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Grinholc, M.

Publications and source records attributed to Grinholc, M..

2 recordsLinked to original sources

Time-resolved transcriptomic mapping reveals conserved stress programs and metabolic rewiring in Escherichia coli under antimicrobial photodynamic and blue light exposure.

Antimicrobial photodynamic inactivation (aPDI) and antimicrobial blue light (aBL) are emerging, resistance-agnostic strategies for controlling bacterial pathogens, yet their systems-level impact on prokaryotic physiology remains incompletely understood. Here, we used time-resolved global transcriptomics to define how Escherichia coli reprograms gene expression in response to diverse photodynamic stresses. E. coli K-12 BW25113 was exposed to five phototreatments differing in photosensitizer chemistry and light wavelength, including rose bengal, TMPyP, new methylene blue, aBL alone, and aBL combined with 5-aminolevulinic acid, and transcriptional responses were profiled after short (30 min) and prolonged (7-8 h) exposure. Short-term phototreatments triggered rapid and extensive transcriptional remodeling, affecting up to [~]58% of the genes and dominated by conserved stress programs including oxidative defense, sulfur metabolism, and a broad downshift in biosynthesis and energy generation. In contrast, prolonged exposure elicited more restrained but highly treatment-specific adaptive responses, characterized by suppression of core energy metabolism, including oxidative phosphorylation and the tricarboxylic acid cycle, coupled with activation of alternative catabolic pathways. Together, these findings reveal a common acute stress architecture across photodynamic modalities followed by divergent long-term adaptive trajectories, providing a systems-level framework for understanding bacterial responses to light-based antimicrobials and informing the rational optimization of photodynamic therapies. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=66 SRC="FIGDIR/small/703343v1_ufig1.gif" ALT="Figure 1"> View larger version (22K): org.highwire.dtl.DTLVardef@a990a1org.highwire.dtl.DTLVardef@5670bcorg.highwire.dtl.DTLVardef@1035840org.highwire.dtl.DTLVardef@96ff67_HPS_FORMAT_FIGEXP M_FIG C_FIG

genomics↗

Cationic heme-mimetic gallium porphyrin kills bacteria and disrupts biofilms

The emergence of antimicrobial resistance in ESKAPE pathogens remains a clinical challenge and limits the utility of conventional antibiotics. Antimicrobial photodynamic inactivation (aPDI) using metal porphyrins is of interest, but the activity of heme-mimetic gallium porphyrins against structured biofilms has not been well defined. In this study, we evaluated a newly synthesized cationic heme-mimetic gallium porphyrin (GaCHP-2-3) activated with visible light against biofilms formed by ESKAPE representatives under static and flow conditions and on titanium surface. Light-activated GaCHP-2-3 reduced biofilm viable counts by up to 4 log10 CFU/mL. Prolonged serial passaging of planktonic bacteria in the presence of GaCHP-2-3 for 20 passages did not yield increases in MIC, indicating no detectable resistance development under these conditions. This work presents GaCHP-2-3 aPDI as a candidate approach for biofilm control and treatment of infections where antibiotic resistance limits the option.

microbiology↗