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Published on: November 16, 2012
Links between S-adenosylmethionine and Agr-based quorum sensing for biofilm development in Listeria monocytogenes
1Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State, MS, USA.
Abstract:
Listeria monocytogenes is the causative agent of human listeriosis which has high hospitalization and mortality rates for individuals with weakened immune systems. The survival and dissemination of L. monocytogenes in adverse environments can be reinforced by the formation of biofilms. Therefore, this study aimed to understand the mechanisms underlying listerial biofilm development. Given that both nutrient availability and quorum sensing (QS) have been known as the factors influencing biofilm development, we hypothesized that the signal from a sentinel metabolite S-adenosylmethionine (SAM) and Agr-based QS could be synchronous in L. monocytogenes to modulate nutrient availability, the synthesis of extracellular polymeric substances (EPSs), and biofilm formation. We performed biofilm assays and quantitative real-time PCR to investigate how biofilm volumes and the expression of genes for the synthesis of EPS were affected by SAM supplementation, agr deletion, or both. We found that exogenously applied SAM induced biofilm formation and that the expression of genes encoding the EPS synthesis machineries was regulated by SAM and/or Agr QS. Moreover, the gene transcription of components acting in the methyl cycle for SAM synthesis and Agr QS was affected by the signals from the other system. In summary, we reveal an interconnection at the transcriptional level between metabolism and QS in L. monocytogenes and highlight the critical role of metabolite-oriented QS in biofilm development.
Insights
S-adenosylmethionine (SAM) and Agr quorum sensing (QS) synchronize in Listeria monocytogenes, controlling nutrient availability and biofilm formation. This metabolite-QS interplay is crucial for bacterial survival and dissemination.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- Listeria monocytogenes causes listeriosis, a severe infection with high mortality, particularly in immunocompromised individuals.
- Biofilm formation enhances the survival and spread of L. monocytogenes in challenging environments.
- Nutrient availability and quorum sensing (QS) are known regulators of biofilm development.
Purpose of the Study:
- To elucidate the mechanisms governing listerial biofilm development.
- To investigate the hypothesis that S-adenosylmethionine (SAM) and Agr-based QS signaling are synchronized in L. monocytogenes.
- To determine how this synchronization modulates nutrient availability, extracellular polymeric substances (EPS) synthesis, and biofilm formation.
Main Methods:
- Biofilm assays were conducted to quantify biofilm formation.
- Quantitative real-time PCR (qRT-PCR) was used to analyze gene expression.
- Experiments involved SAM supplementation, agr deletion, and combined treatments.
Main Results:
- Exogenous SAM application significantly induced biofilm formation in L. monocytogenes.
- The expression of genes involved in EPS synthesis was regulated by both SAM and Agr QS.
- Transcriptional analysis revealed cross-regulation between the SAM synthesis methyl cycle and Agr QS systems.
Conclusions:
- A significant interconnection exists at the transcriptional level between metabolic pathways (SAM synthesis) and QS systems in L. monocytogenes.
- Metabolite-oriented QS, influenced by SAM, plays a critical role in bacterial biofilm development.
- Understanding this interplay offers potential targets for controlling L. monocytogenes infections.
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