Microbiology Department, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387, Krakow, Poland.
Virogenetics Laboratory of Virology, Malopolska Centre of Biotechnology, Jagiellonian University, Gronostajowa 7a, 30-387, Krakow, Poland.
Sci Rep. 2018 May 8;8(1):7124. doi: 10.1038/s41598-018-25640-0.
The Coronaviridae family clusters a number of large RNA viruses, which share several structural and functional features. However, members of this family recognize different cellular receptors and exploit different entry routes, what affects their species specificity and virulence. The aim of this study was to determine how human coronavirus OC43 enters the susceptible cell. Using confocal microscopy and molecular biology tools we visualized early events during infection. We found that the virus employs caveolin-1 dependent endocytosis for the entry and the scission of virus-containing vesicles from the cell surface is dynamin-dependent. Furthermore, the vesicle internalization process requires actin cytoskeleton rearrangements. With our research we strove to broaden the understanding of the infection process, which in future may be beneficial for the development of a potential therapeutics.
冠状病毒科聚集了许多大型 RNA 病毒,这些病毒具有一些共同的结构和功能特征。然而,该科的成员识别不同的细胞受体并利用不同的进入途径,这影响了它们的物种特异性和毒力。本研究旨在确定人冠状病毒 OC43 如何进入易感细胞。我们使用共聚焦显微镜和分子生物学工具来观察感染过程中的早期事件。我们发现,病毒利用网格蛋白依赖的内吞作用进入细胞,病毒囊泡与细胞膜的分离是依赖于动力蛋白的。此外,囊泡的内化过程需要肌动蛋白细胞骨架的重排。通过我们的研究,我们努力加深对感染过程的理解,这在未来可能有益于开发潜在的治疗方法。