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Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements

Horizontal gene transfer (HGT) promotes the spread of genes within bacterial communities. Among the HGT mechanisms, natural transformation stands out as being encoded by the bacterial core genome. Natural transformation is often viewed as a way to acquire new genes and to generate genetic mixing wit...

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Autores principales: Carvalho, Gabriel, Fouchet, David, Danesh, Gonché, Godeux, Anne-Sophie, Laaberki, Maria-Halima, Pontier, Dominique, Charpentier, Xavier, Venner, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064763/
https://www.ncbi.nlm.nih.gov/pubmed/32127449
http://dx.doi.org/10.1128/mBio.02443-19
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author Carvalho, Gabriel
Fouchet, David
Danesh, Gonché
Godeux, Anne-Sophie
Laaberki, Maria-Halima
Pontier, Dominique
Charpentier, Xavier
Venner, Samuel
author_facet Carvalho, Gabriel
Fouchet, David
Danesh, Gonché
Godeux, Anne-Sophie
Laaberki, Maria-Halima
Pontier, Dominique
Charpentier, Xavier
Venner, Samuel
author_sort Carvalho, Gabriel
collection PubMed
description Horizontal gene transfer (HGT) promotes the spread of genes within bacterial communities. Among the HGT mechanisms, natural transformation stands out as being encoded by the bacterial core genome. Natural transformation is often viewed as a way to acquire new genes and to generate genetic mixing within bacterial populations. Another recently proposed function is the curing of bacterial genomes of their infectious parasitic mobile genetic elements (MGEs). Here, we propose that these seemingly opposing theoretical points of view can be unified. Although costly for bacterial cells, MGEs can carry functions that are at points in time beneficial to bacteria under stressful conditions (e.g., antibiotic resistance genes). Using computational modeling, we show that, in stochastic environments, an intermediate transformation rate maximizes bacterial fitness by allowing the reversible integration of MGEs carrying resistance genes, although these MGEs are costly for host cell replication. Based on this dual function (MGE acquisition and removal), transformation would be a key mechanism for stabilizing the bacterial genome in the long term, and this would explain its striking conservation.
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spelling pubmed-70647632020-03-13 Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements Carvalho, Gabriel Fouchet, David Danesh, Gonché Godeux, Anne-Sophie Laaberki, Maria-Halima Pontier, Dominique Charpentier, Xavier Venner, Samuel mBio Research Article Horizontal gene transfer (HGT) promotes the spread of genes within bacterial communities. Among the HGT mechanisms, natural transformation stands out as being encoded by the bacterial core genome. Natural transformation is often viewed as a way to acquire new genes and to generate genetic mixing within bacterial populations. Another recently proposed function is the curing of bacterial genomes of their infectious parasitic mobile genetic elements (MGEs). Here, we propose that these seemingly opposing theoretical points of view can be unified. Although costly for bacterial cells, MGEs can carry functions that are at points in time beneficial to bacteria under stressful conditions (e.g., antibiotic resistance genes). Using computational modeling, we show that, in stochastic environments, an intermediate transformation rate maximizes bacterial fitness by allowing the reversible integration of MGEs carrying resistance genes, although these MGEs are costly for host cell replication. Based on this dual function (MGE acquisition and removal), transformation would be a key mechanism for stabilizing the bacterial genome in the long term, and this would explain its striking conservation. American Society for Microbiology 2020-03-03 /pmc/articles/PMC7064763/ /pubmed/32127449 http://dx.doi.org/10.1128/mBio.02443-19 Text en Copyright © 2020 Carvalho 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 Research Article
Carvalho, Gabriel
Fouchet, David
Danesh, Gonché
Godeux, Anne-Sophie
Laaberki, Maria-Halima
Pontier, Dominique
Charpentier, Xavier
Venner, Samuel
Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements
title Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements
title_full Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements
title_fullStr Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements
title_full_unstemmed Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements
title_short Bacterial Transformation Buffers Environmental Fluctuations through the Reversible Integration of Mobile Genetic Elements
title_sort bacterial transformation buffers environmental fluctuations through the reversible integration of mobile genetic elements
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064763/
https://www.ncbi.nlm.nih.gov/pubmed/32127449
http://dx.doi.org/10.1128/mBio.02443-19
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