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Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community

With the growing global threat of antimicrobial resistance, novel strategies are required for combatting resistant pathogens. Combination therapy, in which multiple drugs are used to treat an infection, has proven highly successful in the treatment of cancer and HIV. However, this practice has prove...

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Autores principales: Adamowicz, Elizabeth M., Harcombe, William R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577160/
https://www.ncbi.nlm.nih.gov/pubmed/32778550
http://dx.doi.org/10.1128/AAC.00465-20
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author Adamowicz, Elizabeth M.
Harcombe, William R.
author_facet Adamowicz, Elizabeth M.
Harcombe, William R.
author_sort Adamowicz, Elizabeth M.
collection PubMed
description With the growing global threat of antimicrobial resistance, novel strategies are required for combatting resistant pathogens. Combination therapy, in which multiple drugs are used to treat an infection, has proven highly successful in the treatment of cancer and HIV. However, this practice has proven challenging for the treatment of bacterial infections due to difficulties in selecting the correct combinations and dosages. An additional challenge in infection treatment is the polymicrobial nature of many infections, which may respond to antibiotics differently than a monoculture pathogen. This study tests whether patterns of antibiotic interactions (synergy, antagonism, or independence/additivity) in monoculture can be used to predict antibiotic interactions in an obligate cross-feeding coculture. Using our previously described weakest-link hypothesis, we hypothesized antibiotic interactions in coculture based on the interactions we observed in monoculture. We then compared our predictions to observed antibiotic interactions in coculture. We tested the interactions between 10 previously identified antibiotic combinations using checkerboard assays. Although our antibiotic combinations interacted differently than predicted in our monocultures, our monoculture results were generally sufficient to predict coculture patterns based solely on the weakest-link hypothesis. These results suggest that combination therapy for cross-feeding multispecies infections may be successfully designed based on antibiotic interaction patterns for their component species.
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spelling pubmed-75771602020-10-30 Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community Adamowicz, Elizabeth M. Harcombe, William R. Antimicrob Agents Chemother Mechanisms of Action: Physiological Effects With the growing global threat of antimicrobial resistance, novel strategies are required for combatting resistant pathogens. Combination therapy, in which multiple drugs are used to treat an infection, has proven highly successful in the treatment of cancer and HIV. However, this practice has proven challenging for the treatment of bacterial infections due to difficulties in selecting the correct combinations and dosages. An additional challenge in infection treatment is the polymicrobial nature of many infections, which may respond to antibiotics differently than a monoculture pathogen. This study tests whether patterns of antibiotic interactions (synergy, antagonism, or independence/additivity) in monoculture can be used to predict antibiotic interactions in an obligate cross-feeding coculture. Using our previously described weakest-link hypothesis, we hypothesized antibiotic interactions in coculture based on the interactions we observed in monoculture. We then compared our predictions to observed antibiotic interactions in coculture. We tested the interactions between 10 previously identified antibiotic combinations using checkerboard assays. Although our antibiotic combinations interacted differently than predicted in our monocultures, our monoculture results were generally sufficient to predict coculture patterns based solely on the weakest-link hypothesis. These results suggest that combination therapy for cross-feeding multispecies infections may be successfully designed based on antibiotic interaction patterns for their component species. American Society for Microbiology 2020-10-20 /pmc/articles/PMC7577160/ /pubmed/32778550 http://dx.doi.org/10.1128/AAC.00465-20 Text en Copyright © 2020 Adamowicz and Harcombe. 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 Mechanisms of Action: Physiological Effects
Adamowicz, Elizabeth M.
Harcombe, William R.
Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community
title Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community
title_full Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community
title_fullStr Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community
title_full_unstemmed Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community
title_short Weakest-Link Dynamics Predict Apparent Antibiotic Interactions in a Model Cross-Feeding Community
title_sort weakest-link dynamics predict apparent antibiotic interactions in a model cross-feeding community
topic Mechanisms of Action: Physiological Effects
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577160/
https://www.ncbi.nlm.nih.gov/pubmed/32778550
http://dx.doi.org/10.1128/AAC.00465-20
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