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Quorum sensing modulates the formation of virulent Legionella persisters within infected cells

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 nonreplica...

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Autores principales: Personnic, Nicolas, Striednig, Bianca, Lezan, Emmanuelle, Manske, Christian, Welin, Amanda, Schmidt, Alexander, Hilbi, Hubert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861284/
https://www.ncbi.nlm.nih.gov/pubmed/31740681
http://dx.doi.org/10.1038/s41467-019-13021-8
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author Personnic, Nicolas
Striednig, Bianca
Lezan, Emmanuelle
Manske, Christian
Welin, Amanda
Schmidt, Alexander
Hilbi, Hubert
author_facet Personnic, Nicolas
Striednig, Bianca
Lezan, Emmanuelle
Manske, Christian
Welin, Amanda
Schmidt, Alexander
Hilbi, Hubert
author_sort Personnic, Nicolas
collection PubMed
description 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.
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spelling pubmed-68612842019-11-20 Quorum sensing modulates the formation of virulent Legionella persisters within infected cells Personnic, Nicolas Striednig, Bianca Lezan, Emmanuelle Manske, Christian Welin, Amanda Schmidt, Alexander Hilbi, Hubert Nat Commun Article 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. Nature Publishing Group UK 2019-11-18 /pmc/articles/PMC6861284/ /pubmed/31740681 http://dx.doi.org/10.1038/s41467-019-13021-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Personnic, Nicolas
Striednig, Bianca
Lezan, Emmanuelle
Manske, Christian
Welin, Amanda
Schmidt, Alexander
Hilbi, Hubert
Quorum sensing modulates the formation of virulent Legionella persisters within infected cells
title Quorum sensing modulates the formation of virulent Legionella persisters within infected cells
title_full Quorum sensing modulates the formation of virulent Legionella persisters within infected cells
title_fullStr Quorum sensing modulates the formation of virulent Legionella persisters within infected cells
title_full_unstemmed Quorum sensing modulates the formation of virulent Legionella persisters within infected cells
title_short Quorum sensing modulates the formation of virulent Legionella persisters within infected cells
title_sort quorum sensing modulates the formation of virulent legionella persisters within infected cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6861284/
https://www.ncbi.nlm.nih.gov/pubmed/31740681
http://dx.doi.org/10.1038/s41467-019-13021-8
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