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PMID: 10745228 Published · ppublish English Comparative Study Journal Article

Properties of hepatitis B virus genome recovered from Vietnamese patients with fulminant hepatitis in comparison with those of acute hepatitis.

Journal of medical virology ·Vol. 61 ·No. 1 ·2000-05-00 ·Pages 23-8

Yuasa R, Takahashi K, Dien BV, Binh NH, Morishita T, Sato K, Yamamoto N, Isomura S, Yoshioka K, Ishikawa T, Mishiro S, Kakumu S

Abstract

Among the many mutations found in the hepatitis B virus (HBV) genome, some have been associated with fulminant hepatitis, as exemplified by precore-defective mutations. The aim of this study was to determine whether such mutations also are found in Vietnamese cases of fulminant hepatitis B. The full-genome nucleotide sequence of HBV in three patients with fulminant hepatitis (F-2, F-3, and F-6) and one with acute hepatitis (A-3), who were admitted to Cho Ray Hospital, Ho Chi Minh City, Vietnam was ascertained. Additionally, two patients with fulminant hepatitis (F-1 and F-7) and three with acute hepatitis (A-1, A-2, and A-5) were examined only for the precore/core region of HBV. Remarkably, the nonsense mutation at precore codon 28 (Trp82Stop) was found in four of the five patients with fulminant hepatitis, while all the acute hepatitis patients harbored wild type (one had a mixture of wild and mutant types). The missense mutations within the core region, Ile97Leu and Pro130Ile/Thr/Ser, were also remarkable in fulminant hepatitis. Only F-2 was free from these precore/core mutations, but F-2 was unique in that it possessed a chimeric genotype: it could be classified into genotype C as a whole, but its X region was of genotype B, like the other four fulminant hepatitis isolates (F-1, F-3, F-6, and F-7). The codon 41 of the X protein was Pro in all three fulminant hepatitis cases examined for this region, while it was Ser in the wild-type isolates of genotype B. Of note as negative data, the mutations C1653T and T1753M of the enhancer II (Enh II) and A1762T and G1764A of the precore/core promoter regions, once reported to be relevant to severe or fulminant hepatitis, were not found in the present cases. The results with the Vietnamese cases of fulminant hepatitis corroborated results of previous studies with respect to the mutations Trp28Stop of precore and Ile97Leu and Pro130Ile/Thr/Ser of core, but not for the mutations within Enh II and precore/core promoter region. Whether the Ser41Pro mutation in the X region of genotype B HBV is Vietnam-specific or disease-specific deserves further investigation.

MeSH Terms
Adult Amino Acid Sequence Female Genome, Viral Hepatitis B/pathology,virology Hepatitis B virus/genetics,isolation & purification Humans Male Molecular Sequence Data Phylogeny Promoter Regions, Genetic Sequence Analysis, DNA Sequence Homology, Amino Acid Vietnam Viral Core Proteins/genetics
Chemicals
Viral Core Proteins
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Yuasa R
First Department of Internal Medicine, Research Center for Infectious Disease, Aichi Medical University, Aichi, Japan.
Takahashi K
Dien B V
Binh N H
Morishita T
Sato K
Yamamoto N
Isomura S
Yoshioka K
Ishikawa T
Mishiro S
Kakumu S
Article Info
Journal
Journal of medical virology
Abbr.
J Med Virol
ISSN
0146-6615
Published
2000-05-00
Pages
23-8
Language
English
Region
United States
NLM ID
7705876
Subset
IM
Databases
GENBANK
AB031260, AB031261, AB031262, AB031263, AB031264, AB031265, AB031266, AB031267, AB031268
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