首页> 外文期刊>Archives of virology >Improvement of a serodiagnostic strategy for foot-and-mouth disease virus surveillance in cattle under systematic vaccination: a combined system of an indirect ELISA-3ABC with an enzyme-linked immunoelectrotransfer blot assay.
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Improvement of a serodiagnostic strategy for foot-and-mouth disease virus surveillance in cattle under systematic vaccination: a combined system of an indirect ELISA-3ABC with an enzyme-linked immunoelectrotransfer blot assay.

机译:在系统接种疫苗的情况下改善牛口蹄疫病毒监测的血清诊断策略:间接ELISA-3ABC与酶联免疫电转移印迹法的组合系统。

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摘要

Foot-and-mouth disease (FMD) recombinant non-capsideal viral antigens 3A, 3B, 2C, 3D and 3ABC were assessed individually in an indirect enzyme-linked immunosorbent assay (I-ELISA) for their ability to screen for persistent infection-specific antibodies in cattle, regardless of vaccination condition. Results of sequential serum samples from non-vaccinated animals with experimentally induced persistent infection, and their correlation with virus isolation, indicated that the polypeptides 3A, 3B and 3ABC showed the most adequate characteristics for further field studies. Reliable performance of the I-ELISA with the selected antigen 3ABC was indicated by the distinct patterns observed for the frequency distribution values of naive and true positive samples. For regularly vaccinated livestock, a clear negative profile was proved in samples from regions without recent history of FMD. In contrast, at 90 and 900 days post-outbreak, coexistence of a positive and a negative population was established. These findings indicated that, irrespective of vaccination, the test allowed a classification of the herd-disease status. A high degree of agreement was observed between I-ELISA-3ABC and EITB results for clearly reactive and non-reactive sera. For samples with reactivity values close to that of the cut-off, the EITB profiles upheld the definition of the infection condition. On this basis, screening by I-ELISA-3ABC, together with confirmation of suspect or positive samples by EITB is proposed as an adequate and accurate approach for large-scale epidemiological surveillance.
机译:在间接酶联免疫吸附试验(I-ELISA)中分别评估了口蹄疫(FMD)重组无病毒病毒非抗原3A,3B,2C,3D和3ABC的能力,以筛选其持续感染特异性的能力牛中的抗体,无论接种条件如何。从实验预防性持续感染的非疫苗接种动物获得的连续血清样品的结果及其与病毒分离的相关性表明,多肽3A,3B和3ABC显示出最合适的特性,可用于进一步的田间研究。观察到的纯天然样品和真实阳性样品的频率分布值的不同模式表明了使用所选抗原3ABC进行I-ELISA的可靠性能。对于定期接种疫苗的牲畜,在没有口蹄疫近期病史的地区的样本中证实存在明显的阴性特征。相反,在暴发后90天和900天,建立了阳性种群和阴性种群的共存。这些发现表明,不管是否接种疫苗,该测试都可以对畜群疾病状态进行分类。在I-ELISA-3ABC和EITB结果之间,观察到明显的反应性和非反应性血清高度吻合。对于具有接近临界值的反应性值的样品,EITB曲线支持感染条件的定义。在此基础上,提出了通过I-ELISA-3ABC进行筛查以及通过EITB确认可疑或阳性样本的方法,是进行大规模流行病学监测的适当而准确的方法。

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