4.8 Article

Droplet printing reveals the importance of micron-scale structure for bacterial ecology

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-021-20996-w

Keywords

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Funding

  1. European Research Council Advanced Grant SYN-TISU
  2. European Research Council Advanced Grant [787932]
  3. Wellcome Trust Investigator award [209397/Z/17/Z]
  4. University of Oxford
  5. EPSRC
  6. BBSRC Centre for Doctoral Training in Synthetic Biology [EP/L016494/1]
  7. Clarendon Fund Scholarship
  8. EPSRC Life Sciences Interface Centre for Doctoral Training [EP/F500394/1]
  9. Swiss National Science Foundation Postdoc Mobility Fellowships [P2LAP3_155109, P300PA_167703]
  10. MRC Career Development Award [MR/M009505/1]
  11. Swiss National Science Foundation (SNF) [P2LAP3_155109, P300PA_167703] Funding Source: Swiss National Science Foundation (SNF)
  12. European Research Council (ERC) [787932] Funding Source: European Research Council (ERC)
  13. MRC [MR/M009505/1] Funding Source: UKRI
  14. Wellcome Trust [209397/Z/17/Z] Funding Source: Wellcome Trust

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The spatial arrangement of bacterial strains and species within microbial communities is considered crucial for their ecology. Krishna Kumar et al. use a droplet-based printing method to arrange different bacterial genotypes across a sub-millimetre array, and show that micron-scale changes in spatial distributions can drive major shifts in ecology.
Bacteria often live in diverse communities where the spatial arrangement of strains and species is considered critical for their ecology. However, a test of this hypothesis requires manipulation at the fine scales at which spatial structure naturally occurs. Here we develop a droplet-based printing method to arrange bacterial genotypes across a sub-millimetre array. We print strains of the gut bacterium Escherichia coli that naturally compete with one another using protein toxins. Our experiments reveal that toxin-producing strains largely eliminate susceptible non-producers when genotypes are well-mixed. However, printing strains side-by-side creates an ecological refuge where susceptible strains can persist in large numbers. Moving to competitions between toxin producers reveals that spatial structure can make the difference between one strain winning and mutual destruction. Finally, we print different potential barriers between competing strains to understand how ecological refuges form, which shows that cells closest to a toxin producer mop up the toxin and protect their clonemates. Our work provides a method to generate customised bacterial communities with defined spatial distributions, and reveals that micron-scale changes in these distributions can drive major shifts in ecology. The spatial arrangement of bacterial strains and species within microbial communities is considered crucial for their ecology. Here, Krishna Kumar et al. use a droplet-based printing method to arrange different bacterial genotypes across a sub-millimetre array, and show that micron-scale changes in spatial distributions can drive major shifts in ecology.

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