Cao M, Xiao X, Egbert B, Darragh T M, Yen T S
Department of Pathology, University of California School of Medicine, San Francisco 94143-0506.
J Invest Dermatol. 1989 Mar;92(3):391-2. doi: 10.1111/1523-1747.ep12277232.
A simple and specific method for detecting herpes simplex virus infection in routinely processed paraffin-embedded biopsy specimens is described. DNA is extracted from paraffin blocks, and subjected to DNA amplification with the polymerase chain reaction. After 40 rounds, an amplified band can be detected after agarose gel electrophoresis and ethidium bromide staining. This band is specific for herpes simplex virus, because tissues infected with related viruses do not give this amplified band. We have been able to detect viral DNA in small punch skin biopsies with this procedure, which can take as little as 6 h.
本文描述了一种简单且特异的方法,用于检测常规处理的石蜡包埋活检标本中的单纯疱疹病毒感染。从石蜡块中提取DNA,然后用聚合酶链反应进行DNA扩增。经过40轮循环后,通过琼脂糖凝胶电泳和溴化乙锭染色可检测到一条扩增带。这条带对单纯疱疹病毒具有特异性,因为感染相关病毒的组织不会产生这条扩增带。我们已经能够通过该方法在小的皮肤穿刺活检中检测到病毒DNA,整个过程最短只需6小时。