4.8 Article

Cryo-EM study of slow bee paralysis virus at low pH reveals iflavirus genome release mechanism

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1616562114

关键词

electron microscopy; uncoating; honeybee; structure; virus

资金

  1. Ministry of Education, Youth and Sport of the Czech Republic [LM2015043]
  2. project Central European Institute of Technology [LQ1601]
  3. program Projects of Large Infrastructure for Research, Development, and Innovations [LM2010005]
  4. IT4Innovations Centre of Excellence project [CZ.1.05/1.1.00/02.0070, LM2011033]
  5. European Research Council under the European Union [355855]
  6. European Molecular Biology Organization installation Grant [3041]

向作者/读者索取更多资源

Viruses from the family Iflaviridae are insect pathogens. Many of them, including slow bee paralysis virus (SBPV), cause lethal diseases in honeybees and bumblebees, resulting in agricultural losses. Iflaviruses have nonenveloped icosahedral virions containing single-stranded RNA genomes. However, their genome release mechanism is unknown. Here, we show that low pH promotes SBPV genome release, indicating that the virus may use endosomes to enter host cells. We used cryo-EM to study a heterogeneous population of SBPV virions at pH 5.5. We determined the structures of SBPV particles before and after genome release to resolutions of 3.3 and 3.4 angstrom, respectively. The capsids of SBPV virions in low pH are not expanded. Thus, SBPV does not appear to form altered particles with pores in their capsids before genome release, as is the case in many related picornaviruses. The egress of the genome from SBPV virions is associated with a loss of interpentamer contacts mediated by N-terminal arms of VP2 capsid proteins, which result in the expansion of the capsid. Pores that are 7 angstrom an diameter form around icosahedral threefold symmetry axes. We speculate that they serve as channels for the genome release. Our findings provide an atomic-level characterization of the genome release mechanism of iflaviruses.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据