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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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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. |
format | Online Article Text |
id | pubmed-7064763 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
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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