Reddy P S, Tuboly T, Nagy E, Derbyshire J B
Department of Veterinary Microbiology and Immunology, University of Guelph, Ontario, Canada.
Arch Virol. 1995;140(1):195-200. doi: 10.1007/BF01309735.
The 25R strain of porcine adenovirus type 1 (PAV-1) and the A47 strain of PAV-2 were propagated in ST cells, and DNA was extracted from the infected cells by a modified Hirt method. The DNA of each virus was digested by each of nine restriction endonucleases, and restriction enzyme fragments representing the entire genome were cloned. The genomic size of each virus was approximately 33 kb. Physical maps for the nine restriction endonucleases were constructed from the results of double digestion and Southern blot hybridization experiments, and oriented with respect to the PAV-3 genome. PAV-1 and PAV-2 were found to be related genetically to PAV-3, and there was a closer relationship between PAV-1 and PAV-3 than between PAV-1 and PAV-2 or between PAV-2 and PAV-3.
1型猪腺病毒(PAV - 1)的25R株和2型猪腺病毒的A47株在ST细胞中增殖,并用改良的Hirt方法从感染细胞中提取DNA。每种病毒的DNA用九种限制性内切酶分别进行消化,并克隆代表整个基因组的限制性酶切片段。每种病毒的基因组大小约为33 kb。根据双酶切和Southern印迹杂交实验结果构建了九种限制性内切酶的物理图谱,并相对于PAV - 3基因组进行了定向。发现PAV - 1和PAV - 2在遗传上与PAV - 3相关,并且PAV - 1与PAV - 3之间的关系比PAV - 1与PAV - 2之间或PAV - 2与PAV - 3之间的关系更密切。