کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5806729 | 1555922 | 2014 | 7 صفحه PDF | دانلود رایگان |
- Epstein Barr virus glycoproteins mediating B lymphocyte and epithelial cell entry.
- Epstein Barr virus switching of cellular tropism during infection.
- Viral glycoprotein interaction to promote virus-cell fusion.
- Physiological significance in the infected host.
Epstein Barr virus (EBV) is a highly prevalent human gamma 1 lymphocryptovirus which infects both B lymphocytes and epithelial cells. In the healthy host, infection of these different cell lineages broadly reflects the different phases of the virus lifecycle. Memory B cells are the reservoir for latent EBV, in which viral gene expression is highly restricted to maintain an asymptomatic lifelong infection. In contrast, epithelial cells may be a major site of the virus lytic cycle, where infectious virus is propagated and transmitted via saliva to uninfected hosts. To achieve this dual tropism, EBV has evolved a unique set of glycoproteins in addition to a highly conserved set, which interact with cell lineage-specific receptors and switch cellular tropism during infection.
Journal: Current Opinion in Virology - Volume 4, February 2014, Pages 78-84