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Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes

Blastocystis is a species complex that exhibits extensive genetic diversity, evidenced by its classification into several genetically distinct subtypes (ST). Although several studies have shown the relationships between a specific subtype and gut microbiota, there is no study to show the effect of t...

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Autores principales: Deng, Lei, Wojciech, Lukasz, Png, Chin Wen, Kioh, Yan Qin Dorinda, Ng, Geok Choo, Chan, Eric Chun Yong, Zhang, Yongliang, Gascoigne, Nicholas R. J., Tan, Kevin Shyong Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130167/
https://www.ncbi.nlm.nih.gov/pubmed/37185924
http://dx.doi.org/10.1038/s41522-023-00389-1
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author Deng, Lei
Wojciech, Lukasz
Png, Chin Wen
Kioh, Yan Qin Dorinda
Ng, Geok Choo
Chan, Eric Chun Yong
Zhang, Yongliang
Gascoigne, Nicholas R. J.
Tan, Kevin Shyong Wei
author_facet Deng, Lei
Wojciech, Lukasz
Png, Chin Wen
Kioh, Yan Qin Dorinda
Ng, Geok Choo
Chan, Eric Chun Yong
Zhang, Yongliang
Gascoigne, Nicholas R. J.
Tan, Kevin Shyong Wei
author_sort Deng, Lei
collection PubMed
description Blastocystis is a species complex that exhibits extensive genetic diversity, evidenced by its classification into several genetically distinct subtypes (ST). Although several studies have shown the relationships between a specific subtype and gut microbiota, there is no study to show the effect of the ubiquitous Blastocystis ST1 on the gut microbiota and host health. Here, we show that Blastocystis ST1 colonization increased the proportion of beneficial bacteria Alloprevotella and Akkermansia, and induced Th2 and Treg cell responses in normal healthy mice. ST1-colonized mice showed decreases in the severity of DSS-induced colitis when compared to non-colonized mice. Furthermore, mice transplanted with ST1-altered gut microbiota were refractory to dextran sulfate sodium (DSS)-induced colitis via induction of Treg cells and elevated short-chain fat acid (SCFA) production. Our results suggest that colonization with Blastocystis ST1, one of the most common subtypes in humans, exerts beneficial effects on host health through modulating the gut microbiota and adaptive immune responses.
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spelling pubmed-101301672023-04-27 Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes Deng, Lei Wojciech, Lukasz Png, Chin Wen Kioh, Yan Qin Dorinda Ng, Geok Choo Chan, Eric Chun Yong Zhang, Yongliang Gascoigne, Nicholas R. J. Tan, Kevin Shyong Wei NPJ Biofilms Microbiomes Article Blastocystis is a species complex that exhibits extensive genetic diversity, evidenced by its classification into several genetically distinct subtypes (ST). Although several studies have shown the relationships between a specific subtype and gut microbiota, there is no study to show the effect of the ubiquitous Blastocystis ST1 on the gut microbiota and host health. Here, we show that Blastocystis ST1 colonization increased the proportion of beneficial bacteria Alloprevotella and Akkermansia, and induced Th2 and Treg cell responses in normal healthy mice. ST1-colonized mice showed decreases in the severity of DSS-induced colitis when compared to non-colonized mice. Furthermore, mice transplanted with ST1-altered gut microbiota were refractory to dextran sulfate sodium (DSS)-induced colitis via induction of Treg cells and elevated short-chain fat acid (SCFA) production. Our results suggest that colonization with Blastocystis ST1, one of the most common subtypes in humans, exerts beneficial effects on host health through modulating the gut microbiota and adaptive immune responses. Nature Publishing Group UK 2023-04-25 /pmc/articles/PMC10130167/ /pubmed/37185924 http://dx.doi.org/10.1038/s41522-023-00389-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Deng, Lei
Wojciech, Lukasz
Png, Chin Wen
Kioh, Yan Qin Dorinda
Ng, Geok Choo
Chan, Eric Chun Yong
Zhang, Yongliang
Gascoigne, Nicholas R. J.
Tan, Kevin Shyong Wei
Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes
title Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes
title_full Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes
title_fullStr Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes
title_full_unstemmed Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes
title_short Colonization with ubiquitous protist Blastocystis ST1 ameliorates DSS-induced colitis and promotes beneficial microbiota and immune outcomes
title_sort colonization with ubiquitous protist blastocystis st1 ameliorates dss-induced colitis and promotes beneficial microbiota and immune outcomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130167/
https://www.ncbi.nlm.nih.gov/pubmed/37185924
http://dx.doi.org/10.1038/s41522-023-00389-1
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