EPSTEIN–BARR VIRUS
VIROLOGY
Epstein–Barr virus (EBV) is the etiologic agent of
infectious mononucleosis and African Burkitt’s lymphoma. Its complete
nucleotide sequence of 172 kbp is smaller than other herpes viruses but has
been thoroughly mapped. Although EBV is morphologically simi-lar to the other
herpesviruses, it can be cultured easily only in lymphoblastoid cell lines
derived from B lymphocytes of humans and higher primates. In vivo, EBV is
tropic for both human B lymphocytes and epithelial cells. The former is a
nonproductive infection, while the latter is productive. The virus generally
does not produce cytopathic effects or the characteristic intranuclear
inclusions of other herpesvirus infections. After infection with EBV,
lymphoblastoid cells containing viral genome can be cultivated continuously in
vitro; they are thus transformed, or immortalized. Recent studies suggest that
most of the viral DNA in transformed cells remains in a circular, nonintegrated
form as an epi-some, while a lesser amount is integrated into the host cell
genome. Viral antigen ex-pression has been studied by immunofluorescent
staining of transformed cell lines under various conditions. One group of
proteins, called EBV nuclear antigens (EBNAs), ap-pear in the nucleus prior to
virus-directed protein synthesis. Viral capsid antigen (VCA) can be detected in
cell lines that produce mature virions. Other cell lines, called nonpro-ducers,
contain no mature virions, but express certain virus-associated antigens called
early antigens (EAs). The latter may be seen as diffuse (D) and as restricted
(R) aggre-gates of staining.
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