Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824, USA.
Department of Microbiology, Federal University of Minas Gerais, Belo Horizonte 31270-901, Brazil.
Cell. 2020 May 28;181(5):1046-1061.e6. doi: 10.1016/j.cell.2020.04.032. Epub 2020 May 8.
Since their discovery, giant viruses have expanded our understanding of the principles of virology. Due to their gargantuan size and complexity, little is known about the life cycles of these viruses. To answer outstanding questions regarding giant virus infection mechanisms, we set out to determine biomolecular conditions that promote giant virus genome release. We generated four infection intermediates in Samba virus (Mimivirus genus, lineage A) as visualized by cryoelectron microscopy (cryo-EM), cryoelectron tomography (cryo-ET), and scanning electron microscopy (SEM). Each of these four intermediates reflects similar morphology to a stage that occurs in vivo. We show that these genome release stages are conserved in other mimiviruses. Finally, we identified proteins that are released from Samba and newly discovered Tupanvirus through differential mass spectrometry. Our work revealed the molecular forces that trigger infection are conserved among disparate giant viruses. This study is also the first to identify specific proteins released during the initial stages of giant virus infection.
自发现以来,巨型病毒扩展了我们对病毒学原理的理解。由于它们巨大的体积和复杂性,人们对这些病毒的生命周期知之甚少。为了回答有关巨型病毒感染机制的悬而未决的问题,我们着手确定促进巨型病毒基因组释放的生物分子条件。我们通过冷冻电镜 (cryo-EM)、冷冻电镜断层扫描 (cryo-ET) 和扫描电子显微镜 (SEM) 可视化生成了桑巴病毒 (Mimivirus 属,A 谱系) 的四个感染中间体。这四个中间体中的每一个都反映了与体内发生的阶段相似的形态。我们表明,这些基因组释放阶段在其他拟病毒中是保守的。最后,我们通过差异质谱法鉴定了从桑巴病毒和新发现的图潘病毒中释放的蛋白质。我们的工作揭示了触发感染的分子力在不同的巨型病毒中是保守的。这项研究也是首次鉴定出在巨型病毒感染初期释放的特定蛋白质。