Structure of deformed wing virus, a major honey bee pathogen
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28270616
PubMed Central
PMC5373406
DOI
10.1073/pnas.1615695114
PII: 1615695114
Knihovny.cz E-zdroje
- Klíčová slova
- Apis mellifera, colony collapse disorder, honey bee, structure, virus,
- MeSH
- elektronová kryomikroskopie MeSH
- kapsida ultrastruktura MeSH
- konformace proteinů MeSH
- molekulární modely MeSH
- počítačové zpracování obrazu MeSH
- proteinové domény MeSH
- RNA-viry ultrastruktura MeSH
- sekvence aminokyselin MeSH
- včely virologie MeSH
- virion ultrastruktura MeSH
- virové plášťové proteiny chemie ultrastruktura MeSH
- viry hmyzu ultrastruktura MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- virové plášťové proteiny MeSH
The worldwide population of western honey bees (Apis mellifera) is under pressure from habitat loss, environmental stress, and pathogens, particularly viruses that cause lethal epidemics. Deformed wing virus (DWV) from the family Iflaviridae, together with its vector, the mite Varroa destructor, is likely the major threat to the world's honey bees. However, lack of knowledge of the atomic structures of iflaviruses has hindered the development of effective treatments against them. Here, we present the virion structures of DWV determined to a resolution of 3.1 Å using cryo-electron microscopy and 3.8 Å by X-ray crystallography. The C-terminal extension of capsid protein VP3 folds into a globular protruding (P) domain, exposed on the virion surface. The P domain contains an Asp-His-Ser catalytic triad that is, together with five residues that are spatially close, conserved among iflaviruses. These residues may participate in receptor binding or provide the protease, lipase, or esterase activity required for entry of the virus into a host cell. Furthermore, nucleotides of the DWV RNA genome interact with VP3 subunits. The capsid protein residues involved in the RNA binding are conserved among honey bee iflaviruses, suggesting a putative role of the genome in stabilizing the virion or facilitating capsid assembly. Identifying the RNA-binding and putative catalytic sites within the DWV virion structure enables future analyses of how DWV and other iflaviruses infect insect cells and also opens up possibilities for the development of antiviral treatments.
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PDB
5L8Q, 5MV5, 5MUP, 5MV6, 5G52, 5G51