bioRxivGenomicsPreprint
Chromosomal resolution reveals symbiotic virus colonization of parasitic wasp genomes
Jérémy GauthieriD, Hélène BoulainiD, Joke J.F.A. van VugtiD, Lyam BaudryiD, Emma PersyniD, Jean‐Marc AuryiD, Benjamin NoëliD, Anthony BretaudeauiD, Fabrice LegeaiiD, Sven WarrisiD, Mohamed Amine Chebbi, Géraldine DubreuiliD, Bernard DuviciD, Natacha KremeriD, Philippe GayraliD, Karine MussetiD, Thibaut JosseiD, Diane Bigot, Christophe BressaciD, Sébastien J. M. MoreauiD, Georges Périquet, Myriam Harry, Nicolas MontagnéiD, Isabelle BoulogneiD, Mahnaz Sabeti-AzadiD, , Jean‐Michel DrezeniD
Abstract
Most endogenous viruses, an important proportion of eukaryote genomes, are doomed to slowly decay. Little is known, however, on how they evolve when they confer a benefit to their host. Bracoviruses are essential for the parasitism success of parasitoid wasps, whose genomes they integrated ~103 million years ago. Here we show, from the assembly of a parasitoid wasp genome, for the first time at a chromosomal scale, that symbiotic bracovirus genes spread to and colonized all the chromosomes. Moreover, large viral clusters are stably maintained suggesting strong evolutionary constraints. Genomic comparison with another wasps revealed that this organization was already established ~53 mya. Transcriptomic analyses highlight temporal synchronization of viral gene expression, leading to particle production. Immune genes are not induced, however, indicating the virus is not perceived as foreign by the wasp. This recognition suggests that no conflicts remain between symbiotic partners when benefits to them converge.
- assay: whole-genome sequencing
- research focus: gene regulatory network inference
- research focus: cell-cell communication
- approach: statistical model
- approach: experimental assay
- Citations
- 3
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