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Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data
Advances in genome sequencing technologies and genome-wide association studies (GWAS) have provided unprecedented insights into the molecular basis of microbial phenotypes and enabled the identification of the underlying genetic variants in real populations. However, utilization of genome sequencing...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5311915/ https://www.ncbi.nlm.nih.gov/pubmed/28205635 http://dx.doi.org/10.1038/srep42808 |
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author | Mobegi, Fredrick M. Cremers, Amelieke J. H. de Jonge, Marien I. Bentley, Stephen D. van Hijum, Sacha A. F. T. Zomer, Aldert |
author_facet | Mobegi, Fredrick M. Cremers, Amelieke J. H. de Jonge, Marien I. Bentley, Stephen D. van Hijum, Sacha A. F. T. Zomer, Aldert |
author_sort | Mobegi, Fredrick M. |
collection | PubMed |
description | Advances in genome sequencing technologies and genome-wide association studies (GWAS) have provided unprecedented insights into the molecular basis of microbial phenotypes and enabled the identification of the underlying genetic variants in real populations. However, utilization of genome sequencing in clinical phenotyping of bacteria is challenging due to the lack of reliable and accurate approaches. Here, we report a method for predicting microbial resistance patterns using genome sequencing data. We analyzed whole genome sequences of 1,680 Streptococcus pneumoniae isolates from four independent populations using GWAS and identified probable hotspots of genetic variation which correlate with phenotypes of resistance to essential classes of antibiotics. With the premise that accumulation of putative resistance-conferring SNPs, potentially in combination with specific resistance genes, precedes full resistance, we retrogressively surveyed the hotspot loci and quantified the number of SNPs and/or genes, which if accumulated would confer full resistance to an otherwise susceptible strain. We name this approach the ‘distance to resistance’. It can be used to identify the creep towards complete antibiotics resistance in bacteria using genome sequencing. This approach serves as a basis for the development of future sequencing-based methods for predicting resistance profiles of bacterial strains in hospital microbiology and public health settings. |
format | Online Article Text |
id | pubmed-5311915 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53119152017-02-23 Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data Mobegi, Fredrick M. Cremers, Amelieke J. H. de Jonge, Marien I. Bentley, Stephen D. van Hijum, Sacha A. F. T. Zomer, Aldert Sci Rep Article Advances in genome sequencing technologies and genome-wide association studies (GWAS) have provided unprecedented insights into the molecular basis of microbial phenotypes and enabled the identification of the underlying genetic variants in real populations. However, utilization of genome sequencing in clinical phenotyping of bacteria is challenging due to the lack of reliable and accurate approaches. Here, we report a method for predicting microbial resistance patterns using genome sequencing data. We analyzed whole genome sequences of 1,680 Streptococcus pneumoniae isolates from four independent populations using GWAS and identified probable hotspots of genetic variation which correlate with phenotypes of resistance to essential classes of antibiotics. With the premise that accumulation of putative resistance-conferring SNPs, potentially in combination with specific resistance genes, precedes full resistance, we retrogressively surveyed the hotspot loci and quantified the number of SNPs and/or genes, which if accumulated would confer full resistance to an otherwise susceptible strain. We name this approach the ‘distance to resistance’. It can be used to identify the creep towards complete antibiotics resistance in bacteria using genome sequencing. This approach serves as a basis for the development of future sequencing-based methods for predicting resistance profiles of bacterial strains in hospital microbiology and public health settings. Nature Publishing Group 2017-02-16 /pmc/articles/PMC5311915/ /pubmed/28205635 http://dx.doi.org/10.1038/srep42808 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Mobegi, Fredrick M. Cremers, Amelieke J. H. de Jonge, Marien I. Bentley, Stephen D. van Hijum, Sacha A. F. T. Zomer, Aldert Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data |
title | Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data |
title_full | Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data |
title_fullStr | Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data |
title_full_unstemmed | Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data |
title_short | Deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data |
title_sort | deciphering the distance to antibiotic resistance for the pneumococcus using genome sequencing data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5311915/ https://www.ncbi.nlm.nih.gov/pubmed/28205635 http://dx.doi.org/10.1038/srep42808 |
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