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一种用于检测抗微管抗体的竞争性酶联免疫吸附测定法,该方法使用针对蓝舌病毒非结构蛋白NS1的单克隆抗体。

A competitive ELISA for the detection of anti-tubule antibodies using a monoclonal antibody against bluetongue virus non-structural protein NS1.

作者信息

Anderson J, Mertens P P, Herniman K A

机构信息

AFRC Institute for Animal Health, Pirbright Laboratory, Pirbright Woking, Surrey, UK.

出版信息

J Virol Methods. 1993 Jul;43(2):167-75. doi: 10.1016/0166-0934(93)90074-2.

Abstract

A monoclonal antibody directed against the largest bluetongue virus (BTV) non-structural protein (NS1) was used in a competitive ELISA to detect antibodies to tubules (composed of NS1) in serum samples. Anti-tubule antibodies were detected at approximately 10 days post-infection in BTV infected sheep but no such antibodies were detected in sheep injected with inactivated BTV vaccines. Tubules are also produced during the replication of other related orbiviruses, including epizootic haemorrhagic disease of deer virus (EHDV). However, antibodies to the EHDV tubules were not detected in antisera from EHDV infected animals using the BTV NS1 specific monoclonal antibody and this assay system, confirming the serogroup-specific nature of this assay. This assay may prove useful not only for confirming the inactivated nature of experimental vaccines but also for the detection of viral replication and hence measurement of protection in vaccine potency trials following virulent BTV challenge. If inactivated BTV vaccines are ever widely adopted this test could provide a valuable means of discriminating between vaccinated and infected animals.

摘要

一种针对最大的蓝舌病病毒(BTV)非结构蛋白(NS1)的单克隆抗体被用于竞争性酶联免疫吸附测定(ELISA),以检测血清样本中针对由NS1组成的小管的抗体。在感染BTV的绵羊中,感染后约10天检测到抗小管抗体,但在注射了灭活BTV疫苗的绵羊中未检测到此类抗体。在包括鹿流行性出血病病毒(EHDV)在内的其他相关环状病毒复制过程中也会产生小管。然而,使用BTV NS1特异性单克隆抗体和该检测系统,在EHDV感染动物的抗血清中未检测到针对EHDV小管的抗体,这证实了该检测的血清群特异性。该检测不仅可能被证明对确认实验疫苗的灭活性质有用,而且对检测病毒复制以及因此在强毒BTV攻击后的疫苗效力试验中测量保护作用也有用。如果灭活BTV疫苗被广泛采用,该检测可以提供一种区分接种疫苗动物和感染动物的有价值方法。

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