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Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut

Immigration to a highly industrialized nation has been associated with metabolic disease and simultaneous shifts in microbiota composition, but the underlying mechanisms are challenging to test in human studies. Here, we conducted a pilot study to assess the differential effects of human gut microbi...

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Autores principales: Vangay, Pajau, Ward, Tonya, Lucas, Sarah, Beura, Lalit K., Sabas, Dominique, Abramson, Max, Till, Lisa, Hoops, Susan L., Kashyap, Purna, Hunter, Ryan C., Masopust, David, Knights, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588527/
https://www.ncbi.nlm.nih.gov/pubmed/37853762
http://dx.doi.org/10.1080/19490976.2023.2266627
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author Vangay, Pajau
Ward, Tonya
Lucas, Sarah
Beura, Lalit K.
Sabas, Dominique
Abramson, Max
Till, Lisa
Hoops, Susan L.
Kashyap, Purna
Hunter, Ryan C.
Masopust, David
Knights, Dan
author_facet Vangay, Pajau
Ward, Tonya
Lucas, Sarah
Beura, Lalit K.
Sabas, Dominique
Abramson, Max
Till, Lisa
Hoops, Susan L.
Kashyap, Purna
Hunter, Ryan C.
Masopust, David
Knights, Dan
author_sort Vangay, Pajau
collection PubMed
description Immigration to a highly industrialized nation has been associated with metabolic disease and simultaneous shifts in microbiota composition, but the underlying mechanisms are challenging to test in human studies. Here, we conducted a pilot study to assess the differential effects of human gut microbiota collected from the United States (US) and rural Thailand on the murine gut mucosa and immune system. Colonization of germ-free mice with microbiota from US individuals resulted in an increased accumulation of innate-like CD8 T cells in the small intestine lamina propria and intra-epithelial compartments when compared to colonization with microbiota from Thai individuals. Both TCRγδ and CD8αα T cells showed a marked increase in mice receiving Western microbiota and, interestingly, this phenotype was also associated with an increase in intestinal mucus thickness. Serendipitously, an accidentally infected group of mice corroborated this association between elevated inflammatory response and increased mucus thickness. These results suggest that Western-associated human gut microbes contribute to a pro-inflammatory immune response.
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spelling pubmed-105885272023-10-21 Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut Vangay, Pajau Ward, Tonya Lucas, Sarah Beura, Lalit K. Sabas, Dominique Abramson, Max Till, Lisa Hoops, Susan L. Kashyap, Purna Hunter, Ryan C. Masopust, David Knights, Dan Gut Microbes Brief Report Immigration to a highly industrialized nation has been associated with metabolic disease and simultaneous shifts in microbiota composition, but the underlying mechanisms are challenging to test in human studies. Here, we conducted a pilot study to assess the differential effects of human gut microbiota collected from the United States (US) and rural Thailand on the murine gut mucosa and immune system. Colonization of germ-free mice with microbiota from US individuals resulted in an increased accumulation of innate-like CD8 T cells in the small intestine lamina propria and intra-epithelial compartments when compared to colonization with microbiota from Thai individuals. Both TCRγδ and CD8αα T cells showed a marked increase in mice receiving Western microbiota and, interestingly, this phenotype was also associated with an increase in intestinal mucus thickness. Serendipitously, an accidentally infected group of mice corroborated this association between elevated inflammatory response and increased mucus thickness. These results suggest that Western-associated human gut microbes contribute to a pro-inflammatory immune response. Taylor & Francis 2023-10-18 /pmc/articles/PMC10588527/ /pubmed/37853762 http://dx.doi.org/10.1080/19490976.2023.2266627 Text en © 2023 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Brief Report
Vangay, Pajau
Ward, Tonya
Lucas, Sarah
Beura, Lalit K.
Sabas, Dominique
Abramson, Max
Till, Lisa
Hoops, Susan L.
Kashyap, Purna
Hunter, Ryan C.
Masopust, David
Knights, Dan
Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut
title Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut
title_full Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut
title_fullStr Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut
title_full_unstemmed Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut
title_short Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut
title_sort industrialized human gut microbiota increases cd8+ t cells and mucus thickness in humanized mouse gut
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588527/
https://www.ncbi.nlm.nih.gov/pubmed/37853762
http://dx.doi.org/10.1080/19490976.2023.2266627
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