Tissular Genomic Responses to Oral FB1 Exposure in Pigs

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Dopavogui, Léonie | Polizzi, Arnaud | Fougerat, Anne | Gourbeyre, Pascal | Terciolo, Chloé | Klement, Wendy | Pinton, Philippe | Laffite, Joëlle | Cossalter, Anne Marie | Bailly, Jean-Denis | Puel, Olivier | Lippi, Yannick | Naylies, Claire | Guillou, Hervé | Oswald, Isabelle P. | Loiseau, Nicolas

Edité par CCSD ; MDPI -

International audience. Fumonisin B1 (FB1) is a widespread mycotoxin produced by fungal Fusarium species—mainly in maize, one of the plants most commonly used for food and feed. Pigs and horses are the animal species most susceptible to this mycotoxin. FB1 exposure can cause highly diverse clinical symptoms, including hepatotoxicity, immunotoxicity, and intestinal barrier function disturbance. Inhibition of ceramide synthetase is a well-understood ubiquitous molecular mechanism of FB1 toxicity, but other more tissue-specific effects remain to be elucidated. To investigate the effects of FB1 in different exposed tissues, we cross-analyzed the transcriptomes of fours organs: liver, jejunum, jejunal Peyer’s patches, and spleen. During a four-week study period, pigs were fed a control diet or a FB1-contaminated diet (10 mg/kg feed). In response to oral FB1 exposure, we observed common biological processes in the four organs, including predominant and recurrent processes (extracellular matrix organization, integrin activation, granulocyte chemotaxis, neutrophil migration, and lipid and sterol homeostasis), as well as more tissue-specific processes that appeared to be related to lipid outcomes (cell cycle regulation in jejunum, and gluconeogenesis in liver).

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