Cargando…

Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles

Gut microbiota regulates host metabolism and immunity. The phylogenetic composition of gut microbiota is influenced by diverse factors that include host gender. In this study, the effects of gender on gut microbial composition and its subsequent influence on serum metabolites in pigs were evaluated....

Descripción completa

Detalles Bibliográficos
Autores principales: He, Maozhang, Gao, Jun, Wu, Jinyuan, Zhou, Yunyan, Fu, Hao, Ke, Shanlin, Yang, Hui, Chen, Congying, Huang, Lusheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591444/
https://www.ncbi.nlm.nih.gov/pubmed/31275280
http://dx.doi.org/10.3389/fmicb.2019.01359
_version_ 1783429733485117440
author He, Maozhang
Gao, Jun
Wu, Jinyuan
Zhou, Yunyan
Fu, Hao
Ke, Shanlin
Yang, Hui
Chen, Congying
Huang, Lusheng
author_facet He, Maozhang
Gao, Jun
Wu, Jinyuan
Zhou, Yunyan
Fu, Hao
Ke, Shanlin
Yang, Hui
Chen, Congying
Huang, Lusheng
author_sort He, Maozhang
collection PubMed
description Gut microbiota regulates host metabolism and immunity. The phylogenetic composition of gut microbiota is influenced by diverse factors that include host gender. In this study, the effects of gender on gut microbial composition and its subsequent influence on serum metabolites in pigs were evaluated. The bacterial composition of feces samples was determined by 16S rRNA gene sequencing in 293 pure-bred Duroc pigs (108 gilts and 185 entire boars) and 64 validated pigs from an eight-breed mosaic F(6) population. Twenty-eight F(6) boars were castrated at 80 days of age to evaluate the effects of androgen on gut microbial composition. Untargeted serum metabolite features were determined in 45 boars and 26 gilts by an ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-QTOF/MS). The study observed an obvious influence of host gender on the gut microbial composition and identified numerous sex-biased bacterial taxa. These included Veillonellaceae, Roseburia, Bulleidia, and Escherichia which showed the higher abundance in boars, and Treponema and Bacteroides which were over-represented in gilts. Castration significantly shifted the fecal microbiota composition of the boars toward that of gilts. The predicted functional pathways of the gut microbiome related to obesity and energy harvest were enriched in gilts, and positively associated with gilt-enriched bacteria. Functional pathways related to peptidases and carbohydrate metabolism were enriched in boars and positively associated with boar-enriched bacteria. Serum metabolites related to androgen and cresol metabolism were identified as sex-biased metabolites. Correlation analysis between serum metabolites and sex-biased bacteria identified that the serum concentration of androgen-related metabolites was positively correlated with Bulleidia and Escherichia, but negatively associated with Treponema, suggesting a significant interaction between gut microbiota and host sex hormone metabolism. These results offer basic knowledge of how host gender and gut microbiota influence host metabolism.
format Online
Article
Text
id pubmed-6591444
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-65914442019-07-02 Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles He, Maozhang Gao, Jun Wu, Jinyuan Zhou, Yunyan Fu, Hao Ke, Shanlin Yang, Hui Chen, Congying Huang, Lusheng Front Microbiol Microbiology Gut microbiota regulates host metabolism and immunity. The phylogenetic composition of gut microbiota is influenced by diverse factors that include host gender. In this study, the effects of gender on gut microbial composition and its subsequent influence on serum metabolites in pigs were evaluated. The bacterial composition of feces samples was determined by 16S rRNA gene sequencing in 293 pure-bred Duroc pigs (108 gilts and 185 entire boars) and 64 validated pigs from an eight-breed mosaic F(6) population. Twenty-eight F(6) boars were castrated at 80 days of age to evaluate the effects of androgen on gut microbial composition. Untargeted serum metabolite features were determined in 45 boars and 26 gilts by an ultra-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-QTOF/MS). The study observed an obvious influence of host gender on the gut microbial composition and identified numerous sex-biased bacterial taxa. These included Veillonellaceae, Roseburia, Bulleidia, and Escherichia which showed the higher abundance in boars, and Treponema and Bacteroides which were over-represented in gilts. Castration significantly shifted the fecal microbiota composition of the boars toward that of gilts. The predicted functional pathways of the gut microbiome related to obesity and energy harvest were enriched in gilts, and positively associated with gilt-enriched bacteria. Functional pathways related to peptidases and carbohydrate metabolism were enriched in boars and positively associated with boar-enriched bacteria. Serum metabolites related to androgen and cresol metabolism were identified as sex-biased metabolites. Correlation analysis between serum metabolites and sex-biased bacteria identified that the serum concentration of androgen-related metabolites was positively correlated with Bulleidia and Escherichia, but negatively associated with Treponema, suggesting a significant interaction between gut microbiota and host sex hormone metabolism. These results offer basic knowledge of how host gender and gut microbiota influence host metabolism. Frontiers Media S.A. 2019-06-18 /pmc/articles/PMC6591444/ /pubmed/31275280 http://dx.doi.org/10.3389/fmicb.2019.01359 Text en Copyright © 2019 He, Gao, Wu, Zhou, Fu, Ke, Yang, Chen and Huang. http://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
He, Maozhang
Gao, Jun
Wu, Jinyuan
Zhou, Yunyan
Fu, Hao
Ke, Shanlin
Yang, Hui
Chen, Congying
Huang, Lusheng
Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles
title Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles
title_full Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles
title_fullStr Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles
title_full_unstemmed Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles
title_short Host Gender and Androgen Levels Regulate Gut Bacterial Taxa in Pigs Leading to Sex-Biased Serum Metabolite Profiles
title_sort host gender and androgen levels regulate gut bacterial taxa in pigs leading to sex-biased serum metabolite profiles
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591444/
https://www.ncbi.nlm.nih.gov/pubmed/31275280
http://dx.doi.org/10.3389/fmicb.2019.01359
work_keys_str_mv AT hemaozhang hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT gaojun hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT wujinyuan hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT zhouyunyan hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT fuhao hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT keshanlin hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT yanghui hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT chencongying hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles
AT huanglusheng hostgenderandandrogenlevelsregulategutbacterialtaxainpigsleadingtosexbiasedserummetaboliteprofiles