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Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production
Colonic luminal aromatic amines have been historically considered to be derived from dietary source, especially fermented foods; however, recent studies indicate that the gut microbiota serves as an alternative source of these amines. Herein, we show that five prominent genera of Firmicutes (Blautia...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553188/ https://www.ncbi.nlm.nih.gov/pubmed/36217238 http://dx.doi.org/10.1080/19490976.2022.2128605 |
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author | Sugiyama, Yuta Mori, Yumiko Nara, Misaki Kotani, Yusuke Nagai, Emiko Kawada, Hiroki Kitamura, Mayu Hirano, Rika Shimokawa, Hiromi Nakagawa, Akira Minami, Hiromichi Gotoh, Aina Sakanaka, Mikiyasu Iida, Noriho Koyanagi, Takashi Katayama, Takane Okamoto, Shigefumi Kurihara, Shin |
author_facet | Sugiyama, Yuta Mori, Yumiko Nara, Misaki Kotani, Yusuke Nagai, Emiko Kawada, Hiroki Kitamura, Mayu Hirano, Rika Shimokawa, Hiromi Nakagawa, Akira Minami, Hiromichi Gotoh, Aina Sakanaka, Mikiyasu Iida, Noriho Koyanagi, Takashi Katayama, Takane Okamoto, Shigefumi Kurihara, Shin |
author_sort | Sugiyama, Yuta |
collection | PubMed |
description | Colonic luminal aromatic amines have been historically considered to be derived from dietary source, especially fermented foods; however, recent studies indicate that the gut microbiota serves as an alternative source of these amines. Herein, we show that five prominent genera of Firmicutes (Blautia, Clostridium, Enterococcus, Ruminococcus, and Tyzzerella) have the ability to abundantly produce aromatic amines through the action of aromatic amino acid decarboxylase (AADC). In vitro cultivation of human fecal samples revealed that a significant positive correlation between aadc copy number of Ruminococcus gnavus and phenylethylamine (PEA) production. Furthermore, using genetically engineered Enterococcus faecalis-colonized BALB/cCrSlc mouse model, we showed that the gut bacterial aadc stimulates the production of colonic serotonin, which is reportedly involved in osteoporosis and irritable bowel syndrome. Finally, we showed that human AADC inhibitors carbidopa and benserazide inhibit PEA production in En. faecalis. |
format | Online Article Text |
id | pubmed-9553188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-95531882022-10-12 Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production Sugiyama, Yuta Mori, Yumiko Nara, Misaki Kotani, Yusuke Nagai, Emiko Kawada, Hiroki Kitamura, Mayu Hirano, Rika Shimokawa, Hiromi Nakagawa, Akira Minami, Hiromichi Gotoh, Aina Sakanaka, Mikiyasu Iida, Noriho Koyanagi, Takashi Katayama, Takane Okamoto, Shigefumi Kurihara, Shin Gut Microbes Research Paper Colonic luminal aromatic amines have been historically considered to be derived from dietary source, especially fermented foods; however, recent studies indicate that the gut microbiota serves as an alternative source of these amines. Herein, we show that five prominent genera of Firmicutes (Blautia, Clostridium, Enterococcus, Ruminococcus, and Tyzzerella) have the ability to abundantly produce aromatic amines through the action of aromatic amino acid decarboxylase (AADC). In vitro cultivation of human fecal samples revealed that a significant positive correlation between aadc copy number of Ruminococcus gnavus and phenylethylamine (PEA) production. Furthermore, using genetically engineered Enterococcus faecalis-colonized BALB/cCrSlc mouse model, we showed that the gut bacterial aadc stimulates the production of colonic serotonin, which is reportedly involved in osteoporosis and irritable bowel syndrome. Finally, we showed that human AADC inhibitors carbidopa and benserazide inhibit PEA production in En. faecalis. Taylor & Francis 2022-10-10 /pmc/articles/PMC9553188/ /pubmed/36217238 http://dx.doi.org/10.1080/19490976.2022.2128605 Text en © 2022 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. |
spellingShingle | Research Paper Sugiyama, Yuta Mori, Yumiko Nara, Misaki Kotani, Yusuke Nagai, Emiko Kawada, Hiroki Kitamura, Mayu Hirano, Rika Shimokawa, Hiromi Nakagawa, Akira Minami, Hiromichi Gotoh, Aina Sakanaka, Mikiyasu Iida, Noriho Koyanagi, Takashi Katayama, Takane Okamoto, Shigefumi Kurihara, Shin Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production |
title | Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production |
title_full | Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production |
title_fullStr | Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production |
title_full_unstemmed | Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production |
title_short | Gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production |
title_sort | gut bacterial aromatic amine production: aromatic amino acid decarboxylase and its effects on peripheral serotonin production |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553188/ https://www.ncbi.nlm.nih.gov/pubmed/36217238 http://dx.doi.org/10.1080/19490976.2022.2128605 |
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