The genome formula of a multipartite virus is regulated both at the individual segment and the segment group levels

PLoS Pathog. 2024 Jan 25;20(1):e1011973. doi: 10.1371/journal.ppat.1011973. eCollection 2024 Jan.

Abstract

Differential accumulation of the distinct genome segments is a common feature of viruses with segmented genomes. The reproducible and specific pattern of genome segment accumulation within the host is referred to as the "genome formula". There is speculation and some experimental support for a functional role of the genome formula by modulating gene expression through copy number variations. However, the mechanisms of genome formula regulation have not yet been identified. In this study, we investigated whether the genome formula of the octopartite nanovirus faba bean necrotic stunt virus (FBNSV) is regulated by processes acting at the individual segment vs. viral population levels. We used a leaf infiltration system to show that the two most accumulated genome segments of the FBNSV possess a greater intrinsic accumulation capacity in Vicia faba tissues than the other segments. Nevertheless, processes acting at the individual segment level are insufficient to generate the genome formula, suggesting the involvement of additional mechanisms acting at the supra-segment level. Indeed, the absence of segments with important functions during systemic infection strongly modifies the relative frequency of the others, indicating that the genome formula is a property of the segment group. Together, these results demonstrate that the FBNSV genome formula is shaped by a complex process acting at both the individual segment and the segment group levels.

MeSH terms

  • DNA Copy Number Variations
  • Genome, Viral
  • Nanovirus* / genetics
  • Plant Diseases
  • Plant Leaves / genetics
  • Vicia faba* / genetics

Grants and funding

This work was funded by Agence Nationale pour la Recherche, ANR Reassort ANR-20-CE02-0016 (YM) and ANR Nanovirus ANR-18-CE92-0028 (SB), as well as by the University of Montpellier MUSE, project MULTIVIR (SB). EP, SB and MB acknowledge support from INRAE dpt. SPE; YM, AB and MB from CNRS, and MB from Univ Montpellier. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.