Walling D M, Raab-Traub N
Division of Infectious Diseases, University of North Carolina, Chapel Hill 27599.
J Virol. 1994 Dec;68(12):7909-17. doi: 10.1128/JVI.68.12.7909-7917.1994.
In laboratory lymphoblastoid cell lines and in natural human infections, Epstein-Barr virus (EBV) strains have been identified by DNA restriction fragment length polymorphisms of the BamHI H fragment. Multiple, heterogeneous BamHI H fragments have been detected in oral hairy leukoplakia (HLP), raising the question of EBV coinfection with multiple strains. To investigate whether the heterogeneous BamHI H fragments represent different EBV strains or recombinant variants of the same strain, EBV DNA from HLP lesions was analyzed to characterize the viral strains and determine the source of possible recombinant variants. Clones of heterogeneous BamHI H fragments from a single HLP lesion were determined to have strain identity on the basis of sequence identity of the EBNA-2 genes. Intrastrain homologous recombination within the IR2 internal repeat region and nonhomologous recombination of other sequences accounted for the heterogeneity of the BamHI H fragments. PCR amplification from additional HLP specimens detected similar recombinant variants. A possible example of site-specific recombination joining the BamHI Y portion of the EBNA-2 gene to sequences within the BamHI S fragment was also detected in multiple HLP specimens. These data indicate that intrastrain recombination during productive replication confounds the use of restriction fragment length polymorphism analysis of the BamHI Y and H fragments to identify EBV strains in HLP. In patients with permissive epithelial EBV infections, EBV strains could be more accurately distinguished by sequence identity or divergence within known regions of genetic strain variation.
在实验室淋巴母细胞系和自然人类感染中,通过BamHI H片段的DNA限制性片段长度多态性已鉴定出爱泼斯坦-巴尔病毒(EBV)毒株。在口腔毛状白斑(HLP)中检测到多个异质性的BamHI H片段,这就提出了EBV是否与多种毒株共感染的问题。为了研究这些异质性的BamHI H片段是代表不同的EBV毒株还是同一毒株的重组变体,对HLP病变中的EBV DNA进行了分析,以鉴定病毒毒株并确定可能的重组变体的来源。根据EBNA-2基因的序列同一性,确定来自单个HLP病变的异质性BamHI H片段的克隆具有毒株同一性。IR2内部重复区域内的株内同源重组以及其他序列的非同源重组导致了BamHI H片段的异质性。从其他HLP标本进行的PCR扩增检测到了类似的重组变体。在多个HLP标本中还检测到一个可能的位点特异性重组例子,即将EBNA-2基因的BamHI Y部分与BamHI S片段内的序列连接起来。这些数据表明,在增殖性复制过程中的株内重组混淆了利用BamHI Y和H片段的限制性片段长度多态性分析来鉴定HLP中EBV毒株的方法。在允许上皮细胞发生EBV感染的患者中,通过已知遗传毒株变异区域内的序列同一性或差异,可以更准确地区分EBV毒株。