Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model.

Body fat composition Eubacterium siraeum Metabolomics Metagenomic sequencing Prevotella copri Uremic toxins Urinary carnitine metabolites Western and Mediterranean diet

Journal

Microbiome
ISSN: 2049-2618
Titre abrégé: Microbiome
Pays: England
ID NLM: 101615147

Informations de publication

Date de publication:
05 05 2021
Historique:
received: 12 01 2021
accepted: 01 04 2021
entrez: 6 5 2021
pubmed: 7 5 2021
medline: 20 5 2021
Statut: epublish

Résumé

The objective of this study was to increase understanding of the complex interactions between diet, obesity, and the gut microbiome of adult female non-human primates (NHPs). Subjects consumed either a Western (n=15) or Mediterranean (n=14) diet designed to represent human dietary patterns for 31 months. Body composition was determined using CT, fecal samples were collected, and shotgun metagenomic sequencing was performed. Gut microbiome results were grouped by diet and adiposity. Diet was the main contributor to gut microbiome bacterial diversity. Adiposity within each diet was associated with subtle shifts in the proportional abundance of several taxa. Mediterranean diet-fed NHPs with lower body fat had a greater proportion of Lactobacillus animalis than their higher body fat counterparts. Higher body fat Western diet-fed NHPs had more Ruminococcus champaneliensis and less Bacteroides uniformis than their low body fat counterparts. Western diet-fed NHPs had significantly higher levels of Prevotella copri than Mediterranean diet NHPs. Western diet-fed subjects were stratified by P. copri abundance (P. copri In summary, the data indicate diet to be the major influencer of gut bacterial diversity. However, diet and adiposity must be considered together when analyzing changes in abundance of specific bacterial taxa. Interestingly, P. copri appears to mediate metabolic dysfunction in Western diet-fed NHPs. Video abstract.

Sections du résumé

BACKGROUND
The objective of this study was to increase understanding of the complex interactions between diet, obesity, and the gut microbiome of adult female non-human primates (NHPs). Subjects consumed either a Western (n=15) or Mediterranean (n=14) diet designed to represent human dietary patterns for 31 months. Body composition was determined using CT, fecal samples were collected, and shotgun metagenomic sequencing was performed. Gut microbiome results were grouped by diet and adiposity.
RESULTS
Diet was the main contributor to gut microbiome bacterial diversity. Adiposity within each diet was associated with subtle shifts in the proportional abundance of several taxa. Mediterranean diet-fed NHPs with lower body fat had a greater proportion of Lactobacillus animalis than their higher body fat counterparts. Higher body fat Western diet-fed NHPs had more Ruminococcus champaneliensis and less Bacteroides uniformis than their low body fat counterparts. Western diet-fed NHPs had significantly higher levels of Prevotella copri than Mediterranean diet NHPs. Western diet-fed subjects were stratified by P. copri abundance (P. copri
CONCLUSIONS
In summary, the data indicate diet to be the major influencer of gut bacterial diversity. However, diet and adiposity must be considered together when analyzing changes in abundance of specific bacterial taxa. Interestingly, P. copri appears to mediate metabolic dysfunction in Western diet-fed NHPs. Video abstract.

Identifiants

pubmed: 33952353
doi: 10.1186/s40168-021-01069-y
pii: 10.1186/s40168-021-01069-y
pmc: PMC8101030
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

100

Subventions

Organisme : NIA NIH HHS
ID : P30 AG049638
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA012197
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001420
Pays : United States

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Auteurs

Tiffany M Newman (TM)

Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Carol A Shively (CA)

Department of Pathology, Section of Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Thomas C Register (TC)

Department of Pathology, Section of Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Susan E Appt (SE)

Department of Pathology, Section of Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Hariom Yadav (H)

Department of Neurosurgery and Brain Repair, USF Center for Microbiome Research University of South Florida Morsani College of Medicine, Tampa, FL, USA.
Department of Internal Medicine-Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Rita R Colwell (RR)

CosmosID, Rockville, MD, USA.

Brian Fanelli (B)

CosmosID, Rockville, MD, USA.

Manoj Dadlani (M)

CosmosID, Rockville, MD, USA.

Karlis Graubics (K)

CosmosID, Rockville, MD, USA.

Uyen Thao Nguyen (UT)

Metabolon, Raleigh, NC, USA.

Sivapriya Ramamoorthy (S)

Metabolon, Raleigh, NC, USA.

Beth Uberseder (B)

Department of Pathology, Section of Comparative Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Kenysha Y J Clear (KYJ)

Department of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Adam S Wilson (AS)

Department of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Kimberly D Reeves (KD)

Department of Internal Medicine-Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Mark C Chappell (MC)

Department of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Janet A Tooze (JA)

Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Department of Biostatistics and Data Science, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Katherine L Cook (KL)

Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA. klcook@wakehealth.edu.
Department of Surgery, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA. klcook@wakehealth.edu.
Comprehensive Cancer Center, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA. klcook@wakehealth.edu.
Wake Forest School of Medicine, 575 N. Patterson Ave, Suite 340, Winston-Salem, NC, 27101, USA. klcook@wakehealth.edu.

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