首页> 外文期刊>Veterinary Immunology and Immunopathology >A systemic vaccine based on Escherichia coli O157:H7 bacterial ghosts (BGs) reduces the excretion of E. coli O157:H7 in calves
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A systemic vaccine based on Escherichia coli O157:H7 bacterial ghosts (BGs) reduces the excretion of E. coli O157:H7 in calves

机译:基于大肠杆菌O157:H7细菌幽灵(BG)的系统疫苗可减少犊牛中大肠杆菌O157:H7的排泄

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Cattle are the main reservoir of enterohemorrhagic Escherichia coil O157:H7, a bacterium that, in humans, causes hemorrhagic colitis and hemolytic uremic syndrome (HUS), a life-threatening disease, especially in children and older people. Therefore, the development of vaccines preventing colonization of cattle by E. coil O157:H7 could be a main tool for an HUS control program. In the present study, we evaluated bacterial ghosts (BGs) of E. coil O157:H7 as an experimental vaccine against this pathogen. BGs are empty envelopes of Gram-negative bacteria, which retain the morphological surface make-up of their living counterparts and are produced by controlled expression of the cloned protein E, which causes loss of all the cytoplasm content. In this work, E. coli O157:H7 BGs were used for subcutaneous immunization of calves. The vaccinated animals elicited significant levels of BC-specific IgG but not IgA antibodies in serum. Low levels of IgA and IgG antibodies against BGs were detected in saliva from vaccinated animals. Following oral challenge with E. coil O157:H7, a significant reduction in both the duration and total bacterial shedding was observed in vaccinated calves compared to the nonimmunized group. We demonstrated that systemic vaccination with E. coli O157 BGs provides protection in a bovine experimental model. Further research is needed to reach a higher mucosal immune response leading to an optimal vaccine. (C) 2012 Elsevier B.V
机译:牛是肠出血性大肠杆菌O157:H7的主要贮藏库,该细菌在人类中会引起出血性结肠炎和溶血性尿毒症综合征(HUS),这是一种威胁生命的疾病,尤其是在儿童和老年人中。因此,开发防止大肠杆菌O157:H7感染牛的定植疫苗可能是HUS控制程序的主要工具。在本研究中,我们评估了大肠杆菌O157:H7的细菌幽灵(BG)作为针对这种病原体的实验疫苗。 BG是革兰氏阴性细菌的空包膜,它们保留了它们活着的对应物的表面形态,并由克隆蛋白E的受控表达产生,这导致所有细胞质含量的损失。在这项工作中,大肠杆菌O157:H7 BG用于小牛的皮下免疫。接种疫苗的动物在血清中引起显着水平的BC特异性IgG而非IgA抗体。在接种动物的唾液中检测到低水平的抗BG的IgA和IgG抗体。与未免疫组相比,接种O157:H7大肠杆菌进行口服攻击后,接种牛犊的持续时间和总细菌脱落均显着减少。我们证明了用大肠杆菌O157 BG进行全身接种可在牛实验模型中提供保护。需要进一步研究以获得更高的粘膜免疫应答,从而产生最佳疫苗。 (C)2012 Elsevier B.V

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