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Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance
BACKGROUND: Carbapenem-resistant Enterobacterales (CRE) are an urgent global health threat. Inferring the dynamics of local CRE dissemination is currently limited by our inability to confidently trace the spread of resistance determinants to unrelated bacterial hosts. Whole-genome sequence compariso...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981930/ https://www.ncbi.nlm.nih.gov/pubmed/35379360 http://dx.doi.org/10.1186/s13073-022-01040-y |
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author | Salamzade, Rauf Manson, Abigail L. Walker, Bruce J. Brennan-Krohn, Thea Worby, Colin J. Ma, Peijun He, Lorrie L. Shea, Terrance P. Qu, James Chapman, Sinéad B. Howe, Whitney Young, Sarah K. Wurster, Jenna I. Delaney, Mary L. Kanjilal, Sanjat Onderdonk, Andrew B. Bittencourt, Cassiana E. Gussin, Gabrielle M. Kim, Diane Peterson, Ellena M. Ferraro, Mary Jane Hooper, David C. Shenoy, Erica S. Cuomo, Christina A. Cosimi, Lisa A. Huang, Susan S. Kirby, James E. Pierce, Virginia M. Bhattacharyya, Roby P. Earl, Ashlee M. |
author_facet | Salamzade, Rauf Manson, Abigail L. Walker, Bruce J. Brennan-Krohn, Thea Worby, Colin J. Ma, Peijun He, Lorrie L. Shea, Terrance P. Qu, James Chapman, Sinéad B. Howe, Whitney Young, Sarah K. Wurster, Jenna I. Delaney, Mary L. Kanjilal, Sanjat Onderdonk, Andrew B. Bittencourt, Cassiana E. Gussin, Gabrielle M. Kim, Diane Peterson, Ellena M. Ferraro, Mary Jane Hooper, David C. Shenoy, Erica S. Cuomo, Christina A. Cosimi, Lisa A. Huang, Susan S. Kirby, James E. Pierce, Virginia M. Bhattacharyya, Roby P. Earl, Ashlee M. |
author_sort | Salamzade, Rauf |
collection | PubMed |
description | BACKGROUND: Carbapenem-resistant Enterobacterales (CRE) are an urgent global health threat. Inferring the dynamics of local CRE dissemination is currently limited by our inability to confidently trace the spread of resistance determinants to unrelated bacterial hosts. Whole-genome sequence comparison is useful for identifying CRE clonal transmission and outbreaks, but high-frequency horizontal gene transfer (HGT) of carbapenem resistance genes and subsequent genome rearrangement complicate tracing the local persistence and mobilization of these genes across organisms. METHODS: To overcome this limitation, we developed a new approach to identify recent HGT of large, near-identical plasmid segments across species boundaries, which also allowed us to overcome technical challenges with genome assembly. We applied this to complete and near-complete genome assemblies to examine the local spread of CRE in a systematic, prospective collection of all CRE, as well as time- and species-matched carbapenem-susceptible Enterobacterales, isolated from patients from four US hospitals over nearly 5 years. RESULTS: Our CRE collection comprised a diverse range of species, lineages, and carbapenem resistance mechanisms, many of which were encoded on a variety of promiscuous plasmid types. We found and quantified rearrangement, persistence, and repeated transfer of plasmid segments, including those harboring carbapenemases, between organisms over multiple years. Some plasmid segments were found to be strongly associated with specific locales, thus representing geographic signatures that make it possible to trace recent and localized HGT events. Functional analysis of these signatures revealed genes commonly found in plasmids of nosocomial pathogens, such as functions required for plasmid retention and spread, as well survival against a variety of antibiotic and antiseptics common to the hospital environment. CONCLUSIONS: Collectively, the framework we developed provides a clearer, high-resolution picture of the epidemiology of antibiotic resistance importation, spread, and persistence in patients and healthcare networks. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-022-01040-y. |
format | Online Article Text |
id | pubmed-8981930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89819302022-04-06 Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance Salamzade, Rauf Manson, Abigail L. Walker, Bruce J. Brennan-Krohn, Thea Worby, Colin J. Ma, Peijun He, Lorrie L. Shea, Terrance P. Qu, James Chapman, Sinéad B. Howe, Whitney Young, Sarah K. Wurster, Jenna I. Delaney, Mary L. Kanjilal, Sanjat Onderdonk, Andrew B. Bittencourt, Cassiana E. Gussin, Gabrielle M. Kim, Diane Peterson, Ellena M. Ferraro, Mary Jane Hooper, David C. Shenoy, Erica S. Cuomo, Christina A. Cosimi, Lisa A. Huang, Susan S. Kirby, James E. Pierce, Virginia M. Bhattacharyya, Roby P. Earl, Ashlee M. Genome Med Research BACKGROUND: Carbapenem-resistant Enterobacterales (CRE) are an urgent global health threat. Inferring the dynamics of local CRE dissemination is currently limited by our inability to confidently trace the spread of resistance determinants to unrelated bacterial hosts. Whole-genome sequence comparison is useful for identifying CRE clonal transmission and outbreaks, but high-frequency horizontal gene transfer (HGT) of carbapenem resistance genes and subsequent genome rearrangement complicate tracing the local persistence and mobilization of these genes across organisms. METHODS: To overcome this limitation, we developed a new approach to identify recent HGT of large, near-identical plasmid segments across species boundaries, which also allowed us to overcome technical challenges with genome assembly. We applied this to complete and near-complete genome assemblies to examine the local spread of CRE in a systematic, prospective collection of all CRE, as well as time- and species-matched carbapenem-susceptible Enterobacterales, isolated from patients from four US hospitals over nearly 5 years. RESULTS: Our CRE collection comprised a diverse range of species, lineages, and carbapenem resistance mechanisms, many of which were encoded on a variety of promiscuous plasmid types. We found and quantified rearrangement, persistence, and repeated transfer of plasmid segments, including those harboring carbapenemases, between organisms over multiple years. Some plasmid segments were found to be strongly associated with specific locales, thus representing geographic signatures that make it possible to trace recent and localized HGT events. Functional analysis of these signatures revealed genes commonly found in plasmids of nosocomial pathogens, such as functions required for plasmid retention and spread, as well survival against a variety of antibiotic and antiseptics common to the hospital environment. CONCLUSIONS: Collectively, the framework we developed provides a clearer, high-resolution picture of the epidemiology of antibiotic resistance importation, spread, and persistence in patients and healthcare networks. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13073-022-01040-y. BioMed Central 2022-04-05 /pmc/articles/PMC8981930/ /pubmed/35379360 http://dx.doi.org/10.1186/s13073-022-01040-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Salamzade, Rauf Manson, Abigail L. Walker, Bruce J. Brennan-Krohn, Thea Worby, Colin J. Ma, Peijun He, Lorrie L. Shea, Terrance P. Qu, James Chapman, Sinéad B. Howe, Whitney Young, Sarah K. Wurster, Jenna I. Delaney, Mary L. Kanjilal, Sanjat Onderdonk, Andrew B. Bittencourt, Cassiana E. Gussin, Gabrielle M. Kim, Diane Peterson, Ellena M. Ferraro, Mary Jane Hooper, David C. Shenoy, Erica S. Cuomo, Christina A. Cosimi, Lisa A. Huang, Susan S. Kirby, James E. Pierce, Virginia M. Bhattacharyya, Roby P. Earl, Ashlee M. Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance |
title | Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance |
title_full | Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance |
title_fullStr | Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance |
title_full_unstemmed | Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance |
title_short | Inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance |
title_sort | inter-species geographic signatures for tracing horizontal gene transfer and long-term persistence of carbapenem resistance |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981930/ https://www.ncbi.nlm.nih.gov/pubmed/35379360 http://dx.doi.org/10.1186/s13073-022-01040-y |
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