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Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella
Horizontal gene transfer (HGT) is a powerful evolutionary force facilitating bacterial adaptation and emergence of novel phenotypes. Several factors, including environmental ones, are predicted to restrict HGT, but we lack systematic and experimental data supporting these predictions. Here, we addre...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355182/ https://www.ncbi.nlm.nih.gov/pubmed/37475746 http://dx.doi.org/10.1093/evlett/qrad020 |
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author | Bhatia, Rama P Kirit, Hande Acar Lewis, Cecil M Sankaranarayanan, Krithivasan Bollback, Jonathan P |
author_facet | Bhatia, Rama P Kirit, Hande Acar Lewis, Cecil M Sankaranarayanan, Krithivasan Bollback, Jonathan P |
author_sort | Bhatia, Rama P |
collection | PubMed |
description | Horizontal gene transfer (HGT) is a powerful evolutionary force facilitating bacterial adaptation and emergence of novel phenotypes. Several factors, including environmental ones, are predicted to restrict HGT, but we lack systematic and experimental data supporting these predictions. Here, we address this gap by measuring the relative fitness of 44 genes horizontally transferred from Escherichia coli to Salmonella enterica in infection-relevant environments. We estimated the distribution of fitness effects in each environment and identified that dosage-dependent effects across different environments are a significant barrier to HGT. The majority of genes were found to be deleterious. We also found longer genes had stronger negative fitness consequences than shorter ones, showing that gene length was negatively associated with HGT. Furthermore, fitness effects of transferred genes were found to be environmentally dependent. In summary, a substantial fraction of transferred genes had a significant fitness cost on the recipient, with both gene characteristics and the environment acting as evolutionary barriers to HGT. |
format | Online Article Text |
id | pubmed-10355182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103551822023-07-20 Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella Bhatia, Rama P Kirit, Hande Acar Lewis, Cecil M Sankaranarayanan, Krithivasan Bollback, Jonathan P Evol Lett Letters Horizontal gene transfer (HGT) is a powerful evolutionary force facilitating bacterial adaptation and emergence of novel phenotypes. Several factors, including environmental ones, are predicted to restrict HGT, but we lack systematic and experimental data supporting these predictions. Here, we address this gap by measuring the relative fitness of 44 genes horizontally transferred from Escherichia coli to Salmonella enterica in infection-relevant environments. We estimated the distribution of fitness effects in each environment and identified that dosage-dependent effects across different environments are a significant barrier to HGT. The majority of genes were found to be deleterious. We also found longer genes had stronger negative fitness consequences than shorter ones, showing that gene length was negatively associated with HGT. Furthermore, fitness effects of transferred genes were found to be environmentally dependent. In summary, a substantial fraction of transferred genes had a significant fitness cost on the recipient, with both gene characteristics and the environment acting as evolutionary barriers to HGT. Oxford University Press 2023-05-23 /pmc/articles/PMC10355182/ /pubmed/37475746 http://dx.doi.org/10.1093/evlett/qrad020 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of The Society for the Study of Evolution (SSE) and European Society for Evolutionary Biology (ESEN). https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Letters Bhatia, Rama P Kirit, Hande Acar Lewis, Cecil M Sankaranarayanan, Krithivasan Bollback, Jonathan P Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella |
title | Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella |
title_full | Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella |
title_fullStr | Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella |
title_full_unstemmed | Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella |
title_short | Evolutionary barriers to horizontal gene transfer in macrophage-associated Salmonella |
title_sort | evolutionary barriers to horizontal gene transfer in macrophage-associated salmonella |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10355182/ https://www.ncbi.nlm.nih.gov/pubmed/37475746 http://dx.doi.org/10.1093/evlett/qrad020 |
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