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Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment

Gut microbiota disorders damage the intestinal barrier, which causes intestinal disease. Thus, we screened the microbiota with significant changes using an in situ malignant colorectal cancer (CRC) model. Among the colonies with increased abundance, Akkermansia muciniphila (A. muciniphila) is known...

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Autores principales: Qu, Shuang, Zheng, Yinghui, Huang, Yichun, Feng, Yicheng, Xu, Kunyao, Zhang, Wei, Wang, Yawen, Nie, Kaili, Qin, Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018180/
https://www.ncbi.nlm.nih.gov/pubmed/36937258
http://dx.doi.org/10.3389/fmicb.2023.1111911
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author Qu, Shuang
Zheng, Yinghui
Huang, Yichun
Feng, Yicheng
Xu, Kunyao
Zhang, Wei
Wang, Yawen
Nie, Kaili
Qin, Meng
author_facet Qu, Shuang
Zheng, Yinghui
Huang, Yichun
Feng, Yicheng
Xu, Kunyao
Zhang, Wei
Wang, Yawen
Nie, Kaili
Qin, Meng
author_sort Qu, Shuang
collection PubMed
description Gut microbiota disorders damage the intestinal barrier, which causes intestinal disease. Thus, we screened the microbiota with significant changes using an in situ malignant colorectal cancer (CRC) model. Among the colonies with increased abundance, Akkermansia muciniphila (A. muciniphila) is known for its characteristic of breaking down mucin, which is an essential component of the intestinal barrier. The role of A. muciniphila remains controversial. To investigate the effect of excess A. muciniphila on the intestinal barrier, we established an over-colonized A. muciniphila mouse model by administering a live bacterial suspension after disrupting the original gut microbiome with antibiotics. The results showed that over-colonization of A. muciniphila decreased intestinal mucin content. The mRNA and protein expression levels of tight junction proteins also decreased significantly in the over-colonized A. muciniphila mouse model. Our findings reveal that excess colonization by A. muciniphila breaks the dynamic balance between mucin secretion and degradation, reduces the thickness of the intestinal mucus layer, and damages the intestinal barrier, which would eventually aggravate the development of colitis and CRC. These results will raise awareness about the safety of A. muciniphila serving as a probiotic.
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spelling pubmed-100181802023-03-17 Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment Qu, Shuang Zheng, Yinghui Huang, Yichun Feng, Yicheng Xu, Kunyao Zhang, Wei Wang, Yawen Nie, Kaili Qin, Meng Front Microbiol Microbiology Gut microbiota disorders damage the intestinal barrier, which causes intestinal disease. Thus, we screened the microbiota with significant changes using an in situ malignant colorectal cancer (CRC) model. Among the colonies with increased abundance, Akkermansia muciniphila (A. muciniphila) is known for its characteristic of breaking down mucin, which is an essential component of the intestinal barrier. The role of A. muciniphila remains controversial. To investigate the effect of excess A. muciniphila on the intestinal barrier, we established an over-colonized A. muciniphila mouse model by administering a live bacterial suspension after disrupting the original gut microbiome with antibiotics. The results showed that over-colonization of A. muciniphila decreased intestinal mucin content. The mRNA and protein expression levels of tight junction proteins also decreased significantly in the over-colonized A. muciniphila mouse model. Our findings reveal that excess colonization by A. muciniphila breaks the dynamic balance between mucin secretion and degradation, reduces the thickness of the intestinal mucus layer, and damages the intestinal barrier, which would eventually aggravate the development of colitis and CRC. These results will raise awareness about the safety of A. muciniphila serving as a probiotic. Frontiers Media S.A. 2023-03-02 /pmc/articles/PMC10018180/ /pubmed/36937258 http://dx.doi.org/10.3389/fmicb.2023.1111911 Text en Copyright © 2023 Qu, Zheng, Huang, Feng, Xu, Zhang, Wang, Nie and Qin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Qu, Shuang
Zheng, Yinghui
Huang, Yichun
Feng, Yicheng
Xu, Kunyao
Zhang, Wei
Wang, Yawen
Nie, Kaili
Qin, Meng
Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment
title Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment
title_full Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment
title_fullStr Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment
title_full_unstemmed Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment
title_short Excessive consumption of mucin by over-colonized Akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment
title_sort excessive consumption of mucin by over-colonized akkermansia muciniphila promotes intestinal barrier damage during malignant intestinal environment
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018180/
https://www.ncbi.nlm.nih.gov/pubmed/36937258
http://dx.doi.org/10.3389/fmicb.2023.1111911
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