Cao Ming-Mei, Li Gang, Ren Hao, Pan Wei, Zhao Ping, Qi Zhong-Tian
Department of Microbiology, Second Military Medical University, Shanghai, China.
Virus Genes. 2009 Dec;39(3):324-9. doi: 10.1007/s11262-009-0405-7. Epub 2009 Oct 3.
The GB virus C/hepatitis G virus (GBV-C/HGV) is a Flaviviridae member that despite its nonpathogenicity, has become of great interest given that it could inhibit the replication of the human immunodeficiency virus (HIV). Therefore, a better knowledge of the viral protein E2 has become our aim. In this study, a GBV-C model cell system (HuhEG) which expressing a fusion protein of the GBV-C E2 protein and enhanced green fluorescent protein (EGFP) stably was established. And the expression of these proteins was silenced effectively by the two E2 gene-specific siRNAs and an EGFP gene-specific siRNA. This inhibition is sequence-specific and extensive (90%). This HuhEG/specific siRNAs system can provide an approach for investigating the association between GBV-C E2 and HIV replication, which may be of potential value in the development of novel prophylactic or therapeutic agents for HIV infection.
GB病毒C/庚型肝炎病毒(GBV-C/HGV)是黄病毒科的一个成员,尽管它无致病性,但鉴于其可能抑制人类免疫缺陷病毒(HIV)的复制,已引起了极大关注。因此,更好地了解病毒蛋白E2成为我们的目标。在本研究中,建立了一种稳定表达GBV-C E2蛋白与增强型绿色荧光蛋白(EGFP)融合蛋白的GBV-C模型细胞系统(HuhEG)。并且,两种E2基因特异性小干扰RNA(siRNA)和一种EGFP基因特异性siRNA可有效沉默这些蛋白的表达。这种抑制具有序列特异性且作用广泛(达90%)。这种HuhEG/特异性siRNA系统可为研究GBV-C E2与HIV复制之间的关联提供一种方法,这在开发针对HIV感染的新型预防或治疗药物方面可能具有潜在价值。