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首页> 外文期刊>Viral immunology >Yellow Fever Virus Modulates the Expression of Key Proteins Related to the microRNA Pathway in the Human Hepatocarcinoma Cell Line HepG2
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Yellow Fever Virus Modulates the Expression of Key Proteins Related to the microRNA Pathway in the Human Hepatocarcinoma Cell Line HepG2

机译:黄热病病毒调节与人肝癌细胞系Hepg2中微小Rna途径相关的关键蛋白的表达

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摘要

Yellow fever is a zoonotic disease caused by the yellow fever virus (YFV) and transmitted by mosquitoes of the family Culicidae. It is well known that cellular and viral microRNAs (miRNAs) are involved in modulation of viral and cellular gene expression, as well as immune response, and are considered by the scientific community as possible targets for an effective therapy against viral infections. This regulation may be involved in different levels of infection and clinical symptomatology. We used viral titration techniques, viral kinetics from 24 to 96 hours postinfection (hpi), and analyzed the expression of key proteins related to the miRNA pathway by quantitative reverse transcriptase polymerase chain reaction (qRT-PCR). The expression of Dicer was different when compared over the course of infection by the distinct YFV genotypes. Drosha expression was similar during infection by YFV genotype 1 or 2, with a decrease in their expression over time and a slight increase in 96 hpi. Ago1, Ago2, and Ago4 showed different levels of expression between the viral genotypes: for YFV genotype 1 infection, Ago1 presented a positive expression, while for YFV genotype 2, it showed a negative expression, when compared with negative controls. We conclude that YFV infection modulates the proteins involved in miRNA biogenesis, which can regulate both viral replication and cellular immune response.
机译:黄热病是由黄热病病毒(YFV)引起的一种动物疾病,并由辛酸蚊子的蚊子传播。众所周知,细胞和病毒微小RNA(miRNA)参与病毒和细胞基因表达的调节,以及免疫应答,并被科学界认为是有效治疗病毒感染的靶标。该调节可能涉及不同水平的感染和临床症状。我们使用病毒滴定技术,病毒动力学从24〜96小时开始(HPI),并通过定量逆转录酶聚合酶链反应(QRT-PCR)分析与miRNA途径相关的关键蛋白的表达。在不同的YFV基因型的感染过程中比较时,Dicer的表达是不同的。在YFV基因型1或2的感染期间,Drosha表达类似,随着时间的推移,表达减少,96 HPI略有增加。前1,前2个,在病毒基因型之间表现出不同程度的表达:对于YFV基因型1感染,以往1呈现阳性表达,而对于YFV基因型2,它显示出与阴性对照相比的阴性表达。我们得出结论,YFV感染调节涉及miRNA生物发生的蛋白质,这可以调节病毒复制和细胞免疫应答。

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