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Levels of Epstein-Barr Virus DNA in Lymphoblastoid Cell Lines Are Correlated with Frequencies of Spontaneous Lytic Growth but Not with Levels of Expression of EBNA-1, EBNA-2, or Latent Membrane Protein

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Journal J Virol
Date 1990 Jan 1
PMID 2152830
Citations 12
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Abstract

The process of Epstein-Barr virus (EBV)-induced transformation of human B lymphocytes results in a cell line that is a mixture of latently and lytically infected cells, with the lytic cells composing roughly 5% to less than 0.0001% of the overall population. A set of nine normal lymphoblastoid cell lines that span a 100- to 200-fold range in average EBV DNA content were studied, and the frequency with which these cells entered a lytic phase of viral growth correlated with their EBV DNA copy number (as a population average). However, neither factor correlated with the levels of expression of transcript for the viral genes EBNA-1, EBNA-2, and latent membrane protein, nor did they correlate with the levels of EBNA-2 protein and latent membrane protein. The rate at which a cell line enters into lytic growth spontaneously is therefore not dependent on the overall steady-state levels of expression of these latent-phase genes.

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References
1.
Austin P, Flemington E, Yandava C, Strominger J, Speck S . Complex transcription of the Epstein-Barr virus BamHI fragment H rightward open reading frame 1 (BHRF1) in latently and lytically infected B lymphocytes. Proc Natl Acad Sci U S A. 1988; 85(11):3678-82. PMC: 280281. DOI: 10.1073/pnas.85.11.3678. View

2.
Wang D, Liebowitz D, Wang F, Gregory C, Rickinson A, Larson R . Epstein-Barr virus latent infection membrane protein alters the human B-lymphocyte phenotype: deletion of the amino terminus abolishes activity. J Virol. 1988; 62(11):4173-84. PMC: 253849. DOI: 10.1128/JVI.62.11.4173-4184.1988. View

3.
Hammerschmidt W, Sugden B . Identification and characterization of oriLyt, a lytic origin of DNA replication of Epstein-Barr virus. Cell. 1988; 55(3):427-33. DOI: 10.1016/0092-8674(88)90028-1. View

4.
Knoll B . Isolation and characterization of mutations in the cIII gene of bacteriophage lambda which increase the efficiency of lysogenization of Escherichia coli K-12. Virology. 1979; 92(2):518-31. DOI: 10.1016/0042-6822(79)90154-5. View

5.
Wilson G, Miller G . Recovery of Epstein-Barr virus from nonproducer neonatal human lymphoid cell transformants. Virology. 1979; 95(2):351-8. DOI: 10.1016/0042-6822(79)90490-2. View