Abstract. Four gnotobiotic calves with intestinal lesions induced by third and fourth calf passages of the virus of human infantile gastroenteritis were studied by light microscopy, scanning and transmission electron microscopy, and by immunofluorescence. Calves, 25-72 hours old, were examined 0.5 hours, 3 hours, 7 hours, and 48 hours after the onset of diarrhea. Intestinal histology of infected calves was [2,6,8,9 , 161 has stimulated investigations for finding animal models for the disease. These studies have shown that the human agent can induce diarrhea in newborn piglets [15, 191, monkeys [20] and calves [14].Our study evaluated the lesions caused in calves by this virus and compared them with those caused by the antigenically related calf diarrheal reovirus-like agent.
Materials and MethodsCalves, inocula, and time between onset of diarrhea and death are summarized in table 1.Four gnotobiotic Hereford-Angus crossbred calves were offered 960 milliliters of autoclaved, homogenized cow's milk twice daily. Noninoculated (control) intestines were obtained from two calves (calves 1 and 2) used in reported experiments [ 11, 121; intestines from both calves were examined by light microscopy. The intestine from calf 2 was examined by scanning electron microscopy. Equipment, procedures and isolation units have been described [13].Source and early calf passages of the D strain of the viral agent have been described [8,19,201. The calves were inoculated orally 114) at 8-10 hours old when they were first fed milk. The 30 milliliters of inoculum was 10 milliliters of diarrheic feces with virus passed three or four times in a gnotobiotic calf and 20 milliliters phosphate-buffered saline solution (pH 7.2).Necropsy procedures, bacteriologic culturing and collection of tissues have been described [ 11, 121. Intestines were prepared for scanning electron microscopy [ 101. Tissues (brain, lung, liver, thymus. kidney, spleen, heart, pancreas, rumen, abomasum, thyroid, adrenal gland, and mesenteric lymph nodes and sections from the proximal, middle and distal small intestine and colon) for light microscopy were embedded and sectioned in the usual manner and stained with hematoxylin and eosin (HE).
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