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Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen?

Aerobic bacteria are frequent primocolonizers of the human naive intestine. Their generally accepted role is to eliminate oxygen, which would allow colonization by anaerobes that subsequently dominate bacterial gut populations. In this hypothesis-based study, we revisited this dogma experimentally i...

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Autores principales: Halpern, David, Morvan, Claire, Derré-Bobillot, Aurélie, Meylheuc, Thierry, Guillemet, Mélanie, Rabot, Sylvie, Gruss, Alexandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8103986/
https://www.ncbi.nlm.nih.gov/pubmed/33952662
http://dx.doi.org/10.1128/mSphere.00232-19
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author Halpern, David
Morvan, Claire
Derré-Bobillot, Aurélie
Meylheuc, Thierry
Guillemet, Mélanie
Rabot, Sylvie
Gruss, Alexandra
author_facet Halpern, David
Morvan, Claire
Derré-Bobillot, Aurélie
Meylheuc, Thierry
Guillemet, Mélanie
Rabot, Sylvie
Gruss, Alexandra
author_sort Halpern, David
collection PubMed
description Aerobic bacteria are frequent primocolonizers of the human naive intestine. Their generally accepted role is to eliminate oxygen, which would allow colonization by anaerobes that subsequently dominate bacterial gut populations. In this hypothesis-based study, we revisited this dogma experimentally in a germfree mouse model as a mimic of the germfree newborn. We varied conditions leading to the establishment of the dominant intestinal anaerobe Bacteroides thetaiotaomicron. Two variables were introduced: Bacteroides inoculum size and preestablishment by bacteria capable or not of consuming oxygen. High Bacteroides inoculum size enabled its primocolonization. At low inocula, we show that bacterial preestablishment was decisive for subsequent Bacteroides colonization. However, even non-oxygen-respiring bacteria, a hemA Escherichia coli mutant and the intestinal obligate anaerobe Clostridium scindens, facilitated Bacteroides establishment. These findings, which are supported by recent reports, revise the long-held assumption that oxygen scavenging is the main role for aerobic primocolonizing bacteria. Instead, we suggest that better survival of aerobic bacteria ex vivo during vectorization between hosts could be a reason for their frequent primocolonization.
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spelling pubmed-81039862021-05-21 Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen? Halpern, David Morvan, Claire Derré-Bobillot, Aurélie Meylheuc, Thierry Guillemet, Mélanie Rabot, Sylvie Gruss, Alexandra mSphere Opinion/Hypothesis Aerobic bacteria are frequent primocolonizers of the human naive intestine. Their generally accepted role is to eliminate oxygen, which would allow colonization by anaerobes that subsequently dominate bacterial gut populations. In this hypothesis-based study, we revisited this dogma experimentally in a germfree mouse model as a mimic of the germfree newborn. We varied conditions leading to the establishment of the dominant intestinal anaerobe Bacteroides thetaiotaomicron. Two variables were introduced: Bacteroides inoculum size and preestablishment by bacteria capable or not of consuming oxygen. High Bacteroides inoculum size enabled its primocolonization. At low inocula, we show that bacterial preestablishment was decisive for subsequent Bacteroides colonization. However, even non-oxygen-respiring bacteria, a hemA Escherichia coli mutant and the intestinal obligate anaerobe Clostridium scindens, facilitated Bacteroides establishment. These findings, which are supported by recent reports, revise the long-held assumption that oxygen scavenging is the main role for aerobic primocolonizing bacteria. Instead, we suggest that better survival of aerobic bacteria ex vivo during vectorization between hosts could be a reason for their frequent primocolonization. American Society for Microbiology 2021-05-05 /pmc/articles/PMC8103986/ /pubmed/33952662 http://dx.doi.org/10.1128/mSphere.00232-19 Text en Copyright © 2021 Halpern et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Opinion/Hypothesis
Halpern, David
Morvan, Claire
Derré-Bobillot, Aurélie
Meylheuc, Thierry
Guillemet, Mélanie
Rabot, Sylvie
Gruss, Alexandra
Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen?
title Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen?
title_full Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen?
title_fullStr Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen?
title_full_unstemmed Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen?
title_short Do Primocolonizing Bacteria Enable Bacteroides thetaiotaomicron Intestinal Colonization Independently of the Capacity To Consume Oxygen?
title_sort do primocolonizing bacteria enable bacteroides thetaiotaomicron intestinal colonization independently of the capacity to consume oxygen?
topic Opinion/Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8103986/
https://www.ncbi.nlm.nih.gov/pubmed/33952662
http://dx.doi.org/10.1128/mSphere.00232-19
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