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Veterinary and human toxicology1996; 38(4); 265-270;

Effects of fusarium moniliforme isolates on tissue and serum sphingolipid concentrations in horses.

Abstract: Disruption in sphingolipid (SL) metabolism is a biomarker of exposure to fumonisins. The role of altered SL metabolism in the pathogenesis of fumonisin toxicoses is not understood. A 27-d feeding trial in horses compared the toxic effects of 3 strains of Fusarium moniliforme: RRC 415, cultured from corn in MS; AU 2/3, cultured from feed associated with clinical signs of duodenitis-proximal jejunitis (DPJ) in horses in AL; and MRC 826, cultured from corn in South Africa and shown to cause equine leukoencephalomalacia (ELEM). These were cultured on corn and diluted with clean corn and grain mixed with molasses (sweet feed) to final concentrations of < 1, 65-130 and 200 mg fumonisin B1 (FB1)/kg, respectively. None of the horses developed DPJ, but horses fed MRC 826 had intestinal lesions consistent with DPJ and horses fed AU 2/3 and MRC 826 developed ELEM. Serum SL concentrations were analyzed in horses fed control and F moniliforme culture material, in brain and/or intestinal tissues in healthy horses (euthanized in AL and IL), and in horses fed AU 2/3 and MRC 826. Serum sphinganine (Sa): sphingosine (Szero) ratios were significantly elevated in horses fed AU 2/3 and MRC 826. Sphinganine concentrations were significantly elevated in the hypothalamus-dentate gyrus and brain stem in horses fed AU 2/3, compared to healthy horses. Sphingosine concentrations were significantly elevated in the proximal duodenum and ileum of MRC 826 horses compared to healthy horses. The brain and intestinal tissues in horses with and without pathological lesions did not have changed Sa:S(zero).
Publication Date: 1996-08-01 PubMed ID: 8829343
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The study explores the effects of different strains of Fusarium moniliforme on sphingolipid concentrations in horses. The 27-day feeding trial discovered that the intake of certain strains lead to symptoms consistent with equine toxicoses and significant alterations in serum sphingolipid ratios.

Study Background and Purpose

  • The research was conducted to understand how the ingestion of Fusarium moniliforme (a type of fungus) impacts sphingolipid (SL) concentrations in horses. Disruption of SL metabolism can indicate exposure to fumonisins, which are mycotoxins produced by the fungus.
  • The disturbances in SL metabolism due to fumonisins are considered crucial in the development of fumonisin toxicoses. However, the exact role that SL plays in this disease process is not well understood. This formed the central research question of the study.

Experimental Setup

  • A 27-day feeding trial was conducted involving 3 strains of Fusarium moniliforme. The strains were RRC 415, AU 2/3, and MRC 826, procured from different locations, with each one associated with varying degrees of horse diseases.
  • The experimental feeds were created by growing these strains on corn. This was then diluted with clean corn and grain mixed with molasses to obtain a range of fumonisin B1 (FB1) concentrations. Horses were fed these concoctions.

Observations and Findings

  • None of the horses developed duodenitis-proximal jejunitis (DPJ), which is an inflammation of the intestinal tract. However, horses fed with MRC 826 had intestinal lesions consistent with DPJ, and horses fed with AU 2/3 and MRC 826 developed equine leukoencephalomalacia (ELEM), a neurological disease.
  • Serum SL concentrations showed alterations in horses fed with the Fusarium moniliforme culture material compared to the control group. This alteration was seen predominantly as an increase in the sphinganine (Sa) to sphingosine (So) ratio, within the serum of horses fed with AU 2/3 and MRC 826.
  • There were also significant changes in sphinganine and sphingosine concentrations in various parts of the brain and intestine across the different feeding groups. Most notably, elevated sphinganine concentrations in the hypothalamus-dentate gyrus and brain stem were seen in horses fed with AU 2/3 compared to healthy horses. Horses fed with MRC 826 showed significantly elevated sphingosine concentrations in the proximal duodenum and ileum compared to healthy horses.
  • Interestingly, no changes were observed in the Sa:So ratio in the brain and intestinal tissues of horses with and without pathological lesions. This indicates that while serum sphingolipid levels are affected, tissue ratios remain stable.

Cite This Article

APA
Goel S, Schumacher J, Lenz SD, Kemppainen BW. (1996). Effects of fusarium moniliforme isolates on tissue and serum sphingolipid concentrations in horses. Vet Hum Toxicol, 38(4), 265-270.

Publication

ISSN: 0145-6296
NlmUniqueID: 7704194
Country: United States
Language: English
Volume: 38
Issue: 4
Pages: 265-270

Researcher Affiliations

Goel, S
  • College of Veterinary Medicine, Auburn University, AL 36849, USA.
Schumacher, J
    Lenz, S D
      Kemppainen, B W

        MeSH Terms

        • Animals
        • Brain / drug effects
        • Brain / metabolism
        • Carcinogens, Environmental / toxicity
        • Culture Media
        • Duodenum / drug effects
        • Duodenum / metabolism
        • Enzyme Inhibitors / blood
        • Enzyme Inhibitors / metabolism
        • Fumonisins
        • Fusarium / classification
        • Horse Diseases / etiology
        • Horse Diseases / microbiology
        • Horses
        • Intestinal Mucosa / metabolism
        • Intestines / drug effects
        • Kidney / drug effects
        • Kidney / metabolism
        • Liver / drug effects
        • Liver / metabolism
        • Lung / drug effects
        • Lung / metabolism
        • Mycotoxins / toxicity
        • Sphingosine / analogs & derivatives
        • Sphingosine / blood
        • Sphingosine / metabolism
        • Tissue Distribution

        Citations

        This article has been cited 1 times.
        1. Doi K, Uetsuka K. Mechanisms of mycotoxin-induced neurotoxicity through oxidative stress-associated pathways.. Int J Mol Sci 2011;12(8):5213-37.
          doi: 10.3390/ijms12085213pubmed: 21954354google scholar: lookup