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The Bacillary Postbiotics, Including 2-Undecanone, Suppress the Virulence of Pathogenic Microorganisms
Satish Kumar Rajasekharan1, Moshe Shemesh1
1Department of Food Science, Institute of Postharvest Technology and Food Sciences, Agricultural Research Organization (ARO), The Volcani Institute, Rishon LeZion 7528809, Israel.
Abstract:
Secreted molecules from probiotic Bacilli have often been considered potential pharmaceuticals to fight infections caused by bacterial or yeast pathogens. In the present study, we investigated the antagonistic potential of secreted probiotic filtrates (hereafter, postbiotics) derived from Lactobacillus plantarum cells against pathogenic microorganisms, such as Escherichia coli, Staphylococcus aureus, and Candida albicans. We found that the postbiotics mitigate the biofilms of the tested pathogens with no notable effect on their planktonic growth. In addition, the postbiotics suppressed some virulence traits, for instance, the dendrite swarming motility of E. coli and yeast-to-hyphal switch in C. albicans. Further assays with an active constituent produced by the L. plantarum cells-2-undecanone revealed two significant findings: (i) 2-undecanone inhibits C. albicans biofilms and hyphae in vitro and in a Caenorhabditis elegans model, and (ii) it interacts specifically with Gln 58 amino acid residue of hyphal wall protein-1 (Hwp-1) in molecular docking analysis. The results suggest the targeted mode of antagonistic action of 2-undecanone against C. albicans biofilm. In total, the findings of the study depict an appealing strategy to use postbiotics, including specific ketone molecules, produced by L. plantarum for developing novel antibiofilm and anti-hyphal pharmaceuticals.
Insights
Probiotic postbiotics from Lactobacillus plantarum combat pathogen biofilms and virulence. A key compound, 2-undecanone, specifically targets Candida albicans biofilms and hyphae, offering a novel pharmaceutical strategy.
Area of Science:
- Microbiology
- Biochemistry
- Pharmaceutical Science
Background:
- Secreted molecules from probiotic bacteria, termed postbiotics, are explored for pharmaceutical applications against pathogens.
- Pathogenic bacteria like Escherichia coli and Staphylococcus aureus, and yeast like Candida albicans, pose significant infection risks.
Purpose of the Study:
- To investigate the antagonistic potential of Lactobacillus plantarum-derived postbiotics against pathogenic microorganisms.
- To identify specific compounds within postbiotics responsible for antimicrobial effects and their mechanisms of action.
Main Methods:
- Testing postbiotic filtrates against biofilms and planktonic growth of E. coli, S. aureus, and C. albicans.
- Assessing the impact of postbiotics on pathogen virulence factors, including E. coli swarming motility and C. albicans hyphal switch.
- Investigating the specific compound 2-undecanone for its effects on C. albicans biofilms and hyphae using in vitro and in vivo models, alongside molecular docking.
Main Results:
- L. plantarum postbiotics effectively mitigated pathogen biofilms without affecting planktonic growth.
- Postbiotics suppressed virulence traits such as E. coli swarming motility and C. albicans yeast-to-hyphal transition.
- 2-undecanone demonstrated significant inhibition of C. albicans biofilms and hyphae, interacting with Hwp-1 via molecular docking.
Conclusions:
- L. plantarum postbiotics represent a promising strategy for developing novel antibiofilm and anti-hyphal pharmaceuticals.
- The ketone 2-undecanone exhibits targeted antagonism against C. albicans biofilm formation and hyphal development.
- Findings support the use of specific postbiotic compounds for combating microbial infections and virulence.
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