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用聚合酶链反应检测鸡贫血因子DNA序列

Detection of chicken anaemia agent DNA sequences by the polymerase chain reaction.

作者信息

Tham K M, Stanislawek W L

机构信息

Virology Section, Central Animal Health Laboratory, MAFQual, Upper Hutt, New Zealand.

出版信息

Arch Virol. 1992;127(1-4):245-55. doi: 10.1007/BF01309588.

Abstract

A polymerase chain reaction (PCR) assay was developed for detection of chicken anaemia agent (CAA) DNA. The assay used a single set of 20-base primers complementary to sequences located in the coding regions of the CAA replicative form (RF) DNA genome at positions 485 to 504 and 1048 to 1067. The observed amplification product had the expected size of 583 bp and was confirmed to derive from CAA RF DNA by a unique Hind III restriction enzyme cleavage pattern. The amplified fragment was shown to be specific for CAA RF DNA after chemiluminescence dot blot hybridisation with a digoxigenin-labelled 25-base internal probe. The optimised PCR assay was specific for CAA and highly sensitive, being able to detect a single CAA-infected MDCC-MSB1 cell and at least 100 fg of CAA RF DNA. Preliminary results also showed that the PCR assay can detect CAA DNA in clinical specimens from chicks experimentally infected with CAA.

摘要

开发了一种聚合酶链反应(PCR)检测方法,用于检测鸡贫血因子(CAA)DNA。该检测方法使用了一组20个碱基的引物,它们与CAA复制型(RF)DNA基因组编码区中位于485至504位和1048至1067位的序列互补。观察到的扩增产物大小为预期的583 bp,并通过独特的Hind III限制性内切酶切割模式确认为源自CAA RF DNA。在用地高辛标记的25个碱基的内部探针进行化学发光斑点印迹杂交后,扩增片段显示对CAA RF DNA具有特异性。优化后的PCR检测方法对CAA具有特异性且高度灵敏,能够检测单个感染CAA的MDCC - MSB1细胞以及至少100 fg的CAA RF DNA。初步结果还表明,该PCR检测方法可以检测来自实验感染CAA的雏鸡临床标本中的CAA DNA。

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