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Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production
Bioinformatic and experimental data show that bacteriophages are ubiquitous in human enteric microbiomes. However, there are gaps in understanding the contribution of these viruses in shaping the bacterial strain and species composition of the gut microbiome and how these phages are maintained over...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659284/ https://www.ncbi.nlm.nih.gov/pubmed/37986824 http://dx.doi.org/10.1101/2023.11.08.566299 |
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author | Berryhill, Brandon A. Burke, Kylie B. Fontaine, Jake Brink, Catherine E. Harvill, Mason G. Goldberg, David A. Konstantinidis, Konstantinos T. Levin, Bruce R. Woodworth, Michael H. |
author_facet | Berryhill, Brandon A. Burke, Kylie B. Fontaine, Jake Brink, Catherine E. Harvill, Mason G. Goldberg, David A. Konstantinidis, Konstantinos T. Levin, Bruce R. Woodworth, Michael H. |
author_sort | Berryhill, Brandon A. |
collection | PubMed |
description | Bioinformatic and experimental data show that bacteriophages are ubiquitous in human enteric microbiomes. However, there are gaps in understanding the contribution of these viruses in shaping the bacterial strain and species composition of the gut microbiome and how these phages are maintained over time. To address these questions, we adapted and analyzed the properties of a mathematical model of the population and evolutionary dynamics of bacteria and phage and performed experiments with Escherichia coli and phages isolated from four fecal microbiota transplantation (FMT) doses as representative samples of non-dysbiotic enteric microbiota. Our models predict and experiments confirm that due to production of the O antigen, E. coli in the enteric microbiome are likely to be resistant to infection with co-occurring phages. However, phages can be maintained in these populations in high densities due to high rates of transition between resistant and sensitive states, which we call leaky resistance. Based on these models and observations, we postulate that the phages found in the human gut are likely to play little role in shaping the composition of E. coli in the enteric microbiome in healthy individuals. How general this is for other species of bacteria in enteric microbiota is not yet clear, although O antigen production is broadly conserved across many taxa. |
format | Online Article Text |
id | pubmed-10659284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106592842023-11-20 Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production Berryhill, Brandon A. Burke, Kylie B. Fontaine, Jake Brink, Catherine E. Harvill, Mason G. Goldberg, David A. Konstantinidis, Konstantinos T. Levin, Bruce R. Woodworth, Michael H. bioRxiv Article Bioinformatic and experimental data show that bacteriophages are ubiquitous in human enteric microbiomes. However, there are gaps in understanding the contribution of these viruses in shaping the bacterial strain and species composition of the gut microbiome and how these phages are maintained over time. To address these questions, we adapted and analyzed the properties of a mathematical model of the population and evolutionary dynamics of bacteria and phage and performed experiments with Escherichia coli and phages isolated from four fecal microbiota transplantation (FMT) doses as representative samples of non-dysbiotic enteric microbiota. Our models predict and experiments confirm that due to production of the O antigen, E. coli in the enteric microbiome are likely to be resistant to infection with co-occurring phages. However, phages can be maintained in these populations in high densities due to high rates of transition between resistant and sensitive states, which we call leaky resistance. Based on these models and observations, we postulate that the phages found in the human gut are likely to play little role in shaping the composition of E. coli in the enteric microbiome in healthy individuals. How general this is for other species of bacteria in enteric microbiota is not yet clear, although O antigen production is broadly conserved across many taxa. Cold Spring Harbor Laboratory 2023-11-08 /pmc/articles/PMC10659284/ /pubmed/37986824 http://dx.doi.org/10.1101/2023.11.08.566299 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Berryhill, Brandon A. Burke, Kylie B. Fontaine, Jake Brink, Catherine E. Harvill, Mason G. Goldberg, David A. Konstantinidis, Konstantinos T. Levin, Bruce R. Woodworth, Michael H. Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production |
title | Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production |
title_full | Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production |
title_fullStr | Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production |
title_full_unstemmed | Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production |
title_short | Enteric Populations of Escherichia coli are Likely to be Resistant to Phages Due to O Antigen Production |
title_sort | enteric populations of escherichia coli are likely to be resistant to phages due to o antigen production |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10659284/ https://www.ncbi.nlm.nih.gov/pubmed/37986824 http://dx.doi.org/10.1101/2023.11.08.566299 |
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