Deoxynivalenol (DON), commonly known as vomitoxin, is a mycotoxin produced by Fusarium fungi that frequently contaminates cereal grains such as wheat, maize, and barley.
Due to its heat stability, DON persists in processed foods, raising concerns about its effects on gastrointestinal health, immune function, and neuroinflammation in both humans and animals.
Deoxynivalenol (DON), or vomitoxin, is a trichothecene mycotoxin produced by Fusarium fungi. It commonly contaminates grains such as wheat, barley, oats, rye, and maize. Due to its heat stability, DON persists in processed foods, posing risks to human and animal health.
Alongside DON, its acetylated derivatives—3-acetyl-DON (3-ADON) and 15-acetyl-DON (15-ADON)—and plant-modified DON-3-glucoside contribute to toxicity.
15-ADON is the most toxic of these compounds, with greater effects on intestinal barrier function and systemic inflammation.
DON is associated with health risks in both humans and animals:
The tolerable daily intake (TDI) is 1 μg/kg body weight (bw) per day, based on reduced body weight gain in mice.
Acute exposure (≥ 8 μg/kg bw per meal) can cause nausea, vomiting, diarrhea, and abdominal pain.
Chronic exposure regularly exceeds the TDI in infants, toddlers, and children, raising significant concerns for immune function, growth, and metabolic health.
Maternal exposure to DON has been linked to lower birth weight, shorter birth length, and an increased risk of small-for-gestational-age (SGA) infants and infant mortality.
Key toxicity mechanisms include:
Symptoms of acute exposure can include:
Symptoms of chronic exposure can include:
Affected species may include:
Human exposure through animal products (milk, meat, eggs) is negligible due to low DON bioaccumulation in animal tissues.
System-based effects of DON exposure in humans may include;
Emerging research highlights DON's direct impact on the brain, influencing appetite, neurotransmission, and neuroinflammation:
Appetite Suppression & Nausea: DON activates brainstem structures, leading to anorexia and nausea.
Neuroinflammation: DON increases IL-1β, IL-6, and TNF-α, promoting sickness behavior and metabolic dysregulation.
Neurotransmitter Disruptions: DON alters serotonin and dopamine pathways, contributing to mood changes, appetite loss, and stress reactivity.
DON and its acetylated derivatives directly damage gut barrier function, with 15-ADON showing the highest toxicity:
Cell Proliferation: 15-ADON inhibits intestinal epithelial cell growth more than DON or 3-ADON.
Barrier Function: 15-ADON decreases transepithelial electrical resistance (TEER), increasing paracellular permeability and gut inflammation.
Tight Junction Integrity:
DON exposure may exacerbate inflammatory bowel disease (IBD), irritable bowel syndrome (IBS), and food sensitivities due to its effects on the gut lining.
Increased gut permeability allows microbial toxins and dietary antigens to enter circulation, contributing to chronic inflammation, autoimmunity, and metabolic disorders.
Pregnant women may be at higher risk of inflammatory and metabolic complications from DON-related gut dysfunction.
DON testing is not a routine clinical test but may be considered in specific populations:
Individuals with suspected mycotoxin exposure and/or mycotoxin-related food poisoning: testing may be warranted in cases of gastrointestinal illness where DON contamination is suspected and other causes have been ruled out.
Occupational health monitoring: workers in grain processing, agriculture, and animal feed production may undergo periodic testing to assess exposure levels.
Research studies on mycotoxin exposure: DON testing may be used in epidemiological studies to investigate the impact of mycotoxin exposure on human health.
Routine testing for the general population is not recommended unless specific symptoms, risk factors, or exposure concerns are present.
Urine mycotoxin testing detects the presence of mycotoxins and their metabolites excreted by the body, providing a direct measure of recent exposure. This test may be useful for assessing acute or ongoing exposure to mold toxins but may not reflect total body burden, as detoxification capacity varies among individuals.
Urine samples may be collected in a clinical setting or from the comfort of home; a first-morning void is often recommended.
Serum immune response testing evaluates the body's reaction to mycotoxins by measuring antibodies (IgG, IgA, IgE) against specific mold toxins. This test requires a blood draw via venipuncture and indicates past or chronic exposure and potential immune system activation.
Combining both tests may offer a more comprehensive assessment of mycotoxin-related health effects.
It is important to consult the laboratory company used for their recommended reference range. In general, levels of DON or of antibodies sensitized to DON are expected to be negative, or very low.
Elevated DON levels in biological samples (urine, blood) may indicate recent or current exposure, biological persistence, or an immune response against these compounds.
The presence of DON metabolites, such as de-epoxy-deoxynivalenol (DOM-1), provides a clearer picture of recent ingestion or inhalation of contaminated material.
High levels of DON can be associated with acute mycotoxicosis.
Low or undetectable levels of DON metabolites may indicate:
While low DON levels suggest lower immediate risk, chronic low-level exposure remains an area of research, particularly concerning its potential effects on immune function and gut health over time.
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