Polysaccharide breakdown products drive degradation-dispersal cycles of foraging bacteria through changes in metabolism and motility

Author:

Stubbusch Astrid KM123ORCID,Keegstra Johannes M4ORCID,Schwartzman Julia56ORCID,Pontrelli Sammy7ORCID,Clerc Estelle E4ORCID,Charlton Samuel4ORCID,Stocker Roman4ORCID,Magnabosco Cara3ORCID,Schubert Olga T12ORCID,Ackermann Martin128ORCID,D’Souza Glen G12ORCID

Affiliation:

1. Institute of Biogeochemistry and Pollutant Dynamics, Department of Environmental Systems Science

2. Department of Environmental Microbiology, Eawag: Swiss Federal Institute of Aquatic Science and Technology

3. Geological Institute, Department of Earth Sciences

4. Institute of Environmental Engineering, Department of Civil

5. Department of Civil and Environmental Engineering

6. Department of Biology, University of Southern California

7. Institute of Molecular Systems Biology, Department of Biology

8. Laboratory of Microbial Systems Ecology, School of Architecture

Abstract

Most of Earth’s biomass is composed of polysaccharides. During biomass decomposition, polysaccharides are degraded by heterotrophic bacteria as a nutrient and energy source and are thereby partly remineralized into CO 2 . As polysaccharides are heterogeneously distributed in nature, following the colonization and degradation of a polysaccharide hotspot the cells need to reach new polysaccharide hotspots. Even though many studies indicate that these degradation-dispersal cycles contribute to the carbon flow in marine systems, we know little about how cells alternate between polysaccharide degradation and motility, and which environmental factors trigger this behavioral switch. Here, we studied the growth of the marine bacterium Vibrio cyclitrophicus ZF270 on the abundant marine polysaccharide alginate, both in its soluble polymeric form as well as on its breakdown products. We used microfluidics coupled to time-lapse microscopy to analyze motility and growth of individual cells, and RNA sequencing to study associated changes in gene expression. We found that single cells grow at reduced rate on alginate until they form large groups that cooperatively break down the polymer. Exposing cell groups to digested alginate accelerates cell growth and changes the expression of genes involved in alginate degradation and catabolism, central metabolism, ribosomal biosynthesis, and transport. However, exposure to digested alginate also triggers cells to become motile and disperse from cell groups, proportionally increasing with the group size before the nutrient switch, and this is accompanied by high expression of genes involved in flagellar assembly, chemotaxis, and quorum sensing. We found that motile cells chemotax toward polymeric but not digested alginate, likely enabling them to find new polysaccharide hotspots. Overall, our findings reveal cellular mechanisms that might also underlie bacterial degradation-dispersal cycles, which influence the remineralization of biomass in marine environments.

Publisher

eLife Sciences Publications, Ltd

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