--Rotavirus infection has been reported to induce an inflammatory response in the host cell accompanied by the increased expression or activation of some cellular molecules including ROS, NF-¿B and COX-2. PPAR¿ stimulation and N-acetylcysteine (NAC) treatment have been found to interfere with viral infections including rotavirus infection. Small intestinal villi isolated from in vivo infected mice with rotavirus ECwt were analyzed for the percentage of ECwt-infected cells, the presence of rotavirus antigens, and infectious virion yield following treatment with pioglitazone. Isolated villi were also infected in vitro and treated with PPAR¿ agonists (PGZ, TZD, RGZ, DHA, ALA), all-trans retinoic acid (ATRA) and NAC. After treatments, the expression of cellular proteins including PPAR¿, NF-¿B, PDI, Hsc70 and COX-2 was analyzed using Immunochemistry, ELISA, immunofluorescence and Western blotting. The results showed that rotavirus infection led to an increased accumulation of the cellular proteins studied and ROS. The virus infection-induced accumulation of the cellular proteins studied and ROS was reduced upon pioglitazone treatment, causing also a concomitant reduction of the infectious virion yield. We hypothesized that rotavirus infection is benefiting from the induction of a host cell pro-inflammatory response and that the interference of the inflammatory pathways involved leads to decreased infection.