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Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection
BACKGROUND: Circulating lipoproteins improve the outcome of severe Gram-negative infections through neutralizing lipopolysaccharides (LPS), thus inhibiting the release of proinflammatory cytokines. METHODS/PRINCIPAL FINDINGS: Low density lipoprotein receptor deficient (LDLR−/−) mice, with a 7-fold i...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2617780/ https://www.ncbi.nlm.nih.gov/pubmed/19156198 http://dx.doi.org/10.1371/journal.pone.0004237 |
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author | Netea, Mihai G. Joosten, Leo A. B. Keuter, Monique Wagener, Frank Stalenhoef, Anton F. H. van der Meer, Jos W. M. Kullberg, Bart Jan |
author_facet | Netea, Mihai G. Joosten, Leo A. B. Keuter, Monique Wagener, Frank Stalenhoef, Anton F. H. van der Meer, Jos W. M. Kullberg, Bart Jan |
author_sort | Netea, Mihai G. |
collection | PubMed |
description | BACKGROUND: Circulating lipoproteins improve the outcome of severe Gram-negative infections through neutralizing lipopolysaccharides (LPS), thus inhibiting the release of proinflammatory cytokines. METHODS/PRINCIPAL FINDINGS: Low density lipoprotein receptor deficient (LDLR−/−) mice, with a 7-fold increase in LDL, are resistant against infection with Salmonella typhimurium (survival 100% vs 5%, p<0.001), and 100 to 1000-fold lower bacterial burden in the organs, compared with LDLR+/+ mice. Protection was not due to differences in cytokine production, phagocytosis, and killing of Salmonella organisms. The differences were caused by the excess of lipoproteins, as hyperlipoproteinemic ApoE−/− mice were also highly resistant to Salmonella infection. Lipoproteins protect against infection by interfering with the binding of Salmonella to host cells, and preventing organ invasion. This leads to an altered biodistribution of the microorganisms during the first hours of infection: after intravenous injection of Salmonella into LDLR+/+ mice, the bacteria invaded the liver and spleen within 30 minutes of infection. In contrast, in LDLR−/− mice, Salmonella remained constrained to the circulation from where they were efficiently cleared, with decreased organ invasion. CONCLUSIONS: plasma lipoproteins are a potent host defense mechanism against invasive Salmonella infection, by blocking adhesion of Salmonella to the host cells and subsequent tissue invasion. |
format | Text |
id | pubmed-2617780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26177802009-01-21 Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection Netea, Mihai G. Joosten, Leo A. B. Keuter, Monique Wagener, Frank Stalenhoef, Anton F. H. van der Meer, Jos W. M. Kullberg, Bart Jan PLoS One Research Article BACKGROUND: Circulating lipoproteins improve the outcome of severe Gram-negative infections through neutralizing lipopolysaccharides (LPS), thus inhibiting the release of proinflammatory cytokines. METHODS/PRINCIPAL FINDINGS: Low density lipoprotein receptor deficient (LDLR−/−) mice, with a 7-fold increase in LDL, are resistant against infection with Salmonella typhimurium (survival 100% vs 5%, p<0.001), and 100 to 1000-fold lower bacterial burden in the organs, compared with LDLR+/+ mice. Protection was not due to differences in cytokine production, phagocytosis, and killing of Salmonella organisms. The differences were caused by the excess of lipoproteins, as hyperlipoproteinemic ApoE−/− mice were also highly resistant to Salmonella infection. Lipoproteins protect against infection by interfering with the binding of Salmonella to host cells, and preventing organ invasion. This leads to an altered biodistribution of the microorganisms during the first hours of infection: after intravenous injection of Salmonella into LDLR+/+ mice, the bacteria invaded the liver and spleen within 30 minutes of infection. In contrast, in LDLR−/− mice, Salmonella remained constrained to the circulation from where they were efficiently cleared, with decreased organ invasion. CONCLUSIONS: plasma lipoproteins are a potent host defense mechanism against invasive Salmonella infection, by blocking adhesion of Salmonella to the host cells and subsequent tissue invasion. Public Library of Science 2009-01-21 /pmc/articles/PMC2617780/ /pubmed/19156198 http://dx.doi.org/10.1371/journal.pone.0004237 Text en Netea et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Netea, Mihai G. Joosten, Leo A. B. Keuter, Monique Wagener, Frank Stalenhoef, Anton F. H. van der Meer, Jos W. M. Kullberg, Bart Jan Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection |
title | Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection |
title_full | Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection |
title_fullStr | Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection |
title_full_unstemmed | Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection |
title_short | Circulating Lipoproteins Are a Crucial Component of Host Defense against Invasive Salmonella typhimurium Infection |
title_sort | circulating lipoproteins are a crucial component of host defense against invasive salmonella typhimurium infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2617780/ https://www.ncbi.nlm.nih.gov/pubmed/19156198 http://dx.doi.org/10.1371/journal.pone.0004237 |
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