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利用酶联免疫吸附测定法检测植物病毒之间血清学交叉反应的程度。

Use of ELISA for measuring the extent of serological cross-reactivity between plant viruses.

作者信息

Jaegle M, Van Regenmortel M H

出版信息

J Virol Methods. 1985 Jul;11(3):189-98. doi: 10.1016/0166-0934(85)90107-7.

Abstract

The degree of antigenic relatedness between two plant viruses is commonly expressed by a serological differentiation index (SDI) which corresponds to the average number of two-fold dilution steps separating homologous from heterologous precipitin titers. Results obtained with several tobamo- and tombusviruses indicated that the indirect form of the enzyme-linked immunosorbent assay (ELISA) can also be used for calculating SDI values. This was achieved by comparing the antiserum dilutions that lead to the same absorbance measurements (for instance 1.0) when homologous and heterologous viruses are assayed by ELISA. SDI values calculated from ELISA were similar to those obtained from precipitin tests. Because of its greater sensitivity, ELISA is able to quantify weak cross-reactions that are not detectable by precipitin tests.

摘要

两种植物病毒之间的抗原相关性程度通常用血清学区分指数(SDI)表示,该指数对应于将同源沉淀素滴度与异源沉淀素滴度分开的两倍稀释步骤的平均数量。用几种烟草花叶病毒属病毒和番茄丛矮病毒属病毒获得的结果表明,酶联免疫吸附测定(ELISA)的间接形式也可用于计算SDI值。这是通过比较在ELISA检测同源和异源病毒时导致相同吸光度测量值(例如1.0)的抗血清稀释度来实现的。从ELISA计算得到的SDI值与从沉淀素试验获得的值相似。由于其更高的灵敏度,ELISA能够量化沉淀素试验无法检测到的微弱交叉反应。

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