Hochstein Norbert, Webb Dennis, Hösel Marianna, Seidel Werner, Auerochs Sabrina, Doerfler Walter
Institute for Virology, Erlangen University Medical School, Schlossgarten 4, D-91054 Erlangen, Germany.
J Virol. 2008 Apr;82(8):4159-63. doi: 10.1128/JVI.02657-07. Epub 2008 Feb 6.
Adenovirus type 12 (Ad12) propagation in hamster BHK21 cells is blocked prior to viral DNA replication. The amounts of Ad12 DNA in the nuclei or cytoplasm of hamster cells are about 2 orders of magnitude (2 h postinfection [p.i.]) and 4 to 5 orders of magnitude (48 h p.i.) lower than in permissive human cells. Cell line BHK21-hCAR is transgenic for and expresses the human coxsackie- and adenovirus receptor (hCAR) gene. Nuclear uptake of Ad12 DNA in BHK21-hCAR cells is markedly increased compared to that in naïve BHK21 cells. Ad12 elicits a cytopathic effect in BHK21-hCAR cells but not in BHK21 cells. Quantitative PCR or [(3)H]thymidine labeling followed by zone velocity sedimentation fails to detect Ad12 DNA replication in BHK21 or BHK21-hCAR cells. Newly assembled Ad12 virions cannot be detected. Thus, the block in Ad12 DNA replication in hamster cells is not released by enhanced nuclear import of Ad12 DNA.
12型腺病毒(Ad12)在仓鼠BHK21细胞中的增殖在病毒DNA复制之前就被阻断。仓鼠细胞细胞核或细胞质中Ad12 DNA的量比允许性人类细胞中的量低约2个数量级(感染后2小时 [p.i.])和4至5个数量级(感染后48小时 [p.i.])。细胞系BHK21-hCAR是转入并表达人柯萨奇病毒和腺病毒受体(hCAR)基因的转基因细胞系。与未处理的BHK21细胞相比,BHK21-hCAR细胞中Ad12 DNA的核摄取显著增加。Ad12在BHK21-hCAR细胞中引发细胞病变效应,但在BHK21细胞中则不会。定量PCR或[³H]胸苷标记后进行区带速度沉降未能检测到BHK21或BHK21-hCAR细胞中的Ad12 DNA复制。无法检测到新组装的Ad12病毒粒子。因此,仓鼠细胞中Ad12 DNA复制的阻断不会因Ad12 DNA核输入增强而解除。