Investigating Extracellular DNA Release in Staphylococcus xylosus Biofilm In Vitro.
Sabine LeroyIsabelle LebertCarine AndantPierre MicheauRégine TalonPublished in: Microorganisms (2021)
Staphylococcus xylosus forms biofilm embedded in an extracellular polymeric matrix. As extracellular DNA (eDNA) resulting from cell lysis has been found in several staphylococcal biofilms, we investigated S. xylosus biofilm in vitro by a microscopic approach and identified the mechanisms involved in cell lysis by a transcriptomic approach. Confocal laser scanning microscopy (CLSM) analyses of the biofilms, together with DNA staining and DNase treatment, revealed that eDNA constituted an important component of the matrix. This eDNA resulted from cell lysis by two mechanisms, overexpression of phage-related genes and of cidABC encoding a holin protein that is an effector of murein hydrolase activity. This lysis might furnish nutrients for the remaining cells as highlighted by genes overexpressed in nucleotide salvage, in amino sugar catabolism and in inorganic ion transports. Several genes involved in DNA/RNA repair and genes encoding proteases and chaperones involved in protein turnover were up-regulated. Furthermore, S. xylosus perceived osmotic and oxidative stresses and responded by up-regulating genes involved in osmoprotectant synthesis and in detoxification. This study provides new insight into the physiology of S. xylosus in biofilm.
Keyphrases
- staphylococcus aureus
- candida albicans
- pseudomonas aeruginosa
- single cell
- biofilm formation
- single molecule
- circulating tumor
- cell free
- cell therapy
- high resolution
- optical coherence tomography
- nucleic acid
- mental health
- rna seq
- high throughput
- genome wide
- induced apoptosis
- transcription factor
- methicillin resistant staphylococcus aureus
- amino acid
- high speed
- cell death
- dna methylation
- mass spectrometry
- bone mineral density
- risk assessment
- mesenchymal stem cells
- circulating tumor cells
- protein protein
- dendritic cells
- binding protein
- cell cycle arrest
- heavy metals
- pi k akt
- heat shock
- atomic force microscopy