Engineered bidirectional communication mediates a consensus in a microbial biofilm consortium
Abstract
Microbial consortia form when multiple species colocalize and communally generate a function that none is capable of alone. Consortia abound in nature, and their cooperative metabolic activities influence everything from biodiversity in the global food chain to human weight gain. Here, we present an engineered consortium in which the microbial members communicate with each other and exhibit a "consensus" gene expression response. Two colocalized populations of Escherichia coli converse bidirectionally by exchanging acyl-homoserine lactone signals. The consortium generates the gene-expression response if and only if both populations are present at sufficient cell densities. Because neither population can respond without the other's signal, this consensus function can be considered a logical AND gate in which the inputs are cell populations. The microbial consensus consortium operates in diverse growth modes, including in a biofilm, where it sustains its response for several days.
Additional Information
© 2007 by The National Academy of Sciences of the USA. Edited by Charles R. Cantor, Sequenom, Inc., San Diego, CA, and approved September 10, 2007 (received for review May 7, 2007). Published online before print October 24, 2007, doi: 10.1073/pnas.0704256104. This article is a PNAS Direct Submission. We thank Jared Leadbetter and Ernesto Andrianantoandro for discussions or comments on the manuscript; and Chris Waters, Tracy Teal, and the Caltech Biological Imaging Center for assistance with biofilm imaging. This material is based on work supported by 2005 National Science Foundation Emerging Models and Technologies for Computation Grant CCF-0523195 and 2006 National Institutes of Health Grants R01 GM074712-01A1 and 5R01CA118486-2. Author contributions: K.B. and D.K.K. contributed equally to this work; K.B., D.K.K., R.W., and F.H.A. designed research; K.B. and D.K.K. performed research; K.B. and D.K.K. contributed new reagents/analytic tools; K.B. and D.K.K. analyzed data; and K.B., D.K.K., R.W., and F.H.A. wrote the paper. The authors declare no conflict of interest. This article contains supporting information online at www.pnas.org/cgi/content/full/0704256104/DC1.Attached Files
Published - BREpnas07.pdf
Supplemental Material - BREpnas07fig10.pdf
Supplemental Material - BREpnas07fig11.pdf
Supplemental Material - BREpnas07fig6.pdf
Supplemental Material - BREpnas07fig7.pdf
Supplemental Material - BREpnas07fig8.pdf
Supplemental Material - BREpnas07fig9.pdf
Supplemental Material - BREpnas07sup.pdf
Supplemental Material - BREpnas07table.pdf
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Additional details
- PMCID
- PMC2077251
- Eprint ID
- 11237
- Resolver ID
- CaltechAUTHORS:BREpnas07
- NSF
- CCF-0523195
- NIH
- R01 GM074712-01A1
- NIH
- 5R01CA118486-2
- Created
-
2008-07-26Created from EPrint's datestamp field
- Updated
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2021-11-08Created from EPrint's last_modified field