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Production and Visualization of Bacterial Spheroplasts and Protoplasts to Characterize Antimicrobial Peptide Localization
Published on: August 11, 2018
Antimicrobial activity of prodigiosin is attributable to plasma-membrane damage
Rahul K Suryawanshi1, Chandrashekhar D Patil1, Sunil H Koli1
1a School of Life Sciences, North Maharashtra University , Jalgaon , India.
Abstract:
The bacterial pigment prodigiosin has various biological activities; it is, for instance, an effective antimicrobial. Here, we investigate the primary site targeted by prodigiosin, using the cells of microbial pathogens of humans as model systems: Candida albicans, Escherichia coli, Staphylococcus aureus. Inhibitory concentrations of prodigiosin; leakage of intracellular K+ ions, amino acids, proteins and sugars; impacts on activities of proteases, catalases and oxidases; and changes in surface appearance of pathogen cells were determined. Prodigiosin was highly inhibitory (30% growth rate reduction of C. albicans, E. coli, S. aureus at 0.3, 100 and 0.18 μg ml-1, respectively); caused leakage of intracellular substances (most severe in S. aureus); was highly inhibitory to each enzyme; and caused changes to S. aureus indicative of cell-surface damage. Collectively, these findings suggest that prodigiosin, log Poctanol-water 5.16, is not a toxin but is a hydrophobic stressor able to disrupt the plasma membrane via a chaotropicity-mediated mode-of-action.
Insights
Prodigiosin, a bacterial pigment, acts as a hydrophobic stressor, disrupting microbial plasma membranes. This antimicrobial mechanism explains its effectiveness against pathogens like Candida albicans, Escherichia coli, and Staphylococcus aureus.
Area of Science:
- Microbiology
- Biochemistry
- Pharmacology
Background:
- Prodigiosin is a bacterial pigment with known biological activities, including antimicrobial properties.
- Understanding the precise mechanism of action and cellular targets of prodigiosin is crucial for its therapeutic development.
Purpose of the Study:
- To investigate the primary cellular targets of the bacterial pigment prodigiosin.
- To elucidate the mode of action of prodigiosin against human microbial pathogens.
Main Methods:
- Assessed the inhibitory effects of prodigiosin on the growth of Candida albicans, Escherichia coli, and Staphylococcus aureus.
- Quantified the leakage of intracellular substances (K+ ions, amino acids, proteins, sugars) following prodigiosin treatment.
- Determined the impact of prodigiosin on the activity of key enzymes (proteases, catalases, oxidases).
- Observed changes in the surface morphology of pathogen cells exposed to prodigiosin.
Main Results:
- Prodigiosin exhibited significant growth inhibition against all tested pathogens.
- Prodigiosin induced substantial leakage of intracellular components, most notably from Staphylococcus aureus.
- The pigment strongly inhibited the activity of proteases, catalases, and oxidases.
- Surface damage was observed on Staphylococcus aureus cells, suggesting membrane disruption.
Conclusions:
- Prodigiosin functions as a hydrophobic stressor rather than a direct toxin.
- Its mode of action involves disrupting the plasma membrane through chaotropicity.
- These findings provide a mechanistic basis for prodigiosin's antimicrobial activity.
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