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Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis

Intestinal fungi are increasingly believed to greatly influence gut health. However, the effects of fungi on intestinal inflammation and on gut bacterial constitution are not clear. Here, based on pyrosequencing method, we reveal that fungal compositions vary in different intestinal segments (ileum,...

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Autores principales: Qiu, Xinyun, Zhang, Feng, Yang, Xi, Wu, Na, Jiang, Weiwei, Li, Xia, Li, Xiaoxue, Liu, Yulan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445066/
https://www.ncbi.nlm.nih.gov/pubmed/26013555
http://dx.doi.org/10.1038/srep10416
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author Qiu, Xinyun
Zhang, Feng
Yang, Xi
Wu, Na
Jiang, Weiwei
Li, Xia
Li, Xiaoxue
Liu, Yulan
author_facet Qiu, Xinyun
Zhang, Feng
Yang, Xi
Wu, Na
Jiang, Weiwei
Li, Xia
Li, Xiaoxue
Liu, Yulan
author_sort Qiu, Xinyun
collection PubMed
description Intestinal fungi are increasingly believed to greatly influence gut health. However, the effects of fungi on intestinal inflammation and on gut bacterial constitution are not clear. Here, based on pyrosequencing method, we reveal that fungal compositions vary in different intestinal segments (ileum, cecum, and colon), prefer different colonization locations (mucosa and feces), and are remarkably changed during intestinal inflammation in dextran sulfate sodium (DSS)-colitis mouse models compare to normal controls: Penicillium, Wickerhamomyces, Alternaria, and Candida are increased while Cryptococcus, Phialemonium, Wallemia and an unidentified Saccharomycetales genus are decreased in the guts of DSS-colitis mice. Fungi-depleted mice exhibited aggravated acute DSS-colitis associated with gain of Hallella, Barnesiella, Bacteroides, Alistipes, and Lactobacillus and loss of butyrate-producing Clostridium XIVa, and Anaerostipes compare with normal control. In contrast, bacteria-depleted mice show attenuated acute DSS-colitis. Mice with severely chronic recurrent DSS-colitis show increased plasma (1,3)-β-D-glucan level and fungal translocation into the colonic mucosa, mesenteric lymph nodes and spleen. This work demonstrate the different roles of fungi in acute and chronic recurrent colitis: They are important counterbalance to bacteria in maintaining intestinal micro-ecological homeostasis and health in acutely inflamed intestines, but can harmfully translocate into abnormal sites and could aggravate disease severity in chronic recurrent colitis.
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spelling pubmed-44450662015-06-01 Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis Qiu, Xinyun Zhang, Feng Yang, Xi Wu, Na Jiang, Weiwei Li, Xia Li, Xiaoxue Liu, Yulan Sci Rep Article Intestinal fungi are increasingly believed to greatly influence gut health. However, the effects of fungi on intestinal inflammation and on gut bacterial constitution are not clear. Here, based on pyrosequencing method, we reveal that fungal compositions vary in different intestinal segments (ileum, cecum, and colon), prefer different colonization locations (mucosa and feces), and are remarkably changed during intestinal inflammation in dextran sulfate sodium (DSS)-colitis mouse models compare to normal controls: Penicillium, Wickerhamomyces, Alternaria, and Candida are increased while Cryptococcus, Phialemonium, Wallemia and an unidentified Saccharomycetales genus are decreased in the guts of DSS-colitis mice. Fungi-depleted mice exhibited aggravated acute DSS-colitis associated with gain of Hallella, Barnesiella, Bacteroides, Alistipes, and Lactobacillus and loss of butyrate-producing Clostridium XIVa, and Anaerostipes compare with normal control. In contrast, bacteria-depleted mice show attenuated acute DSS-colitis. Mice with severely chronic recurrent DSS-colitis show increased plasma (1,3)-β-D-glucan level and fungal translocation into the colonic mucosa, mesenteric lymph nodes and spleen. This work demonstrate the different roles of fungi in acute and chronic recurrent colitis: They are important counterbalance to bacteria in maintaining intestinal micro-ecological homeostasis and health in acutely inflamed intestines, but can harmfully translocate into abnormal sites and could aggravate disease severity in chronic recurrent colitis. Nature Publishing Group 2015-05-27 /pmc/articles/PMC4445066/ /pubmed/26013555 http://dx.doi.org/10.1038/srep10416 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Qiu, Xinyun
Zhang, Feng
Yang, Xi
Wu, Na
Jiang, Weiwei
Li, Xia
Li, Xiaoxue
Liu, Yulan
Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis
title Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis
title_full Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis
title_fullStr Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis
title_full_unstemmed Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis
title_short Changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis
title_sort changes in the composition of intestinal fungi and their role in mice with dextran sulfate sodium-induced colitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445066/
https://www.ncbi.nlm.nih.gov/pubmed/26013555
http://dx.doi.org/10.1038/srep10416
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