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Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model

AIM: Sepsis causes a systemic inflammatory reaction by destroying intestinal flora, which leads to a poor prognosis. In this study, we sought to clarify the characteristics of fecal flora and metabolites in a mouse model of sepsis by comprehensive metagenomic and metabolomic analysis. METHODS: We pe...

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Autores principales: Muratsu, Arisa, Ikeda, Mitsunori, Shimizu, Kentaro, Kameoka, Shoichiro, Motooka, Daisuke, Nakamura, Shota, Matsumoto, Hisatake, Ogura, Hiroshi, Shimazu, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238289/
https://www.ncbi.nlm.nih.gov/pubmed/35782956
http://dx.doi.org/10.1002/ams2.770
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author Muratsu, Arisa
Ikeda, Mitsunori
Shimizu, Kentaro
Kameoka, Shoichiro
Motooka, Daisuke
Nakamura, Shota
Matsumoto, Hisatake
Ogura, Hiroshi
Shimazu, Takeshi
author_facet Muratsu, Arisa
Ikeda, Mitsunori
Shimizu, Kentaro
Kameoka, Shoichiro
Motooka, Daisuke
Nakamura, Shota
Matsumoto, Hisatake
Ogura, Hiroshi
Shimazu, Takeshi
author_sort Muratsu, Arisa
collection PubMed
description AIM: Sepsis causes a systemic inflammatory reaction by destroying intestinal flora, which leads to a poor prognosis. In this study, we sought to clarify the characteristics of fecal flora and metabolites in a mouse model of sepsis by comprehensive metagenomic and metabolomic analysis. METHODS: We performed a cecal ligation and puncture model procedure to create a mild sepsis model. We collected fecal samples on day 0 (healthy condition) and days 1 and 7 after the cecal ligation and puncture to determine the microbiome and metabolites. We analyzed fecal flora using 16S rRNA gene sequencing and metabolites using capillary electrophoresis mass spectrometry with time‐of‐flight analysis. RESULTS: The abundance of bacteria belonging to the family Enterobacteriaceae significantly increased, but that of order Clostridiales such as the families Lachnospiraceae and Ruminococcaceae decreased on day 1 after the cecal ligation and puncture compared with those before the cecal ligation and puncture. The family Enterobacteriaceae significantly decreased, but that of order Clostridiales such as the families Lachnospiraceae and Ruminococcaceae increased on day 7 compared with those on day 1 after the cecal ligation and puncture. In the fecal metabolome, 313 metabolites were identified. Particularly, essential amino acids such as valine and non‐essential amino acids such as glycine increased remarkably following injury. Betaine and trimethylamine also increased. In contrast, short‐chain fatty acids such as isovaleric acid, butyric acid, and propionic acid decreased. CONCLUSION: The fecal microbiota following injury showed that Enterobacteriaceae increased in acute phase, and Lachnospiraceae and Ruminococcaceae increased in subacute phase. The metabolites revealed an increase in essential amino acids and choline metabolites and a decrease in short‐chain fatty acids.
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spelling pubmed-92382892022-06-30 Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model Muratsu, Arisa Ikeda, Mitsunori Shimizu, Kentaro Kameoka, Shoichiro Motooka, Daisuke Nakamura, Shota Matsumoto, Hisatake Ogura, Hiroshi Shimazu, Takeshi Acute Med Surg Original Articles AIM: Sepsis causes a systemic inflammatory reaction by destroying intestinal flora, which leads to a poor prognosis. In this study, we sought to clarify the characteristics of fecal flora and metabolites in a mouse model of sepsis by comprehensive metagenomic and metabolomic analysis. METHODS: We performed a cecal ligation and puncture model procedure to create a mild sepsis model. We collected fecal samples on day 0 (healthy condition) and days 1 and 7 after the cecal ligation and puncture to determine the microbiome and metabolites. We analyzed fecal flora using 16S rRNA gene sequencing and metabolites using capillary electrophoresis mass spectrometry with time‐of‐flight analysis. RESULTS: The abundance of bacteria belonging to the family Enterobacteriaceae significantly increased, but that of order Clostridiales such as the families Lachnospiraceae and Ruminococcaceae decreased on day 1 after the cecal ligation and puncture compared with those before the cecal ligation and puncture. The family Enterobacteriaceae significantly decreased, but that of order Clostridiales such as the families Lachnospiraceae and Ruminococcaceae increased on day 7 compared with those on day 1 after the cecal ligation and puncture. In the fecal metabolome, 313 metabolites were identified. Particularly, essential amino acids such as valine and non‐essential amino acids such as glycine increased remarkably following injury. Betaine and trimethylamine also increased. In contrast, short‐chain fatty acids such as isovaleric acid, butyric acid, and propionic acid decreased. CONCLUSION: The fecal microbiota following injury showed that Enterobacteriaceae increased in acute phase, and Lachnospiraceae and Ruminococcaceae increased in subacute phase. The metabolites revealed an increase in essential amino acids and choline metabolites and a decrease in short‐chain fatty acids. John Wiley and Sons Inc. 2022-06-28 /pmc/articles/PMC9238289/ /pubmed/35782956 http://dx.doi.org/10.1002/ams2.770 Text en © 2022 The Authors. Acute Medicine & Surgery published by John Wiley & Sons Australia, Ltd on behalf of Japanese Association for Acute Medicine. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Muratsu, Arisa
Ikeda, Mitsunori
Shimizu, Kentaro
Kameoka, Shoichiro
Motooka, Daisuke
Nakamura, Shota
Matsumoto, Hisatake
Ogura, Hiroshi
Shimazu, Takeshi
Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model
title Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model
title_full Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model
title_fullStr Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model
title_full_unstemmed Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model
title_short Dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model
title_sort dynamic change of fecal microbiota and metabolomics in a polymicrobial murine sepsis model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9238289/
https://www.ncbi.nlm.nih.gov/pubmed/35782956
http://dx.doi.org/10.1002/ams2.770
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