Intracellular competition shapes plasmid population dynamics

From populations of multicellular organisms to selfish genetic elements, conflicts between levels of biological organization are central to evolution. Plasmids are extrachromosomal, self-replicating genetic elements that face selective pressures from their hosts but also compete within the host cell for replication resources. Although theory indicates that within-cell selection matters for plasmid evolution, experimental measurement of these dynamics has remained elusive. We measured within-cell fitness of competing <i>Escherichia coli</i> plasmids and characterized their drift and selective dynamics. We made synthetic plasmid dimers that can be split in a controlled way to create balanced competition, which we probed experimentally. Incompatible plasmids coexist for an extended time owing to methylation-based replication control. Moreover, less transcriptionally active plasmids display a within-cell advantage and fix preferentially, favoring gene loss. Critically, fixation depends nontrivially on the interplay between plasmid transcription and translation. Our results show that plasmid evolution is driven by within- and between-cell dynamics.

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Publication Details

Journal
Science
Published
2025-11-20
DOI
https://doi.org/10.1126/science.adx0665
Citations
4
Primary Topic
Bacterial Genetics and Biotechnology
Type
article
Field-Weighted Citation Impact
7.27
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article

Intracellular competition shapes plasmid population dynamics

Daniel S. Eaton, Michael Baym, Fernando W. Rossine, Carlos Martínez Sánchez et al.
4 citations
Science
Bacterial Genetics and Biotechnology
7.27
article

Intracellular competition shapes plasmid population dynamics

Daniel S. Eaton, Michael Baym, Fernando W. Rossine, Carlos Martínez Sánchez, Johan Paulsson
article en
4 citations

Abstract

From populations of multicellular organisms to selfish genetic elements, conflicts between levels of biological organization are central to evolution. Plasmids are extrachromosomal, self-replicating genetic elements that face selective pressures from their hosts but also compete within the host cell for replication resources. Although theory indicates that within-cell selection matters for plasmid evolution, experimental measurement of these dynamics has remained elusive. We measured within-cell fitness of competing <i>Escherichia coli</i> plasmids and characterized their drift and selective dynamics. We made synthetic plasmid dimers that can be split in a controlled way to create balanced competition, which we probed experimentally. Incompatible plasmids coexist for an extended time owing to methylation-based replication control. Moreover, less transcriptionally active plasmids display a within-cell advantage and fix preferentially, favoring gene loss. Critically, fixation depends nontrivially on the interplay between plasmid transcription and translation. Our results show that plasmid evolution is driven by within- and between-cell dynamics.

ScienceVol. 390(6779)
Harvard University (US), Center for Systems Biology (US)
Openalex Percentile: Top 3%
Bacterial Genetics and Biotechnology
7.27
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