Çağlayan Elif, Turan Kadir
University of Health Sciences Türkiye, Kartal Koşuyolu High Speciality Educational and Research Hospital, Department of Medical Microbiology, İstanbul, Türkiye.
Marmara University, Faculty of Pharmacy, Department of Basic Pharmaceutical Sciences, İstanbul, Türkiye.
Turk J Pharm Sci. 2022 Oct 31;19(5):552-559. doi: 10.4274/tjps.galenos.2021.25664.
Interferons (IFNs) are one of the most important components of innate immunity against viruses, especially those carrying the RNA genomes such as influenza viruses. Upon viral infection, the IFNs are rapidly secreted, inducing the expression of several genes in the target cells and establishing an antiviral state. In this study, the effects of proteins encoded by some IFN-related genes on influenza A virus RNA-dependent RNA polymerase enzyme were investigated. We evaluated the importance of these proteins in the pathogenesis of different influenza A virus types.
The IFN-related genes were amplified by polymerase chain reaction from the HEK293 cDNA library and cloned into pCHA expression vector. The expression of genes and subcellular localizations of the proteins were determined by Western blotting and immunofluorescence staining, respectively. The effects of IFNs-related proteins on virus RdRP enzyme were determined by influenza A virus mini-replicons.
The study revealed that the influenza A virus infections significantly altered the transcript level of the IFN-related , and genes in HEK293 cells. It was determined that the alteration of the gene expression was also related to the virus type. The mini-replicon assays showed that the transient expression of , and have inhibitory effects on WSN and/or DkPen type virus RdRP enzymes. We observed that the proteins except OAS1 inhibited WSN type RdRP enzyme at a higher level than that of DkPen enzyme.
It was concluded that influenza A virus infection significantly alters the IFN-related gene expression in the cells. Most of the proteins encoded from these genes showed an inhibitory effect on the virus RdRP enzymes in the HEK293 cells. The inhibition of the influenza virus RdRP with IFN-related proteins may be the result of direct or indirect interactions between the host proteins and the viral enzyme subunits.
干扰素(IFN)是针对病毒的固有免疫最重要的组成部分之一,尤其是针对那些携带RNA基因组的病毒,如流感病毒。病毒感染后,干扰素会迅速分泌,诱导靶细胞中多个基因的表达,并建立抗病毒状态。在本研究中,研究了一些干扰素相关基因编码的蛋白质对甲型流感病毒RNA依赖性RNA聚合酶的影响。我们评估了这些蛋白质在不同甲型流感病毒类型发病机制中的重要性。
通过聚合酶链反应从HEK293 cDNA文库中扩增干扰素相关基因,并克隆到pCHA表达载体中。分别通过蛋白质印迹法和免疫荧光染色法测定基因的表达和蛋白质的亚细胞定位。通过甲型流感病毒微型复制子测定干扰素相关蛋白质对病毒RdRP酶的影响。
研究表明,甲型流感病毒感染显著改变了HEK293细胞中干扰素相关基因、和的转录水平。确定基因表达的改变也与病毒类型有关。微型复制子试验表明,、和的瞬时表达对WSN和/或DkPen型病毒RdRP酶有抑制作用。我们观察到,除OAS1外,这些蛋白质对WSN型RdRP酶的抑制水平高于DkPen酶。
得出结论,甲型流感病毒感染显著改变细胞中干扰素相关基因的表达。这些基因编码的大多数蛋白质对HEK293细胞中的病毒RdRP酶有抑制作用。干扰素相关蛋白质对流感病毒RdRP的抑制作用可能是宿主蛋白质与病毒酶亚基之间直接或间接相互作用的结果。