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Antimicrobial Resistance Prediction in PATRIC and RAST
The emergence and spread of antimicrobial resistance (AMR) mechanisms in bacterial pathogens, coupled with the dwindling number of effective antibiotics, has created a global health crisis. Being able to identify the genetic mechanisms of AMR and predict the resistance phenotypes of bacterial pathog...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906388/ https://www.ncbi.nlm.nih.gov/pubmed/27297683 http://dx.doi.org/10.1038/srep27930 |
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author | Davis, James J. Boisvert, Sébastien Brettin, Thomas Kenyon, Ronald W. Mao, Chunhong Olson, Robert Overbeek, Ross Santerre, John Shukla, Maulik Wattam, Alice R. Will, Rebecca Xia, Fangfang Stevens, Rick |
author_facet | Davis, James J. Boisvert, Sébastien Brettin, Thomas Kenyon, Ronald W. Mao, Chunhong Olson, Robert Overbeek, Ross Santerre, John Shukla, Maulik Wattam, Alice R. Will, Rebecca Xia, Fangfang Stevens, Rick |
author_sort | Davis, James J. |
collection | PubMed |
description | The emergence and spread of antimicrobial resistance (AMR) mechanisms in bacterial pathogens, coupled with the dwindling number of effective antibiotics, has created a global health crisis. Being able to identify the genetic mechanisms of AMR and predict the resistance phenotypes of bacterial pathogens prior to culturing could inform clinical decision-making and improve reaction time. At PATRIC (http://patricbrc.org/), we have been collecting bacterial genomes with AMR metadata for several years. In order to advance phenotype prediction and the identification of genomic regions relating to AMR, we have updated the PATRIC FTP server to enable access to genomes that are binned by their AMR phenotypes, as well as metadata including minimum inhibitory concentrations. Using this infrastructure, we custom built AdaBoost (adaptive boosting) machine learning classifiers for identifying carbapenem resistance in Acinetobacter baumannii, methicillin resistance in Staphylococcus aureus, and beta-lactam and co-trimoxazole resistance in Streptococcus pneumoniae with accuracies ranging from 88–99%. We also did this for isoniazid, kanamycin, ofloxacin, rifampicin, and streptomycin resistance in Mycobacterium tuberculosis, achieving accuracies ranging from 71–88%. This set of classifiers has been used to provide an initial framework for species-specific AMR phenotype and genomic feature prediction in the RAST and PATRIC annotation services. |
format | Online Article Text |
id | pubmed-4906388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49063882016-06-15 Antimicrobial Resistance Prediction in PATRIC and RAST Davis, James J. Boisvert, Sébastien Brettin, Thomas Kenyon, Ronald W. Mao, Chunhong Olson, Robert Overbeek, Ross Santerre, John Shukla, Maulik Wattam, Alice R. Will, Rebecca Xia, Fangfang Stevens, Rick Sci Rep Article The emergence and spread of antimicrobial resistance (AMR) mechanisms in bacterial pathogens, coupled with the dwindling number of effective antibiotics, has created a global health crisis. Being able to identify the genetic mechanisms of AMR and predict the resistance phenotypes of bacterial pathogens prior to culturing could inform clinical decision-making and improve reaction time. At PATRIC (http://patricbrc.org/), we have been collecting bacterial genomes with AMR metadata for several years. In order to advance phenotype prediction and the identification of genomic regions relating to AMR, we have updated the PATRIC FTP server to enable access to genomes that are binned by their AMR phenotypes, as well as metadata including minimum inhibitory concentrations. Using this infrastructure, we custom built AdaBoost (adaptive boosting) machine learning classifiers for identifying carbapenem resistance in Acinetobacter baumannii, methicillin resistance in Staphylococcus aureus, and beta-lactam and co-trimoxazole resistance in Streptococcus pneumoniae with accuracies ranging from 88–99%. We also did this for isoniazid, kanamycin, ofloxacin, rifampicin, and streptomycin resistance in Mycobacterium tuberculosis, achieving accuracies ranging from 71–88%. This set of classifiers has been used to provide an initial framework for species-specific AMR phenotype and genomic feature prediction in the RAST and PATRIC annotation services. Nature Publishing Group 2016-06-14 /pmc/articles/PMC4906388/ /pubmed/27297683 http://dx.doi.org/10.1038/srep27930 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 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 in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article Davis, James J. Boisvert, Sébastien Brettin, Thomas Kenyon, Ronald W. Mao, Chunhong Olson, Robert Overbeek, Ross Santerre, John Shukla, Maulik Wattam, Alice R. Will, Rebecca Xia, Fangfang Stevens, Rick Antimicrobial Resistance Prediction in PATRIC and RAST |
title | Antimicrobial Resistance Prediction in PATRIC and RAST |
title_full | Antimicrobial Resistance Prediction in PATRIC and RAST |
title_fullStr | Antimicrobial Resistance Prediction in PATRIC and RAST |
title_full_unstemmed | Antimicrobial Resistance Prediction in PATRIC and RAST |
title_short | Antimicrobial Resistance Prediction in PATRIC and RAST |
title_sort | antimicrobial resistance prediction in patric and rast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906388/ https://www.ncbi.nlm.nih.gov/pubmed/27297683 http://dx.doi.org/10.1038/srep27930 |
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