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Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome
The global crisis in antimicrobial resistance continues to grow. Estimating the risks of antibiotic resistance transmission across habitats is hindered by the lack of data on mobility and habitat‐specificity. Metagenomic samples of 6092 are analyzed to delineate the unique core resistomes from human...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667823/ https://www.ncbi.nlm.nih.gov/pubmed/37870180 http://dx.doi.org/10.1002/advs.202303925 |
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author | Zhang, Qi Xu, Nuohan Lei, Chaotang Chen, Bingfeng Wang, Tingzhang Ma, Yunting Lu, Tao Penuelas, Josep Gillings, Michael Zhu, Yong‐Guan Fu, Zhengwei Qian, Haifeng |
author_facet | Zhang, Qi Xu, Nuohan Lei, Chaotang Chen, Bingfeng Wang, Tingzhang Ma, Yunting Lu, Tao Penuelas, Josep Gillings, Michael Zhu, Yong‐Guan Fu, Zhengwei Qian, Haifeng |
author_sort | Zhang, Qi |
collection | PubMed |
description | The global crisis in antimicrobial resistance continues to grow. Estimating the risks of antibiotic resistance transmission across habitats is hindered by the lack of data on mobility and habitat‐specificity. Metagenomic samples of 6092 are analyzed to delineate the unique core resistomes from human feces and seven other habitats. This is found that most resistance genes (≈85%) are transmitted between external habitats and human feces. This suggests that human feces are broadly representative of the global resistome and are potentially a hub for accumulating and disseminating resistance genes. The analysis found that resistance genes with ancient horizontal gene transfer (HGT) events have a higher efficiency of transfer across habitats, suggesting that HGT may be the main driver for forming unique but partly shared resistomes in all habitats. Importantly, the human fecal resistome is historically different and influenced by HGT and age. The most important routes of cross‐transmission of resistance are from the atmosphere, buildings, and animals to humans. These habitats should receive more attention for future prevention of antimicrobial resistance. The study will disentangle transmission routes of resistance genes between humans and other habitats in a One Health framework and can identify strategies for controlling the ongoing dissemination and antibiotic resistance. |
format | Online Article Text |
id | pubmed-10667823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106678232023-10-23 Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome Zhang, Qi Xu, Nuohan Lei, Chaotang Chen, Bingfeng Wang, Tingzhang Ma, Yunting Lu, Tao Penuelas, Josep Gillings, Michael Zhu, Yong‐Guan Fu, Zhengwei Qian, Haifeng Adv Sci (Weinh) Research Articles The global crisis in antimicrobial resistance continues to grow. Estimating the risks of antibiotic resistance transmission across habitats is hindered by the lack of data on mobility and habitat‐specificity. Metagenomic samples of 6092 are analyzed to delineate the unique core resistomes from human feces and seven other habitats. This is found that most resistance genes (≈85%) are transmitted between external habitats and human feces. This suggests that human feces are broadly representative of the global resistome and are potentially a hub for accumulating and disseminating resistance genes. The analysis found that resistance genes with ancient horizontal gene transfer (HGT) events have a higher efficiency of transfer across habitats, suggesting that HGT may be the main driver for forming unique but partly shared resistomes in all habitats. Importantly, the human fecal resistome is historically different and influenced by HGT and age. The most important routes of cross‐transmission of resistance are from the atmosphere, buildings, and animals to humans. These habitats should receive more attention for future prevention of antimicrobial resistance. The study will disentangle transmission routes of resistance genes between humans and other habitats in a One Health framework and can identify strategies for controlling the ongoing dissemination and antibiotic resistance. John Wiley and Sons Inc. 2023-10-23 /pmc/articles/PMC10667823/ /pubmed/37870180 http://dx.doi.org/10.1002/advs.202303925 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Zhang, Qi Xu, Nuohan Lei, Chaotang Chen, Bingfeng Wang, Tingzhang Ma, Yunting Lu, Tao Penuelas, Josep Gillings, Michael Zhu, Yong‐Guan Fu, Zhengwei Qian, Haifeng Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome |
title | Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome |
title_full | Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome |
title_fullStr | Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome |
title_full_unstemmed | Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome |
title_short | Metagenomic Insight into The Global Dissemination of The Antibiotic Resistome |
title_sort | metagenomic insight into the global dissemination of the antibiotic resistome |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667823/ https://www.ncbi.nlm.nih.gov/pubmed/37870180 http://dx.doi.org/10.1002/advs.202303925 |
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