Vaccines containing viruses involved in avian malabsorption syndrome and methods of administration therefor
A malabsorption syndrome technology, applied in the field of vaccines against poultry malabsorption syndrome-related diseases, can solve the problem that the diagnosis has not yet been confirmed
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Embodiment 1
[0053] Materials and Methods
[0054] Inoculum was prepared from intestines (including duodenum and cecum) samples taken from 10 chicks from a site showing clinical symptoms of MAS disorders. The gut samples were stored at -20°C. 100 grams of intestines were homogenized in 100 ml PBS using a laboratory homogenizer. This tissue homogenate (50% w / v) was inoculated to 1-day-old broiler chickens.
[0055] Eighty one-day-old broiler chicks were obtained from a commercial hatchery. These chickens were divided into 2 groups, 40 in each group, and raised in different isolation areas. Paper was laid on the ground of the isolation area to observe the feces. 40 chicks (group 2) were inoculated with 0.5 ml intestinal tissue homogenate by inserting a cannula into the crop. The remaining 40 chicks (group 1) were not inoculated and served as the uninfected control group. The chicks were fed unlimited commercial broiler feed and had free access to water. Prior to this, they had not bee...
Embodiment 2
[0081] The purpose of this study was to investigate whether one infectious agent or multiple infectious agents caused MAS to spread through the peripheral blood. This was done by inoculating 1-day-old broiler chick crops with homogenates of pancreas, yolk sac and liver tissue from infected chicks.
[0082] Twenty 1-day-old broiler chickens (group 1) were inoculated with 0.5 ml of intestinal tissue homogenate (stored at -70°C) by inserting a cannula into their crops, and then housed on the ground covered with sawdust. The chicks were sacrificed on day 4 after inoculation. Carefully remove the liver, pancreas, yolk sac, and intestine to avoid contamination with intestinal material. Intestines were stored at -70°C. The liver, pancreas and yolk sac were homogenized. These tissue homogenates were used to inoculate three new groups (groups 2, 3 and 4) of 20 1-day-old broiler chicks, each of which was inoculated by inserting a cannula into the crop. The groups were housed on sawd...
Embodiment 3
[0122] 50 1-day-old broiler chickens were divided into 5 groups, 10 in each group, and were inoculated as follows by inserting the intubation method into the crop: the first group (infection control) was inoculated with intestinal tissue homogenate; the second group (reovirus) Vaccination 10 6.7 TCID 50 Reovirus; group 3 (adenovirus) inoculated 10 8.2 TCID 50 Adenovirus; group 4 (adenovirus and reovirus) inoculated 10 6.7 TCID 50 Reovirus and 10 8.2 TCID 50 Combination of adenoviruses. Group 5 (uninfected controls) was not vaccinated. The chickens of each group were kept in stainless steel cages in the isolated animal room, with barbed wire and feces collection devices on the bottom of the cages. On days 14 and 22 after inoculation, the chicks of each group were weighed and sacrificed.
[0123] The changes in the longitudinal sections of the two proximal tibial epiphyseal cartilage plates of each bird were observed, and the bone disease was evaluated visually. Intest...
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