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Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality

Infection with Francisella tularensis, the causative agent of the human disease tularemia, results in the overproduction of inflammatory cytokines, termed the cytokine storm. Excess metabolic byproducts of obesity accumulate in obese individuals and activate the same inflammatory signaling pathways...

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Autores principales: Ramos Muniz, Mireya G., Palfreeman, Matthew, Setzu, Nicole, Sanchez, Michelle A., Saenz Portillo, Pamela, Garza, Kristine M., Gosselink, Kristin L., Spencer, Charles T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038682/
https://www.ncbi.nlm.nih.gov/pubmed/30046592
http://dx.doi.org/10.1155/2018/3412732
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author Ramos Muniz, Mireya G.
Palfreeman, Matthew
Setzu, Nicole
Sanchez, Michelle A.
Saenz Portillo, Pamela
Garza, Kristine M.
Gosselink, Kristin L.
Spencer, Charles T.
author_facet Ramos Muniz, Mireya G.
Palfreeman, Matthew
Setzu, Nicole
Sanchez, Michelle A.
Saenz Portillo, Pamela
Garza, Kristine M.
Gosselink, Kristin L.
Spencer, Charles T.
author_sort Ramos Muniz, Mireya G.
collection PubMed
description Infection with Francisella tularensis, the causative agent of the human disease tularemia, results in the overproduction of inflammatory cytokines, termed the cytokine storm. Excess metabolic byproducts of obesity accumulate in obese individuals and activate the same inflammatory signaling pathways as F. tularensis infection. In addition, elevated levels of leptin in obese individuals also increase inflammation. Since leptin is produced by adipocytes, we hypothesized that increased fat of obese females may make them more susceptible to F. tularensis infection compared with lean individuals. Lean and obese female mice were infected with F. tularensis and the immunopathology and susceptibility monitored. Plasma and tissue cytokines were analyzed by multiplex ELISA and real-time RT-PCR, respectively. Obese mice were more sensitive to infection, developing a more intense cytokine storm, which was associated with increased death of obese mice compared with lean mice. This enhanced inflammatory response correlated with in vitro bacteria-infected macrophage cultures where addition of leptin led to increased production of inflammatory cytokines. We conclude that increased basal leptin expression in obese individuals causes a persistent low-level inflammatory response making them more susceptible to F. tularensis infection and heightening the generation of the immunopathological cytokine storm.
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spelling pubmed-60386822018-07-25 Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality Ramos Muniz, Mireya G. Palfreeman, Matthew Setzu, Nicole Sanchez, Michelle A. Saenz Portillo, Pamela Garza, Kristine M. Gosselink, Kristin L. Spencer, Charles T. Biomed Res Int Research Article Infection with Francisella tularensis, the causative agent of the human disease tularemia, results in the overproduction of inflammatory cytokines, termed the cytokine storm. Excess metabolic byproducts of obesity accumulate in obese individuals and activate the same inflammatory signaling pathways as F. tularensis infection. In addition, elevated levels of leptin in obese individuals also increase inflammation. Since leptin is produced by adipocytes, we hypothesized that increased fat of obese females may make them more susceptible to F. tularensis infection compared with lean individuals. Lean and obese female mice were infected with F. tularensis and the immunopathology and susceptibility monitored. Plasma and tissue cytokines were analyzed by multiplex ELISA and real-time RT-PCR, respectively. Obese mice were more sensitive to infection, developing a more intense cytokine storm, which was associated with increased death of obese mice compared with lean mice. This enhanced inflammatory response correlated with in vitro bacteria-infected macrophage cultures where addition of leptin led to increased production of inflammatory cytokines. We conclude that increased basal leptin expression in obese individuals causes a persistent low-level inflammatory response making them more susceptible to F. tularensis infection and heightening the generation of the immunopathological cytokine storm. Hindawi 2018-06-26 /pmc/articles/PMC6038682/ /pubmed/30046592 http://dx.doi.org/10.1155/2018/3412732 Text en Copyright © 2018 Mireya G. Ramos Muniz et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ramos Muniz, Mireya G.
Palfreeman, Matthew
Setzu, Nicole
Sanchez, Michelle A.
Saenz Portillo, Pamela
Garza, Kristine M.
Gosselink, Kristin L.
Spencer, Charles T.
Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality
title Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality
title_full Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality
title_fullStr Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality
title_full_unstemmed Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality
title_short Obesity Exacerbates the Cytokine Storm Elicited by Francisella tularensis Infection of Females and Is Associated with Increased Mortality
title_sort obesity exacerbates the cytokine storm elicited by francisella tularensis infection of females and is associated with increased mortality
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6038682/
https://www.ncbi.nlm.nih.gov/pubmed/30046592
http://dx.doi.org/10.1155/2018/3412732
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