Evidence map›Paper›PMID 27077662›Full record

ArticlePloS one2016

Lineage Tracking for Probing Heritable Phenotypes at Single-Cell Resolution.

Denis Cottinet, Florence Condamine, Nicolas Bremond, Andrew D Griffiths, Paul B Rainey, J Arjan G M de Visser, Jean Baudry, Jérôme Bibette

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Article
  2. Trajectory analysis ofBiomicrofluidics · 2024
    Article
  3. Review
  4. Article
  5. Droplet Microfluidics for Microbial Biotechnology.Advances in biochemical engineering/biotechnology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Sex in a test tube: testing the benefits of in vitro recombination.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
  14. 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

8 authors.

Denis CottinetChemistry Biology Innovation (CNRS UMR 8231), École supérieure de physique et de chimie industrielles de la Ville de Paris (ESPCI ParisTech), PSL* Research University, Paris, France.
Florence CondamineChemistry Biology Innovation (CNRS UMR 8231), École supérieure de physique et de chimie industrielles de la Ville de Paris (ESPCI ParisTech), PSL* Research University, Paris, France.
Nicolas BremondChemistry Biology Innovation (CNRS UMR 8231), École supérieure de physique et de chimie industrielles de la Ville de Paris (ESPCI ParisTech), PSL* Research University, Paris, France.
Andrew D GriffithsChemistry Biology Innovation (CNRS UMR 8231), École supérieure de physique et de chimie industrielles de la Ville de Paris (ESPCI ParisTech), PSL* Research University, Paris, France.
Paul B RaineyChemistry Biology Innovation (CNRS UMR 8231), École supérieure de physique et de chimie industrielles de la Ville de Paris (ESPCI ParisTech), PSL* Research University, Paris, France.
J Arjan G M de VisserLaboratory of Genetics, Wageningen University, Wageningen, The Netherlands.
Jean BaudryChemistry Biology Innovation (CNRS UMR 8231), École supérieure de physique et de chimie industrielles de la Ville de Paris (ESPCI ParisTech), PSL* Research University, Paris, France.
Jérôme BibetteChemistry Biology Innovation (CNRS UMR 8231), École supérieure de physique et de chimie industrielles de la Ville de Paris (ESPCI ParisTech), PSL* Research University, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Determining the phenotype and genotype of single cells is central to understand microbial evolution. DNA sequencing technologies allow the detection of mutants at high resolution, but similar approaches for phenotypic analyses are still lacking. We show that a drop-based millifluidic system enables the detection of heritable phenotypic changes in evolving bacterial populations. At time intervals, cells were sampled and individually compartmentalized in 100 nL drops. Growth through 15 generations was monitored using a fluorescent protein reporter. Amplification of heritable changes-via growth-over multiple generations yields phenotypically distinct clusters reflecting variation relevant for evolution. To demonstrate the utility of this approach, we follow the evolution of Escherichia coli populations during 30 days of starvation. Phenotypic diversity was observed to rapidly increase upon starvation with the emergence of heritable phenotypes. Mutations corresponding to each phenotypic class were identified by DNA sequencing. This scalable lineage-tracking technology opens the door to large-scale phenotyping methods with special utility for microbiology and microbial population biology.

Indexed as

Evolution, MolecularGenome, BacterialCell LineageDNA, BacterialEscherichia coliEscherichia coli ProteinsGenotypeHigh-Throughput Nucleotide SequencingMutationPhenotypeSingle-Cell AnalysisDNA, BacterialEscherichia coli Proteins

Identifiers

PMID27077662
PMCPMC4831777

What OpenQuestion holds

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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.