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Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice

Salmonella enterica serovar Typhimurium (S. Typhimurium) is a Gram-negative bacterium that produces disease in numerous hosts. In mice, oral inoculation is followed by intestinal colonization and subsequent systemic dissemination, which leads to severe pathogenesis without the activation of an effic...

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Autores principales: Salazar, Geraldyne A., Peñaloza, Hernán F., Pardo-Roa, Catalina, Schultz, Bárbara M., Muñoz-Durango, Natalia, Gómez, Roberto S., Salazar, Francisco J., Pizarro, Daniela P., Riedel, Claudia A., González, Pablo A., Alvarez-Lobos, Manuel, Kalergis, Alexis M., Bueno, Susan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539121/
https://www.ncbi.nlm.nih.gov/pubmed/28824622
http://dx.doi.org/10.3389/fimmu.2017.00889
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author Salazar, Geraldyne A.
Peñaloza, Hernán F.
Pardo-Roa, Catalina
Schultz, Bárbara M.
Muñoz-Durango, Natalia
Gómez, Roberto S.
Salazar, Francisco J.
Pizarro, Daniela P.
Riedel, Claudia A.
González, Pablo A.
Alvarez-Lobos, Manuel
Kalergis, Alexis M.
Bueno, Susan M.
author_facet Salazar, Geraldyne A.
Peñaloza, Hernán F.
Pardo-Roa, Catalina
Schultz, Bárbara M.
Muñoz-Durango, Natalia
Gómez, Roberto S.
Salazar, Francisco J.
Pizarro, Daniela P.
Riedel, Claudia A.
González, Pablo A.
Alvarez-Lobos, Manuel
Kalergis, Alexis M.
Bueno, Susan M.
author_sort Salazar, Geraldyne A.
collection PubMed
description Salmonella enterica serovar Typhimurium (S. Typhimurium) is a Gram-negative bacterium that produces disease in numerous hosts. In mice, oral inoculation is followed by intestinal colonization and subsequent systemic dissemination, which leads to severe pathogenesis without the activation of an efficient anti-Salmonella immune response. This feature suggests that the infection caused by S. Typhimurium may promote the production of anti-inflammatory molecules by the host that prevent efficient T cell activation and bacterial clearance. In this study, we describe the contribution of immune cells producing the anti-inflammatory cytokine interleukin-10 (IL-10) to the systemic infection caused by S. Typhimurium in mice. We observed that the production of IL-10 was required by S. Typhimurium to cause a systemic disease, since mice lacking IL-10 (IL-10(−/−)) were significantly more resistant to die after an infection as compared to wild-type (WT) mice. IL-10(−/−) mice had reduced bacterial loads in internal organs and increased levels of pro-inflammatory cytokines in serum at 5 days of infection. Importantly, WT mice showed high bacterial loads in tissues and no increase of cytokines in serum after 5 days of S. Typhimurium infection, except for IL-10. In WT mice, we observed a peak of il-10 messenger RNA production in ileum, spleen, and liver after 5 days of infection. Importantly, the adoptive transfer of T or B cells from WT mice restored the susceptibility of IL-10(−/−) mice to systemic S. Typhimurium infection, suggesting that the generation of regulatory cells in vivo is required to sustain a systemic infection by S. Typhimurium. These findings support the notion that IL-10 production from lymphoid cells is a key process in the infective cycle of S. Typhimurium in mice due to generation of a tolerogenic immune response that prevents bacterial clearance and supports systemic dissemination.
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spelling pubmed-55391212017-08-18 Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice Salazar, Geraldyne A. Peñaloza, Hernán F. Pardo-Roa, Catalina Schultz, Bárbara M. Muñoz-Durango, Natalia Gómez, Roberto S. Salazar, Francisco J. Pizarro, Daniela P. Riedel, Claudia A. González, Pablo A. Alvarez-Lobos, Manuel Kalergis, Alexis M. Bueno, Susan M. Front Immunol Immunology Salmonella enterica serovar Typhimurium (S. Typhimurium) is a Gram-negative bacterium that produces disease in numerous hosts. In mice, oral inoculation is followed by intestinal colonization and subsequent systemic dissemination, which leads to severe pathogenesis without the activation of an efficient anti-Salmonella immune response. This feature suggests that the infection caused by S. Typhimurium may promote the production of anti-inflammatory molecules by the host that prevent efficient T cell activation and bacterial clearance. In this study, we describe the contribution of immune cells producing the anti-inflammatory cytokine interleukin-10 (IL-10) to the systemic infection caused by S. Typhimurium in mice. We observed that the production of IL-10 was required by S. Typhimurium to cause a systemic disease, since mice lacking IL-10 (IL-10(−/−)) were significantly more resistant to die after an infection as compared to wild-type (WT) mice. IL-10(−/−) mice had reduced bacterial loads in internal organs and increased levels of pro-inflammatory cytokines in serum at 5 days of infection. Importantly, WT mice showed high bacterial loads in tissues and no increase of cytokines in serum after 5 days of S. Typhimurium infection, except for IL-10. In WT mice, we observed a peak of il-10 messenger RNA production in ileum, spleen, and liver after 5 days of infection. Importantly, the adoptive transfer of T or B cells from WT mice restored the susceptibility of IL-10(−/−) mice to systemic S. Typhimurium infection, suggesting that the generation of regulatory cells in vivo is required to sustain a systemic infection by S. Typhimurium. These findings support the notion that IL-10 production from lymphoid cells is a key process in the infective cycle of S. Typhimurium in mice due to generation of a tolerogenic immune response that prevents bacterial clearance and supports systemic dissemination. Frontiers Media S.A. 2017-08-02 /pmc/articles/PMC5539121/ /pubmed/28824622 http://dx.doi.org/10.3389/fimmu.2017.00889 Text en Copyright © 2017 Salazar, Peñaloza, Pardo-Roa, Schultz, Muñoz-Durango, Gómez, Salazar, Pizarro, Riedel, González, Alvarez-Lobos, Kalergis and Bueno. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Salazar, Geraldyne A.
Peñaloza, Hernán F.
Pardo-Roa, Catalina
Schultz, Bárbara M.
Muñoz-Durango, Natalia
Gómez, Roberto S.
Salazar, Francisco J.
Pizarro, Daniela P.
Riedel, Claudia A.
González, Pablo A.
Alvarez-Lobos, Manuel
Kalergis, Alexis M.
Bueno, Susan M.
Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice
title Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice
title_full Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice
title_fullStr Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice
title_full_unstemmed Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice
title_short Interleukin-10 Production by T and B Cells Is a Key Factor to Promote Systemic Salmonella enterica Serovar Typhimurium Infection in Mice
title_sort interleukin-10 production by t and b cells is a key factor to promote systemic salmonella enterica serovar typhimurium infection in mice
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539121/
https://www.ncbi.nlm.nih.gov/pubmed/28824622
http://dx.doi.org/10.3389/fimmu.2017.00889
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