Flagellar point mutation causes social aggregation in laboratory-adapted <i>Bacillus subtilis</i> under conditions that promote swimming

Motility allows microbes to explore and maximize success in their environment; however, many laboratory bacterial strains have a reduced or altered capacity for motility. Swimming motility in <i>Bacillus subtilis</i> depends on peritrichous flagella and is carried out individually as cells move by biased random walks toward attractants. Previously, we adapted <i>Bacillus subtilis</i> strain 3610 to the laboratory for 300 generations in lysogeny broth (LB) batch culture and isolated lab-adapted strains. Strain SH2 is motility-defective and in broth culture forms large, frequently spherical aggregates of cells. A single point mutation in the flagellin gene <i>hag</i> that causes amino acid 259 to switch from A to T is necessary and sufficient to cause these social cell aggregates, and aggregation occurs between flagellated cells bearing this point mutation regardless of the strain background. Cells associate when bearing this mutation, but flagellar rotation is needed to pull associating cells into spherical aggregates. Using electron microscopy, we are able to show that the SH2 flagellar filament has limited polymorphism when compared to other flagellar structures. This limited polymorphism hinders the flagellum's ability to function as a motility apparatus but appears to alter its function to that of cell aggregation/adhesion. We speculate that the genotype-specific aggregation of cells producing Hag<sup>A259T</sup> flagella could have increased representation in a batch-culture experiment by allowing similar cells to go through a transfer together and also that this mutation could serve as an early step to evolve sociality in the natural world.IMPORTANCEThe first life forms on this planet were prokaryotic, and the earliest environments were aquatic, and from these relatively simple starting conditions, complex communities of microbes and ultimately multicellular organisms were able to evolve. Usually, motile cells in aqueous environments swim as individuals but become social by giving up motility and secreting extracellular substances to become a biofilm. Here, we identify a single point mutation in the flagellum that is sufficient to allow cells containing this mutation to specifically form large, suspended groups of cells. The specific change in the flagellar filament protein subunits causes a unique change in the flagellar structure. This could represent a distinct way for closely related cells to associate as an early precursor to sociality.

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Publication Details

Journal
Journal of Bacteriology
Published
2024-09-09
DOI
https://doi.org/10.1128/jb.00199-24
Citations
1
Primary Topic
Evolution and Genetic Dynamics
Type
article
Field-Weighted Citation Impact
0.55

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article

Flagellar point mutation causes social aggregation in laboratory-adapted Bacillus subtilis under conditions that promote swimming

Amanda Buck, Jacqueline Boyle, Edward H. Egelman, Abigail Sheridan et al.
1 citations
Journal of Bacteriology
Evolution and Genetic Dynamics
0.55
article

Flagellar point mutation causes social aggregation in laboratory-adapted Bacillus subtilis under conditions that promote swimming

Amanda Buck, Jacqueline Boyle, Edward H. Egelman, Abigail Sheridan, Mark A. B. Kreutzberger, Anna L. McLoon, Veezen Denise Mondelo, Justin Gejo, M. Mason, S. S. Alvi, Shriya Matta
article en
1 citations

Abstract

Motility allows microbes to explore and maximize success in their environment; however, many laboratory bacterial strains have a reduced or altered capacity for motility. Swimming motility in <i>Bacillus subtilis</i> depends on peritrichous flagella and is carried out individually as cells move by biased random walks toward attractants. Previously, we adapted <i>Bacillus subtilis</i> strain 3610 to the laboratory for 300 generations in lysogeny broth (LB) batch culture and isolated lab-adapted strains. Strain SH2 is motility-defective and in broth culture forms large, frequently spherical aggregates of cells. A single point mutation in the flagellin gene <i>hag</i> that causes amino acid 259 to switch from A to T is necessary and sufficient to cause these social cell aggregates, and aggregation occurs between flagellated cells bearing this point mutation regardless of the strain background. Cells associate when bearing this mutation, but flagellar rotation is needed to pull associating cells into spherical aggregates. Using electron microscopy, we are able to show that the SH2 flagellar filament has limited polymorphism when compared to other flagellar structures. This limited polymorphism hinders the flagellum's ability to function as a motility apparatus but appears to alter its function to that of cell aggregation/adhesion. We speculate that the genotype-specific aggregation of cells producing Hag<sup>A259T</sup> flagella could have increased representation in a batch-culture experiment by allowing similar cells to go through a transfer together and also that this mutation could serve as an early step to evolve sociality in the natural world.IMPORTANCEThe first life forms on this planet were prokaryotic, and the earliest environments were aquatic, and from these relatively simple starting conditions, complex communities of microbes and ultimately multicellular organisms were able to evolve. Usually, motile cells in aqueous environments swim as individuals but become social by giving up motility and secreting extracellular substances to become a biofilm. Here, we identify a single point mutation in the flagellum that is sufficient to allow cells containing this mutation to specifically form large, suspended groups of cells. The specific change in the flagellar filament protein subunits causes a unique change in the flagellar structure. This could represent a distinct way for closely related cells to associate as an early precursor to sociality.

Journal of BacteriologyVol. 206(10)
University of Virginia (US), Siena College (US)
National Institutes of Health, National Institute of General Medical Sciences
Life below water
Openalex Percentile: Top 26%
Evolution and Genetic Dynamics
0.55
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