AI Article Synopsis

  • Ochratoxin A (OTA), a mycotoxin from fungi like Aspergillus and Penicillium, was tested in a study on its effects on piglets fed a diet contaminated with low levels of OTA (0.05 mg/kg).
  • After 30 days, the study found significantly higher levels of OTA in the kidney of poisoned piglets, along with changes in around 105 different genes related to immune response and cellular functions.
  • Although OTA did not affect certain kidney functions like urea and creatinine levels, the findings suggest potential early carcinogenic effects and immune response activation that warrant further research regarding implications for human health.

Article Abstract

Ochratoxin A (OTA) is a mycotoxin produced by fungus belonging to Aspergillus and Penicillium genra. The aim of the present paper was to investigate if a low concentration OTA has toxic effect in pigs. Twelve piglets were fed with a control or an OTA (0.05 mg/kg feed) contaminated diet. After 30 days, animals were slaughtered and samples of blood and kidney were used for further analyses. The mycotoxin analyses showed a significant higher (6.25 times) concentration of OTA in the kidney of OTA intoxicated piglets than in control ones. While OTA has no effect on the urea and creatinine concentration, the microarray analysis of the effect of OTA on genome wide expression in the kidney of intoxicated piglets, revealed that approximately 105 different transcripts were significantly altered. As shown by the microarray results, 0.05 mg/kg of OTA can principally interfere with: i) canonical pathways (CD28 Signaling in T Helper Cells, Role of NFAT in Regulation of the Immune Response, Relaxin Signaling, IL-1 Signaling) ii) molecular and cellular function (cellular movement cellular function and maintenance, cellular growth and proliferation cellular assembly and organization, cell death and survival) etc. However, alteration of renal and urological system development and function and renal necrosis predicted through Ingenuity Pathway Analysis (IPA) were not supported by clinical pathological data. In conclusion, OTA toxicity was found even at low concentration of toxin, correlated with the activation of immune response pathways, oxidative stress response and early carcinogenic events. This effect need to be further investigated and analyzed in the context of human health.

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http://dx.doi.org/10.1016/j.toxicon.2017.07.004DOI Listing

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