Synergy in viral–bacterial co-infection expedites algal bloom demise

Algal blooms are hotspots for diverse microbial interactions affecting bloom dynamics. Viral infections often regulate the demise of these blooms, recycling >25% of oceanic fixed carbon. Although these blooms collapse synchronously, only 10-30% of algal cells show active viral infection, suggesting additional mortality agents. Using microbial communities from natural coccolithophore blooms, we discovered that bacteria significantly enhanced virus-mediated algal mortality. We quantified this interaction using two novel metrics: the Synergy Index (SI) measuring viral-bacterial interaction strength, and the Benefit Index (BI) assessing changes in bacterial fitness. We identified Alteromonas bacteria as drivers of viral-bacterial coinfection, with consistently high SI and BI. In natural communities, Alteromonas exhibited chemoattraction towards infected algal cells, leading to their enrichment in bloom demise particles. This viral-bacterial synergy represents a previously unrecognized mortality agent controlling bloom termination, modulating the balance between the carbon-recycling viral shunt and the carbon-exporting viral shuttle pathways, likely influencing global carbon cycling.

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Publication Details

Journal
Nature
Published
2026-11-04
DOI
https://doi.org/10.1038/s41586-026-11243-7
Citations
2
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
5.61

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article

Synergy in viral–bacterial co-infection expedites algal bloom demise

David Zeevi, Guy Schleyer, Inbal Nussbaum, Roman Stocker et al.
2 citations
Nature
Bacteriophages and microbial interactions
5.61
article

Synergy in viral–bacterial co-infection expedites algal bloom demise

David Zeevi, Guy Schleyer, Inbal Nussbaum, Roman Stocker, Noa Barak-Gavish, Assaf Vardi, Estelle E. Clerc, Constanze Kuhlisch, Jean‐Baptiste Raina, Nir Joffe, Daniella Schatz, Eliran Soffer, Tal Sharon Nir-Zadock, Guy Tadmor
article en
2 citations

Abstract

Algal blooms are hotspots for diverse microbial interactions affecting bloom dynamics. Viral infections often regulate the demise of these blooms, recycling >25% of oceanic fixed carbon. Although these blooms collapse synchronously, only 10-30% of algal cells show active viral infection, suggesting additional mortality agents. Using microbial communities from natural coccolithophore blooms, we discovered that bacteria significantly enhanced virus-mediated algal mortality. We quantified this interaction using two novel metrics: the Synergy Index (SI) measuring viral-bacterial interaction strength, and the Benefit Index (BI) assessing changes in bacterial fitness. We identified Alteromonas bacteria as drivers of viral-bacterial coinfection, with consistently high SI and BI. In natural communities, Alteromonas exhibited chemoattraction towards infected algal cells, leading to their enrichment in bloom demise particles. This viral-bacterial synergy represents a previously unrecognized mortality agent controlling bloom termination, modulating the balance between the carbon-recycling viral shunt and the carbon-exporting viral shuttle pathways, likely influencing global carbon cycling.

Nature
Centre National de la Recherche Scientifique (FR), Université de Perpignan (FR), École Pratique des Hautes Études (FR), Université Paris Sciences et Lettres (FR), ETH Zurich (CH), Royal Netherlands Institute for Sea Research (NL), Centre de Recherches Insulaires et Observatoire de l'Environnement (PF), Institute of Environmental Engineering (CH), Institute of Microbiology (CH), Weizmann Institute of Science (IL)
European Commission
Openalex Percentile: Top 7%
Bacteriophages and microbial interactions
5.61
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