ABSTRACT. Epithelial transport and degradation of horseradish peroxidase (HRP), a macromolecular tracer, was studied in conventional and germ-free suckling mice following an experimental infection with rotavirus. Conventional and germ-free mice developed diarrhea from days 2 to 8 postinfection (pi), with growth failure. In mucosal homogenates, infectious virus detected by immunofluorescence on MA 104 cells was present from day 2 through day 8 pi in germ-free mice, but persisted longer (day 13 pi) in conventional mice. Only mild histological lesions were observed during diarrhea, but obvious macrovacuolation of epithelial cells and increased cellular density occurred during the convalescence period (days 9 to 13 pi). Intact and degraded H R P fluxes from mucosa to serosa were measured in vitro on segments of jejunum mounted in Ussing chambers. Both groups of mice developed increased H R P permeability during the experimental period, but at different times after inoculation: during the diarrheal period (days 2 and 3 pi) conventional mouse epithelium absorbed five times more HRP than noninfected controls and during the convalescence period (days 9 to 13 pi) HRP absorption in germ-free mice rose 10-fold as compared to its level before infection. In both cases, this increase in HRP permeability was entirely due to an increase in intact One of the major problems in the management of infant viral enteritis is to find a suitable diet during and after diarrhea. Of particular interest is the question of whether or not intact foreign proteins are overabsorbed during viral enteritis. Epizootic diarrhea of infant mice provides an interesting model for studying the mechanisms by which the epithelial bamer to macromolecules might be altered in viral enteritis. Intestinal permeability to macromolecular marker HRP was previously studied in isolated jejunal epithelium in different physiological and pathological situations (1-3) including coronavirus infection in piglets (4). Our earlier results indicate that HRP is transported through the enterocytes via two functional pathways: a minor pathway allowing intact protein transport and a major pathway including lvsosomal degradation. In mice. these two Dathwavs do not develop in aUparallel manner d;ring the neonatal ieriod (5). Herein we report the gradual evolution of these two pathways during an experimental rotavirus diarrhea in suckling mice. This is one of the most frequently studied animal models, as it displays similarities to infantile gastroenteritis (6-8). Our results indicate that rotavirus infection in mice causes an increase in intact HRP intestinal permeability which is dependent on intestinal microflora.
METHODSHRP absorption, probably via a transcellular route, and dAnimols, Germ-free and conventional C3H/HeJ supplied occurred without any in degraded HRP trans-by Centre de Sklection et d'Elevage des Animaux de Laboratoire, port. These results indicate that in mice, rotavirus infection Orlkans-la Source, France, were used for experimentation. Germcauses a transient ris...