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Triphala Modulates the Membrane Vesicle Transcriptome of Enterococcus durans VIT3 to Influence Antibiotic Response
Venkatramanan Mahendrarajan1, Gomathi Nayagam Sankaranarayanan1, Gothandam Kodiveri Muthukaliannan1
1School of Biosciences and Technology, Vellore Institute of Technology, Tamil Nadu, Tiruvalam Road, Katpadi, India.
Triphala, a herbal formulation, modifies bacterial membrane vesicles (MVs) RNA cargo in Enterococcus durans. This suggests potential for synbiotic strategies to enhance microbial stress resilience.
Area of Science:
- Microbiology
- Molecular Biology
- Herbal Medicine
Background:
- Membrane vesicles (MVs) are key in bacterial communication and host interactions.
- Enterococcus durans is a bacterium relevant to host physiology.
- Triphala is a polyherbal formulation with potential biological activities.
Purpose of the Study:
- To investigate how triphala affects the RNA cargo of MVs from Enterococcus durans.
- To compare the effects of triphala, antibiotics, and their sequential combinations on MV RNA.
- To explore the impact of these treatments on bacterial stress response genes.
Main Methods:
- Isolation and characterization of MVs from Enterococcus durans under various stress conditions.
- Transcriptomic profiling of MV RNA cargo using pooled samples.
- Cytotoxicity assays on CaCo2 cells.
- Network analysis (STRING) to identify gene interactions.
Main Results:
- Triphala pretreatment upregulated genes for oxidative stress defense, envelope integrity, and CRISPR-Cas.
- Antibiotic-first treatments suppressed stress-related genes, highlighting treatment order importance.
- Triphala-antibiotic sequence showed coordinated expression in ATP synthase, arginine deiminase, and CRISPR loci.
- STRING analysis revealed functional clustering of upregulated genes.
Conclusions:
- Triphala can modulate the RNA cargo of bacterial MVs, influencing stress response pathways.
- The order of treatment (triphala vs. antibiotics) significantly impacts gene expression.
- Findings support triphala's potential role in synbiotic strategies for microbial stress resilience.
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