Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats

Hypertension is regulated by immunological components. Spontaneously hypertensive rats (SHR) display a large population of proinflammatory CD161 + immune cells. We investigated the effect of early post-natal gut microbiota on the development of the immune system and resulting hypertension in the SHR...

Full description

Bibliographic Details
Main Authors: Francois M. Abboud, Michael Z. Cicha, Aaron Ericsson, Mark W. Chapleau, Madhu V. Singh
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-10-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphys.2021.752924/full
_version_ 1818401193369534464
author Francois M. Abboud
Francois M. Abboud
Francois M. Abboud
Michael Z. Cicha
Michael Z. Cicha
Aaron Ericsson
Mark W. Chapleau
Mark W. Chapleau
Mark W. Chapleau
Madhu V. Singh
Madhu V. Singh
author_facet Francois M. Abboud
Francois M. Abboud
Francois M. Abboud
Michael Z. Cicha
Michael Z. Cicha
Aaron Ericsson
Mark W. Chapleau
Mark W. Chapleau
Mark W. Chapleau
Madhu V. Singh
Madhu V. Singh
author_sort Francois M. Abboud
collection DOAJ
description Hypertension is regulated by immunological components. Spontaneously hypertensive rats (SHR) display a large population of proinflammatory CD161 + immune cells. We investigated the effect of early post-natal gut microbiota on the development of the immune system and resulting hypertension in the SHR. We first examined the microbial populations in the fecal samples of SHR and normotensive control WKY using 16S rDNA sequencing. We found that in the newborn SHR (1-week old) the gut microbiota was qualitatively and quantitatively different from the newborns of normotensive WKY. The representation of the predominant bacterial phylum Proteobacteria was significantly less in 1-week old SHR pups than in WKY (94.5% Proteobacteria in WKY vs. 65.2% in SHR neonates). Even within the phylum Proteobacteria, the colonizing genera in WKY and SHR differed dramatically. Whereas WKY microbiota was predominantly comprised of Escherichia-Shigella, SHR microbiota was represented by other taxa of Enterobacteriaceae and Pasteurellaceae. In contrast, the representation of phylum Firmicutes in the neonatal SHR gut was greater than WKY. Cross-fostering newborn SHR pups by lactating WKY dams caused a dramatic shift in 1-week old cross-fostered SHR gut microbiota. The two major bacterial taxa of phylum Proteobacteria, Enterobacteriaceae and Pasteurellaceae as well as Lactobacillus intestinalis, Proteus, Romboustia and Rothia were depleted after cross-fostering and were replaced by the predominant genera of WKY (Escherichia-Shigella). A proinflammatory IL-17F producing CD161 + immune cell population in the spleen and aorta of cross-fostered SHR was also reduced (30.7% in self-fostered SHR vs. 12.6% in cross-fostered SHR at 30 weeks of age) as was the systolic blood pressure in adult cross-fostered SHR at 10 weeks of age. Thus, altered composition of gut microbiota of SHR toward WKY at early neonatal age had a long-lasting effect on immune system by reducing proinflammatory immune cells and lowering systolic blood pressure.
first_indexed 2024-12-14T07:48:35Z
format Article
id doaj.art-9f586fd299004aa5b58760fd052fb563
institution Directory Open Access Journal
issn 1664-042X
language English
last_indexed 2024-12-14T07:48:35Z
publishDate 2021-10-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Physiology
spelling doaj.art-9f586fd299004aa5b58760fd052fb5632022-12-21T23:10:48ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2021-10-011210.3389/fphys.2021.752924752924Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive RatsFrancois M. Abboud0Francois M. Abboud1Francois M. Abboud2Michael Z. Cicha3Michael Z. Cicha4Aaron Ericsson5Mark W. Chapleau6Mark W. Chapleau7Mark W. Chapleau8Madhu V. Singh9Madhu V. Singh10Abboud Cardiovascular Research Center, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesDepartment of Molecular Physiology and Biophysics, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesAbboud Cardiovascular Research Center, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesMetagenomics Center, University of Missouri, Columbia, MO, United StatesAbboud Cardiovascular Research Center, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesDepartment of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesDepartment of Molecular Physiology and Biophysics, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesAbboud Cardiovascular Research Center, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesDepartment of Internal Medicine, Division of Endocrinology and Metabolism, Carver College of Medicine, University of Iowa, Iowa City, IA, United StatesHypertension is regulated by immunological components. Spontaneously hypertensive rats (SHR) display a large population of proinflammatory CD161 + immune cells. We investigated the effect of early post-natal gut microbiota on the development of the immune system and resulting hypertension in the SHR. We first examined the microbial populations in the fecal samples of SHR and normotensive control WKY using 16S rDNA sequencing. We found that in the newborn SHR (1-week old) the gut microbiota was qualitatively and quantitatively different from the newborns of normotensive WKY. The representation of the predominant bacterial phylum Proteobacteria was significantly less in 1-week old SHR pups than in WKY (94.5% Proteobacteria in WKY vs. 65.2% in SHR neonates). Even within the phylum Proteobacteria, the colonizing genera in WKY and SHR differed dramatically. Whereas WKY microbiota was predominantly comprised of Escherichia-Shigella, SHR microbiota was represented by other taxa of Enterobacteriaceae and Pasteurellaceae. In contrast, the representation of phylum Firmicutes in the neonatal SHR gut was greater than WKY. Cross-fostering newborn SHR pups by lactating WKY dams caused a dramatic shift in 1-week old cross-fostered SHR gut microbiota. The two major bacterial taxa of phylum Proteobacteria, Enterobacteriaceae and Pasteurellaceae as well as Lactobacillus intestinalis, Proteus, Romboustia and Rothia were depleted after cross-fostering and were replaced by the predominant genera of WKY (Escherichia-Shigella). A proinflammatory IL-17F producing CD161 + immune cell population in the spleen and aorta of cross-fostered SHR was also reduced (30.7% in self-fostered SHR vs. 12.6% in cross-fostered SHR at 30 weeks of age) as was the systolic blood pressure in adult cross-fostered SHR at 10 weeks of age. Thus, altered composition of gut microbiota of SHR toward WKY at early neonatal age had a long-lasting effect on immune system by reducing proinflammatory immune cells and lowering systolic blood pressure.https://www.frontiersin.org/articles/10.3389/fphys.2021.752924/fullmicrobiomeimmune systemgut microbiomehypertensionSHR (spontaneously hypertensive rat)T helper (T) 17 cells
spellingShingle Francois M. Abboud
Francois M. Abboud
Francois M. Abboud
Michael Z. Cicha
Michael Z. Cicha
Aaron Ericsson
Mark W. Chapleau
Mark W. Chapleau
Mark W. Chapleau
Madhu V. Singh
Madhu V. Singh
Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats
Frontiers in Physiology
microbiome
immune system
gut microbiome
hypertension
SHR (spontaneously hypertensive rat)
T helper (T) 17 cells
title Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats
title_full Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats
title_fullStr Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats
title_full_unstemmed Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats
title_short Altering Early Life Gut Microbiota Has Long-Term Effect on Immune System and Hypertension in Spontaneously Hypertensive Rats
title_sort altering early life gut microbiota has long term effect on immune system and hypertension in spontaneously hypertensive rats
topic microbiome
immune system
gut microbiome
hypertension
SHR (spontaneously hypertensive rat)
T helper (T) 17 cells
url https://www.frontiersin.org/articles/10.3389/fphys.2021.752924/full
work_keys_str_mv AT francoismabboud alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT francoismabboud alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT francoismabboud alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT michaelzcicha alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT michaelzcicha alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT aaronericsson alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT markwchapleau alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT markwchapleau alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT markwchapleau alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT madhuvsingh alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats
AT madhuvsingh alteringearlylifegutmicrobiotahaslongtermeffectonimmunesystemandhypertensioninspontaneouslyhypertensiverats