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Replication and gene expression of mutant hepatitis B virus in a transgenic mouse containing the complete viral genome with mutant s gene

机译:包含完整的带有突变S基因的病毒基因组的转基因小鼠中突变乙型肝炎病毒的复制和基因表达

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AIM: To establish the transgenic mouse line harbouring complete hepatitis B virus (HBV) genome with mutant 5 gene (adr subtype). METHODS: Transgenic mice were generated by microinjecting HBV genome into fertilized eggs. Integration, expression, replication of HBV gene and histological changes in transgenic mice were estimated by genomic DNA PCR, serum DNA PCR, Southern blot, ELISA, HE staining, immunohistochemistry and transmission electron microscopy. Transgenic mice with HBsAg positive in serum were bred and analyzed. RESULTS: A total of 288 eggs survived from microinjections were transplanted into the oviducts of 13 pseudopregnant mice and 49 pups were produced. Twenty-six mice were identified to have the integrated HBV gene. Serum HBsAg and HBeAg were detected in 2 of 43 mice. HBsAg and HBcAg in cytoplasm or nuclei of hepatocytes were detected in 10 mice. Founders with HBsAg in serum were named lineages G145R-15 and G145R-18. Of the 16 Fl offsprings generated by G145R-15 founder, 12 were positive for HBV genome with PCR, 10 were positive for HBsAg and HBcAg with immunohistochemistry and 7 were positive for HBsAg and HBeAg with ELISA. Only 1 of 8 Fl offsprings generated by G145R-18 founder was survived and it was detected positive for HBV genome, HBsAg, HBcAg and HBeAg. Both of the two lineages had some pathological characteristics of mild chronic hepatitis B in the liver, such as swelling of hepatocytes and focal hepatocellular necrosis and parenchymal lymphomononuclear cell infiltrate. CONCLUSION: Transgenic mice harbouring HBV with mutant s gene can be generated. The HBV genes are integrated in the transgenic mice genome and can be expressed, replicated, packaged and excreted. HBV DNA can be stably transmitted in the transgenic mice.
机译:目的:建立具有完整的5型突变基因(adr亚型)的乙肝病毒(HBV)基因组的转基因小鼠品系。方法:通过将HBV基因组显微注射到受精卵中产生转基因小鼠。通过基因组DNA PCR,血清DNA PCR,Southern印迹,ELISA,HE染色,免疫组化和透射电镜等方法评估转基因小鼠中HBV基因的整合,表达,复制和组织学变化。繁殖并分析血清中HBsAg阳性的转基因小鼠。结果:共注射288只卵,将其经皮下移植到13只假孕小鼠的输卵管中,产生了49只幼崽。鉴定出26只小鼠具有整合的HBV基因。在43只小鼠中有2只检测到血清HBsAg和HBeAg。在10只小鼠中检测到肝细胞的细胞质或细胞核中的HBsAg和HBcAg。血清中含有HBsAg的创建者被称为谱系G145R-15和G145R-18。由G145R-15创始人产生的16个Fl后代中,PCR检测为HBV基因组阳性12个,免疫组织化学检测为HBsAg和HBcAg阳性10个,ELISA检测为HBsAg和HBeAg阳性的7个。 G145R-18创始人产生的8个Fl后代中只有1个存活下来,并且被检测出对HBV基因组,HBsAg,HBcAg和HBeAg呈阳性。这两个谱系均具有肝中轻度慢性乙型肝炎的某些病理特征,例如肝细胞肿胀和局灶性肝细胞坏死以及实质性淋巴单核细胞浸润。结论:可产生携带突变型s基因的HBV转基因小鼠。 HBV基因整合到转基因小鼠基因组中,可以表达,复制,包装和排泄。 HBV DNA可以在转基因小鼠中稳定地传播。

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