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用于检测猪伪狂犬病病毒抗体的酶联免疫吸附测定法。

Enzyme-linked immunosorbent assay for detecting antibodies to Aujeszky's disease virus in pigs.

作者信息

Todd D, McNair J, McNulty M S, McFerran J B

出版信息

Vet Rec. 1981 Dec 12;109(24):534-7.

PMID:6280368
Abstract

An indirect micro enzyme-linked immunosorbent assay (ELISA) for detecting antibodies to Aujeszky's disease virus in pigs is described. A control antigen prepared from infected cells was included for each serum tested. Of 243 sera from serologically positive farms, 175 (72 per cent) and 147 (60 per cent) were positive by the ELISA test and microtitre serum neutralisation test, respectively. Failure to include a control antigen for each serum would have resulted in 14 sera (6 per cent) being differently recorded. Results for sera from experimental and field infections indicated that seroconversion was more quickly detected by the ELISA test than the microtitre serum neutralisation test. In addition to greater sensitivity the ELISA test has other advantages over the serum neutralisation test. ELISA is a rapid, cheap test which is not dependent on a continuous supply of cell cultures and which can be readily automated.

摘要

本文描述了一种用于检测猪伪狂犬病病毒抗体的间接微量酶联免疫吸附测定(ELISA)方法。对每份检测血清均使用由感染细胞制备的对照抗原。在来自血清学阳性猪场的243份血清中,ELISA试验和微量血清中和试验分别有175份(72%)和147份(60%)呈阳性。若未对每份血清使用对照抗原,将会导致14份血清(6%)记录结果不同。来自实验感染和现场感染血清的结果表明,ELISA试验比微量血清中和试验能更快地检测到血清转化。除了更高的灵敏度外,ELISA试验相对于血清中和试验还有其他优点。ELISA是一种快速、廉价的检测方法,不依赖于细胞培养物的持续供应,并且易于自动化。

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