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通过重组猫免疫缺陷病毒p24抗原检测南非克鲁格国家公园和埃托沙国家公园野生狮子中猫免疫缺陷病毒反应性抗体的发生率。

Incidence of feline immunodeficiency virus reactive antibodies in free-ranging lions of the Kruger National Park and the Etosha National Park in southern Africa detected by recombinant FIV p24 antigen.

作者信息

Spencer J A, Van Dijk A A, Horzinek M C, Egberink H F, Bengis R G, Keet D F, Morikawa S, Bishop D H

机构信息

Department of Infectious Diseases, Faculty of Veterinary Science, University of Pretoria, Onderstepoort, Republic of South Africa.

出版信息

Onderstepoort J Vet Res. 1992 Dec;59(4):315-22.

PMID:1338477
Abstract

Lion sera from the Kruger National Park (KNP) dating back to 1977 and from the Etosha National Park (ENP), obtained from 1989 to 1991, have been analysed by ELISA and Western blot analyses using a genetically engineered antigen representing the p24 structural protein of feline immunodeficiency virus (FIV). It was concluded that some 83% of 98 KNP lion sera reacted with the p24 antigen, while none of 28 ENP lion sera reacted. A few other KNP felids (cheetahs and genets) gave samples that did not react with the FIV p24 antigen. For the KNP lions, apart from a lower prevalence in cubs (50%), no particular trends were demonstrated in terms of age, sex, date or origins of the samples. In Western blot and radio-immunoprecipitation analyses the lion sera reacted with the engineered p24 antigen, as well as with the p15 and p24 gag proteins and the p50 gag precursor protein from FIV, indicating that the agent is probably a lentivirus related to FIV. The ELISA with the engineered p24 antigen required less serum and appears to be more sensitive at detecting FIV-reactive antibodies than assays with available commercial kits.

摘要

对来自克鲁格国家公园(KNP)可追溯到1977年的狮子血清以及1989年至1991年从埃托沙国家公园(ENP)获取的狮子血清,使用代表猫免疫缺陷病毒(FIV)p24结构蛋白的基因工程抗原,通过酶联免疫吸附测定(ELISA)和蛋白质印迹分析进行了检测。结果显示,98份KNP狮子血清中约83%与p24抗原发生反应,而28份ENP狮子血清均未发生反应。其他一些KNP猫科动物(猎豹和灵猫)的样本未与FIV p24抗原发生反应。对于KNP狮子,除了幼崽中患病率较低(50%)外,在样本的年龄、性别、日期或来源方面未显示出特定趋势。在蛋白质印迹和放射免疫沉淀分析中,狮子血清与基因工程p24抗原以及FIV的p15和p24 gag蛋白和p50 gag前体蛋白发生反应,表明该病原体可能是一种与FIV相关的慢病毒。使用基因工程p24抗原的ELISA所需血清较少,并且在检测FIV反应性抗体方面似乎比使用现有商业试剂盒的检测方法更灵敏。

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