Effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on feed intake, serum chemistry, and hematology of horses, and the efficacy of a polymeric glucomannan mycotoxin adsorbent.

The feeding of Fusarium mycotoxin-contaminated grains adversely affects the performance of swine and poultry. Very little information is available, however, on adverse effects associated with feeding these mycotoxin-contaminated grains on the performance of horses. An experiment was conducted to investigate the effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on feed intake, serum immunoglobulin (Ig) concentrations, serum chemistry, and hematology of horses. A polymeric glucomannan mycotoxin adsorbent (GM polymer) was also tested for efficacy in preventing Fusarium mycotoxicoses. Nine mature, nonexercising, light, mixed-breed mares were assigned randomly to one of three dietary treatments for 21 d. The horses were randomly reassigned and the experiment was subsequently replicated in time following a 14-d washout interval. Feed consumed each day was a combination of up to 2.8 kg of concentrates and 5 kg of mixed timothy/alfalfa hay. The concentrates fed included the following: 1) control, 2) blend of contaminated grains (36% contaminated wheat and 53% contaminated corn), and 3) blend of contaminated grains + 0.2% GM polymer. Diets containing contaminated grains averaged 15.0 ppm of deoxynivalenol, 0.8 ppm of 15-acetyldeoxynivalenol, 9.7 ppm of fusaric acid, and 2.0 ppm of zearalenone. Feed intake by all horses fed contaminated grains was reduced (P < 0.001) compared with controls throughout the experiment. Supplementation of 0.2% GM polymer to the contaminated diet increased (P = 0.004) feed intake of horses compared with those fed the unsupplemented contaminated diet. Serum activities of gamma-glutamyltransferase were higher (P = 0.047 and 0.027) in horses fed the diet containing contaminated grain compared with those fed the control diet on d 7 and 14, but not on d 21 (P = 0.273). Supplementation of GM polymer to the contaminated diet decreased (P < 0.05) serum gamma-glutamyltransferase activities of horses compared with those fed unsupplemented contaminated diet on d 7 and 14. Other hematology and serum chemistry measurements including serum IgM, IgG, and IgA, were not affected by diet. It was concluded that the feeding of grains naturally contaminated with Fusarium mycotoxins caused a decrease in feed intake and altered serum gamma glutamyltransferase activities. The supplementation of GM polymer prevented these mycotoxin-induced adverse effects.

[1]  E. Squires,et al.  Effects of feeding a blend of grains naturally contaminated with Fusarium mycotoxins on swine performance, brain regional neurochemistry, and serum chemistry and the efficacy of a polymeric glucomannan mycotoxin adsorbent. , 2002, Journal of animal science.

[2]  T. Smith,et al.  Effect of dietary alfalfa on zearalenone toxicity and metabolism in rats and swine. , 1982, Journal of animal science.

[3]  J. Pestka,et al.  Dysregulation of IgA production and IgA nephropathy induced by the trichothecene vomitoxin. , 1989, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[4]  K. Andrassy,et al.  Massenhaftes Auftreten von Mykotoxikosen im Komitat Hajdu‐Bihar: Mass Incidence of Mycotoxicoses in Hajdu‐Bihar County , 1980 .

[5]  R. Kuehl Design of Experiments: Statistical Principles of Research Design and Analysis , 1999 .

[6]  P. Eyre Equine pulmonary emphysema: a bronchopulmonary mould allergy , 1972, Veterinary Record.

[7]  J. W. Dickens,et al.  Protocols for surveys, sampling, post-collection handling, and analysis of grain samples involved in mycotoxin problems. , 1980, Journal - Association of Official Analytical Chemists.

[8]  M.V.L.N. Raju,et al.  Influence of esterified-glucomannan on performance and organ morphology, serum biochemistry and haematology in broilers exposed to individual and combined mycotoxicosis (aflatoxin, ochratoxin and T-2 toxin) , 2000, British poultry science.

[9]  Prelusky Db The effect of low-level deoxynivalenol on neurotransmitter levels measured in pig cerebral spinal fluid. , 1993 .

[10]  T. Smith,et al.  Effect of fusaric acid on brain regional neurochemistry and vomiting behavior in swine. , 1991, Journal of animal science.

[11]  T. Smith,et al.  Altered Tissue Amino Acid Metabolism in Acute T-2 Toxicosis , 1995, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[12]  J. Heremans,et al.  Immunochemical quantitation of antigens by single radial immunodiffusion. , 1965, Immunochemistry.

[13]  Midori Watanabe,et al.  Quantitative analysis of fusaric acid in the cultural filtrate and soybean [Glycine max] plants inoculated with Fusarium oxysporum var. redolens , 1988 .

[14]  J. Thomson,et al.  Effects of environmental control on pulmonary function of horses affected with chronic obstructive pulmonary disease. , 1984, Equine veterinary journal.

[15]  H. Hidaka,et al.  Fusaric acid, a hypotensive agent produced by fungi. , 1969, The Journal of antibiotics.

[16]  P. Scott,et al.  Improved liquid chromatographic method for determination of aflatoxins in peanut butter and other commodities. , 1984, Journal - Association of Official Analytical Chemists.

[17]  T. Smith,et al.  Fusaric acid content of swine feedstuffs , 1993 .

[18]  J. Forgacs CHAPTER 4. – Stachybotryotoxicosis , 1972 .

[19]  P. Harris Nutrient requirements of horses: National Research Council Chichester: John Wiley/Washington: National Academy Press. 1990. 5th edition. 100 pp. £15.35/US $17.95 (paper) , 1991 .

[20]  A. Ramos,et al.  Prevention of Toxic Effects of Mycotoxins by Means of Nonnutritive Adsorbent Compounds. , 1996, Journal of food protection.

[21]  G. Wood Mycotoxins in foods and feeds in the United States. , 1992, Journal of animal science.

[22]  S. Casteel,et al.  Effect of Feeding Deoxynivalenol (Vomitoxin)-Contaminated Barley to Horses , 1997, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

[23]  J. Fernstrom Tryptophan Availability and Serotonin Synthesis in Brain , 1988 .

[24]  C. Bacon,et al.  Production of fusaric acid by Fusarium species , 1996, Applied and environmental microbiology.

[25]  T. Smith,et al.  Effects of feeding blends of grains naturally contaminated with Fusarium mycotoxins on production and metabolism in broilers. , 2002, Poultry science.

[26]  H. Trenholm,et al.  Effects of feeding diets containing Fusarium (naturally) contaminated wheat or pure deoxynivalenol (DON) in growing pigs , 1994 .

[27]  S. Swanson,et al.  Sex-related reduced weight gains in growing swine fed diets containing deoxynivalenol. , 1985, Journal of animal science.

[28]  T. Smith,et al.  Effect of feeding blends of Fusarium mycotoxin-contaminated grains containing deoxynivalenol and fusaric acid on growth and feed consumption of immature swine. , 1997, Journal of animal science.

[29]  E. M. Wray,et al.  Fusaric acid in Fusarium moniliforme cultures, corn, and feeds toxic to livestock and the neurochemical effects in the brain and pineal gland of rats. , 1995, Natural toxins.

[30]  J. Pestka,et al.  Effects of 8-week exposure of the B6C3F1 mouse to dietary deoxynivalenol (vomitoxin) and zearalenone. , 1986, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

[31]  松井 幸夫,et al.  Quantitative Analysis of Fusaric acid in the Cultural Filtrate and Soybean Plants Inoculated with Fusarium oxysporum var. redolens , 1988 .

[32]  J. Pestka,et al.  Immunomodulation by fungal toxins. , 2000, Journal of toxicology and environmental health. Part B, Critical reviews.

[33]  W. Horwitz Official Methods of Analysis , 1980 .