Chen Ying-Han, Du WenLi, Hagemeijer Marne C, Takvorian Peter M, Pau Cyrilla, Cali Ann, Brantner Christine A, Stempinski Erin S, Connelly Patricia S, Ma Hsin-Chieh, Jiang Ping, Wimmer Eckard, Altan-Bonnet Grégoire, Altan-Bonnet Nihal
Laboratory of Host-Pathogen Dynamics, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892, USA; Federated Department of Biological Sciences, Rutgers University, Newark, NJ 07102, USA.
Laboratory of Host-Pathogen Dynamics, National Heart Lung and Blood Institute, NIH, Bethesda, MD 20892, USA.
Cell. 2015 Feb 12;160(4):619-630. doi: 10.1016/j.cell.2015.01.032.
A central paradigm within virology is that each viral particle largely behaves as an independent infectious unit. Here, we demonstrate that clusters of enteroviral particles are packaged within phosphatidylserine (PS) lipid-enriched vesicles that are non-lytically released from cells and provide greater infection efficiency than free single viral particles. We show that vesicular PS lipids are co-factors to the relevant enterovirus receptors in mediating subsequent infectivity and transmission, in particular to primary human macrophages. We demonstrate that clustered packaging of viral particles within vesicles enables multiple viral RNA genomes to be collectively transferred into single cells. This study reveals a novel mode of viral transmission, where enteroviral genomes are transmitted from cell-to-cell en bloc in membrane-bound PS vesicles instead of as single independent genomes. This has implications for facilitating genetic cooperativity among viral quasispecies as well as enhancing viral replication.
病毒学的一个核心范式是每个病毒粒子在很大程度上表现为一个独立的感染单位。在此,我们证明肠道病毒粒子簇被包裹在富含磷脂酰丝氨酸(PS)脂质的囊泡中,这些囊泡从细胞中以非裂解方式释放,并且比游离的单个病毒粒子具有更高的感染效率。我们表明,囊泡中的PS脂质是相关肠道病毒受体介导后续感染性和传播的辅助因子,特别是对原代人巨噬细胞而言。我们证明病毒粒子在囊泡中的聚集包装能够使多个病毒RNA基因组集体转移到单个细胞中。这项研究揭示了一种新的病毒传播模式,即肠道病毒基因组以膜结合的PS囊泡形式成块地在细胞间传播,而不是作为单个独立的基因组传播。这对于促进病毒准种之间的遗传协同作用以及增强病毒复制具有重要意义。