Varicella-zoster virus (VZV) is a human alpha-herpesvirus that causes varic
ella (chickenpox) at primary infection and may reactivate as herpes tester.
VN is a T-lymphotropic virus in vivo. To investigate the T-cell tropism of
VN, we constructed a recombinant virus expressing green fluorescent protei
n (VZV-GFP) under the CMV IE promoter. Coculture of VZV-GFP-infected fibrob
lasts with II-23 cells, a CD4-positive human T-cell hybridoma, resulted in
transfer of virus to II-23 cells. II-23 cells are susceptible to VZV-GFP in
fection as demonstrated by expression of immediate/early (IE62), early (ORF
4), and late (gE) genes. Recovery of infectious virus was limited, with onl
y 1 to 3 in 10(6) calls releasing infectious virus by plaque assay, indicat
ing that transfer of virus results in a limited productive infection. in vi
tro infection of II-23 cells will be useful for further analysis of VN trop
ism for T-lymphocytes. (C) 2000 Academic Press.