The molecular epidemiology and evolution of Epstein-Barr virus: Sequence variation and genetic recombination in the latent membrane protein-1 gene

被引:72
|
作者
Walling, DM [1 ]
Shebib, N
Weaver, SC
Nichols, CM
Flaitz, CM
Webster-Cyriaque, J
机构
[1] Univ Texas, Med Branch, Dept Internal Med,WHO,Collaborating Ctr Trop Dis, Div Infect Dis,Viral Pathogenesis Labs, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77555 USA
[3] Univ Texas, Bering Community Serv Fdn, Dent Clin, Houston, TX USA
[4] Univ Texas, Dept Stomatol, Div Oral Pathol, Houston, TX USA
[5] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Immunol & Microbiol, Dent Branch, Chapel Hill, NC 27599 USA
来源
JOURNAL OF INFECTIOUS DISEASES | 1999年 / 179卷 / 04期
关键词
D O I
10.1086/314672
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The phylogeny and evolution of Epstein-Barr virus (EBV) genetic variation are poorly understood. EBV latent membrane protein-1 (LMP-1) gene sequences are especially heterogeneous and may be useful as a tool for EBV genotype identification. Therefore, LMP-1 sequences obtained directly from EBV-infected human tissues were examined by PCR amplification and cloning. EBV genotypes were defined as "strains" from among 22 identified LMP-1 sequence patterns. Three molecular mechanisms were identified by which genetic diversity arises in the LMP-1 gene: point mutation, sequence deletion or duplication, and homologous recombination, The rate of LMP-1 gene evolution was found to be accelerated by coinfection with multiple EBV strains. The results of this study refine our understanding of LMP-1 sequence variation and enable accurate discrimination between independent EBV infection events and the consequence of intrahost EBV evolution. Thus, this LMP-1 sequence-based approach to EBV molecular epidemiology will facilitate the study of intrahost EBV infection, coinfection, and persistence.
引用
收藏
页码:763 / 774
页数:12
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