fisher -344大鼠粪便微生物肠道型对高脂肪饮食的性别差异反应

IF 2.5 Q3 ONCOLOGY
Soo In Choi, Nayoung Kim, Ryoung Hee Nam, Ji Hyun Park, Heewon Nho, Jeong Eun Yu, Chin-Hee Song, Sun Min Lee, Dong Ho Lee
{"title":"fisher -344大鼠粪便微生物肠道型对高脂肪饮食的性别差异反应","authors":"Soo In Choi,&nbsp;Nayoung Kim,&nbsp;Ryoung Hee Nam,&nbsp;Ji Hyun Park,&nbsp;Heewon Nho,&nbsp;Jeong Eun Yu,&nbsp;Chin-Hee Song,&nbsp;Sun Min Lee,&nbsp;Dong Ho Lee","doi":"10.15430/JCP.2021.26.4.277","DOIUrl":null,"url":null,"abstract":"<p><p>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 <i>Ruminococcus</i> genus and expression of <i>Tlr2</i> 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.</p>","PeriodicalId":15120,"journal":{"name":"Journal of Cancer Prevention","volume":"26 4","pages":"277-288"},"PeriodicalIF":2.5000,"publicationDate":"2021-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/23/14/jcp-26-4-277.PMC8749319.pdf","citationCount":"1","resultStr":"{\"title\":\"Fecal Microbial Enterotypes Differentially Respond to a High-fat Diet Based on Sex in Fischer-344 Rats.\",\"authors\":\"Soo In Choi,&nbsp;Nayoung Kim,&nbsp;Ryoung Hee Nam,&nbsp;Ji Hyun Park,&nbsp;Heewon Nho,&nbsp;Jeong Eun Yu,&nbsp;Chin-Hee Song,&nbsp;Sun Min Lee,&nbsp;Dong Ho Lee\",\"doi\":\"10.15430/JCP.2021.26.4.277\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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 <i>Ruminococcus</i> genus and expression of <i>Tlr2</i> 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.</p>\",\"PeriodicalId\":15120,\"journal\":{\"name\":\"Journal of Cancer Prevention\",\"volume\":\"26 4\",\"pages\":\"277-288\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2021-12-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/23/14/jcp-26-4-277.PMC8749319.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Cancer Prevention\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15430/JCP.2021.26.4.277\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cancer Prevention","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15430/JCP.2021.26.4.277","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 1

摘要

肠道微生物群与宿主肠道环境相互作用,而宿主肠道环境受性别、年龄和宿主饮食等因素的影响。这些因素引起微生物组成的变化。本研究的目的是确定喂食高脂肪饮食(HFD)的Fisher-344 (F344)大鼠肠道微生物组的差异,这取决于它们的年龄和性别。采用16S rRNA基因测序、通过重建未观察状态对群落进行系统发育调查和肠型(E)评估,分析6、31、74周龄和2岁的雄性和雌性大鼠(对应于5、30、60和80岁的人类)的粪便微生物组。此外,HFD对结肠上皮细胞的影响采用实时定量PCR检测。无论年龄和性别,HFD组α多样性都有所下降。根据整个粪便微生物群的肠型聚类,将雄性大鼠粪便微生物群分为E1和E2肠型,雌性大鼠粪便微生物群分为E1、E2和E3肠型。雌性E3组Ruminococcus属的丰度和Tlr2 mRNA的表达均显著高,这可能反映了对HFD的补偿。此外,雌性E3组的机会致病性菌株与共生菌株的比例低于雌性E2组。HFD对所有评估年龄组的大鼠粪便微生物群都有影响,这可以进一步按性别区分。特别是,与雄性大鼠相比,雌性大鼠对HFD表现出代偿性肠型反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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 (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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
4.00%
发文量
32
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信