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Bacterial chemotaxis in a microfluidic T-maze reveals strong phenotypic heterogeneity in chemotactic sensitivity

Author

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  • M. Mehdi Salek

    (Massachusetts Institute of Technology
    Environmental and Geomatic Engineering, ETH Zurich)

  • Francesco Carrara

    (Massachusetts Institute of Technology
    Environmental and Geomatic Engineering, ETH Zurich)

  • Vicente Fernandez

    (Massachusetts Institute of Technology
    Environmental and Geomatic Engineering, ETH Zurich)

  • Jeffrey S. Guasto

    (Tufts University)

  • Roman Stocker

    (Massachusetts Institute of Technology
    Environmental and Geomatic Engineering, ETH Zurich)

Abstract

Many microorganisms have evolved chemotactic strategies to exploit the microscale heterogeneity that frequently characterizes microbial habitats. Chemotaxis has been primarily studied as an average characteristic of a population, with little regard for variability among individuals. Here, we adopt a classic tool from animal ecology – the T-maze – and implement it at the microscale by using microfluidics to expose bacteria to a sequence of decisions, each consisting of migration up or down a chemical gradient. Single-cell observations of clonal Escherichia coli in the maze, coupled with a mathematical model, reveal that strong heterogeneity in the chemotactic sensitivity coefficient exists even within clonal populations of bacteria. A comparison of different potential sources of heterogeneity reveals that heterogeneity in the T-maze originates primarily from the chemotactic sensitivity coefficient, arising from a distribution of pathway gains. This heterogeneity may have a functional role, for example in the context of migratory bet-hedging strategies.

Suggested Citation

  • M. Mehdi Salek & Francesco Carrara & Vicente Fernandez & Jeffrey S. Guasto & Roman Stocker, 2019. "Bacterial chemotaxis in a microfluidic T-maze reveals strong phenotypic heterogeneity in chemotactic sensitivity," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09521-2
    DOI: 10.1038/s41467-019-09521-2
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