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Updated: Jan 3, 2026

Tractable Mammalian Cell Infections with Protozoan-primed Bacteria
Published on: April 2, 2013
Quorum sensing modulates the formation of virulent Legionella persisters within infected cells
Nicolas Personnic1, Bianca Striednig2, Emmanuelle Lezan3
1Institute for Medical Microbiology, University of Zürich, Gloriastrasse 30, 8006, Zürich, Switzerland. npersonnic@imm.uzh.ch.
Abstract:
The facultative intracellular bacterium Legionella pneumophila replicates in environmental amoebae and in lung macrophages, and causes Legionnaires' disease. Here we show that L. pneumophila reversibly forms replicating and nonreplicating subpopulations of similar size within amoebae. The nonreplicating bacteria are viable and metabolically active, display increased antibiotic tolerance and a distinct proteome, and show high virulence as well as the capacity to form a degradation-resistant compartment. Upon infection of naïve or interferon-γ-activated macrophages, the nonreplicating subpopulation comprises ca. 10% or 50%, respectively, of the total intracellular bacteria; hence, the nonreplicating subpopulation is of similar size in amoebae and activated macrophages. The numbers of nonreplicating bacteria within amoebae are reduced in the absence of the autoinducer synthase LqsA or other components of the Lqs quorum-sensing system. Our results indicate that virulent, antibiotic-tolerant subpopulations of L. pneumophila are formed during infection of evolutionarily distant phagocytes, in a process controlled by the Lqs system.
Insights
Legionella pneumophila forms distinct, antibiotic-tolerant subpopulations during infection. This bacterial adaptation, crucial for virulence, is regulated by the Lqs quorum-sensing system in both amoebae and macrophages.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Cellular Microbiology
Background:
- Legionella pneumophila is an opportunistic pathogen causing Legionnaires' disease.
- It replicates intracellularly in environmental amoebae and human macrophages.
- Understanding bacterial adaptation during infection is critical for disease control.
Purpose of the Study:
- To investigate the formation and characteristics of bacterial subpopulations within host cells.
- To determine the role of the Lqs quorum-sensing system in bacterial adaptation.
- To assess the virulence and antibiotic tolerance of distinct bacterial subpopulations.
Main Methods:
- Comparative analysis of replicating and nonreplicating L. pneumophila subpopulations.
- Proteomic analysis of bacterial populations.
- Infection models using amoebae and macrophages (naïve and IFN-γ-activated).
- Genetic manipulation of the Lqs quorum-sensing system.
Main Results:
- L. pneumophila forms distinct, viable, and metabolically active nonreplicating subpopulations within amoebae.
- These nonreplicating bacteria exhibit increased antibiotic tolerance, distinct proteomes, and enhanced virulence.
- The proportion of nonreplicating bacteria is similar in amoebae and activated macrophages, and is regulated by the Lqs system.
- Nonreplicating bacteria form degradation-resistant compartments.
Conclusions:
- Virulent, antibiotic-tolerant subpopulations of L. pneumophila are formed during infection of phagocytes.
- This bacterial adaptation is conserved across evolutionarily distant host cells.
- The Lqs quorum-sensing system controls the formation of these important subpopulations.
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