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101.
An assessment of the role of dogs, goats and sheep as reservoir hosts of African trypanosomes infective for humans (sleeping sickness) was carried out in Nigeria during a 2-year study period. Twelve stocks of Trypanosoma (Trypanozoon) brucei, 10 stocks of Trypanosoma congolense and 11 stocks of Trypanosoma vivax were isolated from a total of 699 animals, comprising 286 sheep, 221 goats and 192 dogs. The potential infectivity of the isolates for man was tested in vitro using the blood incubation infectivity test. None of the T. brucei group was resistant to the trypanocidal action of human serum; three of the T. congolense group were resistant to human serum. A parallel study of the trypanocidal action of test serum on authenticated T. brucei brucei and T. brucei gambiense showed that the human serum behaved as expected. The possibility is discussed that T. congolense might produce infections in man and should, therefore, be handled carefully both in the laboratory and by veterinarians in the field.  相似文献   
102.
The chicken gut-associated lymphoid tissue is made up of a number of tissues and cells that are responsible for generating mucosal immune responses and maintaining intestinal homeostasis. The normal chicken microbiota also contributes to this via the ability to activate both innate defense mechanisms and adaptive immune responses. If left uncontrolled, immune activation in response to the normal microbiota would pose a risk of excessive inflammation and intestinal damage. Therefore, it is important that immune responses to the normal microbiota be under strict regulatory control. Through studies of mammals, it has been established that the mucosal immune system has specialized regulatory and anti-inflammatory mechanisms for eliminating or tolerating the normal microbiota. The mechanisms that exist in the chicken to control host responses to the normal microbiota, although assumed to be similar to that of mammals, have not yet been fully described. This review summarizes what is currently known about the host response to the intestinal microbiota, particularly in the chicken.  相似文献   
103.
OBJECTIVE: The purpose of this study was to characterize the proliferation and differentiation of primary canine lens epithelial cells (LEC) under standard culture conditions. PROCEDURE: Canine LEC were isolated by mechanical dissection of the canine globe and enzymatic digestion of the lens capsule from fresh lenses. Isolated capsules and cell suspensions were seeded in laminin-coated culture flasks. Canine LEC proliferated and formed monolayers, which could be passaged and maintained for approximately 2 weeks. Cells were characterized morphologically and cell lysates examined for expression of protein markers of epithelial origin and differentiation. RESULTS: Canine LEC exhibit morphologic characteristics of epithelial cells when cultured on laminin/lysine coated flasks. Expression of epithelial cell marker, cytokeratin 5, was highest at passage 1 and diminished with increasing passage number. Expression of gamma-crystallin, a protein found only in differentiated lens fiber cells, increased at passage 6. A laminin/lysine-coated surface supported optimal proliferation of canine LEC. Both an initial seeding density of 1 x 10(5) cells/cm(2) and culture in Dulbecco's modified essential media (DMEM) supplemented with 10% FBS supported a doubling time of less than 48 h in canine LEC. CONCLUSION: This study demonstrates that primary canine LEC retain the characteristics of lens epithelial cells prior to passage 6 under the described culture conditions and represent a suitable in vitro model for investigating lens physiology and cataractogenesis.  相似文献   
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