TY - JOUR
T1 - FLIM of mCherryTYG Deciphers pH Dynamics and Lifestyles of Salmonella Typhimurium
AU - Singh, Moirangthem Kiran
AU - Fernandez, Marion
AU - Dilawari, Rahul
AU - Zangoui, Parisa
AU - Kenney, Linda
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025
Y1 - 2025
N2 - Intracellular pH regulation is fundamental to bacterial adaptation, virulence, and survival in diverse environments. Salmonella Typhimurium, a key human pathogen, exploits host and environmental pH cues to transition between planktonic, biofilm, and virulence-associated states. However, precise tools to monitor bacterial pH dynamics at subcellular resolution have been limited. Herein, we report the application of mCherryTYG, a genetically encoded pH-sensitive fluorophore optimized for fluorescence lifetime imaging microscopy (FLIM), enabling robust and high-resolution pH measurements across diverse conditions. mCherryTYG demonstrated exceptional sensitivity across a broad pH range (5.5-8.5) with consistent lifetime responses and was unaffected by temperature, buffer composition, or ionic strength. Using FLIM, we characterized the pH dynamics of Salmonella across in vitro, host, and biofilm contexts. Under acidic stress in vitro, Salmonella maintained a uniform intracellular pH (∼6.04), providing clarity on previously debated heterogeneity. In infections of HeLa cells, Salmonella existed in distinct pH environments: acidic vacuolar pH (∼5.89) and neutral pH (∼7.10). During the late infection stage, ∼17% of the bacterial population retained an acidic pH. Biofilm studies revealed stratified pH profiles with acidic pH near the bottom and neutral pH at the surface, mirroring patterns observed in other pathogens. In heterologous host models, pH gradients shape bacterial adaptation strategies. In C. elegans, Salmonella experienced a progressive internal pH gradient from neutral pH (∼7.10) in the anterior lumen to acidic pH (∼6.45) in the posterior. Similarly, in zebrafish, Salmonella encountered acidic lysosome-rich enterocytes (∼5.84) and neutral regions (∼7.33) in the anterior gut. This study establishes mCherryTYG-FLIM as a transformative tool for studying bacterial pH regulation, revealing pH as a critical modulator of Salmonella lifestyle transitions between virulence and persistence. Our findings provide new insights into host-microbe interactions and present pH as a promising target for therapeutic interventions against bacterial infections.
AB - Intracellular pH regulation is fundamental to bacterial adaptation, virulence, and survival in diverse environments. Salmonella Typhimurium, a key human pathogen, exploits host and environmental pH cues to transition between planktonic, biofilm, and virulence-associated states. However, precise tools to monitor bacterial pH dynamics at subcellular resolution have been limited. Herein, we report the application of mCherryTYG, a genetically encoded pH-sensitive fluorophore optimized for fluorescence lifetime imaging microscopy (FLIM), enabling robust and high-resolution pH measurements across diverse conditions. mCherryTYG demonstrated exceptional sensitivity across a broad pH range (5.5-8.5) with consistent lifetime responses and was unaffected by temperature, buffer composition, or ionic strength. Using FLIM, we characterized the pH dynamics of Salmonella across in vitro, host, and biofilm contexts. Under acidic stress in vitro, Salmonella maintained a uniform intracellular pH (∼6.04), providing clarity on previously debated heterogeneity. In infections of HeLa cells, Salmonella existed in distinct pH environments: acidic vacuolar pH (∼5.89) and neutral pH (∼7.10). During the late infection stage, ∼17% of the bacterial population retained an acidic pH. Biofilm studies revealed stratified pH profiles with acidic pH near the bottom and neutral pH at the surface, mirroring patterns observed in other pathogens. In heterologous host models, pH gradients shape bacterial adaptation strategies. In C. elegans, Salmonella experienced a progressive internal pH gradient from neutral pH (∼7.10) in the anterior lumen to acidic pH (∼6.45) in the posterior. Similarly, in zebrafish, Salmonella encountered acidic lysosome-rich enterocytes (∼5.84) and neutral regions (∼7.33) in the anterior gut. This study establishes mCherryTYG-FLIM as a transformative tool for studying bacterial pH regulation, revealing pH as a critical modulator of Salmonella lifestyle transitions between virulence and persistence. Our findings provide new insights into host-microbe interactions and present pH as a promising target for therapeutic interventions against bacterial infections.
KW - bacterial lifestyles
KW - biofilms
KW - fluorescence lifetime imaging
KW - pH
KW - phenotypic heterogeneity
KW - Salmonella
KW - zebrafish, C. elegans
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UR - http://www.scopus.com/inward/citedby.url?scp=105007738659&partnerID=8YFLogxK
U2 - 10.1021/acssensors.5c00404
DO - 10.1021/acssensors.5c00404
M3 - Article
C2 - 40478522
AN - SCOPUS:105007738659
SN - 2379-3694
JO - ACS Sensors
JF - ACS Sensors
ER -