NUCLEOTIDE-SEQUENCE ANALYSIS OF A 30-KILOBASE-PAIR REGION OF HUMAN HERPESVIRUS-6B (HHV-6B) GENOME AND STRAIN-SPECIFIC VARIATIONS IN MAJOR IMMEDIATE-EARLY GENES
H. Kosuge et al., NUCLEOTIDE-SEQUENCE ANALYSIS OF A 30-KILOBASE-PAIR REGION OF HUMAN HERPESVIRUS-6B (HHV-6B) GENOME AND STRAIN-SPECIFIC VARIATIONS IN MAJOR IMMEDIATE-EARLY GENES, Virus research, 52(1), 1997, pp. 1-14
Human herpesvirus 6 (HHV-6) is now classified into two distinct varian
ts such as HHV-6 variant A(HHV-6A) and B(HHV-6B) (Ablashi et al., Arch
. Virol. 129, 1993, 1-4) and the DNA of HHV-6A strain U1102 was comple
tely sequenced (Gompels et al., Virology 209, 1995, 29-51). We have se
quenced a 30-kilobase pair (kbp) (genomic positions around 111-141 kb)
of HHV-6B strain HST, and a sequence of this region was compared with
that of HHV-6A strain U1102. Dodecameric repeats, G/T and Kpn repeat
elements, putative major immediate early 1 (MIE1) and major immediate
early 2 (MIE2) genes were found in this region. The DNA sequences of H
HV-6A (U1102) and HHV-6B (HSI) were markedly different in the MIE1 reg
ion, Kpn repeat elements and the putative MIE2 region. Dodecameric rep
eat element was located in the putative MIE2 locus of HHV-6. When prim
ers covering dodecameric repeat region were used to amplify HHV-6 DNA
of clinical isolates from patients with exanthem subitum (ES) by polym
erase chain reaction (PCR), Variations in size of PCR products in each
isolate were found: indicating strain-specific features. Furthermore,
the results of molecular biological analysis by PCR using DNA samples
in a family suggest that HHV-6 infects within a family. (C) 1997 Else
vier Science B.V.