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Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK
Daptomycin (DAP) is key in treating multidrug-resistant Staphylococcus infections. Diminished susceptibility to DAP is emerging among Staphylococcus epidermidis strains although mechanisms for non-susceptibility (NS) remain poorly understood. We report a case of persistent S. epidermidis bacteremia...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658547/ https://www.ncbi.nlm.nih.gov/pubmed/33214904 http://dx.doi.org/10.1093/emph/eoaa031 |
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author | Brazeau, Nicholas F Levinson, Kara J Schranz, Asher Moser, Kara A Hollis, Ian Iyer, Prashanth Chien, Christopher Bowen, Amanda van Duin, David Lachiewicz, Anne Andermann, Tessa Jones, Melissa Miller, Melissa Juliano, Jonathan J Bartelt, Luther A |
author_facet | Brazeau, Nicholas F Levinson, Kara J Schranz, Asher Moser, Kara A Hollis, Ian Iyer, Prashanth Chien, Christopher Bowen, Amanda van Duin, David Lachiewicz, Anne Andermann, Tessa Jones, Melissa Miller, Melissa Juliano, Jonathan J Bartelt, Luther A |
author_sort | Brazeau, Nicholas F |
collection | PubMed |
description | Daptomycin (DAP) is key in treating multidrug-resistant Staphylococcus infections. Diminished susceptibility to DAP is emerging among Staphylococcus epidermidis strains although mechanisms for non-susceptibility (NS) remain poorly understood. We report a case of persistent S. epidermidis bacteremia in which loss of DAP susceptibility arose during prolonged treatment. Whole genome sequencing identified two mutations, Q371del and P415L, in a single-affected gene, WalK, that coincided with the emergence of DAP-NS. Protein modeling of the mutations predicted a disruption of WalK protein configuration. The emergence of mutations in a single-gene during DAP exposure raises concerns in an era of increasingly treatment-resistant infections. Lay summary: Daptomycin is an important antibiotic for fighting Staphylococcus infections. We identified variants in the WalK gene that were coincident with resistance in a clinical Staphylococcus epidermidis infection. Clinicians, hospital epidemiologists, and microbiology laboratories need to be aware of the potential for the evolution of drug resistance during prolonged daptomycin therapy. |
format | Online Article Text |
id | pubmed-7658547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76585472020-11-18 Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK Brazeau, Nicholas F Levinson, Kara J Schranz, Asher Moser, Kara A Hollis, Ian Iyer, Prashanth Chien, Christopher Bowen, Amanda van Duin, David Lachiewicz, Anne Andermann, Tessa Jones, Melissa Miller, Melissa Juliano, Jonathan J Bartelt, Luther A Evol Med Public Health Case Study Daptomycin (DAP) is key in treating multidrug-resistant Staphylococcus infections. Diminished susceptibility to DAP is emerging among Staphylococcus epidermidis strains although mechanisms for non-susceptibility (NS) remain poorly understood. We report a case of persistent S. epidermidis bacteremia in which loss of DAP susceptibility arose during prolonged treatment. Whole genome sequencing identified two mutations, Q371del and P415L, in a single-affected gene, WalK, that coincided with the emergence of DAP-NS. Protein modeling of the mutations predicted a disruption of WalK protein configuration. The emergence of mutations in a single-gene during DAP exposure raises concerns in an era of increasingly treatment-resistant infections. Lay summary: Daptomycin is an important antibiotic for fighting Staphylococcus infections. We identified variants in the WalK gene that were coincident with resistance in a clinical Staphylococcus epidermidis infection. Clinicians, hospital epidemiologists, and microbiology laboratories need to be aware of the potential for the evolution of drug resistance during prolonged daptomycin therapy. Oxford University Press 2020-09-07 /pmc/articles/PMC7658547/ /pubmed/33214904 http://dx.doi.org/10.1093/emph/eoaa031 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Study Brazeau, Nicholas F Levinson, Kara J Schranz, Asher Moser, Kara A Hollis, Ian Iyer, Prashanth Chien, Christopher Bowen, Amanda van Duin, David Lachiewicz, Anne Andermann, Tessa Jones, Melissa Miller, Melissa Juliano, Jonathan J Bartelt, Luther A Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK |
title | Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK |
title_full | Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK |
title_fullStr | Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK |
title_full_unstemmed | Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK |
title_short | Loss of daptomycin susceptibility in clinical Staphylococcus epidermidis infection coincided with variants in WalK |
title_sort | loss of daptomycin susceptibility in clinical staphylococcus epidermidis infection coincided with variants in walk |
topic | Case Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658547/ https://www.ncbi.nlm.nih.gov/pubmed/33214904 http://dx.doi.org/10.1093/emph/eoaa031 |
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