Kaito Masahiko, Ohba Hiroyoshi, Chiba Joe, Kohara Michinori, Tanaka Hideaki, Fujita Naoki, Gabazza Esteban Cesar, Watanabe Shozo, Konishi Masayoshi, Adachi Yukihiko
Department of Gastroenterology and Hepatology, Division of Clinical Medicine and Biomedical Science, Institute of Medical Science, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie 514-8507, Japan.
Med Mol Morphol. 2006 Sep;39(3):136-45. doi: 10.1007/s00795-006-0330-y.
Cell lines (2.2.15 cells) capable of supporting the replication of hepatitis B virus (HBV) DNA and intact viral particles have been established by HBV DNA transfection into HepG2 cells. The purpose of this study was to determine the ultrastructural morphology of native HBV particles without purification in the culture supernatants and in sera from patients. Electron microscopy (EM) and immunogold EM of the samples were carried out using polyclonal and monoclonal anti-hepatitis B surface antigen antibodies. HBV particles in the purified samples from the culture supernatants by density-gradient centrifugation were examined to compare the morphology with that of unpurified samples. EM and immunogold EM studies demonstrated the presence of Dane particles (41.8 nm in diameter), cobra-shaped (head diameter, 42.4 nm), and horn-shaped (head diameter, 43.5 nm) particles in the culture supernatants and in the sera from two patients. The tail of the cobra-like particles had a diameter of 21.0 nm and a length of 214 nm. The hornlike particles had a long branch 20.1 nm in diameter with a length of 189 nm, and a short branch 21.4 nm in diameter with a length of 112 nm. The ratio of Dane particles and cobra- and horn-shaped particles in the supernatants was 5 : 4 : 1. After ultracentrifugation, the cobra- and horn-shaped particles completely disappeared; there were only Dane particles together with spheres of 22 nm and filaments. In conclusion, this study showed for the first time that the native replicative form of HBV is cobra- and horn-shaped.
通过将乙肝病毒(HBV)DNA转染到HepG2细胞中,已建立了能够支持HBV DNA复制及完整病毒颗粒的细胞系(2.2.15细胞)。本研究的目的是确定未经纯化的培养上清液和患者血清中天然HBV颗粒的超微结构形态。使用多克隆和单克隆抗乙肝表面抗原抗体对样本进行电子显微镜(EM)和免疫金EM检测。对通过密度梯度离心从培养上清液中获得的纯化样本中的HBV颗粒进行检测,以将其形态与未纯化样本的形态进行比较。EM和免疫金EM研究表明,在培养上清液和两名患者的血清中存在大球形颗粒(直径41.8 nm)、眼镜蛇形(头部直径42.4 nm)和角形(头部直径43.5 nm)颗粒。眼镜蛇样颗粒的尾部直径为21.0 nm,长度为214 nm。角形颗粒有一个直径20.1 nm、长度189 nm的长分支,以及一个直径21.4 nm、长度112 nm的短分支。上清液中大球形颗粒与眼镜蛇形和角形颗粒的比例为5:4:1。超速离心后,眼镜蛇形和角形颗粒完全消失;仅存在大球形颗粒以及22 nm的球形颗粒和丝状颗粒。总之,本研究首次表明HBV的天然复制形式为眼镜蛇形和角形。