Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783471320579702784 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6861284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT personnicnicolas quorumsensingmodulatestheformationofvirulentlegionellapersisterswithininfectedcells AT striednigbianca quorumsensingmodulatestheformationofvirulentlegionellapersisterswithininfectedcells AT lezanemmanuelle quorumsensingmodulatestheformationofvirulentlegionellapersisterswithininfectedcells AT manskechristian quorumsensingmodulatestheformationofvirulentlegionellapersisterswithininfectedcells AT welinamanda quorumsensingmodulatestheformationofvirulentlegionellapersisterswithininfectedcells AT schmidtalexander quorumsensingmodulatestheformationofvirulentlegionellapersisterswithininfectedcells AT hilbihubert quorumsensingmodulatestheformationofvirulentlegionellapersisterswithininfectedcells |