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一种缺陷型马立克氏病病毒的细胞培养扩增

Cell culture amplification of a defective Marek's disease virus.

作者信息

Carter J K, Silva R F

机构信息

U.S. Department of Agriculture, Regional Poultry Research Laboratory, East Lansing, MI 48823.

出版信息

Virus Genes. 1990 Sep;4(3):225-37. doi: 10.1007/BF00265632.

Abstract

A highly amplified 4-kb EcoRI fragment was present in DNA isolated from high cell culture passaged stocks (greater than 93 passages) of 281MI/1, a serotype 2 Marek's disease virus (MDV). The isolated 4-kb fragment is amplified in the presence of MDV, replicating as a high molecular weight, head-to-tail concatemer. When the 4-kb fragment was cloned into pUC18 and cotransfected with MDV DNA into chicken embryo fibroblast cells, the plasmid clone also replicated as a high molecular weight concatemer.

摘要

在从281MI/1(一种2型马立克氏病病毒(MDV))的高细胞培养传代毒株(传代次数大于93次)中分离得到的DNA中,存在一个高度扩增的4kb EcoRI片段。分离得到的4kb片段在MDV存在的情况下进行扩增,以高分子量的头对头串联体形式复制。当将该4kb片段克隆到pUC18中,并与MDV DNA共转染到鸡胚成纤维细胞中时,该质粒克隆也以高分子量串联体的形式进行复制。

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