, 2004). Since the enterotoxaemia due to C. perfringens types B and C share similar neurological signs while type B produces both beta-toxin and ET whereas the type C synthesizes only the beta-toxin (reviewed by McClane et al., 2006), the question of whether other toxin(s) produced together with ET may explain Tofacitinib cost some of the neurological aspects of the disease was raised. Experiments performed in mice demonstrated that none of the C. perfringens type B or D toxins, except ET, is indispensable for inducing illness. However, the other toxins seem to play a synergistic/potentiating

role together with ET (for the contribution of beta-toxin to the pathogenesis of C. perfringens type B, see Fernandez-Miyakawa et al., 2007a; for the potentiating role of alpha-toxin and perfringolysin-O, see Fernandez-Miyakawa et al., 2008). Sialidases from C. perfringens type D may play a role ( Li et al., 2011), see also below. However, the mechanism underlying the potentiating role of the other toxins of factors is still unclear. Possibly, they may favour dissemination of ET by increasing vascular permeability ( Fernandez-Miyakawa et al., 2008, 2007a). To summarize, administration of ET mimics the naturally occurring disease produced by C. perfringens types B or D. The observed clinical manifestations LBH589 ic50 ( Table 1) indicate prominent alterations in the central nervous system

functions. Sudden death may result from severe brain damage; however, it can be caused by blood pressure elevation or heart failure. In the next paragraphs we summarize how ET can pass from the intestine to the brain and generates damage in the central nervous system. Since ET is produced into the gut lumen, it should first cross the intestinal barrier before being disseminated in the whole organism. Many studies have addressed this step (for reviews see Finnie, 2004; Popoff, 2011a). ET binds to mucosal epithelium of small intestine (Goldstein

et al., 2009). ET induces decrease in the trans-epithelial resistance in a time- and dose-dependent manner (Fernandez-Miyakawa et al., 2003; Goldstein et al., 2009). Since no histological and ultrastructural changes in the intestinal epithelium have been observed (except paravascular oedema and presence of selleck compound apoptotic cells in the lamina propia, Goldstein et al., 2009) ET may cross the intestinal barrier by passing through the paracellular pathway, possibly by opening the mucosa tight junctions (reviewed by Popoff, 2011a, 2011b). However, despite ET decreases trans-epithelial resistance in cultured confluent renal epithelial cells, as the MDCK (Madin–Darby Canine Kidney) cells ( Petit et al., 2003) or mpkCCDc14 immortalized mouse kidney cells ( Chassin et al., 2007), no alteration of the tight junctions is detected between the renal cells.