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Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus
While microbiological resistance to vancomycin in Staphylococcus aureus is rare, clinical vancomycin treatment failures are common, and methicillin-resistant S. aureus (MRSA) strains isolated from patients after prolonged vancomycin treatment failure remain susceptible. Adaptive laboratory evolution...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233327/ https://www.ncbi.nlm.nih.gov/pubmed/34172889 http://dx.doi.org/10.1038/s42003-021-02339-z |
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author | Machado, Henrique Seif, Yara Sakoulas, George Olson, Connor A. Hefner, Ying Anand, Amitesh Jones, Ying Z. Szubin, Richard Palsson, Bernhard O. Nizet, Victor Feist, Adam M. |
author_facet | Machado, Henrique Seif, Yara Sakoulas, George Olson, Connor A. Hefner, Ying Anand, Amitesh Jones, Ying Z. Szubin, Richard Palsson, Bernhard O. Nizet, Victor Feist, Adam M. |
author_sort | Machado, Henrique |
collection | PubMed |
description | While microbiological resistance to vancomycin in Staphylococcus aureus is rare, clinical vancomycin treatment failures are common, and methicillin-resistant S. aureus (MRSA) strains isolated from patients after prolonged vancomycin treatment failure remain susceptible. Adaptive laboratory evolution was utilized to uncover mutational mechanisms associated with MRSA vancomycin resistance in a physiological medium as well as a bacteriological medium used in clinical susceptibility testing. Sequencing of resistant clones revealed shared and media-specific mutational outcomes, with an overlap in cell wall regulons (walKRyycHI, vraSRT). Evolved strains displayed similar properties to resistant clinical isolates in their genetic and phenotypic traits. Importantly, resistant phenotypes that developed in physiological media did not translate into resistance in bacteriological media. Further, a bacteriological media-specific mechanism for vancomycin resistance associated with a mutated mprF was confirmed. This study bridges the gap between the understanding of clinical and microbiological vancomycin resistance in S. aureus and expands the number of allelic variants (18 ± 4 mutations for the top 5 mutated genes) that result in vancomycin resistance phenotypes. |
format | Online Article Text |
id | pubmed-8233327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82333272021-07-09 Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus Machado, Henrique Seif, Yara Sakoulas, George Olson, Connor A. Hefner, Ying Anand, Amitesh Jones, Ying Z. Szubin, Richard Palsson, Bernhard O. Nizet, Victor Feist, Adam M. Commun Biol Article While microbiological resistance to vancomycin in Staphylococcus aureus is rare, clinical vancomycin treatment failures are common, and methicillin-resistant S. aureus (MRSA) strains isolated from patients after prolonged vancomycin treatment failure remain susceptible. Adaptive laboratory evolution was utilized to uncover mutational mechanisms associated with MRSA vancomycin resistance in a physiological medium as well as a bacteriological medium used in clinical susceptibility testing. Sequencing of resistant clones revealed shared and media-specific mutational outcomes, with an overlap in cell wall regulons (walKRyycHI, vraSRT). Evolved strains displayed similar properties to resistant clinical isolates in their genetic and phenotypic traits. Importantly, resistant phenotypes that developed in physiological media did not translate into resistance in bacteriological media. Further, a bacteriological media-specific mechanism for vancomycin resistance associated with a mutated mprF was confirmed. This study bridges the gap between the understanding of clinical and microbiological vancomycin resistance in S. aureus and expands the number of allelic variants (18 ± 4 mutations for the top 5 mutated genes) that result in vancomycin resistance phenotypes. Nature Publishing Group UK 2021-06-25 /pmc/articles/PMC8233327/ /pubmed/34172889 http://dx.doi.org/10.1038/s42003-021-02339-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Machado, Henrique Seif, Yara Sakoulas, George Olson, Connor A. Hefner, Ying Anand, Amitesh Jones, Ying Z. Szubin, Richard Palsson, Bernhard O. Nizet, Victor Feist, Adam M. Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus |
title | Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus |
title_full | Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus |
title_fullStr | Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus |
title_full_unstemmed | Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus |
title_short | Environmental conditions dictate differential evolution of vancomycin resistance in Staphylococcus aureus |
title_sort | environmental conditions dictate differential evolution of vancomycin resistance in staphylococcus aureus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233327/ https://www.ncbi.nlm.nih.gov/pubmed/34172889 http://dx.doi.org/10.1038/s42003-021-02339-z |
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