Salvato in:
Dettagli Bibliografici
Autori principali: Gebhard, L Johanna, Tomaru, Yuji, Okamoto, Kenta, Munke, Anna
Natura: Artículo científico
Lingua:en
Pubblicazione: Virology journal 2025
Soggetti:
Accesso online:https://pubmed.ncbi.nlm.nih.gov/41327231/
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!
_version_ 1868266117074518017
author Gebhard, L Johanna
Tomaru, Yuji
Okamoto, Kenta
Munke, Anna
author_facet Gebhard, L Johanna
Tomaru, Yuji
Okamoto, Kenta
Munke, Anna
Gebhard, L Johanna
Tomaru, Yuji
Okamoto, Kenta
Munke, Anna
collection PubMed - marine biology
contents Structural diversity and conservation among CRESS-DNA bacilladnaviruses revealed through cryo-EM and computational modelling. Gebhard, L Johanna Tomaru, Yuji Okamoto, Kenta Munke, Anna DNA Viruses Capsid Proteins Cryoelectron Microscopy Models, Molecular Genome, Viral Capsid DNA, Viral Computer Simulation Viruses that infect single-celled algae strongly regulate microalgae growth and community composition through cell lysis, enable nutrient recycling in marine ecosystems, and offer valuable insights into early stages of viral evolution. One major group, the Bacilladnaviridae family of single-stranded DNA viruses, infects diatoms in marine environments. Here, we present the capsid structure of Chaetoceros lorenzianus DNA virus (ClorDNAV, Protobacilladnavirus chaelor) determined at 2.2 Å resolution, thereby expanding the known structural diversity within the Cressdnaviricota phylum. The ClorDNAV capsid protein (CP) contains a conserved jelly-roll fold and a surface-exposed projection domain, with both N- and C-termini oriented toward the capsid interior. A low-resolution reconstruction of the genome revealed a spooled arrangement of the outer DNA layer, similar to that observed in Chaetoceros tenuissimus DNA virus type II (CtenDNAV-II). Structural comparison with CtenDNAV-II revealed five key CP differences: the absence of surface-exposed C-terminal tails in ClorDNAV, the presence of a helical domain, differences in the projection domain conformation, variation in the number of β-strands in the jelly-roll fold, and the lack of ion-attributed densities at subunit interfaces. Together with the genome reconstruction, these findings underscore the importance of experimentally determined structures for understanding viral architecture and evolution. To complement these results, we analyzed AlphaFold3-predicted CPs from all classified Bacilladnaviridae genera. These models confirmed the conservation of the jelly-roll fold across the family while revealing variability in the surface-exposed and terminal regions, likely reflecting host-specific adaptations and genome packaging strategies. Together, the experimental and predicted structures provide a comprehensive view of structural conservation and divergence in Bacilladnaviridae. Furthermore, the results provide additional structural evidence for the evolution of ssDNA Bacilladnaviridae from a noda-like ssRNA virus ancestor and suggest a shared genome organization resembling that of double-stranded viruses.
format Artículo científico
id pubmed_41327231
institution PubMed
language en
publishDate 2025
publisher Virology journal
record_format pubmed
spellingShingle Structural diversity and conservation among CRESS-DNA bacilladnaviruses revealed through cryo-EM and computational modelling.
Gebhard, L Johanna
Tomaru, Yuji
Okamoto, Kenta
Munke, Anna
DNA Viruses
Capsid Proteins
Cryoelectron Microscopy
Models, Molecular
Genome, Viral
Capsid
DNA, Viral
Computer Simulation
Structural diversity and conservation among CRESS-DNA bacilladnaviruses revealed through cryo-EM and computational modelling. Gebhard, L Johanna Tomaru, Yuji Okamoto, Kenta Munke, Anna DNA Viruses Capsid Proteins Cryoelectron Microscopy Models, Molecular Genome, Viral Capsid DNA, Viral Computer Simulation Viruses that infect single-celled algae strongly regulate microalgae growth and community composition through cell lysis, enable nutrient recycling in marine ecosystems, and offer valuable insights into early stages of viral evolution. One major group, the Bacilladnaviridae family of single-stranded DNA viruses, infects diatoms in marine environments. Here, we present the capsid structure of Chaetoceros lorenzianus DNA virus (ClorDNAV, Protobacilladnavirus chaelor) determined at 2.2 Å resolution, thereby expanding the known structural diversity within the Cressdnaviricota phylum. The ClorDNAV capsid protein (CP) contains a conserved jelly-roll fold and a surface-exposed projection domain, with both N- and C-termini oriented toward the capsid interior. A low-resolution reconstruction of the genome revealed a spooled arrangement of the outer DNA layer, similar to that observed in Chaetoceros tenuissimus DNA virus type II (CtenDNAV-II). Structural comparison with CtenDNAV-II revealed five key CP differences: the absence of surface-exposed C-terminal tails in ClorDNAV, the presence of a helical domain, differences in the projection domain conformation, variation in the number of β-strands in the jelly-roll fold, and the lack of ion-attributed densities at subunit interfaces. Together with the genome reconstruction, these findings underscore the importance of experimentally determined structures for understanding viral architecture and evolution. To complement these results, we analyzed AlphaFold3-predicted CPs from all classified Bacilladnaviridae genera. These models confirmed the conservation of the jelly-roll fold across the family while revealing variability in the surface-exposed and terminal regions, likely reflecting host-specific adaptations and genome packaging strategies. Together, the experimental and predicted structures provide a comprehensive view of structural conservation and divergence in Bacilladnaviridae. Furthermore, the results provide additional structural evidence for the evolution of ssDNA Bacilladnaviridae from a noda-like ssRNA virus ancestor and suggest a shared genome organization resembling that of double-stranded viruses.
title Structural diversity and conservation among CRESS-DNA bacilladnaviruses revealed through cryo-EM and computational modelling.
topic DNA Viruses
Capsid Proteins
Cryoelectron Microscopy
Models, Molecular
Genome, Viral
Capsid
DNA, Viral
Computer Simulation
url https://pubmed.ncbi.nlm.nih.gov/41327231/