Abstract
The development of microbial communities depends on a combination of complex deterministic and stochastic factors that can dramatically alter the spatial distribution and activities of community members. We have developed a microwell array platform that can be used to rapidly assemble and track thousands of bacterial communities in parallel. This protocol highlights the utility of the platform and describes its use for optically monitoring the development of simple, two-member communities within an ensemble of arrays within the platform. This demonstration uses two mutants of Pseudomonas aeruginosa, part of a series of mutants developed to study Type VI secretion pathogenicity. Chromosomal inserts of either mCherry or GFP genes facilitate the constitutive expression of fluorescent proteins with distinct emission wavelengths that can be used to monitor community member abundance and location within each microwell. This protocol describes a detailed method for assembling mixtures of bacteria into the wells of the array and using time-lapse fluorescence imaging and quantitative image analysis to measure the relative growth of each member population over time. The seeding and assembly of the microwell platform, the imaging procedures necessary for the quantitative analysis of microbial communities within the array, and the methods that can be used to reveal interactions between microbial species area all discussed.
Original language | English |
---|---|
Article number | e55701 |
Journal | Journal of Visualized Experiments |
Volume | 2017 |
Issue number | 124 |
DOIs | |
State | Published - Jun 6 2017 |
Bibliographical note
Publisher Copyright:© 2017 Journal of Visualized Experiments.
Funding
Microwell arrays were fabricated and characterized at the Center for Nanophase Materials Sciences User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy. Financial support for this work was provided through the Oak Ridge National Laboratory Director’s Research and Development Fund. The authors would also like to thank the J. Mougous Laboratory (University of Washington, Seattle, WA) for the supply of P. aeruginosa strains used in these studies.
Funders | Funder number |
---|---|
Center for Nanophase Materials Sciences User Facilities Division | |
Oak Ridge National Laboratory | |
U.S. Department of Energy | |
Basic Energy Sciences | |
University of Washington |
Keywords
- Bioengineering
- Cell array
- Confinement
- Issue 124
- Lift-off
- Microbial community
- Microfabrication
- Microfluidics
- Microwell
- Nanofabrication
- Niche
- Succession