Identification and analysis of a new hepadnavirus in white storks

被引:46
作者
Pult, I
Netter, HJ
Bruns, M
Prassolov, A
Sirma, H
Hohenberg, H
Chang, SF
Frölich, K
Krone, O
Kaleta, EF
Will, H
机构
[1] Univ Hamburg, Heinrich Pette Inst Expt Virol & Immunol, D-20251 Hamburg, Germany
[2] Univ Giessen, Inst Geflugelkrankheiten, D-35392 Giessen, Germany
[3] Inst Zoo & Wildtierforsch, D-10252 Berlin, Germany
[4] Ind Technol Res Inst, Ctr Biomed Engn, Hsinchu 310, Taiwan
[5] Royal Childrens Hosp, Sir Albert Sakzewski Virus Res Ctr, Brisbane, Qld 4029, Australia
基金
英国医学研究理事会;
关键词
hepatitis; avian virus; liver tropism; chronic viral infection; HBV; hepadnaviridae; viral epidemiology; hepadnavirus; hepatopathogenesis; hepatocytes;
D O I
10.1006/viro.2001.1115
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We identified, cloned, and functionally characterized a new avian hepadnavinus infecting storks (STHBV). STHBV has the largest DNA genome of all avian hepadnaviruses and, based on sequence and phylogenetic analysis, is most closely related to, but distinct from, heron hepatitis B virus (HHBV). Unique for STHBV among the other avian hepadnaviruses is a potential HNF1 binding site in the pries promoter. In common only with HHBV, STHBV has a myristylation signal on the S and not the preS protein, two C terminally located glycosylation sites on the precore/core proteins and lacks the phosphorylation site essential for the transcriptional transactivation activity of duck-HBV preS protein. The cloned STHBV genomes were competent in gene expression, replication, and viral particle secretion. STHBV infected primary duck hepatocytes very inefficiently suggesting a restricted host range, similar to other hepadnaviruses. This discovery of stork infections unravels novel evolutionary aspects of hepadnaviruses and provides new opportunities for hepadnavirus research. (C) 2001 Academic Press.
引用
收藏
页码:114 / 128
页数:15
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