Iron limitation differentially affects viral replication in key marine microbes

Viral lysis accounts for much of microbial mortality in the ocean, and iron (Fe) is a critical micronutrient that can limit phytoplankton growth. However, interactions between Fe nutrition of microbes, including both heterotrophic bacteria and phytoplankton, and viral lysis are not well known. Here, we present viral infection dynamics under Fe-limited and Fe-replete conditions for isolates of three types of marine picoplankton, the photosynthetic picoeukaryote <i>Ostreococcus</i>, the cyanobacterium <i>Synechococcus</i>, and the heterotrophic bacterium <i>Vibrio</i>. Iron limitation of <i>Ostreococcus</i> resulted in slowed growth and reduced viral burst sizes; this is similar to prior results from studies of larger eukaryotic phytoplankton, where reduced viral replication under Fe limitation is attributed to the viral reliance on host metabolism and replication machinery. Fe limitation of one <i>Vibrio</i> impacted dynamics of its virus similarly, lengthening the latent period before infected cells burst to release new viruses, and reducing the number of infective particles released upon lysis. In contrast, for another <i>Vibrio</i> isolate, Fe limitation had no discernible effect on replication of its virus. Furthermore, dynamics of three cyanophages that infect the same <i>Synechococcus</i> isolate were not affected by Fe limitation of the host, either in terms of latent period or burst size. The results show that some marine viruses, particularly cyanophages, can replicate efficiently even when host growth is compromised. These findings have implications for marine ecology and carbon cycling in Fe-limited regions of the global ocean.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-10-15
DOI
https://doi.org/10.1073/pnas.2512910122
Citations
1
Primary Topic
Bacteriophages and microbial interactions
Type
article
Field-Weighted Citation Impact
1.72

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article

Iron limitation differentially affects viral replication in key marine microbes

Brady R. Cunningham, Charmaine C. M. Yung, Amy Zimmerman, Alexandra Z. Worden et al.
1 citations
Proceedings of the National Academy of Sciences
Bacteriophages and microbial interactions
1.72
article

Iron limitation differentially affects viral replication in key marine microbes

Brady R. Cunningham, Charmaine C. M. Yung, Amy Zimmerman, Alexandra Z. Worden, Rachel L. Kelly, Kathryn M. Kauffman, Seth G. John
article en
1 citations

Abstract

Viral lysis accounts for much of microbial mortality in the ocean, and iron (Fe) is a critical micronutrient that can limit phytoplankton growth. However, interactions between Fe nutrition of microbes, including both heterotrophic bacteria and phytoplankton, and viral lysis are not well known. Here, we present viral infection dynamics under Fe-limited and Fe-replete conditions for isolates of three types of marine picoplankton, the photosynthetic picoeukaryote <i>Ostreococcus</i>, the cyanobacterium <i>Synechococcus</i>, and the heterotrophic bacterium <i>Vibrio</i>. Iron limitation of <i>Ostreococcus</i> resulted in slowed growth and reduced viral burst sizes; this is similar to prior results from studies of larger eukaryotic phytoplankton, where reduced viral replication under Fe limitation is attributed to the viral reliance on host metabolism and replication machinery. Fe limitation of one <i>Vibrio</i> impacted dynamics of its virus similarly, lengthening the latent period before infected cells burst to release new viruses, and reducing the number of infective particles released upon lysis. In contrast, for another <i>Vibrio</i> isolate, Fe limitation had no discernible effect on replication of its virus. Furthermore, dynamics of three cyanophages that infect the same <i>Synechococcus</i> isolate were not affected by Fe limitation of the host, either in terms of latent period or burst size. The results show that some marine viruses, particularly cyanophages, can replicate efficiently even when host growth is compromised. These findings have implications for marine ecology and carbon cycling in Fe-limited regions of the global ocean.

Proceedings of the National Academy of SciencesVol. 122(42)
University of Southern California (US), Statewide California Earthquake Center (US), Marine Biological Laboratory (US), Pacific Northwest National Laboratory (US), University of South Carolina (US), Hong Kong University of Science and Technology (HK), GEOMAR Helmholtz Centre for Ocean Research Kiel (DE), University at Buffalo, State University of New York (US)
Gordon and Betty Moore Foundation
Openalex Percentile: Top 13%
Bacteriophages and microbial interactions
1.72
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