Bioorthogonal Metabolic Labeling of the Virulence Factor Phenolic Glycolipid in Mycobacteria.
Lindsay E GuzmánC J CambierTan-Yun ChengKubra F NaqviMichael U ShilohD Branch MoodyCarolyn R BertozziPublished in: ACS chemical biology (2024)
Surface lipids on pathogenic mycobacteria modulate infection outcomes by regulating host immune responses. Phenolic glycolipid (PGL) is a host-modulating surface lipid that varies among clinical Mycobacterium tuberculosis strains. PGL is also found in Mycobacterium marinum , where it promotes infection of zebrafish through effects on the innate immune system. Given the important role this lipid plays in the host-pathogen relationship, tools for profiling its abundance, spatial distribution, and dynamics are needed. Here, we report a strategy for imaging PGL in live mycobacteria using bioorthogonal metabolic labeling. We functionalized the PGL precursor p -hydroxybenzoic acid ( p HB) with an azide group (3-azido p HB). When fed to mycobacteria, 3-azido p HB was incorporated into the cell surface, which could then be visualized via the bioorthogonal conjugation of a fluorescent probe. We confirmed that 3-azido p HB incorporates into PGL using mass spectrometry methods and demonstrated selectivity for PGL-producing M. marinum and M. tuberculosis strains. Finally, we applied this metabolic labeling strategy to study the dynamics of PGL within the mycobacterial membrane. This new tool enables visualization of PGL that may facilitate studies of mycobacterial pathogenesis.
Keyphrases
- mycobacterium tuberculosis
- immune response
- escherichia coli
- fluorescent probe
- mass spectrometry
- cell surface
- pulmonary tuberculosis
- high resolution
- fatty acid
- adipose tissue
- microbial community
- skeletal muscle
- hiv aids
- liquid chromatography
- metabolic syndrome
- antibiotic resistance genes
- high performance liquid chromatography
- quantum dots
- weight loss
- drug induced
- gas chromatography
- electron microscopy