猫疱疹病毒1型分离株DNA的内切酶分析。

A Grail, D A Harbour
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引用次数: 9

摘要

用FHV-1标准实验室菌株、B927和50个野生型分离株感染整个猫胚胎细胞制备的dna用多种限制性内切酶酶切。所得片段在琼脂糖凝胶上分离,并进行Southern印迹。为了使片段可视化,B927 DNA通过脉冲场凝胶电泳纯化,用α 32P标记,并用作杂交探针。在大多数酶的作用下,大量分离物显示出一些片段的迁移性改变,并且有一些模糊的条带异质性。少数分离株具有明显的切割模式,特别是使用Bam HI, Cla I和Sac I酶。这表明存在不同的FHV-1菌株,但病毒基因组的变化只是零星发生,因此可能不易检测到。
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Restriction endonuclease analysis of DNA from isolates of feline herpesvirus type 1.

DNAs prepared from whole feline embryo cells infected with a standard laboratory strain of FHV-1, B927, and 50 wild type isolates were digested with a variety of restriction endonucleases. The resulting fragments were separated on agarose gels and Southern blotting performed. To visualize the fragments, B927 DNA was purified by pulsed field gel electrophoresis, labelled with alpha 32P and used as a hybridization probe. With most enzymes a large number of the isolates displayed altered mobilities of several fragments with some fuzzy band heterogeneity. A few isolates gave distinct cleavage patterns, in particular using the enzymes Bam HI, Cla I and Sac I. It is suggested that different strains of FHV-1 exist but that changes in the viral genome occur only sporadically and thus may not be readily detected.

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