Department of Biological Sciences, Fordham University, Bronx, NY 10458, USA.
Viruses. 2022 May 26;14(6):1150. doi: 10.3390/v14061150.
Human Papillomavirus 16 (HPV16) infects mucosal and epithelial cells and has been identified as a high-risk HPV type that is an etiologic agent of human cancers. The initial infectious process, i.e., the binding of the virus particle and its entry into the host cell, has been studied extensively, although it is not fully understood. There is still a gap in understanding the steps by which the virus is able to cross the plasma membrane after receptor binding. In this study, we demonstrate that after HPV16 comes into contact with a plasma membrane receptor, there are cytoskeletal changes resulting in an increase of filopodia numbers. This increase in filopodia numbers was transient and was maintained during the first two hours after virus addition. Our data show that there is a statistically significant increase in infection when filopodia numbers are increased by the addition of drug and virus simultaneously, and a decrease in virus infection when filopodia formation is inhibited. We describe that HPV16 binding results in the activation of Cdc42 GTPase that in turn results in an increase in filopodia. siRNA directed at Cdc42 GTPase resulted in a statistically significant reduction of infection and a corresponding lack of filopodia induction.
人乳头瘤病毒 16(HPV16)感染黏膜和上皮细胞,被确定为高危 HPV 类型,是人类癌症的病因。病毒颗粒的结合及其进入宿主细胞的初始感染过程已被广泛研究,尽管尚未完全了解。对于病毒在受体结合后能够穿过质膜的步骤,人们仍然存在理解上的差距。在这项研究中,我们证明了 HPV16 与质膜受体接触后,细胞骨架发生变化,导致丝状伪足数量增加。这种丝状伪足数量的增加是短暂的,并在病毒添加后的头两个小时内保持。我们的数据表明,当同时添加药物和病毒以增加丝状伪足数量时,感染率会显著增加,而当抑制丝状伪足形成时,病毒感染会减少。我们描述了 HPV16 结合导致 Cdc42 GTPase 的激活,进而导致丝状伪足的增加。针对 Cdc42 GTPase 的 siRNA 导致感染显著减少和相应的丝状伪足诱导缺乏。