在A549细胞培养中敲低FLT4、Nup98和Nup205基因对甲型H1N1流感病毒活性的抑制作用

E. Pashkov, E. Faizuloev, E. Korchevaya, A. Rtishchev, B. Cherepovich, А. V. Sidorov, A. Poddubikov, Е. P. Bystritskaya, Y. Dronina, A. Bykov, O. Svitich, V. Zverev
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引用次数: 2

摘要

目标。目的探讨细胞基因FLT4、Nup98和Nup205对甲型流感病毒在人肺癌细胞株A549中繁殖的影响。这项工作是利用梅奇尼科夫疫苗和血清研究所(俄罗斯)集体使用中心的设备进行的。从转染和感染时刻起3天内收集含病毒液,通过病毒滴定和血凝反应评估病毒繁殖强度。实时逆转录聚合酶链反应(RT-PCR)检测病毒RNA浓度。为了计算组间的统计学差异,采用了非参数Mann-Whitney检验。在以FLT4、Nup98和Nup205基因为靶点的小干扰RNA (sirna)处理的细胞中,在感染的多重性(MOI) = 0.1时,它们的表达和病毒繁殖指标(病毒滴度、血凝活性、病毒RNA浓度)显著降低。此外,研究发现,使用siRNA减少靶基因的表达并不会导致细胞存活率的显著降低。与非特异性siRNA处理的细胞相比,用siRNA FLT4.2、Nup98.1和Nup205处理的细胞在第一天的病毒滴度平均降低了1.0 lg,在第二和第三天,降低了2.2-2.3 lg。在实时RT-PCR中,siRNA Nup98.1(最多190倍)和Nup205(最多30倍)在第一天、第二天和第三天分别显著降低了病毒RNA浓度26倍和29倍、6倍和30倍。对于FLT4.2 siRNA,病毒RNA拷贝数在第1天、第2天和第3天分别减少了23倍、18倍和16倍。在测定病毒的血凝活性时也得到了类似的结果。siRNA Nup205和FLT4.2处理的细胞在第3天的血凝活性下降最为明显(16次)。在siRNA FLT4.1、Nup98.1和Nup98.2处理的细胞中,血凝活性降低了8倍。本研究鉴定了三个细胞基因(FLT4、Nup98和Nup205),它们的表达降低可有效抑制病毒繁殖,并获得了原始siRNA序列。所获得的结果对于开发基于RNA干扰机制的治疗性和预防性药物具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Knockdown of FLT4, Nup98, and Nup205 cellular genes as a suppressor for the viral activity of Influenza A/WSN/33 (H1N1) in A549 cell culture
Objectives. To evaluate the effect of cellular genes FLT4, Nup98, and Nup205 on the reproduction of the influenza A virus in A549 human lung cancer cell line.Methods. The work was carried out using the equipment of the center for collective use of the I.I. Mechnikov Research Institute of Vaccines and Sera (Russia). The virus-containing fluid was collected within three days from the moment of transfection and infection and the intensity of viral reproduction was assessed by viral titration and hemagglutination reaction. The viral RNA concentration was determined by real-time reverse-transcription polymerase chain reaction (RT-PCR). To calculate statistically significant differences between groups, the nonparametric Mann–Whitney test was used.Results. In cells treated with small interfering RNAs (siRNAs) targeted at FLT4, Nup98, and Nup205 genes, a significant decrease in their expression and indicators of viral reproduction (virus titer, hemagglutinating activity, viral RNA concentration) was observed at a multiplicity of infection (MOI) = 0.1. Additionally, it was found that a decrease in the expression of target genes using siRNA does not lead to a significant decrease in cell survival. The viral titer in cells treated with siRNA FLT4.2, Nup98.1, and Nup205 on the first day was lower by an average of 1.0 lg, and on the second and third days, by 2.2–2.3 lg, compared to cells treated with nonspecific siRNA. During real-time RT-PCR, a significant decrease in the concentration of viral RNA was observed with siRNA Nup98.1 (up to 190 times) and Nup205 (up to 30 times) on the first day, 26 and 29 times on the second day, and 6 and 30 times on the third day, respectively. For FLT4.2 siRNA, the number of viral RNA copies decreased by 23, 18, and 16 times on the first, second, and third days. Similar results were obtained when determining the hemagglutinating activity of the virus. The hemagglutinating activity on the third day most strongly decreased in cells treated with siRNA Nup205 and FLT4.2 (16 times). In cells treated with siRNA FLT4.1, Nup98.1, and Nup98.2, hemagglutinating activity decreased by 8 times.Conclusions. In the present study, three cellular genes (FLT4, Nup98, and Nup205) were identified—the decrease in the expression of which effectively suppresses viral reproduction— and the original siRNA sequences were obtained. The results obtained are important for creating therapeutic and prophylactic medication, whose action is based on the RNA interference mechanism.
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