Cell position fates and collective fountain flow in bacterial biofilms revealed by light-sheet microscopy

Author:

Qin Boyang12ORCID,Fei Chenyi13ORCID,Bridges Andrew A.14ORCID,Mashruwala Ameya A.14ORCID,Stone Howard A.2ORCID,Wingreen Ned S.135ORCID,Bassler Bonnie L.14ORCID

Affiliation:

1. Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.

2. Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544, USA.

3. Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.

4. The Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.

5. Princeton Center for Theoretical Science, Princeton University, Princeton, NJ 08544, USA.

Abstract

Biofilm formation from cell fountains Bacteria form three-dimensional communities called biofilms that are ubiquitous in nature and underlie human infections. Medically, biofilms are problematic because they protect resident cells from antibiotics. Although biofilms have been intensively studied, we do not understand how they develop cell by cell. Micron-sized bacteria are densely packed within biofilms, making it exceptionally challenging to track their movements. Qin et al. studied biofilm formation in the pathogen and model biofilm former Vibrio cholerae (see the Perspective by Dal Co and Brenner). The authors combined light-sheet microscopy with cell labeling to map the trajectories of a biofilm founder cell and its descendants in space and time as they built a biofilm. The findings revealed that as the bacteria reproduce, a bacterial “fountain” drives biofilm expansion and dictates the final positions of the offspring. Science , this issue p. 71 ; see also p. 30

Funder

National Science Foundation

National Institutes of Health

Howard Hughes Medical Institute

Alexander von Humboldt-Stiftung

Damon Runyon Cancer Research Foundation

Life Sciences Research Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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