Sugiyama Masaya, Tanaka Yasuhito, Sakamoto Tomoyuki, Maruyama Isao, Shimada Takashi, Takahashi Satoru, Shirai Tomoyuki, Kato Hideaki, Nagao Masataka, Miyakawa Yuzo, Mizokami Masashi
Department of Clinical Molecular Informative Medicine, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Hepatology. 2007 Apr;45(4):929-37. doi: 10.1002/hep.21584.
Of the 8 genotypes of HBV (genotypes A-H), genotype G is unique in that it has an insertion in the core gene and two stop codons in the precore region preventing the synthesis of hepatitis B e antigen. Most individuals with genotype G are coinfected with other genotypes, typically genotype A. Mice with severe combined immunodeficiency disease carrying human hepatocytes were infected with HBV particles propagated in Huh7 cells in culture. Mice monoinfected with genotype G did not raise detectable HBV DNA in serum, although products of the core gene emerged 4 to 8 weeks after inoculation. When they were superinfected with genotype A at week 10, however, HBV DNA of genotype A developed, which was replaced almost completely by that of genotype G within 10 weeks. Such a rapid takeover was also observed in mice initially infected with genotype A or C and superinfected with genotype G. Similar viral dynamics occurred in mice simultaneously coinfected with genotypes G and A. Takeover was markedly enhanced in mice inoculated with a serum passage containing genotype G with a trace of genotype A. Coinfection of mice with genotypes G and A induced abundant cellular steatosis along with increased fibrosis in the liver, which was not detected in mice monoinfected with genotype A or G.
Genotype G can monoinfect chimeric mice at very low levels, and its replication increases maredly when coinfected with other genotypes. Coinfection with genotype G could enhance fibrosis under immunocompromised states.
在乙肝病毒的8种基因型(A - H型)中,G型独具特点,其核心基因有一个插入片段,前核心区有两个终止密码子,可阻止乙肝e抗原的合成。大多数G型基因型感染者同时感染了其他基因型,通常为A型。将携带人类肝细胞的重症联合免疫缺陷病小鼠,感染在培养的Huh7细胞中增殖的乙肝病毒颗粒。单纯感染G型的小鼠血清中未检测到可检测水平的乙肝病毒DNA,尽管接种后4至8周出现了核心基因产物。然而,在第10周用A型超感染这些小鼠时,A型乙肝病毒DNA出现了,并在10周内几乎完全被G型取代。在最初感染A型或C型并被G型超感染的小鼠中也观察到了这种快速取代现象。在同时感染G型和A型的小鼠中也出现了类似的病毒动态变化。在用含有微量A型的G型血清传代接种的小鼠中,这种取代现象明显增强。G型和A型同时感染小鼠会导致肝脏中大量细胞脂肪变性以及纤维化增加,而在单纯感染A型或G型的小鼠中未检测到这种情况。
G型基因型可在极低水平下单纯感染嵌合小鼠,与其他基因型同时感染时其复制会显著增加。在免疫受损状态下,与G型同时感染会加重纤维化。