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Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously

Salmonella infection is a globally important cause of gastroenteritis and systemic disease and is a useful tool to study immune responses in the intestine. Although mechanisms leading to immune responses against Salmonella have been extensively studied, questions remain about how bacteria travel fro...

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Autores principales: Bravo-Blas, Alberto, Utriainen, Lotta, Clay, Slater L., Kästele, Verena, Cerovic, Vuk, Cunningham, Adam F., Henderson, Ian R., Wall, Daniel M., Milling, Simon W. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AAI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305795/
https://www.ncbi.nlm.nih.gov/pubmed/30487173
http://dx.doi.org/10.4049/jimmunol.1701254
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author Bravo-Blas, Alberto
Utriainen, Lotta
Clay, Slater L.
Kästele, Verena
Cerovic, Vuk
Cunningham, Adam F.
Henderson, Ian R.
Wall, Daniel M.
Milling, Simon W. F.
author_facet Bravo-Blas, Alberto
Utriainen, Lotta
Clay, Slater L.
Kästele, Verena
Cerovic, Vuk
Cunningham, Adam F.
Henderson, Ian R.
Wall, Daniel M.
Milling, Simon W. F.
author_sort Bravo-Blas, Alberto
collection PubMed
description Salmonella infection is a globally important cause of gastroenteritis and systemic disease and is a useful tool to study immune responses in the intestine. Although mechanisms leading to immune responses against Salmonella have been extensively studied, questions remain about how bacteria travel from the intestinal mucosa to the mesenteric lymph nodes (MLN), a key site for Ag presentation. In this study, we used a mouse model of infection with Salmonella enterica serovar Typhimurium (STM) to identify changes in intestinal immune cells induced during early infection. We then used fluorescently labeled STM to identify interactions with immune cells from the site of infection through migration in lymph to the MLN. We show that viable STM can be carried in the lymph by any subset of migrating dendritic cells but not by macrophages. Moreover, approximately half of the STM in lymph are not associated with cells at all and travel autonomously. Within the MLN, STM associates with dendritic cells and B cells but predominantly with MLN-resident macrophages. In conclusion, we describe the routes used by STM to spread systemically in the period immediately postinfection. This deeper understanding of the infection process could open new avenues for controlling it.
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spelling pubmed-63057952019-01-03 Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously Bravo-Blas, Alberto Utriainen, Lotta Clay, Slater L. Kästele, Verena Cerovic, Vuk Cunningham, Adam F. Henderson, Ian R. Wall, Daniel M. Milling, Simon W. F. J Immunol Mucosal Immunology Salmonella infection is a globally important cause of gastroenteritis and systemic disease and is a useful tool to study immune responses in the intestine. Although mechanisms leading to immune responses against Salmonella have been extensively studied, questions remain about how bacteria travel from the intestinal mucosa to the mesenteric lymph nodes (MLN), a key site for Ag presentation. In this study, we used a mouse model of infection with Salmonella enterica serovar Typhimurium (STM) to identify changes in intestinal immune cells induced during early infection. We then used fluorescently labeled STM to identify interactions with immune cells from the site of infection through migration in lymph to the MLN. We show that viable STM can be carried in the lymph by any subset of migrating dendritic cells but not by macrophages. Moreover, approximately half of the STM in lymph are not associated with cells at all and travel autonomously. Within the MLN, STM associates with dendritic cells and B cells but predominantly with MLN-resident macrophages. In conclusion, we describe the routes used by STM to spread systemically in the period immediately postinfection. This deeper understanding of the infection process could open new avenues for controlling it. AAI 2019-01-01 2018-11-28 /pmc/articles/PMC6305795/ /pubmed/30487173 http://dx.doi.org/10.4049/jimmunol.1701254 Text en Copyright © 2018 The Authors https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the CC BY 4.0 Unported license.
spellingShingle Mucosal Immunology
Bravo-Blas, Alberto
Utriainen, Lotta
Clay, Slater L.
Kästele, Verena
Cerovic, Vuk
Cunningham, Adam F.
Henderson, Ian R.
Wall, Daniel M.
Milling, Simon W. F.
Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously
title Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously
title_full Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously
title_fullStr Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously
title_full_unstemmed Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously
title_short Salmonella enterica Serovar Typhimurium Travels to Mesenteric Lymph Nodes Both with Host Cells and Autonomously
title_sort salmonella enterica serovar typhimurium travels to mesenteric lymph nodes both with host cells and autonomously
topic Mucosal Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305795/
https://www.ncbi.nlm.nih.gov/pubmed/30487173
http://dx.doi.org/10.4049/jimmunol.1701254
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