Phosphate amendment drives bloom of RNA viruses after soil wet-up
Soil rewetting after a dry period results in a surge of activity and succession in both microbial and DNA virus communities. Less is known about the response of RNA viruses to soil rewetting—while they are highly diverse and widely distributed in soil, they remain understudied. We hypothesized that RNA viruses would show temporal succession following rewetting and that phosphate amendment would influence their trajectory, as viral proliferation may cause phosphorus limitation. Using 39 time-resolved metatranscriptomes and amplicon data, 2190 RNA viral populations were identified across five phyla, with 26 % of these predicted to infect bacteria, and 11 % fungi. Only 1.2 % of viral populations had annotated capsid genes, suggesting most persist via intracellular replication without a free virion phase. Phosphate amendment altered RNA viral community composition within the first week and amended vs. unamended communities remained distinguishable for up to three weeks. While the overall host community remained stable, certain bacterial populations showed reduced abundance in phosphate-amended soils, likely due to increased viral lysis, as RNA bacteriophages proliferated significantly. Notably, 60 % of the viruses with increased abundance under phosphate amendment belonged to basal Lenarviricota clades rather than well-known groups like Leviviricetes . We estimate RNA bacteriophage infections may affect 10 7 –10 9 bacteria per gram of soil, aligning with the total bacterial population (10 7 –10 10 g −1 soil), suggesting that RNA phages significantly influence bacterial communities post-wet-up, with phosphorus availability modulating this effect. • Soil wet-up influences RNA virus dynamics for over a week. • The majority of hosts predicted for RNA viruses were bacteria and fungi. • Phosphate amendment preferentially supports Lenarviricota over other RNA viruses. • 60 % of vOTUs that responded to phosphate were from unknown bacteriophage clades. • Most soil bacteria are predicted to be infected by RNA bacteriophages within a week.
Authors
- Jennifer Pett‐Ridge (ORCID: https://orcid.org/0000-0002-4439-2398)
- Jeffrey A. Kimbrel (ORCID: https://orcid.org/0000-0001-7213-9392)
- Graeme W. Nicol (ORCID: https://orcid.org/0000-0002-3876-022X)
- Ella T. Sieradzki (ORCID: https://orcid.org/0000-0001-7174-3010)
- Steven J. Blazewicz (ORCID: https://orcid.org/0000-0001-7517-1750)
- Gareth Trubl (ORCID: https://orcid.org/0000-0001-5008-1476)
- Erin Nuccio (ORCID: https://orcid.org/0000-0003-0189-183X)
- Greg Allen (ORCID: https://orcid.org/0009-0009-6134-7482)
- Christina Hazard (ORCID: https://orcid.org/0000-0002-0325-5856)
Institutions
- Université Claude Bernard Lyon 1 (FR)
- Lawrence Livermore National Laboratory (US)
- Centre National de la Recherche Scientifique (FR)
- University of California, Merced (US)
- Université de Lyon (FR)
- Aarhus University (DK)
- Centre de Gestion Scientifique (FR)
- Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR)
- Agroécologie (FR)
- VetAgro Sup (FR)
- Innovative Genomics Institute (US)
- Laboratoire Ampère (FR)
- Institut National des Sciences Appliquées de Lyon (FR)
- University of California, Berkeley (US)
Publication Details
- Journal
- Soil Biology and Biochemistry
- Published
- 2025-03-18
- DOI
- https://doi.org/10.1016/j.soilbio.2025.109791
- Citations
- 1
- Primary Topic
- Bacteriophages and microbial interactions
- Type
- article
- Field-Weighted Citation Impact
- 1.72
Funders
- U.S. Department of Energy
- Biological and Environmental Research
- Lawrence Livermore National Laboratory