Hamelin C, Jacques C, Lussier G
Centre de Recherche en Virologie, Institut Armand-Frappier, Laval-des-Rapides, Quebec, Canada.
J Clin Microbiol. 1988 Jan;26(1):31-3. doi: 10.1128/jcm.26.1.31-33.1988.
Restriction endonuclease cleavage site analysis was used to differentiate between mouse adenovirus (MAV) types 1 and 2 strains. Viral DNA of suitable purity and quantity for multiple enzymatic digestions was obtained from cloned CMT-93 mouse tumor cells infected with each type of MAV. Clear differences between the MAV-1 (FL) and MAV-2 (K87) genomes were observed after cleavage with restriction enzymes such as BglII, EcoRI, and PaeR7. Fast electrophoresis of DNA fragments in miniature agarose slab gels allowed rapid and unequivocal identification of the MAV strains. This relatively simple and accurate method should be quite useful to determine the different modes of transmission of mouse adenoviruses and their presence in various animal populations.
限制性内切酶切割位点分析用于区分小鼠腺病毒(MAV)1型和2型毒株。从感染每种MAV的克隆CMT - 93小鼠肿瘤细胞中获得了纯度和数量适合多次酶切的病毒DNA。在用诸如BglII、EcoRI和PaeR7等限制性酶切割后,观察到MAV - 1(FL)和MAV - 2(K87)基因组之间存在明显差异。在微型琼脂糖平板凝胶中对DNA片段进行快速电泳,可快速且明确地鉴定MAV毒株。这种相对简单且准确的方法对于确定小鼠腺病毒的不同传播模式及其在各种动物群体中的存在情况应该非常有用。