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一种基于单克隆抗体的免疫过氧化物酶方法,用于快速检测火鸡出血性肠炎病毒。

A monoclonal antibody-based immunoperoxidase method for rapid detection of haemorrhagic enteritis virus of turkeys.

作者信息

Hussain I, Nagaraja K V

机构信息

Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Minnesota, St Paul 55108.

出版信息

Res Vet Sci. 1993 Jul;55(1):98-103. doi: 10.1016/0034-5288(93)90041-d.

Abstract

An indirect immunoperoxidase (IP) technique involving avidin-biotin peroxidase complex, using a monoclonal antibody was developed for the detection of haemorrhagic enteritis (HE) virus antigen in frozen and formalin-fixed paraffin-embedded tissue sections. This IP procedure was compared with an indirect immunofluorescence antibody technique (IFAT) and an agar gel precipitation test (AGPT). Spleens from turkeys experimentally infected with HE virus were collected and examined for the presence of viral antigen. The IP staining procedure detected HE viral antigen as early as 48 hours after infection and continued to demonstrate the presence of viral antigen for up to 11 days after infection at which time the experiment was terminated. The antigen was detected from three to seven days and from two to nine days after infection by the AGPT and IFAT, respectively. The IFAT and AGPT had sensitivities of 74.19 and 48 per cent, respectively, compared with IP. Because of its high sensitivity and specificity, the IP technique could be useful for studying the pathogenesis and rapid laboratory detection of HE virus.

摘要

一种使用单克隆抗体、涉及抗生物素蛋白-生物素过氧化物酶复合物的间接免疫过氧化物酶(IP)技术被开发出来,用于检测冷冻及经福尔马林固定、石蜡包埋的组织切片中的出血性肠炎(HE)病毒抗原。将该IP程序与间接免疫荧光抗体技术(IFAT)和琼脂凝胶沉淀试验(AGPT)进行了比较。收集经实验感染HE病毒的火鸡脾脏,检测其中病毒抗原的存在情况。IP染色程序在感染后48小时就检测到了HE病毒抗原,并且在感染后长达11天(实验终止时)都持续显示有病毒抗原存在。AGPT和IFAT分别在感染后3至7天和2至9天检测到抗原。与IP相比,IFAT和AGPT的灵敏度分别为74.19%和48%。由于其高灵敏度和特异性,IP技术可能有助于研究HE病毒的发病机制及进行快速实验室检测。

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