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使用具有表面和分泌定位的六钩蚴粘附蛋白(HP6),通过抗原捕获酶联免疫吸附测定法(Ag-ELISA)和聚合酶链反应(PCR)监测牛抗牛带绦虫囊尾蚴病疫苗接种情况。

Ag-ELISA and PCR for monitoring the vaccination of cattle against Taenia saginata cysticercosis using an oncospheral adhesion protein (HP6) with surface and secreted localization.

作者信息

Harrison L J S, Garate T, Bryce D M, Gonzalez L M, Foster-Cuevas M, Wamae L W, Onyango-Abuje J A, Parkhouse R M E

机构信息

University of Edinburgh, Department of Tropical Animal Health, Sir Alexander Robertson Centre for Tropical Veterinary Medicine, Easter Bush Veterinary Centre, Roslin, Midlothian, Scotland, UK.

出版信息

Trop Anim Health Prod. 2005 Feb;37(2):103-20. doi: 10.1023/b:trop.0000048459.98067.99.

Abstract

A Taenia saginata oncosphere-derived adhesion protein (HP6) with surface and secreted localization was used to successfully vaccinate calves against oral challenge with T. saginata eggs. In contrast, vaccination using a combination of T. saginata oncosphere-derived peptides, selected on the basis of their antigenic index, and including three derived from the HP6 molecule (HP6-1, HP6-2 and HP6-3), was unsuccessful. This either indicated that the wrong peptides were selected or, in the case of the HP6 protein, that the protective epitope is conformational in nature. The protection experiments were monitored using a parasite antigen detection ELISA (HP10 Ag-ELISA), which allowed the early determination of the success of the vaccination protocol, subsequently confirmed at autopsy. PCR assays were used for the first time to confirm the presence of T. saginata DNA in lesions recovered at autopsy and thus verify the parasite origin of the lesions.

摘要

一种具有表面和分泌定位的牛带绦虫六钩蚴衍生黏附蛋白(HP6)被用于成功地给小牛接种疫苗,使其抵抗牛带绦虫卵的口服攻击。相比之下,使用基于抗原指数选择的牛带绦虫六钩蚴衍生肽组合进行疫苗接种未成功,其中包括三种源自HP6分子的肽(HP6-1、HP6-2和HP6-3)。这要么表明选择了错误的肽,要么就HP6蛋白而言,表明保护性表位本质上是构象性的。使用寄生虫抗原检测ELISA(HP10 Ag-ELISA)监测保护实验,该方法可早期确定疫苗接种方案是否成功,随后在尸检时得到证实。首次使用PCR检测来确认尸检时回收的病变中是否存在牛带绦虫DNA,从而验证病变的寄生虫来源。

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