4.7 Article

Localized electrical stimulation triggers cell-type-specific proliferation in biofilms

Journal

CELL SYSTEMS
Volume 13, Issue 6, Pages 488-+

Publisher

CELL PRESS
DOI: 10.1016/j.cels.2022.04.001

Keywords

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Funding

  1. Spanish Ministry of Science, Innovation and Universities
  2. FEDER [PGC2018-101251-B-I00, CEX2018-000792-M]
  3. Generalitat de Catalunya (ICREA Academia program)
  4. Burroughs Wellcome Fund Career Award at the Scientific Interface
  5. National Science Foundation [2027108]
  6. National Institute of General Medical Sciences [R01 GM121888, R35 GM139645, R35GM142584-01]
  7. Defense Advanced Research Projects Agency [HR0011-16-2-0035]
  8. Direct For Mathematical & Physical Scien
  9. Division Of Materials Research [2027108] Funding Source: National Science Foundation

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This study developed an experimental platform combining a microfluidic chip with a multielectrode array to enable localized electrochemical stimulation of bacterial biofilms and simultaneous measurement of physiological response. The findings show that the stimulation of an electrode can selectively promote the proliferation of a specific bacterial cell type, revealing the potential control of biofilm composition and development through electronic interface.
Biological systems ranging from bacteria to mammals utilize electrochemical signaling. Although artificial electrochemical signals have been utilized to characterize neural tissue responses, the effects of such stimuli on non-neural systems remain unclear. To pursue this question, we developed an experimental platform that combines a microfluidic chip with a multielectrode array (MiCMA) to enable localized electrochemical stimulation of bacterial biofilms. The device also allows for the simultaneous measurement of the physiological response within the biofilm with single-cell resolution. We find that the stimulation of an electrode locally changes the ratio of the two major cell types comprising Bacillus subtilis biofilms, namely motile and extra cellular-matrix-producing cells. Specifically, stimulation promotes the proliferation of motile cells but not matrix cells, even though these two cell types are genetically identical and reside in the same microenvironment. Our work thus reveals that an electronic interface can selectively target bacterial cell types, enabling the control of biofilm composition and development.

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