The seminars take place on the Montpellier Institut Agro/INRAE Campus of La Gaillarde (2, place P. Viala Montpellier)

Thursday march 19 , 2026– 14h – Amphi 206

Stéphane Blanc
stephane.blanc@inrae.fr
UMR PHIM, Univ Montpellier, INRAE, CIRAD, IRD, Institut Agro, Montpellier, France

What we can learn in virology from multipartite viruses

Multipartite viruses, with genomes split across multiple segments each encapsidated in separate particles, deviate sharply from classical viral architectures. In these systems, full genetic information is recovered only at the population level. Theoretical models predict that such viruses—especially those with more than three or four segments—should be nonviable due to high loss risk during transmission. Yet, they comprise ~17% of all known viral species. Using a nanovirus with eight genomic segments, we have experimentally challenged prevailing assumptions in virology. We showed that spatial co-localization of all segments in single host cells is not essential: distinct genes act cooperatively at a supracellular scale. Similarly, segments’ transfer between hosts by aphid vectors does not require co-transmission. They can be separately acquired from different infected plants by one or multiple vectors and reassembled into a complete genome. Furthermore, we uncovered that segment abundance varies with the host plant, suggesting a mutation-free mechanism for tuning gene expression through gene dosing. This flexibility may confer a benefit in fluctuating environments. These findings prompt a broader question: are such collective, flexible strategies unique to multipartite viruses, or do they reveal a more general, overlooked mode of viral organization?

Mots clés: Multipartite viruses, pluricellularity, gene copy number variation, gene network, population genetics

Contact : Alexandre Martinière