Cargando…

Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA

BACKGROUND: Fitness costs imposed on bacteria by antibiotic resistance mechanisms are believed to hamper their dissemination. The scale of these costs is highly variable. Some, including resistance of Staphylococcus aureus to the clinically important antibiotic mupirocin, have been reported as being...

Descripción completa

Detalles Bibliográficos
Autores principales: Yokoyama, Maho, Stevens, Emily, Laabei, Maisem, Bacon, Leann, Heesom, Kate, Bayliss, Sion, Ooi, Nicola, O’Neill, Alex J., Murray, Ewan, Williams, Paul, Lubben, Anneke, Reeksting, Shaun, Meric, Guillaume, Pascoe, Ben, Sheppard, Samuel K., Recker, Mario, Hurst, Laurence D., Massey, Ruth C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052701/
https://www.ncbi.nlm.nih.gov/pubmed/30021593
http://dx.doi.org/10.1186/s13059-018-1469-2
_version_ 1783340713156542464
author Yokoyama, Maho
Stevens, Emily
Laabei, Maisem
Bacon, Leann
Heesom, Kate
Bayliss, Sion
Ooi, Nicola
O’Neill, Alex J.
Murray, Ewan
Williams, Paul
Lubben, Anneke
Reeksting, Shaun
Meric, Guillaume
Pascoe, Ben
Sheppard, Samuel K.
Recker, Mario
Hurst, Laurence D.
Massey, Ruth C.
author_facet Yokoyama, Maho
Stevens, Emily
Laabei, Maisem
Bacon, Leann
Heesom, Kate
Bayliss, Sion
Ooi, Nicola
O’Neill, Alex J.
Murray, Ewan
Williams, Paul
Lubben, Anneke
Reeksting, Shaun
Meric, Guillaume
Pascoe, Ben
Sheppard, Samuel K.
Recker, Mario
Hurst, Laurence D.
Massey, Ruth C.
author_sort Yokoyama, Maho
collection PubMed
description BACKGROUND: Fitness costs imposed on bacteria by antibiotic resistance mechanisms are believed to hamper their dissemination. The scale of these costs is highly variable. Some, including resistance of Staphylococcus aureus to the clinically important antibiotic mupirocin, have been reported as being cost-free, which suggests that there are few barriers preventing their global spread. However, this is not supported by surveillance data in healthy communities, which indicate that this resistance mechanism is relatively unsuccessful. RESULTS: Epistasis analysis on two collections of MRSA provides an explanation for this discord, where the mupirocin resistance-conferring mutation of the ileS gene appears to affect the levels of toxins produced by S. aureus when combined with specific polymorphisms at other loci. Proteomic analysis demonstrates that the activity of the secretory apparatus of the PSM family of toxins is affected by mupirocin resistance. As an energetically costly activity, this reduction in toxicity masks the fitness costs associated with this resistance mutation, a cost that becomes apparent when toxin production becomes necessary. This hidden fitness cost provides a likely explanation for why this mupirocin-resistance mechanism is not more prevalent, given the widespread use of this antibiotic. CONCLUSIONS: With dwindling pools of antibiotics available for use, information on the fitness consequences of the acquisition of resistance may need to be considered when designing antibiotic prescribing policies. However, this study suggests there are levels of depth that we do not understand, and that holistic, surveillance and functional genomics approaches are required to gain this crucial information. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1469-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6052701
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-60527012018-07-23 Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA Yokoyama, Maho Stevens, Emily Laabei, Maisem Bacon, Leann Heesom, Kate Bayliss, Sion Ooi, Nicola O’Neill, Alex J. Murray, Ewan Williams, Paul Lubben, Anneke Reeksting, Shaun Meric, Guillaume Pascoe, Ben Sheppard, Samuel K. Recker, Mario Hurst, Laurence D. Massey, Ruth C. Genome Biol Research BACKGROUND: Fitness costs imposed on bacteria by antibiotic resistance mechanisms are believed to hamper their dissemination. The scale of these costs is highly variable. Some, including resistance of Staphylococcus aureus to the clinically important antibiotic mupirocin, have been reported as being cost-free, which suggests that there are few barriers preventing their global spread. However, this is not supported by surveillance data in healthy communities, which indicate that this resistance mechanism is relatively unsuccessful. RESULTS: Epistasis analysis on two collections of MRSA provides an explanation for this discord, where the mupirocin resistance-conferring mutation of the ileS gene appears to affect the levels of toxins produced by S. aureus when combined with specific polymorphisms at other loci. Proteomic analysis demonstrates that the activity of the secretory apparatus of the PSM family of toxins is affected by mupirocin resistance. As an energetically costly activity, this reduction in toxicity masks the fitness costs associated with this resistance mutation, a cost that becomes apparent when toxin production becomes necessary. This hidden fitness cost provides a likely explanation for why this mupirocin-resistance mechanism is not more prevalent, given the widespread use of this antibiotic. CONCLUSIONS: With dwindling pools of antibiotics available for use, information on the fitness consequences of the acquisition of resistance may need to be considered when designing antibiotic prescribing policies. However, this study suggests there are levels of depth that we do not understand, and that holistic, surveillance and functional genomics approaches are required to gain this crucial information. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13059-018-1469-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-18 /pmc/articles/PMC6052701/ /pubmed/30021593 http://dx.doi.org/10.1186/s13059-018-1469-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Yokoyama, Maho
Stevens, Emily
Laabei, Maisem
Bacon, Leann
Heesom, Kate
Bayliss, Sion
Ooi, Nicola
O’Neill, Alex J.
Murray, Ewan
Williams, Paul
Lubben, Anneke
Reeksting, Shaun
Meric, Guillaume
Pascoe, Ben
Sheppard, Samuel K.
Recker, Mario
Hurst, Laurence D.
Massey, Ruth C.
Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA
title Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA
title_full Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA
title_fullStr Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA
title_full_unstemmed Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA
title_short Epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of MRSA
title_sort epistasis analysis uncovers hidden antibiotic resistance-associated fitness costs hampering the evolution of mrsa
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052701/
https://www.ncbi.nlm.nih.gov/pubmed/30021593
http://dx.doi.org/10.1186/s13059-018-1469-2
work_keys_str_mv AT yokoyamamaho epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT stevensemily epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT laabeimaisem epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT baconleann epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT heesomkate epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT baylisssion epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT ooinicola epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT oneillalexj epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT murrayewan epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT williamspaul epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT lubbenanneke epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT reekstingshaun epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT mericguillaume epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT pascoeben epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT sheppardsamuelk epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT reckermario epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT hurstlaurenced epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa
AT masseyruthc epistasisanalysisuncovershiddenantibioticresistanceassociatedfitnesscostshamperingtheevolutionofmrsa