Hepatitis E virus (HEV) genome was detected by reverse transcriptase-p
olymerase chain reaction (RT-PCR) in fecal samples of two sporadic cas
es of hepatitis E in Cairo Egypt. Sequence of the complete putative st
ructural region [open reading frame (ORF)-2] and complete region of un
known function (ORF-3) was determined for the two HEV isolates. Phylog
enetic analysis of the nucleotide sequences was performed using neighb
or joining or maximum parsimony methods of tree reconstruction. Direct
correspondence between the HEV evolutionary trees and geographic orig
in of the HEV isolates was observed. Three genotypes of HEV were ident
ified: genotype I (Asia-Africa), genotype II (US), and genotype III (M
exico). Genotype I was further divided into two subgenotypes (Asia and
Africa). In the Asian subgenotype, three smaller genetic clusters wer
e observed (China-like sequences, Burma-like sequences, and sequence f
rom a fulminant case of HEV). The segregation of all these genetic clu
sters was supported by the high level of bootstrap probabilities. Four
regions of the HEV genome were used for phylogenetic analysis. In all
four regions, Egyptian HEV isolates were grouped in a separate Africa
n clade. J. Med. Virol. 57:68-74, 1999. Published 1999 Wiley-Liss, Inc
.