Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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
_version_ 1783713827004612608
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
work_keys_str_mv AT machadohenrique environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT seifyara environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT sakoulasgeorge environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT olsonconnora environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT hefnerying environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT anandamitesh environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT jonesyingz environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT szubinrichard environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT palssonbernhardo environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT nizetvictor environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus
AT feistadamm environmentalconditionsdictatedifferentialevolutionofvancomycinresistanceinstaphylococcusaureus