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Updated: Jun 16, 2025

Bile Salt-induced Biofilm Formation in Enteric Pathogens: Techniques for Identification and Quantification
Published on: May 6, 2018
Extracellular DNA filaments associated with surface polysaccharide II give Clostridioides difficile biofilm matrix a
Tania Kamwouo1, Sylvie Bouttier2, Séverine Domenichini3
1Micalis Institute, Université Paris-Saclay, INRAE, AgroParisTech, 17 avenue des Sciences, Orsay, France.
Abstract:
Clostridioides difficile is an anaerobic, spore-forming, Gram-positive bacterium, and a leading cause of healthcare-associated intestinal infections. Recurrences occur frequently, most of them being relapses. Apart from spores, C. difficile biofilm is hypothesized as a reservoir for relapses. Thus, increased knowledge on in vitro biofilm formation and characteristics is required. We finely characterized the matrix components in 4 C. difficile strains. Confocal microscopy revealed for the first time the presence of eDNA filaments connecting bacteria, with a spider's web-like organization. Biofilm disruption with DNase I suggests that eDNA, even in low abundance, plays a key role in the biofilm scaffold, maintaining biofilm cohesion by connecting bacteria. Observation of strong overlapping staining, particularly in the highest biofilm-producing strain tested between eDNA and polysaccharide II or lipoprotein CD1687, suggests that interactions between these components may enhance biofilm cohesion. Whereas autolysis does not appear to be a major way of matrix component release under our conditions, eDNA was sometimes associated with lipidic round shapes that can evoke vesicle structures. Together, these results suggest that the bacterial aggregation and structuring of the C. difficile biofilm involve several components of the matrix, including eDNA, interacting with each other to build the scaffold of biofilm.
Insights
Clostridioides difficile biofilms use extracellular DNA (eDNA) to connect bacteria and maintain structure. This eDNA, along with other matrix components, is crucial for biofilm cohesion and may contribute to recurrent infections.
Area of Science:
- Microbiology
- Bacterial pathogenesis
- Biofilm formation
Background:
- Clostridioides difficile is a major cause of healthcare-associated intestinal infections.
- Recurrent infections are common, with biofilms potentially acting as reservoirs.
- Understanding C. difficile biofilm structure is essential for developing new treatments.
Purpose of the Study:
- To characterize the matrix components of C. difficile biofilms.
- To investigate the role of extracellular DNA (eDNA) in biofilm structure and cohesion.
- To explore interactions between matrix components in C. difficile biofilms.
Main Methods:
- Culturing of 4 C. difficile strains.
- Confocal microscopy to visualize biofilm matrix.
- Treatment with DNase I to assess eDNA's role.
- Staining for eDNA, polysaccharide II, and lipoprotein CD1687.
Main Results:
- eDNA filaments form a connecting, spider's web-like network within the biofilm.
- DNase I treatment disrupted biofilm, indicating eDNA's key role in cohesion.
- Overlapping staining suggests interactions between eDNA, polysaccharide II, and CD1687 enhance cohesion.
- eDNA was sometimes associated with vesicle-like structures.
Conclusions:
- eDNA is a critical structural component of C. difficile biofilms.
- Interactions between eDNA and other matrix molecules contribute to biofilm cohesion.
- These findings provide insights into biofilm formation and potential targets for preventing recurrent C. difficile infections.
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