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Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota

The intestinal microbiota plays important roles in digestion and resistance against entero-pathogens. As with other ecosystems, its species composition is resilient against small disturbances but strong perturbations such as antibiotics can affect the consortium dramatically. Antibiotic cessation do...

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Detalles Bibliográficos
Autores principales: Bucci, Vanni, Bradde, Serena, Biroli, Giulio, Xavier, Joao B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343147/
https://www.ncbi.nlm.nih.gov/pubmed/22577356
http://dx.doi.org/10.1371/journal.pcbi.1002497
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author Bucci, Vanni
Bradde, Serena
Biroli, Giulio
Xavier, Joao B.
author_facet Bucci, Vanni
Bradde, Serena
Biroli, Giulio
Xavier, Joao B.
author_sort Bucci, Vanni
collection PubMed
description The intestinal microbiota plays important roles in digestion and resistance against entero-pathogens. As with other ecosystems, its species composition is resilient against small disturbances but strong perturbations such as antibiotics can affect the consortium dramatically. Antibiotic cessation does not necessarily restore pre-treatment conditions and disturbed microbiota are often susceptible to pathogen invasion. Here we propose a mathematical model to explain how antibiotic-mediated switches in the microbiota composition can result from simple social interactions between antibiotic-tolerant and antibiotic-sensitive bacterial groups. We build a two-species (e.g. two functional-groups) model and identify regions of domination by antibiotic-sensitive or antibiotic-tolerant bacteria, as well as a region of multistability where domination by either group is possible. Using a new framework that we derived from statistical physics, we calculate the duration of each microbiota composition state. This is shown to depend on the balance between random fluctuations in the bacterial densities and the strength of microbial interactions. The singular value decomposition of recent metagenomic data confirms our assumption of grouping microbes as antibiotic-tolerant or antibiotic-sensitive in response to a single antibiotic. Our methodology can be extended to multiple bacterial groups and thus it provides an ecological formalism to help interpret the present surge in microbiome data.
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spelling pubmed-33431472012-05-10 Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota Bucci, Vanni Bradde, Serena Biroli, Giulio Xavier, Joao B. PLoS Comput Biol Research Article The intestinal microbiota plays important roles in digestion and resistance against entero-pathogens. As with other ecosystems, its species composition is resilient against small disturbances but strong perturbations such as antibiotics can affect the consortium dramatically. Antibiotic cessation does not necessarily restore pre-treatment conditions and disturbed microbiota are often susceptible to pathogen invasion. Here we propose a mathematical model to explain how antibiotic-mediated switches in the microbiota composition can result from simple social interactions between antibiotic-tolerant and antibiotic-sensitive bacterial groups. We build a two-species (e.g. two functional-groups) model and identify regions of domination by antibiotic-sensitive or antibiotic-tolerant bacteria, as well as a region of multistability where domination by either group is possible. Using a new framework that we derived from statistical physics, we calculate the duration of each microbiota composition state. This is shown to depend on the balance between random fluctuations in the bacterial densities and the strength of microbial interactions. The singular value decomposition of recent metagenomic data confirms our assumption of grouping microbes as antibiotic-tolerant or antibiotic-sensitive in response to a single antibiotic. Our methodology can be extended to multiple bacterial groups and thus it provides an ecological formalism to help interpret the present surge in microbiome data. Public Library of Science 2012-04-26 /pmc/articles/PMC3343147/ /pubmed/22577356 http://dx.doi.org/10.1371/journal.pcbi.1002497 Text en Bucci et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bucci, Vanni
Bradde, Serena
Biroli, Giulio
Xavier, Joao B.
Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota
title Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota
title_full Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota
title_fullStr Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota
title_full_unstemmed Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota
title_short Social Interaction, Noise and Antibiotic-Mediated Switches in the Intestinal Microbiota
title_sort social interaction, noise and antibiotic-mediated switches in the intestinal microbiota
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343147/
https://www.ncbi.nlm.nih.gov/pubmed/22577356
http://dx.doi.org/10.1371/journal.pcbi.1002497
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