e 2024

Cryo-electron microscopy analysis of virus replication in vivo

HOMOLA, Miroslav

Basic information

Original name

Cryo-electron microscopy analysis of virus replication in vivo

Name in Czech

Kryo-elektronová analýza virového replikačního cyklu in vivo

Authors

HOMOLA, Miroslav

Edition

171 pp. 2024

Other information

Language

English

Type of outcome

Survey and educational texts

Country of publisher

Czech Republic

Confidentiality degree

is not subject to a state or trade secret

References:

Organization

Středoevropský technologický institut – Repository – Repository

Keywords in English

Cryo-electron microscopy; Cryo-electron tomography; Subtomogram averaging; Emiliania huxleyi; Emiliania huxleyi virus 201; Virion structure; Viral life cycle.

Links

LX22NPO5103, research and development project.
Changed: 6/12/2024 00:50, RNDr. Daniel Jakubík

Abstract

V originále

The globally distributed marine alga Emiliania huxleyi produces reflective calcite disks (coccoliths) that increase the albedo of ocean water and thus reduce the heat absorption in the ocean, which cools the Earth’s climate. The population density of E. huxleyi is restricted by Nucleocytoviricota viruses, including E. huxleyi virus 201 (EhV-201). Despite the impact of E. huxleyi viruses on the climate, there is limited information about their structure and replication. Here we show that the dsDNA genome inside the EhV-201 virion is protected by an inner membrane, capsid, and outer membrane decorated with numerous transmembrane proteins. The virions are prone to deformation, and parts of their capsids deviate from the icosahedral arrangement. EhV-201 virions infect E. huxleyi by using their fivefold vertex to bind to a host cell and fuse the virus inner membrane with the plasma membrane. Whereas the replication of EhV-201 probably occurs in the nucleus, virions assemble in the cytoplasm at the surface of endoplasmic reticulum-derived membrane segments. Genome packaging initiates synchronously with the capsid assembly and completes through an aperture in the forming capsid. Upon the completion of genome packaging, the capsids change conformation, which enables them to acquire an outer membrane by budding into intracellular vesicles. EhV-201 infection induces a loss of surface protective layers from E. huxleyi cells, which allows the continuous release of virions by exocytosis. Our results provide insight into how EhVs bypass the surface protective layers of E. huxleyi and exploit the organelles of an infected cell for progeny assembly

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