O. Lungu et al., REACTIVATED AND LATENT VARICELLA-ZOSTER VIRUS IN HUMAN DORSAL-ROOT GANGLIA, Proceedings of the National Academy of Sciences of the United Statesof America, 92(24), 1995, pp. 10980-10984
Ganglia obtained at autopsy were examined by in situ hybridization fro
m one patient with tester (also called herpes tester or shingles), two
varicella-zoster virus (VZV)-seropositive patients without clinical e
vidence of zoster, one VZV-seronegative child, and one fetus. Ganglia
positive for VZV had a hybridization signal in both neuronal and nonne
uronal satellite cells. Ganglia obtained from the fetus and from the s
eronegative infant were consistently negative for VZV. Two striking ob
servations were evident regarding the presence of VZV DNA in ganglia o
btained from the individual with tester at the time of death. First, g
anglia innervating the sites of reactivation and ganglia innervating a
djacent sites yielded strongly positive signals in neurons and satelli
te cells, whereas ganglia from distant sites were rarely positive, Sec
ond, VZV DNA was found in both the nuclei and the cytoplasm of neurons
innervating areas of tester, However, in neurons innervating tester-f
ree areas, VZV DNA was found only in the nucleus of neurons and their
supporting satellite cells, Immunohistochemistry with a fluorescent mo
noclonal antibody to the VZV glycoprotein gpI, a late virus protein, r
evealed a positive signal in the cytoplasm of ganglia with clinical ev
idence of reactivation, These results illustrate that both neuronal an
d satellite cells become latently infected following primary VZV infec
tion, The presence of VZV DNA and gpI in the cytoplasm of neurons demo
nstrates productive infection following reactivation at the site of la
tency.