Alimentarius Commission is an international body established by the United Nations' Food and Agriculture Organization and the World Health Organization to develop harmonized international food standards, guidelines, and codes of practice to protect the health of the consumers and to ensure fair practices in the food trade. Codex has published a Code of Practice to reduce and prevent mycotoxin contamination in cereals (for example, wheat, corn, oats, and barley)Footnote 2. This Code of Practice acknowledges that the complete elimination of mycotoxins from foods is not possible but it provides guidance on ways to control and manage the mycotoxin levels at the farm level and after harvest (for example, during processing, storage, and transport).

There are now more than 300 known mycotoxins of widely different chemical structures and differing modes of action - some target the kidney, liver, or immune system and some are carcinogenic. Common mycotoxins include aflatoxins, ochratoxin A, ergot alkaloids, fumonisins, trichothecenes (such as deoxynivalenol which is also known as vomitoxin) and zearalenoneFootnote 1.

Please see Appendix A for a description of the different mycotoxins included in this study and their health effects.

What did we sample

A variety of domestic and imported corn products, crackers, other grain (non-staple) products, pasta and gluten-free products were sampled between April 1, 2018 and March 31, 2019. Samples of products were collected from local/regional retail locations located in 6 major cities across Canada. These cities encompassed 4 Canadian geographical areas:

  • Atlantic (Halifax);
  • Quebec (Montreal);
  • Ontario (Toronto, Ottawa); and,
  • the West (Vancouver, and Calgary).

The number of samples collected from these cities was in proportion to the relative population of the respective areas. The shelf life, storage conditions, and the cost of the food on the open market were not considered in this survey.

Table 1. Distribution of samples based on product type and origin
Product type Number of domestic samples Number of imported Table Note a samples Number of samples of unspecified Table Note b origin Total number of samples
Corn products 12 80 44 136
Crackers 7 41 54 102
Gluten-free products 17 35 18 70
Other grains 73 76 148 297
Pasta 46 73 26 145
Grand total 155 305 290 750

Table Notes

Table Note a

Imported from at least  27 countries.

Return to table note a  referrer

Table Note b

Unspecified refers to those samples for which the country of origin could not be assigned from the product label or available sample information.

Return to table note b  referrer

How were samples analyzed and assessed

Samples were analyzed by an ISO/IEC 17025 accredited food testing laboratory under contract with the Government of Canada. See Appendix A for a list of the pesticides analyzed. The results are based on the food products as sold and not necessarily as they would be consumed.

Health Canada has not established tolerances or standards for the majority of the mycotoxins in the grain products targeted in this survey. In 2009, Health Canada proposed maximum levels (ML) for OTA in a variety of foods. An ML of 3 ppb has been proposed for grains for direct consumption and derived cereal products (for example flour, bread, breakfast cereal), an ML of 7 ppb has been proposed for wheat bran and an ML of 0.5 ppb has been proposed for infant formulas and cereal-based foodsFootnote 3. These MLs as well as an industry guidance value for OTA in unprocessed cereal grains are still under consideration.

In the absence of applicable tolerances or standards, high levels of mycotoxins may be assessed by Health Canada's Bureau of Chemical Safety (BCS) on a case-by-case basis using the most current scientific data available.

What were the survey results


A total of 750 samples were analyzed for the presence of mycotoxins. The products sampled were separated into 5 product types: corn products, crackers, other grain products, pasta, and gluten-free products. Mycotoxins were detected in 388 samples (52%). A total of 17 different mycotoxins were detected in the product types sampled by this survey. Aflatoxin G2, 3-Ac-DON, 15-Ac-DON, NEO, DAS, FUS-X, alpha-zeranol, and beta-zeranol were not detected in any of the samples. Table 2 illustrates the number of samples with detectable levels of mycotoxins for all of the product types. Pasta and gluten-free products have the highest and lowest percentage of detectable mycotoxins, respectively.

Table 2. Results of multi-mycotoxin testing in grain-based products
Product type Number of samples Number (percentage) of samples with detected mycotoxin(s) Number (percentage) of samples with no detected mycotoxin(s) Number of mycotoxins per sample
Corn products 136 92 (68%) 44 (32%) 1-9
Crackers 102 70 (69%) 32 (31%) 1-2
Gluten-free products 70 17 (24%) 53 (76%) 1-4
Other grains 297 103 (35%) 194 (65%) 1-4
Pasta 145 104 (72%) 41 (28%) 1-5
Grand total 750 386 (51%) 364 (49%) 1-9

As can be seen from Table 2, up to 9 mycotoxins were detected per sample. These may consist of mycotoxin families (3 forms of aflatoxin or 3 forms of fumonisin) or discrete mycotoxins (for example, sterigmatocystin). The mycotoxin detected most frequently was deoxynivalenol in a total of 306 samples (41%). The least commonly detected mycotoxin was aflatoxin B2; detected in only 1 sample. The levels of mycotoxins ranged from 0.4 ppb to 2570 ppb.

What do the survey results mean

In comparison to previous survey yearsFootnote 4, Footnote 5, Footnote 6, Footnote 7 the detection rates for mycotoxins in various types of grain-based foods were consistent, with the exception of cyclopiazonic acid and zearalenone and its derivatives (Table 3). This may be related to differences in product types, conditions during a specific cultivation year, and source of the grains. Health Canada has not set or proposed limits for any of the mycotoxins for these surveys, with the exception of OTA. The compliance rate for grain based products for OTA (99.1%) was comparable to previous survey years (97.3% to 99.6%). As observed in previous surveys, DON was the most commonly observed mycotoxin. HC determined the levels of mycotoxins in the grain-based foods observed in the current survey are not expected to pose a concern to human health, therefore there were no recalls resulting from this survey.

Table 3. Mycotoxin testing results in grain-based products from various survey years
Survey author Year Analyte Number of samples Number of samples with detectable mycotoxins (percentage) Maximum mycotoxin level (ppb) Average* mycotoxin level (ppb)
CFIA 2018 Aflatoxins B1, B2, and G1 750 11 (1.5) 30 4.4
CFIA 2017 Aflatoxins B1, B2, and G1 748 4 (0.5) 4.6 4.3
CFIA 2016 Aflatoxins B1, B2, and G1 751 4 (0.5) 7.6 5.0
CFIA 2015 Aflatoxins B1, B2, and G1 745 6 (0.8) 1.4 0.9
CFIA 2013 to 2015 Aflatoxins B1, B2, and G1 2235 57 (2.5) 17 3.6
CFIA 2015 to 2019 3- and 15-acetyldeoxynivalenol 2994 0 (0) - -
CFIA 2013 to 2015 3- and 15-acetyldeoxynivalenol 2235 8 (0.004) 53 35.25
CFIA 2018 Deoxynivalenol 750 306 (41) 2570 282
CFIA 2017 Deoxynivalenol 748 440 (59) 1000 160
CFIA 2016 Deoxynivalenol 751 245 (33) 1360 176
CFIA 2015 Deoxynivalenol 745 203 (27) 3900 232
CFIA 2013 to 2015 Deoxynivalenol 2235 1044 (46) 2330 176
CFIA 2018 Diacetoxyscirpenol 750 0 (0) - -
CFIA 2017 Diacetoxyscirpenol 748 0 (0) - -
CFIA 2016 Diacetoxyscirpenol 751 1 (0.1) 10 10
CFIA 2015 Diacetoxyscirpenol 745 4 (0.5) 250 115
CFIA 2013 to 2015 Diacetoxyscirpenol 2235 0 (0.0) - -
Fusarenone-X 750 0 (0) - -
CFIA 2017 Fusarenone-X 748 0 (0) - -
CFIA 2016 Fusarenone-X 751 1 (0.1) 23 23
CFIA 2015 Fusarenone-X 745 0 (0) - -
CFIA 2013 to 2015 Fusarenone-X 2235 0 (0.0) - -
    Neosolaniol 750 0 (0.0) - -
CFIA 2017 Neosolaniol 748 1 (0.1) 20 20
CFIA 2016 Neosolaniol 751 0 (0) - -
CFIA 2015 Neosolaniol 745 0 (0) - -
CFIA 2013 to 2015 Neosolaniol 2235 1 (0.0004) 30 30
CFIA 2018 Nivalenol 750 7 (0.9) 86 22
CFIA 2017 Nivalenol 748 6 (0.8) 47 28
CFIA 2016 Nivalenol 751 0 (0) - -
CFIA 2015 Nivalenol 745 1 (0.1) 17 17
CFIA 2013 to 2015 Nivalenol 2235 4 (0.002) 98 42
CFIA 2018 Ergot Alkaloids 750 46 (6.1) 664 79
CFIA 2017 Ergot Alkaloids 748 231 (31) 1060 60
CFIA 2016 Ergot Alkaloids 751 63 (8.4) 1530 138
CFIA 2015 Ergot Alkaloids 745 85 (11) 1145 110
CFIA 2013 to 2015 Ergot Alkaloids 2235 478 (21.4) 1078 62
CFIA 2018 Fumonisins B1, B2 and B3 750 105 (14) 3503 280
CFIA 2017 Fumonisins B1, B2 and B3 748 21 (2.8) 864 90
CFIA 2016 Fumonisins B1, B2 and B3 751 48 (6.4) 2209 430
CFIA 2015 Fumonisins B1, B2 and B3 745 30 (4.0) 1142 214
CFIA 2013 to 2015 Fumonisins B1, B2 and B3 2235 233 (10) 2062 187
CFIA 2011 Fumonisins B1and B2 274 161 (59) 4442 253
CFIA 2018 HT-2 and T-2 toxin 750 8 (1.1) 98 37
CFIA 2017 HT-2 and T-2 toxin 748 8 (1.1) 98 15
CFIA 2016 HT-2 and T-2 toxin 751 19 (2.5) 85 21
CFIA 2015 HT-2 and T-2 toxin 745 11 (1.5) 32 17
CFIA 2013 to 2015 HT-2 and T-2 toxin 2235 66 (2.9) 271 28
CFIA 2018 Cyclopiazonic acid 750 18 (2.4) 47 11
CFIA 2017 Cyclopiazonic acid 748 4 (0.5) 6.5 2.5
CFIA 2016 Cyclopiazonic acid 751 1 (0.1) 2.5 2.5
CFIA 2015 Cyclopiazonic acid 745 5 (0.7) 3.1 1.9
CFIA 2013 to 2015 Cyclopiazonic acid 2235 35 (1.5) 8.3 2.7
CFIA 2018 Ochratoxin A 750 20 (2.7) 34 4.2
CFIA 2017 Ochratoxin A 748 35 (4.7) 267 10
CFIA 2016 Ochratoxin A 751 20 (2.7) 20 2.7
CFIA 2015 Ochratoxin A 745 36 (4.8) 36 4.8
CFIA 2013 to 2015 Ochratoxin A 2235 128 (5.7) 34 2.6
CFIA 2018 Sterigmatocystin 750 12 (1.6) 12 2.7
CFIA 2017 Sterigmatocystin 748 26 (3.5) 12 2.8
CFIA 2016 Sterigmatocystin 751 40 (5.3) 34 3.0
CFIA 2015 Sterigmatocystin 745 32 (4.3) 28 5.7
CFIA 2013 to 2015 Sterigmatocystin 2235 41 (1.8) 18 3.1
CFIA 2018 Zearalenone, α-zearalenol and β-zearalenol 750 34 (4.5) 450 44
CFIA 2017 Zearalenone, α-zearalenol and β-zearalenol 748 12 (1.6) 199 46
CFIA 2016 Zearalenone, α-zearalenol and β-zearalenol 751 23 (3.1) 145 39
CFIA 2015 Zearalenone, α-zearalenol and β-zearalenol 745 23 (3.1) 477 88
CFIA 2013 to 2015 Zearalenone, α-zearalenol and β-zearalenol 2235 93 (4.0) 577 50

*Average of positive results only.

Appendix A

1 Aflatoxins

Aflatoxins are a family of naturally-occurring, toxic secondary metabolites produced by Aspergillus flavus and A. parasiticus fungiFootnote 8. Aflatoxin-producing fungi may contaminate agricultural products (such as corn, nuts, spices, dried fruit) if grown, transported, stored, or processed under hot, humid conditions for prolonged periods of time, or with pest pressures resulting in bruising or cuts on the commodityFootnote 8, Footnote 9. Drought pressure on corn is also a major risk factor for the occurrence of aflatoxins in the fieldFootnote 8,Footnote 9,Footnote 10. Due to the cooler Canadian climate, domestically-grown agricultural commodities (and products) are less likely to contain aflatoxins than those imported from warmer climates. Aflatoxins are not destroyed by heating, cooking or most other processing methodsFootnote 11.

One aflatoxin form, aflatoxin B1, is among the most potent naturally-occurring liver carcinogens knownFootnote 12. The International Agency for Research on Cancer (IARC) classified aflatoxins to be carcinogenic to humans (Group 1 carcinogen)Footnote 13. Chronic exposure to aflatoxins has also been associated with growth impairment in children living in developing countries where exposure to aflatoxins is relatively high. Aflatoxins have been shown to cause immune suppression in experimental animalsFootnote 14, Footnote 15, Footnote 16, Footnote 17.Short-term exposure to high levels of aflatoxins can cause illness in humans which is characterized by vomiting, abdominal pain, convulsions, coma and death. The illness is very rare in the developed worldFootnote 18. This study included aflatoxins B1, B2, G1 and G2.

2 Cyclopiazonic Acid

Cyclopiazonic acid (CPA) is produced by Penicillium cyclopium, Penicillium species (for example, P. commune and P. camembertii), Aspergillus flavus and A. versicolor. Cyclopiazonic acid has been detected in corn, millet, peanuts, pulses, cheese, ham, sausage, hot dogs, tomato and milkFootnote 19

There is little information available regarding potential human health effects associated with CPA. However, it has been linked to 'Kodua' poisoning in India resulting from ingestion of contaminated millet seeds. The symptoms included sleepiness, tremors and giddiness which lasted 1-3 days, followed by complete recoveryFootnote 20. Experimental animal studies indicate that CPA is toxic only when ingested in high concentrations. Repeat exposure to high doses of CPA show a range of effects such as neurotoxicity, liver and kidney damage, weight loss, diarrhea, dehydration, convulsions and death in several different speciesFootnote 21.

3 Ergot Alkaloids

Ergot alkaloids are formed by fungi of the Claviceps species, particularly C. purpurea. These fungi parasitize the seed heads of cereals, replacing individual grain kernels with discoloured fungal structures (dark purple or black) known as sclerotia or ergot bodies. The predominant ergot alkaloids present in ergot bodies are ergometrine, ergotamine, ergosine, ergocristine, ergocryptine and ergocornine (only ergosine, ergocristine and ergocryptine were successfully included in the current multi-mycotoxin method). The type and levels of these alkaloids in ergot bodies vary considerably depending on the fungal strain, the host species, the weather conditions and geographic region. Wet weather and soil favour the growth of ergot bodies. These bodies are harvested with the cereals and can thus lead to contamination of cereal based food and feed products with ergot alkaloids. The cleaning methods used during grain processing usually remove the ergot bodies from the grainFootnote 22.

Long-term exposure to ergot alkaloids causes ergotism, also known as ergotoxicosis, ergot poisoning and Saint Anthony's FireFootnote 23,Footnote 24. The symptoms can include fevers, hallucinations, swollen or rigid limbs, severe inflammation sometimes followed by loss of affected tissues and deathFootnote 25. Experimental animal studies indicate the ergot alkaloids act on a number of neurotransmitter receptors which with repeat dosing results in restricted blood flow, particularly of the limbs, weight loss and changes in the levels of some hormones in ratsFootnote 26. This study included ergosine, ergocristine and ergocryptine.

4 Fumonisins

Fusarium moniliforme and Fusarium proliferatum are plant pathogens common in grain-growing regions throughout the world. These pathogens can infect grain crops either in the field (pre-harvest) or during storage (post-harvest). The moulds proliferate if grains are grown in hot, dry weather followed by very humid conditions. Mould growth is also favoured by storage under wet conditions. The plant pathogens produce mycotoxins known as fumonisins. Corn is the grain most vulnerable to fumonisin contaminationFootnote 27. The levels of fumonisins can be quite high, even in the absence of visible signs of mould proliferationFootnote 28. There are several forms of fumonisin: fumonisins B1, B2 and B3 are the most prevalent. While studies have focused on fumonisin B1, available data suggests that fumonisins B2 and B3 have a similar toxicological profileFootnote 29,Footnote 30,Footnote 31,Footnote 32. Fumonisins are heat-stable up to 150°C and are unaffected by mechanical forces (such as grinding), but can be reduced by alkaline treatment (a traditional means of preparing corn masa and other corn-based products such as tacos)Footnote 33.

Although fumonisin contamination is mainly observed in corn, some scientific studies have shown the presence of fumonisins in red wineFootnote 34, sorghumFootnote 35, white beans, wheatFootnote 29, barleyFootnote 29, soybeansFootnote 29, figsFootnote 29, riceFootnote 36, black teaFootnote 29, and medicinal herbsFootnote 29.

The ingestion of foods containing fumonisins may be harmful to human health. Health effects which have been observed in specific populations where corn is a major component of the diet and where the climate may favor fumonisin proliferation include esophageal cancer in South Africa and ChinaFootnote 28, Footnote 37, neural tube defects in Central America and the southwestern USFootnote 32. The precise biological effects of fumonisins are complex and relate to their interference with cell metabolismFootnote 27. Experimental animal studies have revealed that fumonisins induce liver and kidney damage in many speciesFootnote 38. Fumonisin B1 has been classified by IARC as possibly carcinogenic to humans based on evidence in experimental animal studiesFootnote 39. This study included fumonisins B1, B2 and B3.

5 Ochratoxin A (OTA)

OTA is a naturally occurring metabolite of Aspergillus and Penicillium moulds. Under favourable moisture and temperature conditions, the fungi can grow on stored material and produce OTAFootnote 40. OTA has been widely detected in cereal grains (wheat, corn, oat, and barley), green coffee, grape juice, beer, wines, cocoa, dried fruits, and nutsFootnote 41. OTA is heat-stable and is only partially destroyed under normal cooking or processing conditionsFootnote 42.

The International Agency for Research on Cancer (IARC) has classified OTA as a possible human carcinogen based largely on data from animal studiesFootnote 43. The mechanism by which OTA causes kidney tumours in rodents has yet to be fully explained. In animal studies, OTA has also been shown to have effects on the kidneys, the developing fetus, and the immune system. Health Canada completed a risk assessment for OTA, and as a result, has proposed maximum levels for OTA in various food commoditiesFootnote 3 as well as an industry guidance value for OTA in unprocessed cereal grainsFootnote 3.

6 Sterigmatocystin

Sterigmatocystin is a mycotoxin produced mainly by various Aspergillus species. It can also be produced by species such as Bipolaris, Chaetomium, and Emiricella. It has been detected in grains, corn, bread, cheese, spices, coffee beans, soybeans, and pistachio nuts. Wet, warm, conditions favour sterigmatocystin productionFootnote 44.

The IARC has classified sterigmatocystin as a possible human carcinogenFootnote 45. It also has properties capable of causing DNA mutations. It is acutely toxic to animals, with the liver and kidneys as its principle targets. This toxin is structurally similar to aflatoxin, however, tests in rats have shown that it is ten times less lethal following acute exposure to high doses and ten to a hundred times less effective at inducing liver cancerFootnote 41. Its human health effects have not been well-studied.

7 Trichothecenes

This large family of mycotoxins are typically found in cereal grains (notably wheat, barley, and corn), and have been detected in their derived products (flours, meals, bran, grits, cereals, and beer). These toxins are produced by various species of Fusarium mould in some crops prior to harvest. These toxins are observed in grains suffering from Fusarium head blight (FHB) in the field. Wet, warm weather conditions in the field will favour the development of FHB, and subsequently the production of trichothecenesFootnote 46. The trichothecenes are heat-stable and are only partially destroyed under normal cooking or processing conditionsFootnote 47. The most widely commonly occurring trichothenece is DON.

The human health effects of nivalenolFootnote 48, fusarenoneFootnote 49, 3-Ac-DONFootnote 46, 15-Ac-DONFootnote 46, neosolaniol NEOFootnote 46 and DASFootnote 46 are not as well-studied as those of DON. DON is not known to be carcinogenic, but it has been associated with acute and chronic health effects. Outbreaks in Asia, attributed to the consumption of grains with high levels of DON, are associated with short-term human illness, involving nausea, vomiting, abdominal pain, headache and dizziness. In experimental animal studies, long-term exposures to low levels of DON are associated with decreased food intake, weight loss, and effects on the immune systemFootnote 50.

T-2 and HT-2 toxins are formed when grain crops remain in the field at or after harvest for extended periods, especially in cold weather, or in grain that becomes wet during storage. They have been detected in wheat, corn, oats, barley, rice, beans, and soybeans and some cereal-based products. Oats are most likely to contain these toxins but they have been detected frequently at lower concentrations in barley. Wheat is only rarely contaminated with these toxinsFootnote 51.

The human health effects associated with chronic exposure to HT-2 and T-2 are not known. In animals, these toxins inhibit DNA, RNA and protein synthesis and are cytotoxic. IARC considers HT-2/T-2 toxins not classifiable as to their carcinogenicity to humans based on the lack of available human carcinogenicity data and only limited evidence in experimental animalsFootnote 52,Footnote 53. This study examined nivalenol, fusarenone, 3-Ac-DON, 15-Ac-DON, NEO, DAS, DON, HT-2 and T-2.

8 Zearalenone and Related Compounds

Zearalenone (ZEN) is a mycotoxin produced mainly by Fusarium species. It has been detected in wheat, barley, rice, corn, and other cereals. It is heat-resistant and can be found in finished grain-based products. ZEN is metabolised to α-zearalenol (α-ZOL) and β-zearalenol (β-ZOL)Footnote 54,Footnote 55,Footnote 56.

ZEN is not an acute toxin. ZEN is an estrogenic compound and its major metabolites are more potent estrogenic compounds. It causes infertility in sheep, cattle and pigs, and may lead to earlier sexual maturation in some animals. In experimental animal studies, high oral doses of ZEN have also been shown to be genotoxic, toxic to the liver, and affect blood and the immune systemFootnote 53,Footnote 57. IARC concluded that there is limited evidence of the carcinogenicity of ZENFootnote 58. ZEN has been considered a possible contributing agent in the outbreaks of early puberty in thousands of girls in Puerto Rico and may play a role in human breast and cervical cancer in highly exposed populationsFootnote 52.

This study examined ZEN α-ZOL, and β-ZOL.