International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi 110067, India.
School of Science and Tropical Medicine & Biology Platform, Monash University, Malaysia, Bandar Sunway, Selangor, DE 47500, Malaysia.
Viruses. 2018 Nov 18;10(11):650. doi: 10.3390/v10110650.
Influenza still remains one of the most challenging diseases, posing a significant threat to public health. Host lipid rafts play a critical role in influenza A virus (IAV) assembly and budding, however, their role in polyvalent IAV host binding and endocytosis had remained elusive until now. In the present study, we observed co-localization of IAV with a lipid raft marker ganglioside, GM1, on the host surface. Further, we isolated the lipid raft micro-domains from IAV infected cells and detected IAV protein in the raft fraction. Finally, raft disruption using Methyl-β-Cyclodextrin revealed significant reduction in IAV host binding, suggesting utilization of host rafts for polyvalent binding on the host cell surface. In addition to this, cyclodextrin mediated inhibition of raft-dependent endocytosis showed significantly reduced IAV internalization. Interestingly, exposure of cells to cyclodextrin two hours post-IAV binding showed no such reduction in IAV entry, indicating use of raft-dependent endocytosis for host entry. In summary, this study demonstrates that host lipid rafts are selected by IAV as a host attachment factors for multivalent binding, and IAV utilizes these micro-domains to exploit raft-dependent endocytosis for host internalization, a virus entry route previously unknown for IAV.
流感仍然是最具挑战性的疾病之一,对公共卫生构成重大威胁。宿主脂筏在甲型流感病毒(IAV)的组装和出芽中起着至关重要的作用,然而,它们在多价 IAV 宿主结合和内吞作用中的作用至今仍未被揭示。在本研究中,我们观察到 IAV 与宿主表面的脂筏标记神经节苷脂 GM1 共定位。此外,我们从感染 IAV 的细胞中分离出脂筏微区,并在筏区检测到 IAV 蛋白。最后,用甲基-β-环糊精破坏筏可以显著减少 IAV 与宿主的结合,表明宿主筏在宿主细胞表面的多价结合中被利用。除此之外,环糊精介导的筏依赖的内吞作用抑制导致 IAV 内化显著减少。有趣的是,细胞在 IAV 结合后两小时暴露于环糊精中,IAV 进入并没有减少,表明 IAV 利用依赖于筏的内吞作用进入宿主。总之,这项研究表明,宿主脂筏被 IAV 选择作为多价结合的宿主附着因子,IAV 利用这些微区利用依赖于筏的内吞作用进行宿主内化,这是以前未知的 IAV 进入宿主的途径。