# Restraining Staphylococcus aureus Virulence Factors and Quorum Sensing through Lactic Acid Bacteria Supernatant Extracts

**Authors:** Myriam Anabel Díaz, Esteban Gabriel Vega-Hissi, María Amparo Blázquez, María Rosa Alberto, Mario Eduardo Arena

PMC · DOI: 10.3390/antibiotics13040297 · Antibiotics · 2024-03-25

## TL;DR

Scientists found that extracts from lactic acid bacteria can inhibit harmful traits of Staphylococcus aureus, including biofilm formation and toxin production.

## Contribution

This study identifies 2,5-diketopiperazines as antivirulence and antibiofilm agents against antibiotic-resistant S. aureus.

## Key findings

- Lactic acid bacteria extracts inhibit biofilm formation and disrupt mature biofilms of S. aureus.
- Extracts reduce α-hemolysin production and coagulase activity in S. aureus.
- Molecular docking suggests 2,5-diketopiperazines interact with key S. aureus proteins like SarA and AgrA.

## Abstract

The escalating prevalence of antibiotic-resistant bacteria poses a grave threat to human health, necessitating the exploration of novel alternatives to conventional antibiotics. This study investigated the impact of extracts derived from the supernatant of four lactic acid bacteria strains on factors contributing to the pathogenicity of three Staphylococcus aureus strains. The study evaluated the influence of lactic acid bacteria supernatant extracts on the growth, biofilm biomass formation, biofilm metabolic activity, and biofilm integrity of the S. aureus strains. Additionally, the impact on virulence factors (hemolysin and coagulase) was examined. Gas chromatography coupled with mass spectrometry was used to identify the bioactive compounds in the extracts, while molecular docking analyses explored potential interactions. Predominantly, the extracts contain eight 2,5-diketopiperazines, which are cyclic forms of peptides. The extracts demonstrated inhibitory effects on biofilm formation, the ability to disrupt mature biofilms, and reduce the biofilm cell metabolic activity of the S. aureus strains. Furthermore, they exhibited the ability to inhibit α-hemolysin production and reduce coagulase activity. An in silico docking analysis reveals promising interactions between 2,5-diketopiperazines and key proteins (SarA and AgrA) in S. aureus, confirming their antivirulence and antibiofilm activities. These findings suggest that 2,5-diketopiperazines could serve as a promising lead compound in the fight against antibiotic-resistant S. aureus.

## Linked entities

- **Proteins:** ZFYVE9 (zinc finger FYVE-type containing 9), agrA (quorum-sensing response regulator AgrA)
- **Species:** Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Genes:** alpha-hemolysin [NCBI Gene 28381283], coagulase [NCBI Gene 28379458]
- **Species:** Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11047364/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC11047364/full.md

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Source: https://tomesphere.com/paper/PMC11047364