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建立人肝癌细胞系 Huh-7 中持续性 HCV 基因型 3a 感染的细胞培养模型。

Development of persistent HCV genotype 3a infection cell culture model in huh-7 cell.

机构信息

Applied and Functional Genomics Lab, Centre of Excellence in Molecular Biology, 87-West Canal Bank Road, 53700 Lahore, Pakistan.

出版信息

Virol J. 2012 Jan 10;9:11. doi: 10.1186/1743-422X-9-11.

Abstract

BACKGROUND

Hepatitis C virus (HCV) is one of the major health concerns globally, with genotype 3a as the most prevalent in Pakistan. Lack of efficient HCV genotype 3a small animal models as well as genomic replicons has hampered the complete understanding of its life cycle, pathogenesis and therapeutic options. In this study we aimed to develop a persistent HCV genotype 3a infectious cell culture model.

METHODS

We inoculated Huh-7 cells with HCV genotype 3a serum. Cells and media supernatant were collected at different time periods up to 40th day post infection. Culture media supernatant was also collected to find out its ability to infect naive Huh-7 cells.

RESULTS

HCV replication was confirmed at both RNA and protein level through Real Time RCR and western blot using HCV core as marker. In order to validate the persistence of our model for HCV genotype 3a replication we inhibited the HCV replication through core specific siRNAs. The HCV RNA was detected intracellularly from the day one post infection up till 40th day, while HCV core protein was detected from the second day up to 40th day consistently. In culture media supernatant HCV RNA was also actively detected conferring its ability to infect the naive Huh-7 cells. Furthermore, core specific siRNA showed significant inhibition at 24th hour post transfection both at RNA and protein level with progressive increase in the expression of core gene after 3rd day. It clearly depicts that the Huh-7 successfully retained the HCV replication after degradation of siRNA.

CONCLUSION

Finally, we report that our persistent infection cell culture model consistently replicate HCV genotype 3a for more than 1 month.

摘要

背景

丙型肝炎病毒(HCV)是全球主要的健康关注点之一,基因型 3a 是巴基斯坦最常见的类型。缺乏有效的 HCV 基因型 3a 小动物模型和基因组复制子,阻碍了对其生命周期、发病机制和治疗选择的全面理解。在这项研究中,我们旨在开发一种持续的 HCV 基因型 3a 感染性细胞培养模型。

方法

我们用 HCV 基因型 3a 血清接种 Huh-7 细胞。在感染后不同时间(最长达 40 天)收集细胞和培养基上清液。还收集培养基上清液以确定其感染幼稚 Huh-7 细胞的能力。

结果

通过实时 RCR 和使用 HCV 核心作为标记的 Western blot 在 RNA 和蛋白质水平上均证实了 HCV 的复制。为了验证我们的 HCV 基因型 3a 复制持久性模型,我们通过核心特异性 siRNA 抑制 HCV 复制。从感染后第一天到第 40 天,在细胞内检测到 HCV RNA,而 HCV 核心蛋白从第二天到第 40 天持续检测到。在培养基上清液中,也积极检测到 HCV RNA,证明其具有感染幼稚 Huh-7 细胞的能力。此外,核心特异性 siRNA 在转染后 24 小时在 RNA 和蛋白质水平上均显示出显著的抑制作用,并且在第 3 天后核心基因的表达逐渐增加。这清楚地表明,在 siRNA 降解后,Huh-7 成功地保留了 HCV 的复制。

结论

最后,我们报告说,我们的持续感染细胞培养模型能够持续复制 HCV 基因型 3a 超过 1 个月。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e50/3292816/d234e58f489a/1743-422X-9-11-1.jpg

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