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Impact of gut permeability on the breast microbiome using a non-human primate model

We previously demonstrated in non-human primates (NHP) that Mediterranean diet consumption shifted the proportional abundance of Lactobacillus in the breast and gut. This data highlights a potential link about gut-breast microbiome interconnectivity. To address this question, we compared bacterial p...

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Autores principales: Bawaneh, Alaa, Shively, Carol A., Tooze, Janet Austin, Cook, Katherine Loree
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990890/
https://www.ncbi.nlm.nih.gov/pubmed/36891249
http://dx.doi.org/10.1017/gmb.2022.9
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author Bawaneh, Alaa
Shively, Carol A.
Tooze, Janet Austin
Cook, Katherine Loree
author_facet Bawaneh, Alaa
Shively, Carol A.
Tooze, Janet Austin
Cook, Katherine Loree
author_sort Bawaneh, Alaa
collection PubMed
description We previously demonstrated in non-human primates (NHP) that Mediterranean diet consumption shifted the proportional abundance of Lactobacillus in the breast and gut. This data highlights a potential link about gut-breast microbiome interconnectivity. To address this question, we compared bacterial populations identified in matched breast and faecal samples from our NHP study. Dietary pattern concurrently shifted two species in both regions; Streptococcus lutetiensis and Ruminococcus torques. While we observe similar trends in Lactobacillus abundances in the breast and gut, the species identified in each region vary; Mediterranean diet increased Lactobacillus_unspecified species in breast but regulated L. animalis and L. reuteri in the gut.We also investigated the impact of gut permeability on the breast microbiome. Regardless of dietary pattern, subjects that displayed increased physiological measures of gut permeability (elevated plasma lipopolysaccharide, decreased villi length, and decreased goblet cells) displayed a significantly different breast microbiome. Gut barrier dysfunction was associated with increased α-diversity and significant different β-diversity in the breast tissue. Taken together our data supports the presence of a breast microbiome influenced by diet that largely varies from the gut microbiome population but is, however, sensitive to gut permeability.
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spelling pubmed-99908902023-03-07 Impact of gut permeability on the breast microbiome using a non-human primate model Bawaneh, Alaa Shively, Carol A. Tooze, Janet Austin Cook, Katherine Loree Gut Microbiome (Camb) Article We previously demonstrated in non-human primates (NHP) that Mediterranean diet consumption shifted the proportional abundance of Lactobacillus in the breast and gut. This data highlights a potential link about gut-breast microbiome interconnectivity. To address this question, we compared bacterial populations identified in matched breast and faecal samples from our NHP study. Dietary pattern concurrently shifted two species in both regions; Streptococcus lutetiensis and Ruminococcus torques. While we observe similar trends in Lactobacillus abundances in the breast and gut, the species identified in each region vary; Mediterranean diet increased Lactobacillus_unspecified species in breast but regulated L. animalis and L. reuteri in the gut.We also investigated the impact of gut permeability on the breast microbiome. Regardless of dietary pattern, subjects that displayed increased physiological measures of gut permeability (elevated plasma lipopolysaccharide, decreased villi length, and decreased goblet cells) displayed a significantly different breast microbiome. Gut barrier dysfunction was associated with increased α-diversity and significant different β-diversity in the breast tissue. Taken together our data supports the presence of a breast microbiome influenced by diet that largely varies from the gut microbiome population but is, however, sensitive to gut permeability. 2022 2022-11-09 /pmc/articles/PMC9990890/ /pubmed/36891249 http://dx.doi.org/10.1017/gmb.2022.9 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Article
Bawaneh, Alaa
Shively, Carol A.
Tooze, Janet Austin
Cook, Katherine Loree
Impact of gut permeability on the breast microbiome using a non-human primate model
title Impact of gut permeability on the breast microbiome using a non-human primate model
title_full Impact of gut permeability on the breast microbiome using a non-human primate model
title_fullStr Impact of gut permeability on the breast microbiome using a non-human primate model
title_full_unstemmed Impact of gut permeability on the breast microbiome using a non-human primate model
title_short Impact of gut permeability on the breast microbiome using a non-human primate model
title_sort impact of gut permeability on the breast microbiome using a non-human primate model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9990890/
https://www.ncbi.nlm.nih.gov/pubmed/36891249
http://dx.doi.org/10.1017/gmb.2022.9
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