Evidence map›Paper›PMID 30517696›Full record

ArticleMolecular biology and evolution2019

Segregational Drift and the Interplay between Plasmid Copy Number and Evolvability.

Judith Ilhan, Anne Kupczok, Christian Woehle, Tanita Wein, Nils F Hülter, Philip Rosenstiel, Giddy Landan, Itzhak Mizrahi, Tal Dagan

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Plasmid mutation rates scale with copy number.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. ACCIO: An Assembly-Based Tool Enabling Plasmid Detection.medRxiv : the preprint server for health sciences · 2025
    Article
  6. Article
  7. Article
  8. Universal rules govern plasmid copy number.Nature communications · 2025
    Article
  9. Article
  10. Article
  11. Birmingham-group IncP-1Microbial genomics · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Rational evolution for altering the ligand preference of estrogen receptor alpha.Protein science : a publication of the Protein Society · 2024
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Judith IlhanInstitute of Microbiology, Kiel University, Kiel, Germany.
Anne KupczokInstitute of Microbiology, Kiel University, Kiel, Germany.
Christian WoehleInstitute of Microbiology, Kiel University, Kiel, Germany.
Tanita WeinInstitute of Microbiology, Kiel University, Kiel, Germany.
Nils F HülterInstitute of Microbiology, Kiel University, Kiel, Germany.
Philip RosenstielInstitute of Clinical Molecular Biology, Kiel University, Kiel, Germany.
Giddy LandanInstitute of Microbiology, Kiel University, Kiel, Germany.
Itzhak MizrahiThe Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Tal DaganInstitute of Microbiology, Kiel University, Kiel, Germany.
Kiel University · DEBen-Gurion University of the Negev · IL

Funding

European Research Council 281357
6 · The paper itself

Abstract

The ubiquity of plasmids in all prokaryotic phyla and habitats and their ability to transfer between cells marks them as prominent constituents of prokaryotic genomes. Many plasmids are found in their host cell in multiple copies. This leads to an increased mutational supply of plasmid-encoded genes and genetically heterogeneous plasmid genomes. Nonetheless, the segregation of plasmid copies into daughter cells during cell division is considered to occur in the absence of selection on the plasmid alleles. We investigate the implications of random genetic drift of multicopy plasmids during cell division-termed here "segregational drift"-to plasmid evolution. Performing experimental evolution of low- and high-copy non-mobile plasmids in Escherichia coli, we find that the evolutionary rate of multicopy plasmids does not reflect the increased mutational supply expected according to their copy number. In addition, simulated evolution of multicopy plasmid alleles demonstrates that segregational drift leads to increased loss frequency and extended fixation time of plasmid mutations in comparison to haploid chromosomes. Furthermore, an examination of the experimentally evolved hosts reveals a significant impact of the plasmid type on the host chromosome evolution. Our study demonstrates that segregational drift of multicopy plasmids interferes with the retention and fixation of novel plasmid variants. Depending on the selection pressure on newly emerging variants, plasmid genomes may evolve slower than haploid chromosomes, regardless of their higher mutational supply. We suggest that plasmid copy number is an important determinant of plasmid evolvability due to the manifestation of segregational drift.

Indexed as

Biological EvolutionGenetic DriftModels, GeneticChromosomes, BacterialEscherichia coliGene FrequencyPlasmidsbacterial evolutionmitochondria heteroplasmypopulation genetics

Identifiers

PMID30517696
PMCPMC6389322
OpenAlexW2949773829

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.