Department of Biosciences and Biomedical Engineering, Indian Institute of Technology Indore, Simrol, Indore, 453552, India.
Institute of Anatomy and Cell Biology, Julius-Maximilians-University Würzburg, Würzburg, 97070, Germany.
Microb Pathog. 2023 Jan;174:105946. doi: 10.1016/j.micpath.2022.105946. Epub 2022 Dec 13.
Viruses utilize clever strategies of interacting with various cellular factors, to remodel an organelle function, for the establishment of successful infection. In recent decades, numerous studies revealed the exploitation of the peroxisomal compartment by viruses. Epstein-Barr virus (EBV) is a ubiquitous virus linked with various cancers and neurological disorders. Till now, there is no report regarding the impacts of EBV infection on peroxisomal compartment. Therefore, we investigate the modulation of peroxisomal proteins in EBV transformed cell lines and during acute EBV infection. EBV positive Burkitt lymphoma cells of different origins as EBV transformed cells along with EBV negative Burkitt lymphoma cells as a control were used in this study. For acute EBV infection experiments, we infected peripheral blood mononuclear cells with EBV for three days. Thereafter, analyzed the gene expression patterns of peroxisomal proteins using qPCR. In addition, quantification of lipid content was performed by using fluorescence microscopy and biochemical assay. Our results revealed that, the peroxisomal proteins were distinctly regulated in EBV transformed cells and during acute EBV infection. Interestingly, PEX19 was significantly upregulated in EBV infected cells. Further, in correlation with the altered expression of peroxisomes proteins involved in lipid metabolism, the EBV transformed cells showed lower lipid abundance. Conversely, the lipid levels were increased during acute EBV infection. Our study highlights the importance of investigating the manipulation of the peroxisomal compartment by putting forward various differentially expressed proteins upon EBV infection. This study provides a base for further investigation to delve deeper into EBV and peroxisomal interactions. The future research in this direction could provide involvement of novel signaling pathways to understand molecular changes during EBV mediated pathologies.
病毒利用巧妙的策略与各种细胞因子相互作用,重塑细胞器功能,从而成功感染。近几十年来,大量研究揭示了病毒对过氧化物酶体 compartment 的利用。Epstein-Barr 病毒(EBV)是一种普遍存在的病毒,与多种癌症和神经紊乱有关。到目前为止,还没有关于 EBV 感染对过氧化物酶体 compartment 的影响的报告。因此,我们研究了 EBV 转化细胞系和急性 EBV 感染过程中过氧化物酶体蛋白的调节。本研究使用了不同来源的 EBV 阳性 Burkitt 淋巴瘤细胞作为 EBV 转化细胞,以及 EBV 阴性 Burkitt 淋巴瘤细胞作为对照。对于急性 EBV 感染实验,我们用 EBV 感染外周血单核细胞 3 天。然后,使用 qPCR 分析过氧化物酶体蛋白的基因表达模式。此外,通过荧光显微镜和生化测定法进行脂质含量的定量。我们的结果表明,过氧化物酶体蛋白在 EBV 转化细胞和急性 EBV 感染过程中明显受到调节。有趣的是,PEX19 在 EBV 感染的细胞中显著上调。此外,与参与脂质代谢的过氧化物酶体蛋白表达的改变相关,EBV 转化细胞显示出较低的脂质丰度。相反,在急性 EBV 感染期间,脂质水平增加。我们的研究强调了研究 EBV 感染时过氧化物酶体 compartment 操纵的重要性,提出了各种差异表达的蛋白质。这项研究为进一步研究 EBV 与过氧化物酶体的相互作用提供了基础。在这一方向的未来研究可以提供新的信号通路的参与,以了解 EBV 介导的病理过程中的分子变化。