Lineage Tracking for Probing Heritable Phenotypes at Single-Cell Resolution

PLoS One. 2016 Apr 14;11(4):e0152395. doi: 10.1371/journal.pone.0152395. eCollection 2016.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Lineage / genetics*
  • DNA, Bacterial / genetics
  • Escherichia coli / genetics*
  • Escherichia coli / growth & development
  • Escherichia coli Proteins / genetics*
  • Evolution, Molecular*
  • Genome, Bacterial*
  • Genotype
  • High-Throughput Nucleotide Sequencing / methods*
  • Mutation / genetics
  • Phenotype
  • Single-Cell Analysis / methods*

Substances

  • DNA, Bacterial
  • Escherichia coli Proteins

Grants and funding

This work was supported by the European Community’s Seventh Framework Programme (FP7/2007¬2013) under grant agreement no. [225167] (eFlux), by a PhD grant from Université Pierre Marie Curie (Paris, France). PBR holds an International Blaise Pascal Research Chair funded by the French State and the Ile-de-France, managed by the Fondation de l’Ecole Normale Supérieure.