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首页> 外文期刊>Journal of Virological Methods >Development and evaluation of an IgM-capture ELISA for detection of recent infection with bluetongue viruses in cattle.
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Development and evaluation of an IgM-capture ELISA for detection of recent infection with bluetongue viruses in cattle.

机译:IgM捕获ELISA的开发和评估,用于检测牛最近感染蓝舌病毒。

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摘要

An IgM-capture enzyme-linked immunosorbent assay (ELISA) was developed for the detection of recent infection of bluetongue virus (BTV) in cattle. The test is based on the use of biotinylated capture anti-bovine IgM antibodies bound to a streptavidin-coated ELISA plate. The captured IgM antibodies were detected by application of BTV VP7 antigen and a VP7 antigen-specific monoclonal antibody. The IgM-capture ELISA was compared with the competitive ELISA by testing serum samples from groups of calves infected experimentally with five USA and 19 South Africa serotypes of BTV. The IgM-capture ELISA was able to detect bovine anti-VP7 antibodies from all animals infected with the 24 BTV serotypes at 10 days post-infection, whereas the competitive ELISA was not. When the detectable IgM diminished after 40 days post-infection by the IgM-capture ELISA, the IgG anti-VP7 antibodies remained high. The IgM-capture ELISA is sensitive and can be applied for the detection of recent infection of BTV in cattle.
机译:一种IgM捕获酶联免疫吸附测定(ELISA)用于检测牛最近感染蓝舌病毒(BTV)。该测试基于与链霉亲和素包被的ELISA板结合的生物素化捕获抗牛IgM抗体的使用。通过应用BTV VP7抗原和VP7抗原特异性单克隆抗体检测捕获的IgM抗体。通过测试实验性感染了五种美国和19种南非BTV血清型的小牛群的血清样品,将IgM捕获ELISA与竞争性ELISA进行了比较。 IgM捕获ELISA能够在感染后第10天从感染了24种BTV血清型的所有动物中检测牛抗VP7抗体,而竞争性ELISA不能。当通过IgM捕获ELISA感染后40天后可检测的IgM减少时,IgG抗VP7抗体仍然很高。 IgM捕获ELISA是灵敏的,可用于检测牛近期感染BTV。

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