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A novel Epstein-Barr virus-like virus, HVMNE, in a Macaca nemestrina with mycosis fungoides

  1. Author:
    Rivadeneira, E. D.
    Ferrari, M. G.
    Jarrett, R. F.
    Armstrong, A. A.
    Markham, P.
    Birkebak, T.
    Takemoto, S.
    Johnson-Delaney, C.
    Pecon-Slattery, J.
    Clark, E. A.
    Franchini, G.
  2. Author Address

    Franchini G NCI, Sect Anin Models & Retrovirus Vaccines, Basic Res Labs, Div Basic Sci,NIH 41 Lib Dr,Bldg 41,Room D804 Bethesda, MD 20892 USA NCI, Sect Anin Models & Retrovirus Vaccines, Basic Res Labs, Div Basic Sci,NIH Bethesda, MD 20892 USA Univ Glasgow, Dept Vet Pathol Glasgow Lanark Scotland Adv Biotechnol Lab Rockville, MD USA Univ Washington, Dept Comparat Med Seattle, WA 98195 USA Univ Washington, Washington Reg Primate Res Ctr Seattle, WA 98195 USA NCI, Frederick Canc Res & Dev Ctr Frederick, MD USA
    1. Year: 1999
  1. Journal: Blood
    1. 94
    2. 6
    3. Pages: 2090-2101
  2. Type of Article: Article
  1. Abstract:

    Epstein-Barr virus (EBV) infection of humans has been associated with the development of lymphoid malignancies mainly of B-cell lineage, although occasionally T-cell lymphomas have been reported. We describe here the characterization of a novel EBV-like virus (HVMNE) isolated from a simian T-cell lymphotropic virus type I/II (STLV-I/II) seronegative pigtailed macaque (Macaca nemestrina) with a cutaneous T-cell lymphoma. Immunohistochemistry studies on the skin lesions demonstrated that the infiltrating cells were of the CD3(+)/CD8(+) phenotype. Two primary transformed CD8(+); T-cell lines were obtained from cultures of peripheral blood mononuclear cells (PBMC) and skin, and, with time, both cell lines became interleukin-2-independent and acquired the constitutive activation of STAT proteins. Polymerase chain reaction analysis of the DNA from the cell lines and tissues from the lymphomatous animal demonstrated the presence of a 536-bp DNA fragment that was 90% identical to EBV polymerase gene sequences, whereas the same DNA was consistently negative for STLV-I/II sequences. Electron microscopy performed on both cell lines, after sodium butyrate treatment, showed the presence of a herpes-like virus that was designated HVMNE according to the existing nomenclature, In situ hybridization studies using EBV Epstein-Barr viral-encoded RNA probes showed viral RNA expression in both CD8(+) T-cell lines as well as in the infiltrating CD8(+) T cells of skin-tissue biopsies. Phylogenetic analysis of a 465-bp fragment from the polymerase gene of HVMNE placed this virus within the Lymphocryptovirus genus and demonstrated that HVMNE is a distinct virus, clearly related to human EBV and other EBV-like herpesviruses found in nonhuman primates. (C) 1999 by The American Society of Hematology. [References: 58]

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