Evidence map›Paper›PMID 32094541›Full record

ArticleNature ecology & evolution2020

Chromosomal barcoding of E. coli populations reveals lineage diversity dynamics at high resolution.

Weronika Jasinska, Michael Manhart, Jesse Lerner, Louis Gauthier, Adrian W R Serohijos, Shimon Bershtein

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature ecology & evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Direct estimation of genotype fitness from time series.bioRxiv : the preprint server for biology · 2026
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  7. Contrasting pH optima of β-lactamases CTX-M and CMY influenceApplied and environmental microbiology · 2026
    Article
  8. Review
  9. Review
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  13. Article
  14. Article
  15. AInfection and immunity · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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

6 authors at 3 institutions in 4 countries.

Weronika Jasinska *Department of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Michael Manhart *Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-3791-9056
Jesse LernerDepartment of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Louis GauthierDepartment of Biochemistry, University of Montreal, Montreal, Quebec, Canada.ORCID http://orcid.org/0000-0003-1009-068X
Adrian W R SerohijosDepartment of Biochemistry, University of Montreal, Montreal, Quebec, Canada.ORCID http://orcid.org/0000-0001-8369-982X
Shimon BershteinDepartment of Life Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel. shimonb@bgu.ac.il.ORCID http://orcid.org/0000-0003-4322-1025
Ben-Gurion University of the Negev · ILUniversité de Montréal · CAHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evolutionary dynamics in large asexual populations is strongly influenced by multiple competing beneficial lineages, most of which segregate at very low frequencies. However, technical barriers to tracking a large number of these rare lineages in bacterial populations have so far prevented a detailed elucidation of evolutionary dynamics. Here, we overcome this hurdle by developing a chromosomal-barcoding technique that allows simultaneous tracking of approximately 450,000 distinct lineages in Escherichia coli, which we use to test the effect of sub-inhibitory concentrations of common antibiotics on the evolutionary dynamics of low-frequency lineages. We find that populations lose lineage diversity at distinct rates that correspond to their antibiotic regimen. We also determine that some lineages have similar fates across independent experiments. By analysing the trajectory dynamics, we attribute the reproducible fates of these lineages to the presence of pre-existing beneficial mutations, and we demonstrate how the relative contribution of pre-existing and de novo mutations varies across drug regimens. Finally, we reproduce the observed lineage dynamics by simulations. Altogether, our results provide a valuable methodology for studying bacterial evolution as well as insights into evolution under sub-inhibitory antibiotic levels.

Indexed as

Escherichia coliEvolution, MolecularAnti-Bacterial AgentsMutationAnti-Bacterial Agents

Identifiers

PMID32094541
OpenAlexW3006915344

What OpenQuestion holds

Textmetadata
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.