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A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim
Adjuvants can be used to potentiate the function of antibiotics whose efficacy has been reduced by acquired or intrinsic resistance. In the present study, we discovered that human milk oligosaccharides (HMOs) sensitize strains of group B Streptococcus (GBS) to trimethoprim (TMP), an antibiotic to wh...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078465/ https://www.ncbi.nlm.nih.gov/pubmed/32184236 http://dx.doi.org/10.1128/mBio.00076-20 |
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author | Chambers, Schuyler A. Moore, Rebecca E. Craft, Kelly M. Thomas, Harrison C. Das, Rishub Manning, Shannon D. Codreanu, Simona G. Sherrod, Stacy D. Aronoff, David M. McLean, John A. Gaddy, Jennifer A. Townsend, Steven D. |
author_facet | Chambers, Schuyler A. Moore, Rebecca E. Craft, Kelly M. Thomas, Harrison C. Das, Rishub Manning, Shannon D. Codreanu, Simona G. Sherrod, Stacy D. Aronoff, David M. McLean, John A. Gaddy, Jennifer A. Townsend, Steven D. |
author_sort | Chambers, Schuyler A. |
collection | PubMed |
description | Adjuvants can be used to potentiate the function of antibiotics whose efficacy has been reduced by acquired or intrinsic resistance. In the present study, we discovered that human milk oligosaccharides (HMOs) sensitize strains of group B Streptococcus (GBS) to trimethoprim (TMP), an antibiotic to which GBS is intrinsically resistant. Reductions in the MIC of TMP reached as high as 512-fold across a diverse panel of isolates. To better understand HMOs’ mechanism of action, we characterized the metabolic response of GBS to HMO treatment using ultrahigh-performance liquid chromatography–high-resolution tandem mass spectrometry (UPLC-HRMS/MS) analysis. These data showed that when challenged by HMOs, GBS undergoes significant perturbations in metabolic pathways related to the biosynthesis and incorporation of macromolecules involved in membrane construction. This study represents reports the metabolic characterization of a cell that is perturbed by HMOs. |
format | Online Article Text |
id | pubmed-7078465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-70784652020-03-31 A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim Chambers, Schuyler A. Moore, Rebecca E. Craft, Kelly M. Thomas, Harrison C. Das, Rishub Manning, Shannon D. Codreanu, Simona G. Sherrod, Stacy D. Aronoff, David M. McLean, John A. Gaddy, Jennifer A. Townsend, Steven D. mBio Research Article Adjuvants can be used to potentiate the function of antibiotics whose efficacy has been reduced by acquired or intrinsic resistance. In the present study, we discovered that human milk oligosaccharides (HMOs) sensitize strains of group B Streptococcus (GBS) to trimethoprim (TMP), an antibiotic to which GBS is intrinsically resistant. Reductions in the MIC of TMP reached as high as 512-fold across a diverse panel of isolates. To better understand HMOs’ mechanism of action, we characterized the metabolic response of GBS to HMO treatment using ultrahigh-performance liquid chromatography–high-resolution tandem mass spectrometry (UPLC-HRMS/MS) analysis. These data showed that when challenged by HMOs, GBS undergoes significant perturbations in metabolic pathways related to the biosynthesis and incorporation of macromolecules involved in membrane construction. This study represents reports the metabolic characterization of a cell that is perturbed by HMOs. American Society for Microbiology 2020-03-17 /pmc/articles/PMC7078465/ /pubmed/32184236 http://dx.doi.org/10.1128/mBio.00076-20 Text en Copyright © 2020 Chambers et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Chambers, Schuyler A. Moore, Rebecca E. Craft, Kelly M. Thomas, Harrison C. Das, Rishub Manning, Shannon D. Codreanu, Simona G. Sherrod, Stacy D. Aronoff, David M. McLean, John A. Gaddy, Jennifer A. Townsend, Steven D. A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim |
title | A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim |
title_full | A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim |
title_fullStr | A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim |
title_full_unstemmed | A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim |
title_short | A Solution to Antifolate Resistance in Group B Streptococcus: Untargeted Metabolomics Identifies Human Milk Oligosaccharide-Induced Perturbations That Result in Potentiation of Trimethoprim |
title_sort | solution to antifolate resistance in group b streptococcus: untargeted metabolomics identifies human milk oligosaccharide-induced perturbations that result in potentiation of trimethoprim |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078465/ https://www.ncbi.nlm.nih.gov/pubmed/32184236 http://dx.doi.org/10.1128/mBio.00076-20 |
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