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Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus

NorA is the best studied efflux system of Staphylococcus aureus and therefore frequently used as a model for investigating efflux-mediated resistance in this pathogen. NorA activity is associated with resistance to fluoroquinolones, several antiseptics and disinfectants and several reports have poin...

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Autores principales: Costa, Sofia Santos, Sobkowiak, Benjamin, Parreira, Ricardo, Edgeworth, Jonathan D., Viveiros, Miguel, Clark, Taane G., Couto, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333699/
https://www.ncbi.nlm.nih.gov/pubmed/30687388
http://dx.doi.org/10.3389/fgene.2018.00710
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author Costa, Sofia Santos
Sobkowiak, Benjamin
Parreira, Ricardo
Edgeworth, Jonathan D.
Viveiros, Miguel
Clark, Taane G.
Couto, Isabel
author_facet Costa, Sofia Santos
Sobkowiak, Benjamin
Parreira, Ricardo
Edgeworth, Jonathan D.
Viveiros, Miguel
Clark, Taane G.
Couto, Isabel
author_sort Costa, Sofia Santos
collection PubMed
description NorA is the best studied efflux system of Staphylococcus aureus and therefore frequently used as a model for investigating efflux-mediated resistance in this pathogen. NorA activity is associated with resistance to fluoroquinolones, several antiseptics and disinfectants and several reports have pointed out the role of efflux systems, including NorA, as a first-line response to antimicrobials in S. aureus. Genetic diversity studies of the gene norA have described three alleles; norAI, norAII and norAIII. However, the epidemiology of these alleles and their impact on NorA activity remains unclear. Additionally, increasing studies do not account for norA variability when establishing relations between resistance phenotypes and norA presence or reported absence, which actually corresponds, as we now demonstrate, to different norA alleles. In the present study we assessed the variability of the norA gene present in the genome of over 1,000 S. aureus isolates, corresponding to 112 S. aureus strains with whole genome sequences publicly available; 917 MRSA strains sourced from a London-based study and nine MRSA isolates collected in a major Hospital in Lisbon, Portugal. Our analyses show that norA is part of the core genome of S. aureus. It also suggests that occurrence of norA variants reflects the population structure of this major pathogen. Overall, this work highlights the ubiquitous nature of norA in S. aureus which must be taken into account when studying the role played by this important determinant on S. aureus resistance to antimicrobials.
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spelling pubmed-63336992019-01-25 Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus Costa, Sofia Santos Sobkowiak, Benjamin Parreira, Ricardo Edgeworth, Jonathan D. Viveiros, Miguel Clark, Taane G. Couto, Isabel Front Genet Genetics NorA is the best studied efflux system of Staphylococcus aureus and therefore frequently used as a model for investigating efflux-mediated resistance in this pathogen. NorA activity is associated with resistance to fluoroquinolones, several antiseptics and disinfectants and several reports have pointed out the role of efflux systems, including NorA, as a first-line response to antimicrobials in S. aureus. Genetic diversity studies of the gene norA have described three alleles; norAI, norAII and norAIII. However, the epidemiology of these alleles and their impact on NorA activity remains unclear. Additionally, increasing studies do not account for norA variability when establishing relations between resistance phenotypes and norA presence or reported absence, which actually corresponds, as we now demonstrate, to different norA alleles. In the present study we assessed the variability of the norA gene present in the genome of over 1,000 S. aureus isolates, corresponding to 112 S. aureus strains with whole genome sequences publicly available; 917 MRSA strains sourced from a London-based study and nine MRSA isolates collected in a major Hospital in Lisbon, Portugal. Our analyses show that norA is part of the core genome of S. aureus. It also suggests that occurrence of norA variants reflects the population structure of this major pathogen. Overall, this work highlights the ubiquitous nature of norA in S. aureus which must be taken into account when studying the role played by this important determinant on S. aureus resistance to antimicrobials. Frontiers Media S.A. 2019-01-09 /pmc/articles/PMC6333699/ /pubmed/30687388 http://dx.doi.org/10.3389/fgene.2018.00710 Text en Copyright © 2019 Costa, Sobkowiak, Parreira, Edgeworth, Viveiros, Clark and Couto. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Costa, Sofia Santos
Sobkowiak, Benjamin
Parreira, Ricardo
Edgeworth, Jonathan D.
Viveiros, Miguel
Clark, Taane G.
Couto, Isabel
Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus
title Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus
title_full Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus
title_fullStr Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus
title_full_unstemmed Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus
title_short Genetic Diversity of norA, Coding for a Main Efflux Pump of Staphylococcus aureus
title_sort genetic diversity of nora, coding for a main efflux pump of staphylococcus aureus
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333699/
https://www.ncbi.nlm.nih.gov/pubmed/30687388
http://dx.doi.org/10.3389/fgene.2018.00710
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