Sugiyama Masaya, Tanaka Yasuhito, Kurbanov Fuat, Nakayama Nobuaki, Mochida Satoshi, Mizokami Masashi
Department of Clinical Molecular Informative Medicine, Nagoya City University Graduate School of Medical Sciences, Kawasumi, Mizuho, Nagoya 467-8601, Japan.
Virology. 2007 Sep 1;365(2):285-91. doi: 10.1016/j.virol.2007.04.004. Epub 2007 May 10.
Little is known about specific naturally occurring mutations of hepatitis B virus (HBV) and underlying mechanisms of their association with fulminant hepatitis. A HBV clone isolated from a patient with fulminant hepatitis was analyzed, and the features of the particular mutations observed around furin cleavage site in core region (A2339G/G2345A) were assessed using an in vitro replication model. The clone belonged to genotype B with precore stop codon mutation (G1896A). Replication efficiency of 1.24-fold HBV genome in Huh-7 cells was increased in the presence of A2339G. Further in vitro studies using furin inhibitor indicated that the effect of the mutation was probably associated with accumulation of the full-length core protein without cleavage by furin-like protease, suggesting that a processing of the core protein might play an important role in regulation of viral replication. In conclusion, the A2339G mutation was considered as one of the viral factors involved in high replication efficiency.
关于乙型肝炎病毒(HBV)特定的自然发生突变及其与暴发性肝炎关联的潜在机制,人们了解甚少。对从一名暴发性肝炎患者分离出的HBV克隆进行了分析,并使用体外复制模型评估了在核心区域弗林蛋白酶切割位点(A2339G/G2345A)周围观察到的特定突变的特征。该克隆属于伴有前核心终止密码子突变(G1896A)的B基因型。在存在A2339G的情况下,Huh-7细胞中HBV基因组的复制效率提高了1.24倍。使用弗林蛋白酶抑制剂的进一步体外研究表明,该突变的作用可能与全长核心蛋白在未被弗林蛋白酶样蛋白酶切割的情况下积累有关,这表明核心蛋白的加工可能在病毒复制调节中起重要作用。总之,A2339G突变被认为是涉及高复制效率的病毒因素之一。