Secreted nucleases reclaim extracellular DNA during biofilm development

DNA is the genetic code found inside all living cells and its molecular stability can also be utilized outside the cell. While extracellular DNA (eDNA) has been identified as a structural polymer in bacterial biofilms, whether it persists stably throughout development remains unclear. Here, we report that eDNA is temporarily invested in the biofilm matrix before being reclaimed later in development. Specifically, by imaging eDNA dynamics within undomesticated Bacillus subtilis biofilms, we found eDNA is produced during biofilm establishment before being globally degraded in a spatiotemporally coordinated pulse. We identified YhcR, a secreted Ca<sup>2+</sup>-dependent nuclease, as responsible for eDNA degradation in pellicle biofilms. YhcR cooperates with two other nucleases, NucA and NucB, to reclaim eDNA for its phosphate content in colony biofilms. Our results identify extracellular nucleases that are crucial for eDNA reclamation during biofilm development and we therefore propose a new role for eDNA as a dynamic metabolic reservoir.

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Publication Details

Journal
npj Biofilms and Microbiomes
Published
2024-10-07
DOI
https://doi.org/10.1038/s41522-024-00575-9
Citations
12
Primary Topic
Bacterial biofilms and quorum sensing
Type
article
Field-Weighted Citation Impact
2.81

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article

Secreted nucleases reclaim extracellular DNA during biofilm development

Garth Fisher, Blake A. Everett, Stephen M. Lander, Peter Tran et al.
12 citations
npj Biofilms and Microbiomes
Bacterial biofilms and quorum sensing
2.81
article

Secreted nucleases reclaim extracellular DNA during biofilm development

Garth Fisher, Blake A. Everett, Stephen M. Lander, Peter Tran, Arthur Prindle
article en
12 citations

Abstract

DNA is the genetic code found inside all living cells and its molecular stability can also be utilized outside the cell. While extracellular DNA (eDNA) has been identified as a structural polymer in bacterial biofilms, whether it persists stably throughout development remains unclear. Here, we report that eDNA is temporarily invested in the biofilm matrix before being reclaimed later in development. Specifically, by imaging eDNA dynamics within undomesticated Bacillus subtilis biofilms, we found eDNA is produced during biofilm establishment before being globally degraded in a spatiotemporally coordinated pulse. We identified YhcR, a secreted Ca<sup>2+</sup>-dependent nuclease, as responsible for eDNA degradation in pellicle biofilms. YhcR cooperates with two other nucleases, NucA and NucB, to reclaim eDNA for its phosphate content in colony biofilms. Our results identify extracellular nucleases that are crucial for eDNA reclamation during biofilm development and we therefore propose a new role for eDNA as a dynamic metabolic reservoir.

npj Biofilms and MicrobiomesVol. 10(1)
Northwestern University (US), Chan Zuckerberg Initiative (United States) (US)
National Science Foundation, Northwestern University, National Institutes of Health, National Cancer Institute, National Institute of General Medical Sciences, Army Research Office
Openalex Percentile: Top 9%
Bacterial biofilms and quorum sensing
2.81
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Secreted nucleases reclaim extracellular DNA during biofilm development — Garth Fisher, Blake A. Everett, et al. · npj Biofilms and Microbiomes (2024) | TGRS Research Map | TGRS