The nucleotide sequence of Hepatitis E virus (HEV) serous isolates (G-9 and
G-20) from Guangzhou, South China, which has been reported previously, are
divergent significantly from those of other reported HEV isolates. in orde
r to investigate more extensively the Guangzhou isolate, the 93G strain was
isolated from the faecal sample of the same individual as G-9 by A549 cell
culture and identified immunologically and by molecular biological techniq
ues. The results showed that strain 93G could be propagated in an A549 cell
line causing cytopathic effects. The viral particles were aggregated by a
specific antibody to HEV Chinese Xinjiang strain (87A) observed using immun
oelectron microscopy and were similar morphologically to HEV from other sou
rces. In this study, an indirect fluorescent antibody assay was first devel
oped to examine HEV antigen in the infected cells, by immunofluorescence in
the cytoplasm and on the surface membrane of the cells. The 58-kDa and 82-
kDa native structural proteins of HEV were also identified in this study by
Western blotting. The 93G genome showed high homology (93%) with G-9 previ
ously reported but was also as divergent from the Burmese, Mexican, Chinese
Xinjiang isolates and the recently reported US-1 isolate, as was G-9. The
data presented indicate that 93G propagated in A549 cells, together with it
s related serum isolate G-9, represents another HEV strain circulating in C
hina and is responsible for some sporadic hepatitis E infections. (C) 2000
Wiley-Liss, Inc.