EventsViruses 2026 – New Horizons in Virology
Published
This submission belongs to the session S4. Structure and Mechanisms of Virus Replication of the event Viruses 2026 – New Horizons in Virology
Published date
09 Mar, 2026
Academic Editor
author-avatarEric Freed
Citation
Anne-Laure Favier, Marcel Zimmeck, Emmanuelle Quemin, Maria Girleanu, Olivier Le Bihan, Xavier Holy, Gaelle Frenois.Veyrat, Frédéric Iseni, Pierre Legrand, Jean-Nicolas Tournier, Exploring the native poxvirus structure in BioSafety level 3, in Proceedings of Viruses 2026 – New Horizons in Virology, Barcelona, 11 March–13 March 2026, MDPI: Basel, Switzerland
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Exploring the native poxvirus structure in BioSafety level 3

Maria Girleanu 1
Olivier Le Bihan 1
Xavier Holy 1
Frédéric Iseni 3
Emmanuelle Quemin 2
1. Unité d’Imagerie, Institut de Recherche Biomédicale des Armées (IRBA), Brétigny-sur-Orge, France, France
2. Department of Virology, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France, France
3. Centre national de référence LE des Orthopoxvirus, IRBA, Brétigny-sur-Orge, France, France
4. Centre national de référence LE des Orthopoxvirus, IRBA, Brétigny-sur-Orge, France,, France
5. Synchrotron SOLEIL, HelioBio group, Saint-Aubin, France, France
Abstract

Poxviruses represent a large family of dsDNA viruses that can pose a significant threat to public health due to their ability to infect a broad range of hosts and spread in human populations. Vaccinia virus (VACV) has become a model to study poxvirus biology and pathogenicity. However, the diversity of this viral family remains overlooked and knowledge about other members is critically lacking. We decided to study the intricate structural details of three poxviruses using state-of-the-art cryo-electron tomography (cryoET) and advanced subvolume averaging processing. At IRBA, we developed a dedicated sample preparation workflow to be able to analyze native poxvirus samples of purified infectious particles in biological safety level 3 environment. By elucidating virion structures at high resolution and in the native environment, we aim at increasing our understanding of poxvirus diversity at the structural level to improve our preparedness and provide new targets for the future development of antiviral strategies.

Keywords
poxvirus
VACV
electron microscopy
BSL3
cryoEM
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