Microbead-Encapsulated Luminescent Bioreporter Screening of P. aeruginosa via Its Secreted Quorum-Sensing Molecules.
Abraham Abbey PaulYael Schlichter KadoshAriel KushmaroRobert S MarksPublished in: Biosensors (2024)
Pseudomonas aeruginosa is an opportunistic Gram-negative bacterium that remains a prevalent clinical and environmental challenge. Quorum-sensing (QS) molecules are effective biomarkers in pinpointing the presence of P. aeruginosa . This study aimed to develop a convenient-to-use, whole-cell biosensor using P. aeruginosa reporters individually encapsulated within alginate-poly-L-lysine (alginate-PLL) microbeads to specifically detect the presence of bacterial autoinducers. The PLL-reinforced microbeads were prepared using a two-step method involving ionic cross-linking and subsequent coating with thin layers of PLL. The alginate-PLL beads showed good stability in the presence of a known cation scavenger (sodium citrate), which typically limits the widespread applications of calcium alginate. In media containing synthetic autoinducers-such as N-(3-oxo dodecanoyl) homoserine lactone (3-oxo-C 12 -HSL) and N -butanoyl-L-homoserine lactone (C 4 -HSL), or the cell-free supernatants of planktonic or the flow-cell biofilm effluent of wild P. aeruginosa (PAO1)-the encapsulated bacteria enabled a dose-dependent detection of the presence of these QS molecules. The prepared bioreporter beads remained stable during prolonged storage at 4 and -80 °C and were ready for on-the-spot sensing without the need for recovery. The proof-of-concept, optical fiber-based, and whole-cell biosensor developed here demonstrates the practicality of the encapsulated bioreporter for bacterial detection based on specific QS molecules.
Keyphrases
- pseudomonas aeruginosa
- single cell
- gram negative
- cell free
- label free
- sensitive detection
- cell therapy
- gold nanoparticles
- quantum dots
- multidrug resistant
- cystic fibrosis
- high resolution
- staphylococcus aureus
- tissue engineering
- stem cells
- wound healing
- biofilm formation
- escherichia coli
- mass spectrometry
- loop mediated isothermal amplification
- acinetobacter baumannii
- real time pcr
- high speed
- genetic diversity