Pult I, Netter H J, Bruns M, Prassolov A, Sirma H, Hohenberg H, Chang S F, Frölich K, Krone O, Kaleta E F, Will H
Heinrich-Pette-Institut für Experimentelle Virologie und Immunologie an der Universität Hamburg, Martinistrasse 52, 20251 Hamburg, Germany.
Virology. 2001 Oct 10;289(1):114-28. doi: 10.1006/viro.2001.1115.
We identified, cloned, and functionally characterized a new avian hepadnavirus 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 preS 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.
我们鉴定、克隆并对一种感染鹳的新型禽嗜肝DNA病毒(STHBV)进行了功能特性分析。STHBV拥有所有禽嗜肝DNA病毒中最大的DNA基因组,基于序列和系统发育分析,它与鹭乙肝病毒(HHBV)关系最为密切,但又有所不同。在其他禽嗜肝DNA病毒中,STHBV独有的特征是前S启动子中存在一个潜在的肝细胞核因子1(HNF1)结合位点。仅与HHBV相同的是,STHBV在S蛋白而非前S蛋白上有一个肉豆蔻酰化信号,在前核心/核心蛋白上有两个位于C末端的糖基化位点,并且缺乏鸭乙肝病毒前S蛋白转录反式激活活性所必需的磷酸化位点。克隆的STHBV基因组具有基因表达、复制和病毒颗粒分泌的能力。STHBV感染原代鸭肝细胞的效率非常低,这表明其宿主范围有限,与其他嗜肝DNA病毒类似。鹳感染的这一发现揭示了嗜肝DNA病毒新的进化方面,并为嗜肝DNA病毒研究提供了新的机会。