Issue 3, 2025

A simple three-dimensional microfluidic platform for studying chemotaxis and cell sorting

Abstract

Microbial chemotaxis plays a key role in a diversity of biological and ecological processes. Although microfluidics-based assays have been applied to investigate bacterial chemotaxis, retrieving chemotactic cells off-chip based on their dynamic chemotactic responses remains limited. Here, we present a simple three-dimensional microfluidic platform capable of programmable delivery of solutions, maintaining static, stable gradients for over 20 hours, followed by active sorting and retrieval of bacteria based on their chemotactic phenotypes. Using this platform, we revealed the swimming features of individual E. coli cells in response to chemoattractant and observed rapid bacterial adaptation to the gradients. Furthermore, the robust performance of the platform allowed us to investigate complex natural microbial communities. Exemplified by sorting bacteria towards soluble cellulose and lignin compounds, we found only a small percentage (<20%) of chemotactic bacteria from a leaf mould microbiota exhibited cellulolytic or lignin-degradation abilities. These findings highlight that chemotaxis does not always align with degradation abilities. Interestingly, a new Erwinia aphidicola strain was discovered with substantial cellulose degradation capabilities. These results illustrate the strong potential of this microfluidic platform for investigating broad processes involving bacterial chemotaxis and for discovering functional microbes.

Graphical abstract: A simple three-dimensional microfluidic platform for studying chemotaxis and cell sorting

Supplementary files

Article information

Article type
Paper
Submitted
21 Oct 2024
Accepted
31 Dec 2024
First published
06 Jan 2025
This article is Open Access
Creative Commons BY license

Lab Chip, 2025,25, 343-353

A simple three-dimensional microfluidic platform for studying chemotaxis and cell sorting

X. Li, Y. Song, A. Glidle, C. Smith, W. Sloan, M. Cusack and H. Yin, Lab Chip, 2025, 25, 343 DOI: 10.1039/D4LC00892H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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