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Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli
There is urgent need to develop novel treatment strategies to reduce antimicrobial resistance. Collateral sensitivity (CS), where resistance to one antimicrobial increases susceptibility to other drugs, might enable selection against resistance during treatment. However, the success of this approach...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131505/ https://www.ncbi.nlm.nih.gov/pubmed/30202004 http://dx.doi.org/10.1038/s41467-018-06143-y |
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author | Podnecky, Nicole L. Fredheim, Elizabeth G. A. Kloos, Julia Sørum, Vidar Primicerio, Raul Roberts, Adam P. Rozen, Daniel E. Samuelsen, Ørjan Johnsen, Pål J. |
author_facet | Podnecky, Nicole L. Fredheim, Elizabeth G. A. Kloos, Julia Sørum, Vidar Primicerio, Raul Roberts, Adam P. Rozen, Daniel E. Samuelsen, Ørjan Johnsen, Pål J. |
author_sort | Podnecky, Nicole L. |
collection | PubMed |
description | There is urgent need to develop novel treatment strategies to reduce antimicrobial resistance. Collateral sensitivity (CS), where resistance to one antimicrobial increases susceptibility to other drugs, might enable selection against resistance during treatment. However, the success of this approach would depend on the conservation of CS networks across genetically diverse bacterial strains. Here, we examine CS conservation across diverse Escherichia coli strains isolated from urinary tract infections. We determine collateral susceptibilities of mutants resistant to relevant antimicrobials against 16 antibiotics. Multivariate statistical analyses show that resistance mechanisms, in particular efflux-related mutations, as well as the relative fitness of resistant strains, are principal contributors to collateral responses. Moreover, collateral responses shift the mutant selection window, suggesting that CS-informed therapies may affect evolutionary trajectories of antimicrobial resistance. Our data allow optimism for CS-informed therapy and further suggest that rapid detection of resistance mechanisms is important to accurately predict collateral responses. |
format | Online Article Text |
id | pubmed-6131505 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61315052018-09-12 Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli Podnecky, Nicole L. Fredheim, Elizabeth G. A. Kloos, Julia Sørum, Vidar Primicerio, Raul Roberts, Adam P. Rozen, Daniel E. Samuelsen, Ørjan Johnsen, Pål J. Nat Commun Article There is urgent need to develop novel treatment strategies to reduce antimicrobial resistance. Collateral sensitivity (CS), where resistance to one antimicrobial increases susceptibility to other drugs, might enable selection against resistance during treatment. However, the success of this approach would depend on the conservation of CS networks across genetically diverse bacterial strains. Here, we examine CS conservation across diverse Escherichia coli strains isolated from urinary tract infections. We determine collateral susceptibilities of mutants resistant to relevant antimicrobials against 16 antibiotics. Multivariate statistical analyses show that resistance mechanisms, in particular efflux-related mutations, as well as the relative fitness of resistant strains, are principal contributors to collateral responses. Moreover, collateral responses shift the mutant selection window, suggesting that CS-informed therapies may affect evolutionary trajectories of antimicrobial resistance. Our data allow optimism for CS-informed therapy and further suggest that rapid detection of resistance mechanisms is important to accurately predict collateral responses. Nature Publishing Group UK 2018-09-10 /pmc/articles/PMC6131505/ /pubmed/30202004 http://dx.doi.org/10.1038/s41467-018-06143-y Text en © The Author(s) 2018 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 Podnecky, Nicole L. Fredheim, Elizabeth G. A. Kloos, Julia Sørum, Vidar Primicerio, Raul Roberts, Adam P. Rozen, Daniel E. Samuelsen, Ørjan Johnsen, Pål J. Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli |
title | Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli |
title_full | Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli |
title_fullStr | Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli |
title_full_unstemmed | Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli |
title_short | Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli |
title_sort | conserved collateral antibiotic susceptibility networks in diverse clinical strains of escherichia coli |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131505/ https://www.ncbi.nlm.nih.gov/pubmed/30202004 http://dx.doi.org/10.1038/s41467-018-06143-y |
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