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Physiopathological effects ofEscherichia coliO157:H7 inoculation in weaned calves fed with colostrum containing antibodies to EspB and Intimin
Escherichia coliO157:H7 is responsible for severe intestinal disease and hemolytic uremic syndrome (HUS), a serious systemic complication which particularly affects children. Cattle are the primary reservoir forE. coliO157:H7 and the main source of infection for humans. In this study, we evaluated t...
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Published in: | Vaccine 2014-06, Vol.32 (30), p.3823 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Escherichia coliO157:H7 is responsible for severe intestinal disease and hemolytic uremic syndrome (HUS), a serious systemic complication which particularly affects children. Cattle are the primary reservoir forE. coliO157:H7 and the main source of infection for humans. In this study, we evaluated the ability of transferred maternal colostral antibodies against γ-Intimin C280and EspB, to protect young weaned calves fromE. coliO157:H7 infection. Hyperimmune colostra were obtained by immunization of pregnant cows with a mix of the mentioned antigens. All vaccinated cows mounted a significant IgG response against γ-Intimin C280, and EspB in sera and colostra. Colostrum-fed calves also exhibited high serum IgG titers against γ-Intimin C280and EspB along with a rise in mucosal γ-Intimin C280-specific IgG antibodies at recto-anal junction and ileum. Additionally, 70 day-old calves received a challenge withE. coliO157:H7 but no reduction in total bacterial shedding or frequency ofE. coliO157:H7 excretion from these calves was observed. Most tissue samples showed granulocyte focal infiltrations of the lamina propria and enterocyte erosion. In conclusion, up to the 70th day, the passively acquired γ-Intimin-C280and EspB-IgG antibodies present in sera and recto-anal mucosa reached a titer insufficient to reduce EHEC O157 shedding and damages of experimentally inoculated young calves. |
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ISSN: | 0264-410X 1873-2518 |
DOI: | 10.1016/j.vaccine.2014.04.073 |