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Resource limitation prevents the emergence of drug resistance by intensifying within-host competition
Slowing the evolution of antimicrobial resistance is essential if we are to continue to successfully treat infectious diseases. Whether a drug-resistant mutant grows to high densities, and so sickens the patient and spreads to new hosts, is determined by the competitive interactions it has with drug...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748215/ https://www.ncbi.nlm.nih.gov/pubmed/29233945 http://dx.doi.org/10.1073/pnas.1715874115 |
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author | Wale, Nina Sim, Derek G. Jones, Matthew J. Salathe, Rahel Day, Troy Read, Andrew F. |
author_facet | Wale, Nina Sim, Derek G. Jones, Matthew J. Salathe, Rahel Day, Troy Read, Andrew F. |
author_sort | Wale, Nina |
collection | PubMed |
description | Slowing the evolution of antimicrobial resistance is essential if we are to continue to successfully treat infectious diseases. Whether a drug-resistant mutant grows to high densities, and so sickens the patient and spreads to new hosts, is determined by the competitive interactions it has with drug-susceptible pathogens within the host. Competitive interactions thus represent a good target for resistance management strategies. Using an in vivo model of malaria infection, we show that limiting a resource that is disproportionately required by resistant parasites retards the evolution of drug resistance by intensifying competitive interactions between susceptible and resistant parasites. Resource limitation prevented resistance emergence regardless of whether resistant mutants arose de novo or were experimentally added before drug treatment. Our work provides proof of principle that chemotherapy paired with an “ecological” intervention can slow the evolution of resistance to antimicrobial drugs, even when resistant pathogens are present at high frequencies. It also suggests that a broad range of previously untapped compounds could be used for treating infectious diseases. |
format | Online Article Text |
id | pubmed-5748215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-57482152018-01-09 Resource limitation prevents the emergence of drug resistance by intensifying within-host competition Wale, Nina Sim, Derek G. Jones, Matthew J. Salathe, Rahel Day, Troy Read, Andrew F. Proc Natl Acad Sci U S A Biological Sciences Slowing the evolution of antimicrobial resistance is essential if we are to continue to successfully treat infectious diseases. Whether a drug-resistant mutant grows to high densities, and so sickens the patient and spreads to new hosts, is determined by the competitive interactions it has with drug-susceptible pathogens within the host. Competitive interactions thus represent a good target for resistance management strategies. Using an in vivo model of malaria infection, we show that limiting a resource that is disproportionately required by resistant parasites retards the evolution of drug resistance by intensifying competitive interactions between susceptible and resistant parasites. Resource limitation prevented resistance emergence regardless of whether resistant mutants arose de novo or were experimentally added before drug treatment. Our work provides proof of principle that chemotherapy paired with an “ecological” intervention can slow the evolution of resistance to antimicrobial drugs, even when resistant pathogens are present at high frequencies. It also suggests that a broad range of previously untapped compounds could be used for treating infectious diseases. National Academy of Sciences 2017-12-26 2017-12-12 /pmc/articles/PMC5748215/ /pubmed/29233945 http://dx.doi.org/10.1073/pnas.1715874115 Text en Copyright © 2017 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Wale, Nina Sim, Derek G. Jones, Matthew J. Salathe, Rahel Day, Troy Read, Andrew F. Resource limitation prevents the emergence of drug resistance by intensifying within-host competition |
title | Resource limitation prevents the emergence of drug resistance by intensifying within-host competition |
title_full | Resource limitation prevents the emergence of drug resistance by intensifying within-host competition |
title_fullStr | Resource limitation prevents the emergence of drug resistance by intensifying within-host competition |
title_full_unstemmed | Resource limitation prevents the emergence of drug resistance by intensifying within-host competition |
title_short | Resource limitation prevents the emergence of drug resistance by intensifying within-host competition |
title_sort | resource limitation prevents the emergence of drug resistance by intensifying within-host competition |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5748215/ https://www.ncbi.nlm.nih.gov/pubmed/29233945 http://dx.doi.org/10.1073/pnas.1715874115 |
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