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Salmonella enters a dormant state within human epithelial cells for persistent infection

Salmonella Typhimurium (S. Typhimurium) is an enteric bacterium capable of invading a wide range of hosts, including rodents and humans. It targets different host cell types showing different intracellular lifestyles. S. Typhimurium colonizes different intracellular niches and is able to either acti...

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Autores principales: Luk, Chak Hon, Valenzuela, Camila, Gil, Magdalena, Swistak, Léa, Bomme, Perrine, Chang, Yuen-Yan, Mallet, Adeline, Enninga, Jost
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115778/
https://www.ncbi.nlm.nih.gov/pubmed/33930101
http://dx.doi.org/10.1371/journal.ppat.1009550
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author Luk, Chak Hon
Valenzuela, Camila
Gil, Magdalena
Swistak, Léa
Bomme, Perrine
Chang, Yuen-Yan
Mallet, Adeline
Enninga, Jost
author_facet Luk, Chak Hon
Valenzuela, Camila
Gil, Magdalena
Swistak, Léa
Bomme, Perrine
Chang, Yuen-Yan
Mallet, Adeline
Enninga, Jost
author_sort Luk, Chak Hon
collection PubMed
description Salmonella Typhimurium (S. Typhimurium) is an enteric bacterium capable of invading a wide range of hosts, including rodents and humans. It targets different host cell types showing different intracellular lifestyles. S. Typhimurium colonizes different intracellular niches and is able to either actively divide at various rates or remain dormant to persist. A comprehensive tool to determine these distinct S. Typhimurium lifestyles remains lacking. Here we developed a novel fluorescent reporter, Salmonella INtracellular Analyzer (SINA), compatible for fluorescence microscopy and flow cytometry in single-bacterium level quantification. This identified a S. Typhimurium subpopulation in infected epithelial cells that exhibits a unique phenotype in comparison to the previously documented vacuolar or cytosolic S. Typhimurium. This subpopulation entered a dormant state in a vesicular compartment distinct from the conventional Salmonella-containing vacuoles (SCV) as well as the previously reported niche of dormant S. Typhimurium in macrophages. The dormant S. Typhimurium inside enterocytes were viable and expressed Salmonella Pathogenicity Island 2 (SPI-2) virulence factors at later time points. We found that the formation of these dormant S. Typhimurium is not triggered by the loss of SPI-2 effector secretion but it is regulated by (p)ppGpp-mediated stringent response through RelA and SpoT. We predict that intraepithelial dormant S. Typhimurium represents an important pathogen niche and provides an alternative strategy for S. Typhimurium pathogenicity and its persistence.
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spelling pubmed-81157782021-05-24 Salmonella enters a dormant state within human epithelial cells for persistent infection Luk, Chak Hon Valenzuela, Camila Gil, Magdalena Swistak, Léa Bomme, Perrine Chang, Yuen-Yan Mallet, Adeline Enninga, Jost PLoS Pathog Research Article Salmonella Typhimurium (S. Typhimurium) is an enteric bacterium capable of invading a wide range of hosts, including rodents and humans. It targets different host cell types showing different intracellular lifestyles. S. Typhimurium colonizes different intracellular niches and is able to either actively divide at various rates or remain dormant to persist. A comprehensive tool to determine these distinct S. Typhimurium lifestyles remains lacking. Here we developed a novel fluorescent reporter, Salmonella INtracellular Analyzer (SINA), compatible for fluorescence microscopy and flow cytometry in single-bacterium level quantification. This identified a S. Typhimurium subpopulation in infected epithelial cells that exhibits a unique phenotype in comparison to the previously documented vacuolar or cytosolic S. Typhimurium. This subpopulation entered a dormant state in a vesicular compartment distinct from the conventional Salmonella-containing vacuoles (SCV) as well as the previously reported niche of dormant S. Typhimurium in macrophages. The dormant S. Typhimurium inside enterocytes were viable and expressed Salmonella Pathogenicity Island 2 (SPI-2) virulence factors at later time points. We found that the formation of these dormant S. Typhimurium is not triggered by the loss of SPI-2 effector secretion but it is regulated by (p)ppGpp-mediated stringent response through RelA and SpoT. We predict that intraepithelial dormant S. Typhimurium represents an important pathogen niche and provides an alternative strategy for S. Typhimurium pathogenicity and its persistence. Public Library of Science 2021-04-30 /pmc/articles/PMC8115778/ /pubmed/33930101 http://dx.doi.org/10.1371/journal.ppat.1009550 Text en © 2021 Luk et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Luk, Chak Hon
Valenzuela, Camila
Gil, Magdalena
Swistak, Léa
Bomme, Perrine
Chang, Yuen-Yan
Mallet, Adeline
Enninga, Jost
Salmonella enters a dormant state within human epithelial cells for persistent infection
title Salmonella enters a dormant state within human epithelial cells for persistent infection
title_full Salmonella enters a dormant state within human epithelial cells for persistent infection
title_fullStr Salmonella enters a dormant state within human epithelial cells for persistent infection
title_full_unstemmed Salmonella enters a dormant state within human epithelial cells for persistent infection
title_short Salmonella enters a dormant state within human epithelial cells for persistent infection
title_sort salmonella enters a dormant state within human epithelial cells for persistent infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115778/
https://www.ncbi.nlm.nih.gov/pubmed/33930101
http://dx.doi.org/10.1371/journal.ppat.1009550
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