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The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria
Antimicrobial resistance (AMR) in bacteria is a major public health problem. The main route for AMR acquisition in clinically important bacteria is the horizontal transfer of plasmids carrying resistance genes. AMR plasmids allow bacteria to survive antibiotics, but they also entail physiological al...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Microbiology Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433420/ https://www.ncbi.nlm.nih.gov/pubmed/37505800 http://dx.doi.org/10.1099/mic.0.001369 |
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author | Fernández-Calvet, Ariadna Toribio-Celestino, Laura Alonso-del Valle, Aida Sastre-Dominguez, Jorge Valdes-Chiara, Paula San Millan, Alvaro DelaFuente, Javier |
author_facet | Fernández-Calvet, Ariadna Toribio-Celestino, Laura Alonso-del Valle, Aida Sastre-Dominguez, Jorge Valdes-Chiara, Paula San Millan, Alvaro DelaFuente, Javier |
author_sort | Fernández-Calvet, Ariadna |
collection | PubMed |
description | Antimicrobial resistance (AMR) in bacteria is a major public health problem. The main route for AMR acquisition in clinically important bacteria is the horizontal transfer of plasmids carrying resistance genes. AMR plasmids allow bacteria to survive antibiotics, but they also entail physiological alterations in the host cell. Multiple studies over the last few years have indicated that these alterations can translate into a fitness cost when antibiotics are absent. However, due to technical limitations, most of these studies are based on analysing new associations between plasmids and bacteria generated in vitro, and we know very little about the effects of plasmids in their native bacterial hosts. In this study, we used a CRISPR-Cas9-tool to selectively cure plasmids from clinical enterobacteria to overcome this limitation. Using this approach, we were able to study the fitness effects of the carbapenem resistance plasmid pOXA-48 in 35 pOXA-48-carrying isolates recovered from hospitalized patients. Our results revealed that pOXA-48 produces variable effects across the collection of wild-type enterobacterial strains naturally carrying the plasmid, ranging from fitness costs to fitness benefits. Importantly, the plasmid was only associated with a significant fitness reduction in four out of 35 clones, and produced no significant changes in fitness in the great majority of isolates. Our results suggest that plasmids produce neutral fitness effects in most native bacterial hosts, helping to explain the great prevalence of plasmids in natural microbial communities. |
format | Online Article Text |
id | pubmed-10433420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104334202023-08-18 The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria Fernández-Calvet, Ariadna Toribio-Celestino, Laura Alonso-del Valle, Aida Sastre-Dominguez, Jorge Valdes-Chiara, Paula San Millan, Alvaro DelaFuente, Javier Microbiology (Reading) Microbial Evolution Antimicrobial resistance (AMR) in bacteria is a major public health problem. The main route for AMR acquisition in clinically important bacteria is the horizontal transfer of plasmids carrying resistance genes. AMR plasmids allow bacteria to survive antibiotics, but they also entail physiological alterations in the host cell. Multiple studies over the last few years have indicated that these alterations can translate into a fitness cost when antibiotics are absent. However, due to technical limitations, most of these studies are based on analysing new associations between plasmids and bacteria generated in vitro, and we know very little about the effects of plasmids in their native bacterial hosts. In this study, we used a CRISPR-Cas9-tool to selectively cure plasmids from clinical enterobacteria to overcome this limitation. Using this approach, we were able to study the fitness effects of the carbapenem resistance plasmid pOXA-48 in 35 pOXA-48-carrying isolates recovered from hospitalized patients. Our results revealed that pOXA-48 produces variable effects across the collection of wild-type enterobacterial strains naturally carrying the plasmid, ranging from fitness costs to fitness benefits. Importantly, the plasmid was only associated with a significant fitness reduction in four out of 35 clones, and produced no significant changes in fitness in the great majority of isolates. Our results suggest that plasmids produce neutral fitness effects in most native bacterial hosts, helping to explain the great prevalence of plasmids in natural microbial communities. Microbiology Society 2023-07-28 /pmc/articles/PMC10433420/ /pubmed/37505800 http://dx.doi.org/10.1099/mic.0.001369 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution. |
spellingShingle | Microbial Evolution Fernández-Calvet, Ariadna Toribio-Celestino, Laura Alonso-del Valle, Aida Sastre-Dominguez, Jorge Valdes-Chiara, Paula San Millan, Alvaro DelaFuente, Javier The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria |
title | The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria |
title_full | The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria |
title_fullStr | The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria |
title_full_unstemmed | The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria |
title_short | The distribution of fitness effects of plasmid pOXA-48 in clinical enterobacteria |
title_sort | distribution of fitness effects of plasmid poxa-48 in clinical enterobacteria |
topic | Microbial Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433420/ https://www.ncbi.nlm.nih.gov/pubmed/37505800 http://dx.doi.org/10.1099/mic.0.001369 |
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