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Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy
Now more than ever there is a demand to understand the mechanisms surrounding antibiotic resistance and look for alternative ways to impact phenotypic antibiotic outcome. Cellular energetics can be impacted by many bacteriostatic and bactericidal antibiotics, which affect metabolism and energy outpu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736855/ https://www.ncbi.nlm.nih.gov/pubmed/33318549 http://dx.doi.org/10.1038/s41598-020-78855-5 |
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author | Smith, Helen Grant, Sharon Parker, Joanne Murphy, Richard |
author_facet | Smith, Helen Grant, Sharon Parker, Joanne Murphy, Richard |
author_sort | Smith, Helen |
collection | PubMed |
description | Now more than ever there is a demand to understand the mechanisms surrounding antibiotic resistance and look for alternative ways to impact phenotypic antibiotic outcome. Cellular energetics can be impacted by many bacteriostatic and bactericidal antibiotics, which affect metabolism and energy output, resulting in a reduction of cell growth or induction of cell death respectively. In this study, we provide evidence that a mannan rich fraction (MRF) from the cell wall of Saccharomyces cerevisiae modulates growth of antibiotic susceptible and resistant Escherichia coli and potentiates bactericidal antibiotic efficiency through modulation of bacterial cellular respiration. The role of MRF in modulating bactericidal impact and cellular metabolic state were assessed in E. coli by monitoring microbial growth and by measuring oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) using the Seahorse XFe96 Analyser, respectively. This work further illustrates the link between bacterial susceptibility to antibiotics (phenotypic resistance) and resistance through modulation of bacterial metabolism. This is the first example of yeast MRF enabling collateral sensitivity to antibiotics in vitro and supports the search for alternative strategies to promote animal health without contributing to the growing issue of antimicrobial resistance. |
format | Online Article Text |
id | pubmed-7736855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77368552020-12-15 Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy Smith, Helen Grant, Sharon Parker, Joanne Murphy, Richard Sci Rep Article Now more than ever there is a demand to understand the mechanisms surrounding antibiotic resistance and look for alternative ways to impact phenotypic antibiotic outcome. Cellular energetics can be impacted by many bacteriostatic and bactericidal antibiotics, which affect metabolism and energy output, resulting in a reduction of cell growth or induction of cell death respectively. In this study, we provide evidence that a mannan rich fraction (MRF) from the cell wall of Saccharomyces cerevisiae modulates growth of antibiotic susceptible and resistant Escherichia coli and potentiates bactericidal antibiotic efficiency through modulation of bacterial cellular respiration. The role of MRF in modulating bactericidal impact and cellular metabolic state were assessed in E. coli by monitoring microbial growth and by measuring oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) using the Seahorse XFe96 Analyser, respectively. This work further illustrates the link between bacterial susceptibility to antibiotics (phenotypic resistance) and resistance through modulation of bacterial metabolism. This is the first example of yeast MRF enabling collateral sensitivity to antibiotics in vitro and supports the search for alternative strategies to promote animal health without contributing to the growing issue of antimicrobial resistance. Nature Publishing Group UK 2020-12-14 /pmc/articles/PMC7736855/ /pubmed/33318549 http://dx.doi.org/10.1038/s41598-020-78855-5 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Smith, Helen Grant, Sharon Parker, Joanne Murphy, Richard Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy |
title | Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy |
title_full | Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy |
title_fullStr | Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy |
title_full_unstemmed | Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy |
title_short | Yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy |
title_sort | yeast cell wall mannan rich fraction modulates bacterial cellular respiration potentiating antibiotic efficacy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736855/ https://www.ncbi.nlm.nih.gov/pubmed/33318549 http://dx.doi.org/10.1038/s41598-020-78855-5 |
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