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

ABSTRACT: 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 diet...

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Autores principales: Newman, Tiffany M., Shively, Carol A., Register, Thomas C., Appt, Susan E., Yadav, Hariom, Colwell, Rita R., Fanelli, Brian, Dadlani, Manoj, Graubics, Karlis, Nguyen, Uyen Thao, Ramamoorthy, Sivapriya, Uberseder, Beth, Clear, Kenysha Y. J., Wilson, Adam S., Reeves, Kimberly D., Chappell, Mark C., Tooze, Janet A., Cook, Katherine L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101030/
https://www.ncbi.nlm.nih.gov/pubmed/33952353
http://dx.doi.org/10.1186/s40168-021-01069-y
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author Newman, Tiffany M.
Shively, Carol A.
Register, Thomas C.
Appt, Susan E.
Yadav, Hariom
Colwell, Rita R.
Fanelli, Brian
Dadlani, Manoj
Graubics, Karlis
Nguyen, Uyen Thao
Ramamoorthy, Sivapriya
Uberseder, Beth
Clear, Kenysha Y. J.
Wilson, Adam S.
Reeves, Kimberly D.
Chappell, Mark C.
Tooze, Janet A.
Cook, Katherine L.
author_facet Newman, Tiffany M.
Shively, Carol A.
Register, Thomas C.
Appt, Susan E.
Yadav, Hariom
Colwell, Rita R.
Fanelli, Brian
Dadlani, Manoj
Graubics, Karlis
Nguyen, Uyen Thao
Ramamoorthy, Sivapriya
Uberseder, Beth
Clear, Kenysha Y. J.
Wilson, Adam S.
Reeves, Kimberly D.
Chappell, Mark C.
Tooze, Janet A.
Cook, Katherine L.
author_sort Newman, Tiffany M.
collection PubMed
description ABSTRACT: 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(HIGH) versus P. copri(LOW)), which was not associated with adiposity. Overall, Western diet-fed animals in the P. copri(HIGH) group showed greater proportional abundance of B. ovatus, B. faecis, P. stercorea, P. brevis, and Faecalibacterium prausnitzii than those in the Western P. copri(LOW) group. Western diet P. copri(LOW) subjects had a greater proportion of Eubacterium siraeum. E. siraeum negatively correlated with P. copri proportional abundance regardless of dietary consumption. In the Western diet group, Shannon diversity was significantly higher in P. copri(LOW) when compared to P. copri(HIGH) subjects. Furthermore, gut E. siraeum abundance positively correlated with HDL plasma cholesterol indicating that those in the P. copri(LOW) population may represent a more metabolically healthy population. Untargeted metabolomics on urine and plasma from Western diet-fed P. copri(HIGH) and P. copri(LOW) subjects suggest early kidney dysfunction in Western diet-fed P. copri(HIGH) subjects. 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01069-y.
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spelling pubmed-81010302021-05-06 Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model Newman, Tiffany M. Shively, Carol A. Register, Thomas C. Appt, Susan E. Yadav, Hariom Colwell, Rita R. Fanelli, Brian Dadlani, Manoj Graubics, Karlis Nguyen, Uyen Thao Ramamoorthy, Sivapriya Uberseder, Beth Clear, Kenysha Y. J. Wilson, Adam S. Reeves, Kimberly D. Chappell, Mark C. Tooze, Janet A. Cook, Katherine L. Microbiome Research ABSTRACT: 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(HIGH) versus P. copri(LOW)), which was not associated with adiposity. Overall, Western diet-fed animals in the P. copri(HIGH) group showed greater proportional abundance of B. ovatus, B. faecis, P. stercorea, P. brevis, and Faecalibacterium prausnitzii than those in the Western P. copri(LOW) group. Western diet P. copri(LOW) subjects had a greater proportion of Eubacterium siraeum. E. siraeum negatively correlated with P. copri proportional abundance regardless of dietary consumption. In the Western diet group, Shannon diversity was significantly higher in P. copri(LOW) when compared to P. copri(HIGH) subjects. Furthermore, gut E. siraeum abundance positively correlated with HDL plasma cholesterol indicating that those in the P. copri(LOW) population may represent a more metabolically healthy population. Untargeted metabolomics on urine and plasma from Western diet-fed P. copri(HIGH) and P. copri(LOW) subjects suggest early kidney dysfunction in Western diet-fed P. copri(HIGH) subjects. 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-021-01069-y. BioMed Central 2021-05-05 /pmc/articles/PMC8101030/ /pubmed/33952353 http://dx.doi.org/10.1186/s40168-021-01069-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Newman, Tiffany M.
Shively, Carol A.
Register, Thomas C.
Appt, Susan E.
Yadav, Hariom
Colwell, Rita R.
Fanelli, Brian
Dadlani, Manoj
Graubics, Karlis
Nguyen, Uyen Thao
Ramamoorthy, Sivapriya
Uberseder, Beth
Clear, Kenysha Y. J.
Wilson, Adam S.
Reeves, Kimberly D.
Chappell, Mark C.
Tooze, Janet A.
Cook, Katherine L.
Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model
title Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model
title_full Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model
title_fullStr Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model
title_full_unstemmed Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model
title_short Diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model
title_sort diet, obesity, and the gut microbiome as determinants modulating metabolic outcomes in a non-human primate model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101030/
https://www.ncbi.nlm.nih.gov/pubmed/33952353
http://dx.doi.org/10.1186/s40168-021-01069-y
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