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Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus

Staphylococcus aureus is a commensal colonizing the skin and mucous membranes. It can also act as a pathogen, and is the most common microorganism isolated from prosthetic joint infections (PJIs). The aim of this study was to explore the genomic relatedness between commensal and PJI S. aureus strain...

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Autores principales: Wildeman, Peter, Tevell, Staffan, Eriksson, Carl, Lagos, Amaya Campillay, Söderquist, Bo, Stenmark, Bianca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125104/
https://www.ncbi.nlm.nih.gov/pubmed/32246045
http://dx.doi.org/10.1038/s41598-020-62751-z
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author Wildeman, Peter
Tevell, Staffan
Eriksson, Carl
Lagos, Amaya Campillay
Söderquist, Bo
Stenmark, Bianca
author_facet Wildeman, Peter
Tevell, Staffan
Eriksson, Carl
Lagos, Amaya Campillay
Söderquist, Bo
Stenmark, Bianca
author_sort Wildeman, Peter
collection PubMed
description Staphylococcus aureus is a commensal colonizing the skin and mucous membranes. It can also act as a pathogen, and is the most common microorganism isolated from prosthetic joint infections (PJIs). The aim of this study was to explore the genomic relatedness between commensal and PJI S. aureus strains as well as microbial traits and host-related risk factors for treatment failure. Whole-genome sequencing (WGS) was performed on S. aureus isolates obtained from PJIs (n = 100) and control isolates from nares (n = 101). Corresponding clinical data for the PJI patients were extracted from medical records. No PJI-specific clusters were found in the WGS phylogeny, and the distribution of the various clonal complexes and prevalence of virulence genes among isolates from PJIs and nares was almost equal. Isolates from patients with treatment success and failure were genetically very similar, while the presence of an antibiotic-resistant phenotype and the use of non-biofilm-active antimicrobial treatment were both associated with failure.In conclusion, commensal and PJI isolates of S. aureus in arthroplasty patients were genetically indistinguishable, suggesting that commensal S. aureus clones are capable of causing PJIs. Furthermore, no association between genetic traits and outcome could be demonstrated, stressing the importance of patient-related factors in the treatment of S. aureus PJIs.
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spelling pubmed-71251042020-04-08 Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus Wildeman, Peter Tevell, Staffan Eriksson, Carl Lagos, Amaya Campillay Söderquist, Bo Stenmark, Bianca Sci Rep Article Staphylococcus aureus is a commensal colonizing the skin and mucous membranes. It can also act as a pathogen, and is the most common microorganism isolated from prosthetic joint infections (PJIs). The aim of this study was to explore the genomic relatedness between commensal and PJI S. aureus strains as well as microbial traits and host-related risk factors for treatment failure. Whole-genome sequencing (WGS) was performed on S. aureus isolates obtained from PJIs (n = 100) and control isolates from nares (n = 101). Corresponding clinical data for the PJI patients were extracted from medical records. No PJI-specific clusters were found in the WGS phylogeny, and the distribution of the various clonal complexes and prevalence of virulence genes among isolates from PJIs and nares was almost equal. Isolates from patients with treatment success and failure were genetically very similar, while the presence of an antibiotic-resistant phenotype and the use of non-biofilm-active antimicrobial treatment were both associated with failure.In conclusion, commensal and PJI isolates of S. aureus in arthroplasty patients were genetically indistinguishable, suggesting that commensal S. aureus clones are capable of causing PJIs. Furthermore, no association between genetic traits and outcome could be demonstrated, stressing the importance of patient-related factors in the treatment of S. aureus PJIs. Nature Publishing Group UK 2020-04-03 /pmc/articles/PMC7125104/ /pubmed/32246045 http://dx.doi.org/10.1038/s41598-020-62751-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wildeman, Peter
Tevell, Staffan
Eriksson, Carl
Lagos, Amaya Campillay
Söderquist, Bo
Stenmark, Bianca
Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus
title Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus
title_full Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus
title_fullStr Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus
title_full_unstemmed Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus
title_short Genomic characterization and outcome of prosthetic joint infections caused by Staphylococcus aureus
title_sort genomic characterization and outcome of prosthetic joint infections caused by staphylococcus aureus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7125104/
https://www.ncbi.nlm.nih.gov/pubmed/32246045
http://dx.doi.org/10.1038/s41598-020-62751-z
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