Nanoscaled Discovery of a Shunt Rifamycin from Salinispora arenicola Using a Three-Color GFP-Tagged Staphylococcus aureus Macrophage Infection Assay.
Nhan T PhamJoana AlvesFiona A SargisonReiko CullumJan WildenhainWilliam FenicalMark S ButlerDavid A MeadBrendan M DugganJ Ross FitzgeraldJames J La ClairManfred AuerPublished in: ACS infectious diseases (2023)
Antimicrobial resistance has emerged as a global public health threat, and development of novel therapeutics for treating infections caused by multi-drug resistant bacteria is urgent. Staphylococcus aureus is a major human and animal pathogen, responsible for high levels of morbidity and mortality worldwide. The intracellular survival of S. aureus in macrophages contributes to immune evasion, dissemination, and resilience to antibiotic treatment. Here, we present a confocal fluorescence imaging assay for monitoring macrophage infection by green fluorescent protein (GFP)-tagged S. aureus as a front-line tool to identify antibiotic leads. The assay was employed in combination with nanoscaled chemical analyses to facilitate the discovery of a new, active rifamycin analogue. Our findings indicate a promising new approach for the identification of antimicrobial compounds with macrophage intracellular activity. The antibiotic identified here may represent a useful addition to our armory in tackling the silent pandemic of antimicrobial resistance.
Keyphrases
- antimicrobial resistance
- staphylococcus aureus
- drug resistant
- high throughput
- fluorescence imaging
- public health
- small molecule
- multidrug resistant
- adipose tissue
- acinetobacter baumannii
- endothelial cells
- biofilm formation
- sars cov
- coronavirus disease
- photodynamic therapy
- protein protein
- reactive oxygen species
- optical coherence tomography
- candida albicans
- single cell
- climate change
- social support
- pulmonary artery
- depressive symptoms
- escherichia coli
- replacement therapy
- smoking cessation
- raman spectroscopy