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Microbial Reprogramming Inhibits Western Diet-Associated Obesity
A recent epidemiological study showed that eating ‘fast food’ items such as potato chips increased likelihood of obesity, whereas eating yogurt prevented age-associated weight gain in humans. It was demonstrated previously in animal models of obesity that the immune system plays a critical role in t...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707834/ https://www.ncbi.nlm.nih.gov/pubmed/23874682 http://dx.doi.org/10.1371/journal.pone.0068596 |
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author | Poutahidis, Theofilos Kleinewietfeld, Markus Smillie, Christopher Levkovich, Tatiana Perrotta, Alison Bhela, Siddheshvar Varian, Bernard J. Ibrahim, Yassin M. Lakritz, Jessica R. Kearney, Sean M. Chatzigiagkos, Antonis Hafler, David A. Alm, Eric J. Erdman, Susan E. |
author_facet | Poutahidis, Theofilos Kleinewietfeld, Markus Smillie, Christopher Levkovich, Tatiana Perrotta, Alison Bhela, Siddheshvar Varian, Bernard J. Ibrahim, Yassin M. Lakritz, Jessica R. Kearney, Sean M. Chatzigiagkos, Antonis Hafler, David A. Alm, Eric J. Erdman, Susan E. |
author_sort | Poutahidis, Theofilos |
collection | PubMed |
description | A recent epidemiological study showed that eating ‘fast food’ items such as potato chips increased likelihood of obesity, whereas eating yogurt prevented age-associated weight gain in humans. It was demonstrated previously in animal models of obesity that the immune system plays a critical role in this process. Here we examined human subjects and mouse models consuming Westernized ‘fast food’ diet, and found CD4(+) T helper (Th)17-biased immunity and changes in microbial communities and abdominal fat with obesity after eating the Western chow. In striking contrast, eating probiotic yogurt together with Western chow inhibited age-associated weight gain. We went on to test whether a bacteria found in yogurt may serve to lessen fat pathology by using purified Lactobacillus reuteri ATCC 6475 in drinking water. Surprisingly, we discovered that oral L. reuteri therapy alone was sufficient to change the pro-inflammatory immune cell profile and prevent abdominal fat pathology and age-associated weight gain in mice regardless of their baseline diet. These beneficial microbe effects were transferable into naïve recipient animals by purified CD4(+) T cells alone. Specifically, bacterial effects depended upon active immune tolerance by induction of Foxp3(+) regulatory T cells (Treg) and interleukin (Il)-10, without significantly changing the gut microbial ecology or reducing ad libitum caloric intake. Our finding that microbial targeting restored CD4(+) T cell balance and yielded significantly leaner animals regardless of their dietary ‘fast food’ indiscretions suggests population-based approaches for weight management and enhancing public health in industrialized societies. |
format | Online Article Text |
id | pubmed-3707834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37078342013-07-19 Microbial Reprogramming Inhibits Western Diet-Associated Obesity Poutahidis, Theofilos Kleinewietfeld, Markus Smillie, Christopher Levkovich, Tatiana Perrotta, Alison Bhela, Siddheshvar Varian, Bernard J. Ibrahim, Yassin M. Lakritz, Jessica R. Kearney, Sean M. Chatzigiagkos, Antonis Hafler, David A. Alm, Eric J. Erdman, Susan E. PLoS One Research Article A recent epidemiological study showed that eating ‘fast food’ items such as potato chips increased likelihood of obesity, whereas eating yogurt prevented age-associated weight gain in humans. It was demonstrated previously in animal models of obesity that the immune system plays a critical role in this process. Here we examined human subjects and mouse models consuming Westernized ‘fast food’ diet, and found CD4(+) T helper (Th)17-biased immunity and changes in microbial communities and abdominal fat with obesity after eating the Western chow. In striking contrast, eating probiotic yogurt together with Western chow inhibited age-associated weight gain. We went on to test whether a bacteria found in yogurt may serve to lessen fat pathology by using purified Lactobacillus reuteri ATCC 6475 in drinking water. Surprisingly, we discovered that oral L. reuteri therapy alone was sufficient to change the pro-inflammatory immune cell profile and prevent abdominal fat pathology and age-associated weight gain in mice regardless of their baseline diet. These beneficial microbe effects were transferable into naïve recipient animals by purified CD4(+) T cells alone. Specifically, bacterial effects depended upon active immune tolerance by induction of Foxp3(+) regulatory T cells (Treg) and interleukin (Il)-10, without significantly changing the gut microbial ecology or reducing ad libitum caloric intake. Our finding that microbial targeting restored CD4(+) T cell balance and yielded significantly leaner animals regardless of their dietary ‘fast food’ indiscretions suggests population-based approaches for weight management and enhancing public health in industrialized societies. Public Library of Science 2013-07-10 /pmc/articles/PMC3707834/ /pubmed/23874682 http://dx.doi.org/10.1371/journal.pone.0068596 Text en © 2013 Poutahidis 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 Poutahidis, Theofilos Kleinewietfeld, Markus Smillie, Christopher Levkovich, Tatiana Perrotta, Alison Bhela, Siddheshvar Varian, Bernard J. Ibrahim, Yassin M. Lakritz, Jessica R. Kearney, Sean M. Chatzigiagkos, Antonis Hafler, David A. Alm, Eric J. Erdman, Susan E. Microbial Reprogramming Inhibits Western Diet-Associated Obesity |
title | Microbial Reprogramming Inhibits Western Diet-Associated Obesity |
title_full | Microbial Reprogramming Inhibits Western Diet-Associated Obesity |
title_fullStr | Microbial Reprogramming Inhibits Western Diet-Associated Obesity |
title_full_unstemmed | Microbial Reprogramming Inhibits Western Diet-Associated Obesity |
title_short | Microbial Reprogramming Inhibits Western Diet-Associated Obesity |
title_sort | microbial reprogramming inhibits western diet-associated obesity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3707834/ https://www.ncbi.nlm.nih.gov/pubmed/23874682 http://dx.doi.org/10.1371/journal.pone.0068596 |
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