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Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids

Plasmids are extrachromosomal genetic elements in prokaryotes that have been recognized as important drivers of microbial ecology and evolution. Plasmids are found in multiple copies inside their host cell where independent emergence of mutations may lead to intracellular genetic heterogeneity. The...

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Autores principales: Garoña, Ana, Hülter, Nils F, Romero Picazo, Devani, Dagan, Tal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662611/
https://www.ncbi.nlm.nih.gov/pubmed/34550379
http://dx.doi.org/10.1093/molbev/msab283
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author Garoña, Ana
Hülter, Nils F
Romero Picazo, Devani
Dagan, Tal
author_facet Garoña, Ana
Hülter, Nils F
Romero Picazo, Devani
Dagan, Tal
author_sort Garoña, Ana
collection PubMed
description Plasmids are extrachromosomal genetic elements in prokaryotes that have been recognized as important drivers of microbial ecology and evolution. Plasmids are found in multiple copies inside their host cell where independent emergence of mutations may lead to intracellular genetic heterogeneity. The intracellular plasmid diversity is thus subject to changes upon cell division. However, the effect of plasmid segregation on plasmid evolution remains understudied. Here, we show that genetic drift during cell division—segregational drift—leads to the rapid extinction of novel plasmid alleles. We established a novel experimental approach to control plasmid allele frequency at the levels of a single cell and the whole population. Following the dynamics of plasmid alleles in an evolution experiment, we find that the mode of plasmid inheritance—random or clustered—is an important determinant of plasmid allele dynamics. Phylogenetic reconstruction of our model plasmid in clinical isolates furthermore reveals a slow evolutionary rate of plasmid-encoded genes in comparison to chromosomal genes. Our study provides empirical evidence that genetic drift in plasmid evolution occurs at multiple levels: the host cell and the population of hosts. Segregational drift has implications for the evolutionary rate heterogeneity of extrachromosomal genetic elements.
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spelling pubmed-86626112021-12-10 Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids Garoña, Ana Hülter, Nils F Romero Picazo, Devani Dagan, Tal Mol Biol Evol Discoveries Plasmids are extrachromosomal genetic elements in prokaryotes that have been recognized as important drivers of microbial ecology and evolution. Plasmids are found in multiple copies inside their host cell where independent emergence of mutations may lead to intracellular genetic heterogeneity. The intracellular plasmid diversity is thus subject to changes upon cell division. However, the effect of plasmid segregation on plasmid evolution remains understudied. Here, we show that genetic drift during cell division—segregational drift—leads to the rapid extinction of novel plasmid alleles. We established a novel experimental approach to control plasmid allele frequency at the levels of a single cell and the whole population. Following the dynamics of plasmid alleles in an evolution experiment, we find that the mode of plasmid inheritance—random or clustered—is an important determinant of plasmid allele dynamics. Phylogenetic reconstruction of our model plasmid in clinical isolates furthermore reveals a slow evolutionary rate of plasmid-encoded genes in comparison to chromosomal genes. Our study provides empirical evidence that genetic drift in plasmid evolution occurs at multiple levels: the host cell and the population of hosts. Segregational drift has implications for the evolutionary rate heterogeneity of extrachromosomal genetic elements. Oxford University Press 2021-09-22 /pmc/articles/PMC8662611/ /pubmed/34550379 http://dx.doi.org/10.1093/molbev/msab283 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Garoña, Ana
Hülter, Nils F
Romero Picazo, Devani
Dagan, Tal
Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids
title Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids
title_full Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids
title_fullStr Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids
title_full_unstemmed Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids
title_short Segregational Drift Constrains the Evolutionary Rate of Prokaryotic Plasmids
title_sort segregational drift constrains the evolutionary rate of prokaryotic plasmids
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8662611/
https://www.ncbi.nlm.nih.gov/pubmed/34550379
http://dx.doi.org/10.1093/molbev/msab283
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