Cargando…

Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women

OBJECTIVES: More than 40% of U.S. adults are obese. Obesity, and in particular abdominal obesity, is associated with increased risk for developing a variety of chronic diseases. Obesity, aging, and menopause are each associated with differential shifts in the gut microbiome. We examined the associat...

Descripción completa

Detalles Bibliográficos
Autores principales: Cook, Katherine, Ochs-Balcom, Heather, Hovey, Kathleen, Wactawski-Wende, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194030/
http://dx.doi.org/10.1093/cdn/nzac069.006
_version_ 1784726618418184192
author Cook, Katherine
Ochs-Balcom, Heather
Hovey, Kathleen
Wactawski-Wende, Jean
author_facet Cook, Katherine
Ochs-Balcom, Heather
Hovey, Kathleen
Wactawski-Wende, Jean
author_sort Cook, Katherine
collection PubMed
description OBJECTIVES: More than 40% of U.S. adults are obese. Obesity, and in particular abdominal obesity, is associated with increased risk for developing a variety of chronic diseases. Obesity, aging, and menopause are each associated with differential shifts in the gut microbiome. We examined the association of visceral adiposity tissue (VAT) and the gut bacterial and phage microbiome. METHODS: We selected postmenopausal women (mean age 78 yrs) from the extremes of VAT (n = 25 per group; low VAT area (45.6 ± 12.5 cm(2)) and high VAT area (179.6 ± 30.4 cm(2))) using data from dual x-ray absorptiometry (DXA) scans and performed shotgun metagenomic sequencing on fecal DNA collected at the time of DXA scan. Women with history of hypertension, diabetes, hormone therapy use, or antibiotic use within 90 days from sample collection were excluded. DNA libraries were prepared using the Illumina Nextera XT library preparation kit and libraries were sequenced on an Illumina HiSeq platform to generate 150-bp paired-ends reads. We examined the α-diversity (Shannon or Chao1), principal coordinate analysis β-diversity distances, and prevalence of microbiome taxa comparing the high vs. low VAT groups. RESULTS: There was no significant difference in α-diversity or β-diversity between VAT groups. At the phyla level, women with high VAT displayed elevated Bacteroidetes and Proteobacteria proportional abundance (p < 0.05). At the species level, women with low VAT displayed significantly elevated proportional abundance of Alistipes shahii, Anaerostipes hadrus, and Blautia wexlerae. Women with high VAT area displayed significantly elevated Parabacteroides distasonis, Bacteroides uniformis, and Roseburia intestinalis. Women with high VAT displayed elevated proportional abundance of Escherichia phage TL-2011b (p < 0.05). CONCLUSIONS: Data suggest that postmenopausal women with high VAT display a differential bacterial microbiome and phage profile compared to postmenopausal women with low VAT, consistent with changes seen with age. Moreover, we identified an elevated proportional abundance of Alistipes shahii, Anaerostipes hadrus, and Blautia wexlerae in women with low VAT, suggesting potential for anti-obesity activity of these microbes in postmenopausal women. FUNDING SOURCES: DOD BCRP Breakthrough Award to KLC. The WHI program is funded by the NHLBI/NIH. NIDCR/NIH R01 to JW-W.
format Online
Article
Text
id pubmed-9194030
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-91940302022-06-14 Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women Cook, Katherine Ochs-Balcom, Heather Hovey, Kathleen Wactawski-Wende, Jean Curr Dev Nutr Nutritional Microbiology/Microbiome OBJECTIVES: More than 40% of U.S. adults are obese. Obesity, and in particular abdominal obesity, is associated with increased risk for developing a variety of chronic diseases. Obesity, aging, and menopause are each associated with differential shifts in the gut microbiome. We examined the association of visceral adiposity tissue (VAT) and the gut bacterial and phage microbiome. METHODS: We selected postmenopausal women (mean age 78 yrs) from the extremes of VAT (n = 25 per group; low VAT area (45.6 ± 12.5 cm(2)) and high VAT area (179.6 ± 30.4 cm(2))) using data from dual x-ray absorptiometry (DXA) scans and performed shotgun metagenomic sequencing on fecal DNA collected at the time of DXA scan. Women with history of hypertension, diabetes, hormone therapy use, or antibiotic use within 90 days from sample collection were excluded. DNA libraries were prepared using the Illumina Nextera XT library preparation kit and libraries were sequenced on an Illumina HiSeq platform to generate 150-bp paired-ends reads. We examined the α-diversity (Shannon or Chao1), principal coordinate analysis β-diversity distances, and prevalence of microbiome taxa comparing the high vs. low VAT groups. RESULTS: There was no significant difference in α-diversity or β-diversity between VAT groups. At the phyla level, women with high VAT displayed elevated Bacteroidetes and Proteobacteria proportional abundance (p < 0.05). At the species level, women with low VAT displayed significantly elevated proportional abundance of Alistipes shahii, Anaerostipes hadrus, and Blautia wexlerae. Women with high VAT area displayed significantly elevated Parabacteroides distasonis, Bacteroides uniformis, and Roseburia intestinalis. Women with high VAT displayed elevated proportional abundance of Escherichia phage TL-2011b (p < 0.05). CONCLUSIONS: Data suggest that postmenopausal women with high VAT display a differential bacterial microbiome and phage profile compared to postmenopausal women with low VAT, consistent with changes seen with age. Moreover, we identified an elevated proportional abundance of Alistipes shahii, Anaerostipes hadrus, and Blautia wexlerae in women with low VAT, suggesting potential for anti-obesity activity of these microbes in postmenopausal women. FUNDING SOURCES: DOD BCRP Breakthrough Award to KLC. The WHI program is funded by the NHLBI/NIH. NIDCR/NIH R01 to JW-W. Oxford University Press 2022-06-14 /pmc/articles/PMC9194030/ http://dx.doi.org/10.1093/cdn/nzac069.006 Text en © The Author 2022. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology. 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 (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Nutritional Microbiology/Microbiome
Cook, Katherine
Ochs-Balcom, Heather
Hovey, Kathleen
Wactawski-Wende, Jean
Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women
title Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women
title_full Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women
title_fullStr Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women
title_full_unstemmed Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women
title_short Visceral Adiposity Is Associated With Shifts in the Gut Bacterial and Phage Microbiome in Postmenopausal Women
title_sort visceral adiposity is associated with shifts in the gut bacterial and phage microbiome in postmenopausal women
topic Nutritional Microbiology/Microbiome
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194030/
http://dx.doi.org/10.1093/cdn/nzac069.006
work_keys_str_mv AT cookkatherine visceraladiposityisassociatedwithshiftsinthegutbacterialandphagemicrobiomeinpostmenopausalwomen
AT ochsbalcomheather visceraladiposityisassociatedwithshiftsinthegutbacterialandphagemicrobiomeinpostmenopausalwomen
AT hoveykathleen visceraladiposityisassociatedwithshiftsinthegutbacterialandphagemicrobiomeinpostmenopausalwomen
AT wactawskiwendejean visceraladiposityisassociatedwithshiftsinthegutbacterialandphagemicrobiomeinpostmenopausalwomen