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Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates

BACKGROUND: The microbial community composition of urban environments is primarily determined by human activity. The use of metagenomics to explore how microbial communities are shaped in a city provides a novel input that can improve decisions on public health measures, architectural design, and ur...

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Autores principales: Salazar, Cecilia, Giménez, Matias, Riera, Nadia, Parada, Andrés, Puig, Josefina, Galiana, Antonio, Grill, Fabio, Vieytes, Mariela, Mason, Christopher E., Antelo, Verónica, D’Alessandro, Bruno, Risso, Jimena, Iraola, Gregorio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715416/
https://www.ncbi.nlm.nih.gov/pubmed/36457116
http://dx.doi.org/10.1186/s40168-022-01407-8
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author Salazar, Cecilia
Giménez, Matias
Riera, Nadia
Parada, Andrés
Puig, Josefina
Galiana, Antonio
Grill, Fabio
Vieytes, Mariela
Mason, Christopher E.
Antelo, Verónica
D’Alessandro, Bruno
Risso, Jimena
Iraola, Gregorio
author_facet Salazar, Cecilia
Giménez, Matias
Riera, Nadia
Parada, Andrés
Puig, Josefina
Galiana, Antonio
Grill, Fabio
Vieytes, Mariela
Mason, Christopher E.
Antelo, Verónica
D’Alessandro, Bruno
Risso, Jimena
Iraola, Gregorio
author_sort Salazar, Cecilia
collection PubMed
description BACKGROUND: The microbial community composition of urban environments is primarily determined by human activity. The use of metagenomics to explore how microbial communities are shaped in a city provides a novel input that can improve decisions on public health measures, architectural design, and urban resilience. Of note, the sewage system in a city acts as a complex reservoir of bacteria, pharmaceuticals, and antimicrobial resistant (AMR) genes that can be an important source of epidemiological information. Hospital effluents are rich in patient-derived bacteria and can thus readily become a birthplace and hotspot reservoir for antibiotic resistant pathogens which are eventually incorporated into the environment. Yet, the scope to which nosocomial outbreaks impact the urban environment is still poorly understood. RESULTS: In this work, we extensively show that different urban waters from creeks, beaches, sewage spillways and collector pipes enclose discrete microbial communities that are characterized by a differential degree of contamination and admixture with human-derived bacteria. The abundance of human bacteria correlates with the abundance of AMR genes in the environment, with beta-lactamases being the top-contributing class to distinguish low vs. highly-impacted urban environments. Indeed, the abundance of beta-lactamase resistance and carbapenem resistance determinants in the urban environment significantly increased in a 1-year period. This was in line with a pronounced increase of nosocomial carbapenem-resistant infections reported during the same period that was mainly driven by an outbreak-causing, carbapenemase-producing Klebsiella pneumoniae (KPC) ST-11 strain. Genome-resolved metagenomics of urban waters before and after this outbreak, coupled with high-resolution whole-genome sequencing, confirmed the dissemination of the ST-11 strain and a novel KPC megaplasmid from the hospital to the urban environment. City-wide analysis showed that geospatial dissemination of the KPC megaplasmid in the urban environment inversely depended on the sewage system infrastructure. CONCLUSIONS: We show how urban metagenomics and outbreak genomic surveillance can be coupled to generate relevant information for infection control, antibiotic stewardship, and pathogen epidemiology. Our results highlight the need to better characterize and understand how human-derived bacteria and antimicrobial resistance disseminate in the urban environment to incorporate this information in the development of effluent treatment infrastructure and public health policies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01407-8.
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spelling pubmed-97154162022-12-02 Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates Salazar, Cecilia Giménez, Matias Riera, Nadia Parada, Andrés Puig, Josefina Galiana, Antonio Grill, Fabio Vieytes, Mariela Mason, Christopher E. Antelo, Verónica D’Alessandro, Bruno Risso, Jimena Iraola, Gregorio Microbiome Research BACKGROUND: The microbial community composition of urban environments is primarily determined by human activity. The use of metagenomics to explore how microbial communities are shaped in a city provides a novel input that can improve decisions on public health measures, architectural design, and urban resilience. Of note, the sewage system in a city acts as a complex reservoir of bacteria, pharmaceuticals, and antimicrobial resistant (AMR) genes that can be an important source of epidemiological information. Hospital effluents are rich in patient-derived bacteria and can thus readily become a birthplace and hotspot reservoir for antibiotic resistant pathogens which are eventually incorporated into the environment. Yet, the scope to which nosocomial outbreaks impact the urban environment is still poorly understood. RESULTS: In this work, we extensively show that different urban waters from creeks, beaches, sewage spillways and collector pipes enclose discrete microbial communities that are characterized by a differential degree of contamination and admixture with human-derived bacteria. The abundance of human bacteria correlates with the abundance of AMR genes in the environment, with beta-lactamases being the top-contributing class to distinguish low vs. highly-impacted urban environments. Indeed, the abundance of beta-lactamase resistance and carbapenem resistance determinants in the urban environment significantly increased in a 1-year period. This was in line with a pronounced increase of nosocomial carbapenem-resistant infections reported during the same period that was mainly driven by an outbreak-causing, carbapenemase-producing Klebsiella pneumoniae (KPC) ST-11 strain. Genome-resolved metagenomics of urban waters before and after this outbreak, coupled with high-resolution whole-genome sequencing, confirmed the dissemination of the ST-11 strain and a novel KPC megaplasmid from the hospital to the urban environment. City-wide analysis showed that geospatial dissemination of the KPC megaplasmid in the urban environment inversely depended on the sewage system infrastructure. CONCLUSIONS: We show how urban metagenomics and outbreak genomic surveillance can be coupled to generate relevant information for infection control, antibiotic stewardship, and pathogen epidemiology. Our results highlight the need to better characterize and understand how human-derived bacteria and antimicrobial resistance disseminate in the urban environment to incorporate this information in the development of effluent treatment infrastructure and public health policies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01407-8. BioMed Central 2022-12-02 /pmc/articles/PMC9715416/ /pubmed/36457116 http://dx.doi.org/10.1186/s40168-022-01407-8 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
Salazar, Cecilia
Giménez, Matias
Riera, Nadia
Parada, Andrés
Puig, Josefina
Galiana, Antonio
Grill, Fabio
Vieytes, Mariela
Mason, Christopher E.
Antelo, Verónica
D’Alessandro, Bruno
Risso, Jimena
Iraola, Gregorio
Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates
title Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates
title_full Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates
title_fullStr Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates
title_full_unstemmed Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates
title_short Human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates
title_sort human microbiota drives hospital-associated antimicrobial resistance dissemination in the urban environment and mirrors patient case rates
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715416/
https://www.ncbi.nlm.nih.gov/pubmed/36457116
http://dx.doi.org/10.1186/s40168-022-01407-8
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