Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance

Recent preclinical data suggest that alterations in the gut microbiota may be an important factor linking obesity to vascular dysfunction, an early sign of cardiovascular disease. The purpose of this study was to begin translation of these preclinical data by examining whether vascular phenotypes in...

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Main Authors: S. Raj J. Trikha, Dustin M. Lee, Kayl E. Ecton, Scott D. Wrigley, Allegra R. Vazquez, Nicole S. Litwin, Keely N. Thomas, Yuren Wei, Micah L. Battson, Sarah A. Johnson, Kristine A. Kuhn, Sean P. Colgan, Christopher L. Gentile, Tiffany L. Weir
Format: Article
Language:English
Published: Taylor & Francis Group 2021-01-01
Series:Gut Microbes
Subjects:
Online Access:http://dx.doi.org/10.1080/19490976.2021.1940791
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spelling doaj-4f206cc49e2045d0abc57ae69c5f7c7e2021-08-09T15:50:07ZengTaylor & Francis GroupGut Microbes1949-09761949-09842021-01-0113110.1080/19490976.2021.19407911940791Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intoleranceS. Raj J. Trikha0Dustin M. Lee1Kayl E. Ecton2Scott D. Wrigley3Allegra R. Vazquez4Nicole S. Litwin5Keely N. Thomas6Yuren Wei7Micah L. Battson8Sarah A. Johnson9Kristine A. Kuhn10Sean P. Colgan11Christopher L. Gentile12Tiffany L. Weir13Colorado State UniversityBrooke Army Medical CenterColorado State UniversityColorado State UniversityColorado State UniversityUniversity of California San DiegoColorado State UniversityColorado State UniversityMetropolitan State UniversityColorado State UniversityUniversity of Colorado School of MedicineUniversity of Colorado School of MedicineColorado State UniversityColorado State UniversityRecent preclinical data suggest that alterations in the gut microbiota may be an important factor linking obesity to vascular dysfunction, an early sign of cardiovascular disease. The purpose of this study was to begin translation of these preclinical data by examining whether vascular phenotypes in humans are transmissible through the gut microbiota. We hypothesized that germ-free mice colonized with gut microbiota from obese individuals would display diminished vascular function compared to germ-free mice receiving microbiota from lean individuals. We transplanted fecal material from obese and lean age-and sex-matched participants with disparate vascular function to germ-free mice. Using Principle Component Analysis, the microbiota of colonized mice separated by donor group along the first principle component, accounting for between 70–93% of the total variability in the dataset. The microbiota of mice receiving transplants from lean individuals was also characterized by increased alpha diversity, as well as increased relative abundance of potentially beneficial bacteria, including Bifidobacterium, Lactobacillus, and Bacteroides ovatis. Endothelium-dependent dilation, aortic pulse wave velocity and glucose tolerance were significantly altered in mice receiving microbiota from the obese donor relative to those receiving microbiota from the lean donor or those remaining germ-free. These data indicate that the obesity-associated human gut microbiota is sufficient to alter the vascular phenotype in germ-free mice in the absence of differences in body weight or dietary manipulation, and provide justification for future clinical trials to test the efficacy of microbiota-targeted therapies in the prevention or treatment of cardiovascular disease.http://dx.doi.org/10.1080/19490976.2021.1940791vascular functionpulse wave velocityendothelial functionobesitymicrobiotacardiovascular disease
collection DOAJ
language English
format Article
sources DOAJ
author S. Raj J. Trikha
Dustin M. Lee
Kayl E. Ecton
Scott D. Wrigley
Allegra R. Vazquez
Nicole S. Litwin
Keely N. Thomas
Yuren Wei
Micah L. Battson
Sarah A. Johnson
Kristine A. Kuhn
Sean P. Colgan
Christopher L. Gentile
Tiffany L. Weir
spellingShingle S. Raj J. Trikha
Dustin M. Lee
Kayl E. Ecton
Scott D. Wrigley
Allegra R. Vazquez
Nicole S. Litwin
Keely N. Thomas
Yuren Wei
Micah L. Battson
Sarah A. Johnson
Kristine A. Kuhn
Sean P. Colgan
Christopher L. Gentile
Tiffany L. Weir
Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance
Gut Microbes
vascular function
pulse wave velocity
endothelial function
obesity
microbiota
cardiovascular disease
author_facet S. Raj J. Trikha
Dustin M. Lee
Kayl E. Ecton
Scott D. Wrigley
Allegra R. Vazquez
Nicole S. Litwin
Keely N. Thomas
Yuren Wei
Micah L. Battson
Sarah A. Johnson
Kristine A. Kuhn
Sean P. Colgan
Christopher L. Gentile
Tiffany L. Weir
author_sort S. Raj J. Trikha
title Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance
title_short Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance
title_full Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance
title_fullStr Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance
title_full_unstemmed Transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance
title_sort transplantation of an obesity-associated human gut microbiota to mice induces vascular dysfunction and glucose intolerance
publisher Taylor & Francis Group
series Gut Microbes
issn 1949-0976
1949-0984
publishDate 2021-01-01
description Recent preclinical data suggest that alterations in the gut microbiota may be an important factor linking obesity to vascular dysfunction, an early sign of cardiovascular disease. The purpose of this study was to begin translation of these preclinical data by examining whether vascular phenotypes in humans are transmissible through the gut microbiota. We hypothesized that germ-free mice colonized with gut microbiota from obese individuals would display diminished vascular function compared to germ-free mice receiving microbiota from lean individuals. We transplanted fecal material from obese and lean age-and sex-matched participants with disparate vascular function to germ-free mice. Using Principle Component Analysis, the microbiota of colonized mice separated by donor group along the first principle component, accounting for between 70–93% of the total variability in the dataset. The microbiota of mice receiving transplants from lean individuals was also characterized by increased alpha diversity, as well as increased relative abundance of potentially beneficial bacteria, including Bifidobacterium, Lactobacillus, and Bacteroides ovatis. Endothelium-dependent dilation, aortic pulse wave velocity and glucose tolerance were significantly altered in mice receiving microbiota from the obese donor relative to those receiving microbiota from the lean donor or those remaining germ-free. These data indicate that the obesity-associated human gut microbiota is sufficient to alter the vascular phenotype in germ-free mice in the absence of differences in body weight or dietary manipulation, and provide justification for future clinical trials to test the efficacy of microbiota-targeted therapies in the prevention or treatment of cardiovascular disease.
topic vascular function
pulse wave velocity
endothelial function
obesity
microbiota
cardiovascular disease
url http://dx.doi.org/10.1080/19490976.2021.1940791
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