Plasmid mutation rates scale with copy number

P Paula Ramiro-Martínez (Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria) I Ignacio de Quinto (Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria) L Laura Jaraba-Soto (Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria) V Val F. Lanza (Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria) C Cristina Herencias-Rodríguez (Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria) A Adrián González Casanova (Department of Applied Mathematics, School of Mathematical and Statistical Sciences, and Center for Mechanisms of Evolution (Biodesign Institute), Arizona State University) R Rafael Peña-Miller (Programa de Biología de Sistemas, Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México) J Jerónimo Rodríguez-Beltrán (Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria)

Abstract

Plasmids are extrachromosomal DNA molecules that spread by horizontal transfer and shape bacterial evolution. Plasmids are typically present at multiple copies per bacterial cell, and these extra copies increase the supply of plasmid mutations, potentially accelerating their evolution. However, the segregation of plasmid copies to daughter cells is random, introducing an additional layer of genetic drift, termed segregational drift, that might delay plasmid evolution. The interplay between plasmid mutational supply and segregational drift determines the evolutionary rate of plasmid-encoded genes, yet the relative contribution of these opposite forces in plasmid evolution remains unclear. Here, we develop a population genetics framework to predict the rate of plasmid mutations in bacterial populations and validate these predictions using computational, experimental, and bioinformatic approaches. Our findings show that plasmid mutation rates scale logarithmically with copy number and that the supply of new mutations consistently surpasses the impact of segregational drift across all copy numbers. These results underscore plasmids as powerful drivers of bacterial evolvability, where they can potentiate the evolution of critical traits such as antibiotic resistance.

Article Details

Volume / Issue Vol. 123, Issue 4
Published January 27, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (8)

P

Paula Ramiro-Martínez

Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria

I

Ignacio de Quinto

Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria

L

Laura Jaraba-Soto

Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria

V

Val F. Lanza

Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria

C

Cristina Herencias-Rodríguez

Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria

A

Adrián González Casanova

Department of Applied Mathematics, School of Mathematical and Statistical Sciences, and Center for Mechanisms of Evolution (Biodesign Institute), Arizona State University

R

Rafael Peña-Miller

Programa de Biología de Sistemas, Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México

J

Jerónimo Rodríguez-Beltrán

Microbiology Department, Hospital Universitario Ramón y Cajal-Instituto Ramón y Cajal de Investigación Sanitaria