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A supramolecular platform technology for bacterial cell surface modification
- Source :
- ACS Infectious Diseases, 6(7), 1734-1744. AMER CHEMICAL SOC, ACS Infectious Diseases
- Publication Year :
- 2020
- Publisher :
- AMER CHEMICAL SOC, 2020.
-
Abstract
- In an era of antimicrobial resistance, a better understanding of the interaction between bacteria and the sentinel immune system is needed to discover new therapeutic targets for combating bacterial infectious disease. Sentinel immune cells such as macrophages phagocytose intact bacteria and thereby initiate ensuing immune responses. The bacterial surface composition is a key element that determines the macrophage signaling. To study the role of the bacterial cell surface composition in immune recognition, we developed a platform technology for altering bacterial surfaces in a controlled manner with versatile chemical scaffolds. We show that these scaffolds are efficiently loaded onto both Gram-positive and -negative bacteria and that their presence does not impair the capacity of monocyte-derived macrophages to phagocytose bacteria and subsequently signal to other components of the immune system. We believe this technology thus presents a useful tool to study the role of bacterial cell surface composition in disease etiology and potentially in novel interventions utilizing intact bacteria for vaccination.
- Subjects :
- 0301 basic medicine
Technology
Phagocytosis
infectious disease
030106 microbiology
Article
Bacterial cell structure
supramolecular chemistry
immune response
03 medical and health sciences
Antibiotic resistance
Immune system
bacteria
biology
Chemistry
Macrophages
biology.organism_classification
Disease etiology
Cell biology
030104 developmental biology
Infectious Diseases
Infectious disease (medical specialty)
Surface modification
surface modification
Bacteria
Signal Transduction
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- ACS Infectious Diseases, 6(7), 1734-1744. AMER CHEMICAL SOC, ACS Infectious Diseases
- Accession number :
- edsair.doi.dedup.....74080121b68dc785574c4f68f67c2ff4