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Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages

We need to find ways of enhancing the potency of existing antibiotics, and, with this in mind, we begin with an unusual question: how low can antibiotic dosages be and yet bacterial clearance still be observed? Seeking to optimise the simultaneous use of two antibiotics, we use the minimal dose at w...

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Autores principales: Fuentes-Hernandez, Ayari, Plucain, Jessica, Gori, Fabio, Pena-Miller, Rafael, Reding, Carlos, Jansen, Gunther, Schulenburg, Hinrich, Gudelj, Ivana, Beardmore, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390231/
https://www.ncbi.nlm.nih.gov/pubmed/25853342
http://dx.doi.org/10.1371/journal.pbio.1002104
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author Fuentes-Hernandez, Ayari
Plucain, Jessica
Gori, Fabio
Pena-Miller, Rafael
Reding, Carlos
Jansen, Gunther
Schulenburg, Hinrich
Gudelj, Ivana
Beardmore, Robert
author_facet Fuentes-Hernandez, Ayari
Plucain, Jessica
Gori, Fabio
Pena-Miller, Rafael
Reding, Carlos
Jansen, Gunther
Schulenburg, Hinrich
Gudelj, Ivana
Beardmore, Robert
author_sort Fuentes-Hernandez, Ayari
collection PubMed
description We need to find ways of enhancing the potency of existing antibiotics, and, with this in mind, we begin with an unusual question: how low can antibiotic dosages be and yet bacterial clearance still be observed? Seeking to optimise the simultaneous use of two antibiotics, we use the minimal dose at which clearance is observed in an in vitro experimental model of antibiotic treatment as a criterion to distinguish the best and worst treatments of a bacterium, Escherichia coli. Our aim is to compare a combination treatment consisting of two synergistic antibiotics to so-called sequential treatments in which the choice of antibiotic to administer can change with each round of treatment. Using mathematical predictions validated by the E. coli treatment model, we show that clearance of the bacterium can be achieved using sequential treatments at antibiotic dosages so low that the equivalent two-drug combination treatments are ineffective. Seeking to treat the bacterium in testing circumstances, we purposefully study an E. coli strain that has a multidrug pump encoded in its chromosome that effluxes both antibiotics. Genomic amplifications that increase the number of pumps expressed per cell can cause the failure of high-dose combination treatments, yet, as we show, sequentially treated populations can still collapse. However, dual resistance due to the pump means that the antibiotics must be carefully deployed and not all sublethal sequential treatments succeed. A screen of 136 96-h-long sequential treatments determined five of these that could clear the bacterium at sublethal dosages in all replicate populations, even though none had done so by 24 h. These successes can be attributed to a collateral sensitivity whereby cross-resistance due to the duplicated pump proves insufficient to stop a reduction in E. coli growth rate following drug exchanges, a reduction that proves large enough for appropriately chosen drug switches to clear the bacterium.
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spelling pubmed-43902312015-04-21 Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages Fuentes-Hernandez, Ayari Plucain, Jessica Gori, Fabio Pena-Miller, Rafael Reding, Carlos Jansen, Gunther Schulenburg, Hinrich Gudelj, Ivana Beardmore, Robert PLoS Biol Research Article We need to find ways of enhancing the potency of existing antibiotics, and, with this in mind, we begin with an unusual question: how low can antibiotic dosages be and yet bacterial clearance still be observed? Seeking to optimise the simultaneous use of two antibiotics, we use the minimal dose at which clearance is observed in an in vitro experimental model of antibiotic treatment as a criterion to distinguish the best and worst treatments of a bacterium, Escherichia coli. Our aim is to compare a combination treatment consisting of two synergistic antibiotics to so-called sequential treatments in which the choice of antibiotic to administer can change with each round of treatment. Using mathematical predictions validated by the E. coli treatment model, we show that clearance of the bacterium can be achieved using sequential treatments at antibiotic dosages so low that the equivalent two-drug combination treatments are ineffective. Seeking to treat the bacterium in testing circumstances, we purposefully study an E. coli strain that has a multidrug pump encoded in its chromosome that effluxes both antibiotics. Genomic amplifications that increase the number of pumps expressed per cell can cause the failure of high-dose combination treatments, yet, as we show, sequentially treated populations can still collapse. However, dual resistance due to the pump means that the antibiotics must be carefully deployed and not all sublethal sequential treatments succeed. A screen of 136 96-h-long sequential treatments determined five of these that could clear the bacterium at sublethal dosages in all replicate populations, even though none had done so by 24 h. These successes can be attributed to a collateral sensitivity whereby cross-resistance due to the duplicated pump proves insufficient to stop a reduction in E. coli growth rate following drug exchanges, a reduction that proves large enough for appropriately chosen drug switches to clear the bacterium. Public Library of Science 2015-04-08 /pmc/articles/PMC4390231/ /pubmed/25853342 http://dx.doi.org/10.1371/journal.pbio.1002104 Text en © 2015 Fuentes-Hernandez et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fuentes-Hernandez, Ayari
Plucain, Jessica
Gori, Fabio
Pena-Miller, Rafael
Reding, Carlos
Jansen, Gunther
Schulenburg, Hinrich
Gudelj, Ivana
Beardmore, Robert
Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages
title Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages
title_full Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages
title_fullStr Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages
title_full_unstemmed Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages
title_short Using a Sequential Regimen to Eliminate Bacteria at Sublethal Antibiotic Dosages
title_sort using a sequential regimen to eliminate bacteria at sublethal antibiotic dosages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4390231/
https://www.ncbi.nlm.nih.gov/pubmed/25853342
http://dx.doi.org/10.1371/journal.pbio.1002104
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