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Antibiotic resistance genes are differentially mobilized according to resistance mechanism
BACKGROUND: Screening for antibiotic resistance genes (ARGs) in especially environmental samples with (meta)genomic sequencing is associated with false-positive predictions of phenotypic resistance. This stems from the fact that most acquired ARGs require being overexpressed before conferring resist...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338424/ https://www.ncbi.nlm.nih.gov/pubmed/35906888 http://dx.doi.org/10.1093/gigascience/giac072 |
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author | Nielsen, Tue Kjærgaard Browne, Patrick Denis Hansen, Lars Hestbjerg |
author_facet | Nielsen, Tue Kjærgaard Browne, Patrick Denis Hansen, Lars Hestbjerg |
author_sort | Nielsen, Tue Kjærgaard |
collection | PubMed |
description | BACKGROUND: Screening for antibiotic resistance genes (ARGs) in especially environmental samples with (meta)genomic sequencing is associated with false-positive predictions of phenotypic resistance. This stems from the fact that most acquired ARGs require being overexpressed before conferring resistance, which is often caused by decontextualization of putative ARGs by mobile genetic elements (MGEs). Consequent overexpression of ARGs can be caused by strong promoters often present in insertion sequence (IS) elements and integrons and the copy number effect of plasmids, which may contribute to high expression of accessory genes. RESULTS: Here, we screen all complete bacterial RefSeq genomes for ARGs. The genetic contexts of detected ARGs are investigated for IS elements, integrons, plasmids, and phylogenetic dispersion. The ARG-MOB scale is proposed, which indicates how mobilized detected ARGs are in bacterial genomes. It is concluded that antibiotic efflux genes are rarely mobilized and even 80% of β-lactamases have never, or very rarely, been mobilized in the 15,790 studied genomes. However, some ARGs are indeed mobilized and co-occur with IS elements, plasmids, and integrons. CONCLUSIONS: In this study, ARGs in all complete bacterial genomes are classified by their association with MGEs, using the proposed ARG-MOB scale. These results have consequences for the design and interpretation of studies screening for resistance determinants, as mobilized ARGs pose a more concrete risk to human health. An interactive table of all results is provided for future studies targeting highly mobilized ARGs. |
format | Online Article Text |
id | pubmed-9338424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-93384242022-08-01 Antibiotic resistance genes are differentially mobilized according to resistance mechanism Nielsen, Tue Kjærgaard Browne, Patrick Denis Hansen, Lars Hestbjerg Gigascience Research BACKGROUND: Screening for antibiotic resistance genes (ARGs) in especially environmental samples with (meta)genomic sequencing is associated with false-positive predictions of phenotypic resistance. This stems from the fact that most acquired ARGs require being overexpressed before conferring resistance, which is often caused by decontextualization of putative ARGs by mobile genetic elements (MGEs). Consequent overexpression of ARGs can be caused by strong promoters often present in insertion sequence (IS) elements and integrons and the copy number effect of plasmids, which may contribute to high expression of accessory genes. RESULTS: Here, we screen all complete bacterial RefSeq genomes for ARGs. The genetic contexts of detected ARGs are investigated for IS elements, integrons, plasmids, and phylogenetic dispersion. The ARG-MOB scale is proposed, which indicates how mobilized detected ARGs are in bacterial genomes. It is concluded that antibiotic efflux genes are rarely mobilized and even 80% of β-lactamases have never, or very rarely, been mobilized in the 15,790 studied genomes. However, some ARGs are indeed mobilized and co-occur with IS elements, plasmids, and integrons. CONCLUSIONS: In this study, ARGs in all complete bacterial genomes are classified by their association with MGEs, using the proposed ARG-MOB scale. These results have consequences for the design and interpretation of studies screening for resistance determinants, as mobilized ARGs pose a more concrete risk to human health. An interactive table of all results is provided for future studies targeting highly mobilized ARGs. Oxford University Press 2022-07-30 /pmc/articles/PMC9338424/ /pubmed/35906888 http://dx.doi.org/10.1093/gigascience/giac072 Text en © The Author(s) 2022. Published by Oxford University Press GigaScience. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Nielsen, Tue Kjærgaard Browne, Patrick Denis Hansen, Lars Hestbjerg Antibiotic resistance genes are differentially mobilized according to resistance mechanism |
title | Antibiotic resistance genes are differentially mobilized according to
resistance mechanism |
title_full | Antibiotic resistance genes are differentially mobilized according to
resistance mechanism |
title_fullStr | Antibiotic resistance genes are differentially mobilized according to
resistance mechanism |
title_full_unstemmed | Antibiotic resistance genes are differentially mobilized according to
resistance mechanism |
title_short | Antibiotic resistance genes are differentially mobilized according to
resistance mechanism |
title_sort | antibiotic resistance genes are differentially mobilized according to
resistance mechanism |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338424/ https://www.ncbi.nlm.nih.gov/pubmed/35906888 http://dx.doi.org/10.1093/gigascience/giac072 |
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