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. 2025 Apr 26;8:100235. doi: 10.1016/j.crtox.2025.100235

Table 3.

Overview of available literature for experimental cattle exposed to dietary FUM.

Reference No. of cattle (dose groups) Body weight (BW, kg) Exposure duration (days) Average FUM content:
FB1 + FB2 + FB3,
(mg FUM/kg BW)a
Employed toxicological tests Statistically significant findings associated with FUM
Studies used as basis of current US FDA ML for fumonisin
Osweiler et al. (1993) 18 (3) 231 ± 5.7 31 • Control: < 0.13 • Feed intake • Liver function tests
• Weight gain
• Treatment 1: 0.78 • Hematology test • Neutrophil function
• Treatment 2: 3.7 • Liver function test • Lymphocyte blastogenesis
• Neutrophil function test
• Lymphocyte blastogenesis
• Histopathological analysis
Smith & Thakur (1996)b 6 (2) 217 30 • Control: < 0.13
• Treatment: 5.15
• Liver function test • Liver function tests
• Organ-to-BW ratio
• Feed-to-tissue ratio
• Histopathological analysis
Baker & Rottinghaus (1999)b 5 (2) 86 to 127 239 to 253 • Control: < 0.13
• Treatment: 11
• Liver function test
• Biomarker analysis
• Histopathological analysis
• Hematology test

• Liver function tests
Literature advances since 2001
Jennings et al. (2020) 50 (5) 361 ± 6.4 110 • Control: 0.2
• Treatment 1: 0.67
• Treatment 2: 1.02
• Treatment 3: 1.69
• Treatment 4: 2.72
• Feed intake
• Performace test
• Weight gain
• Biomarker analysis
• Carcass grading & evaluation
• Histopathological analysis &
scoring

• Biomarker analysis


a

Average dietary FUM concentration is calculated with the assumption that experimental cattle consumed 2.5% of BW per day.

b

Studies did not investigate FUM concentrations proximate to the present regulatory limit of 0.75 mg/kg BW/d and were excluded.