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Skin test with recombinant protein of Mycobacterium bovis as antigen in Cavia porcellus

机译:以牛分枝杆菌的重组蛋白为抗原的豚鼠皮肤测试

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The intradermal skin test for diagnosis of bovine tuberculosis has been used the purified protein derivative (PPD) of Mycobacterium bovis, that is able to induce a hypersensitivity reaction in infected animals. However, shows low specificity due to the occurrence of cross reactions with other mycobacteria Thus, the aim of this study was to produce recombinant proteins (ESAT-6, PE13, PE5 and ESX-1) of Mycobacterium bovis and assess them as antigens in skin test using guinea pigs (Cavia parcellus) as a model, and check if the conditions employed in the purification (native or denaturing condition) interfere in the antigenic performance of these proteins. The proteins were tested in guinea pigs previously sensitized with inactivated M. bovis strain AN5, individually (160 mu g/mu l), or as a mixed cocktail (40 mu g each). The cocktail of proteins induced hypersensitivity reactions in sensitized animals significantly (p=0.002) higher than those observed in non-sensitized animals, allowing differentiation. On the other hand, the proteins individually were not able to promote this differentiation. The conditions of solubilization and purification influenced the antigenic performance of the protein ESAT-6, since, when produced in denaturing condition triggered nonspecific reaction in non-sensitized animals. Whereas when produced under native conditions and used at concentrations (6, 12, 24 and 48 mu g/mu l) induced a significant response only in sensitized animals, confirming its potential as antigen.
机译:牛结核分枝杆菌的纯化蛋白衍生物(PPD)已被用于诊断牛结核的皮内皮肤试验,该衍生物能够在被感染的动物中引起超敏反应。但是,由于与其他分枝杆菌发生交叉反应而显示出低特异性。因此,本研究的目的是生产牛分枝杆菌的重组蛋白(ESAT-6,PE13,PE5和ESX-1)并将其评估为皮肤抗原使用豚鼠(Cavia parcellus)作为模型进行测试,并检查纯化中使用的条件(天然或变性条件)是否干扰了这些蛋白的抗原性能。在事先用灭活的牛分枝杆菌AN5致敏的豚鼠中分别测试蛋白质(160微克/微升)或混合鸡尾酒(每种40微克)。蛋白质混合物在致敏动物中诱导的超敏反应显着(p = 0.002)高于未致敏动物中观察到的超敏反应,从而可以分化。另一方面,蛋白质单独不能促进这种分化。增溶和纯化的条件影响了ESAT-6蛋白的抗原性能,因为在变性条件下生产时,会在非致敏动物中引发非特异性反应。而在天然条件下生产并以浓度(6、12、24和48微克/微升)使用时,仅在致敏动物中引起显着反应,从而证实其作为抗原的潜力。

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