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Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus

Plasmids have largely contributed to the spread of antimicrobial resistance genes among Staphylococcus strains. Knowledge about the fitness cost that plasmids confer on clinical staphylococcal isolates and the coevolutionary dynamics that drive plasmid maintenance is still scarce. In this study, we...

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Autores principales: Dorado-Morales, Pedro, Garcillán-Barcia, M. Pilar, Lasa, Iñigo, Solano, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8545097/
https://www.ncbi.nlm.nih.gov/pubmed/33622733
http://dx.doi.org/10.1128/mBio.03094-20
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author Dorado-Morales, Pedro
Garcillán-Barcia, M. Pilar
Lasa, Iñigo
Solano, Cristina
author_facet Dorado-Morales, Pedro
Garcillán-Barcia, M. Pilar
Lasa, Iñigo
Solano, Cristina
author_sort Dorado-Morales, Pedro
collection PubMed
description Plasmids have largely contributed to the spread of antimicrobial resistance genes among Staphylococcus strains. Knowledge about the fitness cost that plasmids confer on clinical staphylococcal isolates and the coevolutionary dynamics that drive plasmid maintenance is still scarce. In this study, we aimed to analyze the initial fitness cost of plasmids in the bacterial pathogen Staphylococcus aureus and the plasmid-host adaptations that occur over time. For that, we first designed a CRISPR (clustered regularly interspaced palindromic repeats)-based tool that enables the removal of native S. aureus plasmids and then transferred three different plasmids isolated from clinical S. aureus strains to the same-background clinical cured strain. One of the plasmids, pUR2940, obtained from a livestock-associated methicillin-resistant S. aureus (LA-MRSA) ST398 strain, imposed a significant fitness cost on both its native and the new host. Experimental evolution in a nonselective medium resulted in a high rate pUR2940 loss and selected for clones with an alleviated fitness cost in which compensatory adaptation occurred via deletion of a 12.8-kb plasmid fragment, contained between two ISSau10 insertion sequences and harboring several antimicrobial resistance genes. Overall, our results describe the relevance of plasmid-borne insertion sequences in plasmid rearrangement and maintenance and suggest the potential benefits of reducing the use of antibiotics both in animal and clinical settings for the loss of clinical multidrug resistance plasmids.
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spelling pubmed-85450972021-10-27 Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus Dorado-Morales, Pedro Garcillán-Barcia, M. Pilar Lasa, Iñigo Solano, Cristina mBio Research Article Plasmids have largely contributed to the spread of antimicrobial resistance genes among Staphylococcus strains. Knowledge about the fitness cost that plasmids confer on clinical staphylococcal isolates and the coevolutionary dynamics that drive plasmid maintenance is still scarce. In this study, we aimed to analyze the initial fitness cost of plasmids in the bacterial pathogen Staphylococcus aureus and the plasmid-host adaptations that occur over time. For that, we first designed a CRISPR (clustered regularly interspaced palindromic repeats)-based tool that enables the removal of native S. aureus plasmids and then transferred three different plasmids isolated from clinical S. aureus strains to the same-background clinical cured strain. One of the plasmids, pUR2940, obtained from a livestock-associated methicillin-resistant S. aureus (LA-MRSA) ST398 strain, imposed a significant fitness cost on both its native and the new host. Experimental evolution in a nonselective medium resulted in a high rate pUR2940 loss and selected for clones with an alleviated fitness cost in which compensatory adaptation occurred via deletion of a 12.8-kb plasmid fragment, contained between two ISSau10 insertion sequences and harboring several antimicrobial resistance genes. Overall, our results describe the relevance of plasmid-borne insertion sequences in plasmid rearrangement and maintenance and suggest the potential benefits of reducing the use of antibiotics both in animal and clinical settings for the loss of clinical multidrug resistance plasmids. American Society for Microbiology 2021-02-23 /pmc/articles/PMC8545097/ /pubmed/33622733 http://dx.doi.org/10.1128/mBio.03094-20 Text en Copyright © 2021 Dorado-Morales 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
Dorado-Morales, Pedro
Garcillán-Barcia, M. Pilar
Lasa, Iñigo
Solano, Cristina
Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus
title Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus
title_full Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus
title_fullStr Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus
title_full_unstemmed Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus
title_short Fitness Cost Evolution of Natural Plasmids of Staphylococcus aureus
title_sort fitness cost evolution of natural plasmids of staphylococcus aureus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8545097/
https://www.ncbi.nlm.nih.gov/pubmed/33622733
http://dx.doi.org/10.1128/mBio.03094-20
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