Based on computer analysis of hydrophobicity and prediction of seconda
ry structures for the full-length putative proteins encoded by open re
ading frame-1 (ORF-1), ORF-2 and ORF-3 of hepatitis E virus (HEV), we
selected antigenic regions with hydrophilicity, beta-turn, and beta-sh
eet, and synthesized 7 peptides of possible epitope-containing regions
of the polypeptide encoded by all 3 ORFs of HEV genomic RNA by Merrif
ield's method of solid-phase synthesis. The synthetic peptides were sc
reened and identified by solid-phase enzyme-linked immunosorbent assay
(ELISA). Three of the peptides (EH(174) from ORF-1, EH(286) from ORF-
2 and EH(362) from ORF-3) showed antigenic activity and possible appli
cation for the development of anti-HEV test kits (the peptide-based EL
ISA). The laboratory experiments and clinical trials showed that the k
its, using a set of 3 synthetic HEV peptides as coating antigens, were
of high specificity and exhibited good reproducibility. The small-sca
le seroepidemiological survey indicated high seroprevalence (14.3%) of
anti-HEV in Tibetan populations. Additionally, the results also demon
strated good agreement with clinical findings, suggesting that the tes
t kits will be of major use for immunodiagnosis and seroepidemiologica
l surveys of HEV infection.