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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AAI
2019
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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. |
format | Online Article Text |
id | pubmed-6305795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | AAI |
record_format | MEDLINE/PubMed |
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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