Cargando…

Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species

Surveillance programs for managing antimicrobial resistance (AMR) have yielded thousands of genomes suited for data-driven mechanism discovery. We present a workflow integrating pangenomics, gene annotation, and machine learning to identify AMR genes at scale. When applied to 12 species, 27,155 geno...

Descripción completa

Detalles Bibliográficos
Autores principales: Hyun, Jason C., Monk, Jonathan M., Szubin, Richard, Hefner, Ying, Palsson, Bernhard O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673929/
https://www.ncbi.nlm.nih.gov/pubmed/38001096
http://dx.doi.org/10.1038/s41467-023-43549-9
_version_ 1785149662244634624
author Hyun, Jason C.
Monk, Jonathan M.
Szubin, Richard
Hefner, Ying
Palsson, Bernhard O.
author_facet Hyun, Jason C.
Monk, Jonathan M.
Szubin, Richard
Hefner, Ying
Palsson, Bernhard O.
author_sort Hyun, Jason C.
collection PubMed
description Surveillance programs for managing antimicrobial resistance (AMR) have yielded thousands of genomes suited for data-driven mechanism discovery. We present a workflow integrating pangenomics, gene annotation, and machine learning to identify AMR genes at scale. When applied to 12 species, 27,155 genomes, and 69 drugs, we 1) find AMR gene transfer mostly confined within related species, with 925 genes in multiple species but just eight in multiple phylogenetic classes, 2) demonstrate that discovery-oriented support vector machines outperform contemporary methods at recovering known AMR genes, recovering 263 genes compared to 145 by Pyseer, and 3) identify 142 AMR gene candidates. Validation of two candidates in E. coli BW25113 reveals cases of conditional resistance: ΔcycA confers ciprofloxacin resistance in minimal media with D-serine, and frdD V111D confers ampicillin resistance in the presence of ampC by modifying the overlapping promoter. We expect this approach to be adaptable to other species and phenotypes.
format Online
Article
Text
id pubmed-10673929
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-106739292023-11-24 Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species Hyun, Jason C. Monk, Jonathan M. Szubin, Richard Hefner, Ying Palsson, Bernhard O. Nat Commun Article Surveillance programs for managing antimicrobial resistance (AMR) have yielded thousands of genomes suited for data-driven mechanism discovery. We present a workflow integrating pangenomics, gene annotation, and machine learning to identify AMR genes at scale. When applied to 12 species, 27,155 genomes, and 69 drugs, we 1) find AMR gene transfer mostly confined within related species, with 925 genes in multiple species but just eight in multiple phylogenetic classes, 2) demonstrate that discovery-oriented support vector machines outperform contemporary methods at recovering known AMR genes, recovering 263 genes compared to 145 by Pyseer, and 3) identify 142 AMR gene candidates. Validation of two candidates in E. coli BW25113 reveals cases of conditional resistance: ΔcycA confers ciprofloxacin resistance in minimal media with D-serine, and frdD V111D confers ampicillin resistance in the presence of ampC by modifying the overlapping promoter. We expect this approach to be adaptable to other species and phenotypes. Nature Publishing Group UK 2023-11-24 /pmc/articles/PMC10673929/ /pubmed/38001096 http://dx.doi.org/10.1038/s41467-023-43549-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hyun, Jason C.
Monk, Jonathan M.
Szubin, Richard
Hefner, Ying
Palsson, Bernhard O.
Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species
title Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species
title_full Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species
title_fullStr Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species
title_full_unstemmed Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species
title_short Global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species
title_sort global pathogenomic analysis identifies known and candidate genetic antimicrobial resistance determinants in twelve species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10673929/
https://www.ncbi.nlm.nih.gov/pubmed/38001096
http://dx.doi.org/10.1038/s41467-023-43549-9
work_keys_str_mv AT hyunjasonc globalpathogenomicanalysisidentifiesknownandcandidategeneticantimicrobialresistancedeterminantsintwelvespecies
AT monkjonathanm globalpathogenomicanalysisidentifiesknownandcandidategeneticantimicrobialresistancedeterminantsintwelvespecies
AT szubinrichard globalpathogenomicanalysisidentifiesknownandcandidategeneticantimicrobialresistancedeterminantsintwelvespecies
AT hefnerying globalpathogenomicanalysisidentifiesknownandcandidategeneticantimicrobialresistancedeterminantsintwelvespecies
AT palssonbernhardo globalpathogenomicanalysisidentifiesknownandcandidategeneticantimicrobialresistancedeterminantsintwelvespecies