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Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics
Plasmid-borne colistin resistance mediated by mcr-1 may contribute to the dissemination of pan-resistant Gram-negative bacteria. Here, we show that mcr-1 confers resistance to colistin-induced lysis and bacterial cell death, but provides minimal protection from the ability of colistin to disrupt the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792607/ https://www.ncbi.nlm.nih.gov/pubmed/29386620 http://dx.doi.org/10.1038/s41467-018-02875-z |
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author | MacNair, Craig R. Stokes, Jonathan M. Carfrae, Lindsey A. Fiebig-Comyn, Aline A. Coombes, Brian K. Mulvey, Michael R. Brown, Eric D. |
author_facet | MacNair, Craig R. Stokes, Jonathan M. Carfrae, Lindsey A. Fiebig-Comyn, Aline A. Coombes, Brian K. Mulvey, Michael R. Brown, Eric D. |
author_sort | MacNair, Craig R. |
collection | PubMed |
description | Plasmid-borne colistin resistance mediated by mcr-1 may contribute to the dissemination of pan-resistant Gram-negative bacteria. Here, we show that mcr-1 confers resistance to colistin-induced lysis and bacterial cell death, but provides minimal protection from the ability of colistin to disrupt the Gram-negative outer membrane. Indeed, for colistin-resistant strains of Enterobacteriaceae expressing plasmid-borne mcr-1, clinically relevant concentrations of colistin potentiate the action of antibiotics that, by themselves, are not active against Gram-negative bacteria. The result is that several antibiotics, in combination with colistin, display growth-inhibition at levels below their corresponding clinical breakpoints. Furthermore, colistin and clarithromycin combination therapy displays efficacy against mcr-1-positive Klebsiella pneumoniae in murine thigh and bacteremia infection models at clinically relevant doses. Altogether, these data suggest that the use of colistin in combination with antibiotics that are typically active against Gram-positive bacteria poses a viable therapeutic alternative for highly drug-resistant Gram-negative pathogens expressing mcr-1. |
format | Online Article Text |
id | pubmed-5792607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57926072018-02-02 Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics MacNair, Craig R. Stokes, Jonathan M. Carfrae, Lindsey A. Fiebig-Comyn, Aline A. Coombes, Brian K. Mulvey, Michael R. Brown, Eric D. Nat Commun Article Plasmid-borne colistin resistance mediated by mcr-1 may contribute to the dissemination of pan-resistant Gram-negative bacteria. Here, we show that mcr-1 confers resistance to colistin-induced lysis and bacterial cell death, but provides minimal protection from the ability of colistin to disrupt the Gram-negative outer membrane. Indeed, for colistin-resistant strains of Enterobacteriaceae expressing plasmid-borne mcr-1, clinically relevant concentrations of colistin potentiate the action of antibiotics that, by themselves, are not active against Gram-negative bacteria. The result is that several antibiotics, in combination with colistin, display growth-inhibition at levels below their corresponding clinical breakpoints. Furthermore, colistin and clarithromycin combination therapy displays efficacy against mcr-1-positive Klebsiella pneumoniae in murine thigh and bacteremia infection models at clinically relevant doses. Altogether, these data suggest that the use of colistin in combination with antibiotics that are typically active against Gram-positive bacteria poses a viable therapeutic alternative for highly drug-resistant Gram-negative pathogens expressing mcr-1. Nature Publishing Group UK 2018-01-31 /pmc/articles/PMC5792607/ /pubmed/29386620 http://dx.doi.org/10.1038/s41467-018-02875-z Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article MacNair, Craig R. Stokes, Jonathan M. Carfrae, Lindsey A. Fiebig-Comyn, Aline A. Coombes, Brian K. Mulvey, Michael R. Brown, Eric D. Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics |
title | Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics |
title_full | Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics |
title_fullStr | Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics |
title_full_unstemmed | Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics |
title_short | Overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics |
title_sort | overcoming mcr-1 mediated colistin resistance with colistin in combination with other antibiotics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5792607/ https://www.ncbi.nlm.nih.gov/pubmed/29386620 http://dx.doi.org/10.1038/s41467-018-02875-z |
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