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Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats

The gut microbiota interacts with the host gut environment, which is influenced by such factors as sex, age, and host diet. These factors induce changes in the microbial composition. The aim of this study was to identify differences in the gut microbiome of Fisher-344 (F344) rats fed a high-fat diet...

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Autores principales: Choi, Soo In, Kim, Nayoung, Nam, Ryoung Hee, Park, Ji Hyun, Nho, Heewon, Yu, Jeong Eun, Song, Chin-Hee, Lee, Sun Min, Lee, Dong Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Cancer Prevention 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749319/
https://www.ncbi.nlm.nih.gov/pubmed/35047454
http://dx.doi.org/10.15430/JCP.2021.26.4.277
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author Choi, Soo In
Kim, Nayoung
Nam, Ryoung Hee
Park, Ji Hyun
Nho, Heewon
Yu, Jeong Eun
Song, Chin-Hee
Lee, Sun Min
Lee, Dong Ho
author_facet Choi, Soo In
Kim, Nayoung
Nam, Ryoung Hee
Park, Ji Hyun
Nho, Heewon
Yu, Jeong Eun
Song, Chin-Hee
Lee, Sun Min
Lee, Dong Ho
author_sort Choi, Soo In
collection PubMed
description The gut microbiota interacts with the host gut environment, which is influenced by such factors as sex, age, and host diet. These factors induce changes in the microbial composition. The aim of this study was to identify differences in the gut microbiome of Fisher-344 (F344) rats fed a high-fat diet (HFD), depending on their age and sex. Fecal microbiomes from 6-, 31-, and 74-week-old, and 2-year-old both male and female rats (corresponding to 5-, 30-, 60-, and 80-year-old humans) were analyzed using 16S rRNA gene sequencing, phylogenetic investigation of communities by reconstruction of unobserved states, and enterotype (E) assessment. Moreover, the effect of an HFD on colonic epithelial cells was measured using real-time quantitative PCR. Alpha diversity decreased in the HFD group regardless of age and sex. Based on the enterotype clustering of the whole fecal microbiome, clusters from male rats were divided into E1 and E2 enterotypes, while clusters from female rats were divided into E1, E2, and E3 enterotypes. The female E3 group showed a significantly high abundance in the Ruminococcus genus and expression of Tlr2 mRNA, which may reflect compensation to the HFD. Moreover, the female E3 group showed a lower ratio of opportunistic pathogenic strains to commensal strains compared to the female E2 group. Administration of an HFD influenced the rat fecal microbiota in all assessed age groups, which could be further differentiated by sex. In particular, female rats showed a compensatory enterotype response to an HFD compared to male rats.
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spelling pubmed-87493192022-01-18 Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats Choi, Soo In Kim, Nayoung Nam, Ryoung Hee Park, Ji Hyun Nho, Heewon Yu, Jeong Eun Song, Chin-Hee Lee, Sun Min Lee, Dong Ho J Cancer Prev Original Article The gut microbiota interacts with the host gut environment, which is influenced by such factors as sex, age, and host diet. These factors induce changes in the microbial composition. The aim of this study was to identify differences in the gut microbiome of Fisher-344 (F344) rats fed a high-fat diet (HFD), depending on their age and sex. Fecal microbiomes from 6-, 31-, and 74-week-old, and 2-year-old both male and female rats (corresponding to 5-, 30-, 60-, and 80-year-old humans) were analyzed using 16S rRNA gene sequencing, phylogenetic investigation of communities by reconstruction of unobserved states, and enterotype (E) assessment. Moreover, the effect of an HFD on colonic epithelial cells was measured using real-time quantitative PCR. Alpha diversity decreased in the HFD group regardless of age and sex. Based on the enterotype clustering of the whole fecal microbiome, clusters from male rats were divided into E1 and E2 enterotypes, while clusters from female rats were divided into E1, E2, and E3 enterotypes. The female E3 group showed a significantly high abundance in the Ruminococcus genus and expression of Tlr2 mRNA, which may reflect compensation to the HFD. Moreover, the female E3 group showed a lower ratio of opportunistic pathogenic strains to commensal strains compared to the female E2 group. Administration of an HFD influenced the rat fecal microbiota in all assessed age groups, which could be further differentiated by sex. In particular, female rats showed a compensatory enterotype response to an HFD compared to male rats. Korean Society of Cancer Prevention 2021-12-30 2021-12-30 /pmc/articles/PMC8749319/ /pubmed/35047454 http://dx.doi.org/10.15430/JCP.2021.26.4.277 Text en Copyright © 2021 Korean Society of Cancer Prevention https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Soo In
Kim, Nayoung
Nam, Ryoung Hee
Park, Ji Hyun
Nho, Heewon
Yu, Jeong Eun
Song, Chin-Hee
Lee, Sun Min
Lee, Dong Ho
Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats
title Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats
title_full Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats
title_fullStr Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats
title_full_unstemmed Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats
title_short Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats
title_sort fecal microbial enterotypes differentially respond to a high-fat diet based on sex in fischer-344 rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8749319/
https://www.ncbi.nlm.nih.gov/pubmed/35047454
http://dx.doi.org/10.15430/JCP.2021.26.4.277
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