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Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics
Antimicrobial resistance (AMR) in soils represents a serious risk to human health through the food chain and human–nature contact. However, the active antibiotic-resistant bacteria (ARB) residing in soils that primarily drive AMR dissemination are poorly explored. Here, single-cell Raman-D(2)O coupl...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546533/ https://www.ncbi.nlm.nih.gov/pubmed/36161886 http://dx.doi.org/10.1073/pnas.2201473119 |
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author | Li, Hong-Zhe Yang, Kai Liao, Hu Lassen, Simon Bo Su, Jian-Qiang Zhang, Xian Cui, Li Zhu, Yong-Guan |
author_facet | Li, Hong-Zhe Yang, Kai Liao, Hu Lassen, Simon Bo Su, Jian-Qiang Zhang, Xian Cui, Li Zhu, Yong-Guan |
author_sort | Li, Hong-Zhe |
collection | PubMed |
description | Antimicrobial resistance (AMR) in soils represents a serious risk to human health through the food chain and human–nature contact. However, the active antibiotic-resistant bacteria (ARB) residing in soils that primarily drive AMR dissemination are poorly explored. Here, single-cell Raman-D(2)O coupled with targeted metagenomics is developed as a culture-independent approach to phenotypically and genotypically profiling active ARB against clinical antibiotics in a wide range of soils. This method quantifies the prevalence (contamination degree) and activity (spread potential) of soil ARB and reveals a clear elevation with increasing anthropogenic activities such as farming and the creation of pollution, thereby constituting a factor that is critical for the assessment of AMR risks. Further targeted sorting and metagenomic sequencing of the most active soil ARB uncover several uncultured genera and a pathogenic strain. Furthermore, the underlying resistance genes, virulence factor genes, and associated mobile genetic elements (including plasmids, insertion sequences, and prophages) are fully deciphered at the single-cell level. This study advances our understanding of the soil active AMR repertoire by linking the resistant phenome to the genome. It will aid in the risk assessment of environmental AMR and guide the combat under the One Health framework. |
format | Online Article Text |
id | pubmed-9546533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-95465332023-03-26 Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics Li, Hong-Zhe Yang, Kai Liao, Hu Lassen, Simon Bo Su, Jian-Qiang Zhang, Xian Cui, Li Zhu, Yong-Guan Proc Natl Acad Sci U S A Biological Sciences Antimicrobial resistance (AMR) in soils represents a serious risk to human health through the food chain and human–nature contact. However, the active antibiotic-resistant bacteria (ARB) residing in soils that primarily drive AMR dissemination are poorly explored. Here, single-cell Raman-D(2)O coupled with targeted metagenomics is developed as a culture-independent approach to phenotypically and genotypically profiling active ARB against clinical antibiotics in a wide range of soils. This method quantifies the prevalence (contamination degree) and activity (spread potential) of soil ARB and reveals a clear elevation with increasing anthropogenic activities such as farming and the creation of pollution, thereby constituting a factor that is critical for the assessment of AMR risks. Further targeted sorting and metagenomic sequencing of the most active soil ARB uncover several uncultured genera and a pathogenic strain. Furthermore, the underlying resistance genes, virulence factor genes, and associated mobile genetic elements (including plasmids, insertion sequences, and prophages) are fully deciphered at the single-cell level. This study advances our understanding of the soil active AMR repertoire by linking the resistant phenome to the genome. It will aid in the risk assessment of environmental AMR and guide the combat under the One Health framework. National Academy of Sciences 2022-09-26 2022-10-04 /pmc/articles/PMC9546533/ /pubmed/36161886 http://dx.doi.org/10.1073/pnas.2201473119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Li, Hong-Zhe Yang, Kai Liao, Hu Lassen, Simon Bo Su, Jian-Qiang Zhang, Xian Cui, Li Zhu, Yong-Guan Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics |
title | Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics |
title_full | Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics |
title_fullStr | Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics |
title_full_unstemmed | Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics |
title_short | Active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics |
title_sort | active antibiotic resistome in soils unraveled by single-cell isotope probing and targeted metagenomics |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546533/ https://www.ncbi.nlm.nih.gov/pubmed/36161886 http://dx.doi.org/10.1073/pnas.2201473119 |
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