Grail A, Harbour D A
Department of Veterinary Medicine, University of Bristol, Langford, U.K.
Nihon Juigaku Zasshi. 1990 Oct;52(5):1007-13. doi: 10.1292/jvms1939.52.1007.
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.
从感染了FHV-1标准实验室毒株B927的全猫胚胎细胞以及50株野生型分离株中提取的DNA,用多种限制性内切酶进行消化。将得到的片段在琼脂糖凝胶上分离并进行Southern印迹分析。为了观察这些片段,通过脉冲场凝胶电泳纯化B927 DNA,用α-32P标记并用作杂交探针。使用大多数酶时,大量分离株显示出几个片段迁移率改变,伴有一些模糊的条带异质性。少数分离株呈现出独特的切割模式,特别是使用Bam HI、Cla I和Sac I酶时。这表明存在不同的FHV-1毒株,但病毒基因组的变化只是偶尔发生,因此可能不容易被检测到。