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Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces

Bacterial pathogens that infect patients also contaminate hospital surfaces. These contaminants impact hospital infection control and epidemiology, prompting quantitative examination of their transmission dynamics. Here we investigate spatiotemporal and phylogenetic relationships of multidrug resist...

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Autores principales: D’Souza, Alaric W., Potter, Robert F., Wallace, Meghan, Shupe, Angela, Patel, Sanket, Sun, Xiaoqing, Gul, Danish, Kwon, Jennie H., Andleeb, Saadia, Burnham, Carey-Ann D., Dantas, Gautam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783542/
https://www.ncbi.nlm.nih.gov/pubmed/31594927
http://dx.doi.org/10.1038/s41467-019-12563-1
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author D’Souza, Alaric W.
Potter, Robert F.
Wallace, Meghan
Shupe, Angela
Patel, Sanket
Sun, Xiaoqing
Gul, Danish
Kwon, Jennie H.
Andleeb, Saadia
Burnham, Carey-Ann D.
Dantas, Gautam
author_facet D’Souza, Alaric W.
Potter, Robert F.
Wallace, Meghan
Shupe, Angela
Patel, Sanket
Sun, Xiaoqing
Gul, Danish
Kwon, Jennie H.
Andleeb, Saadia
Burnham, Carey-Ann D.
Dantas, Gautam
author_sort D’Souza, Alaric W.
collection PubMed
description Bacterial pathogens that infect patients also contaminate hospital surfaces. These contaminants impact hospital infection control and epidemiology, prompting quantitative examination of their transmission dynamics. Here we investigate spatiotemporal and phylogenetic relationships of multidrug resistant (MDR) bacteria on intensive care unit surfaces from two hospitals in the United States (US) and Pakistan collected over one year. MDR bacteria isolated from 3.3% and 86.7% of US and Pakistani surfaces, respectively, include common nosocomial pathogens, rare opportunistic pathogens, and novel taxa. Common nosocomial isolates are dominated by single lineages of different clones, are phenotypically MDR, and have high resistance gene burdens. Many resistance genes (e.g., bla(NDM), bla(OXA) carbapenamases), are shared by multiple species and flanked by mobilization elements. We identify Acinetobacter baumannii and Enterococcus faecium co-association on multiple surfaces, and demonstrate these species establish synergistic biofilms in vitro. Our results highlight substantial MDR pathogen burdens in hospital built-environments, provide evidence for spatiotemporal-dependent transmission, and demonstrate potential mechanisms for multi-species surface persistence.
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spelling pubmed-67835422019-10-10 Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces D’Souza, Alaric W. Potter, Robert F. Wallace, Meghan Shupe, Angela Patel, Sanket Sun, Xiaoqing Gul, Danish Kwon, Jennie H. Andleeb, Saadia Burnham, Carey-Ann D. Dantas, Gautam Nat Commun Article Bacterial pathogens that infect patients also contaminate hospital surfaces. These contaminants impact hospital infection control and epidemiology, prompting quantitative examination of their transmission dynamics. Here we investigate spatiotemporal and phylogenetic relationships of multidrug resistant (MDR) bacteria on intensive care unit surfaces from two hospitals in the United States (US) and Pakistan collected over one year. MDR bacteria isolated from 3.3% and 86.7% of US and Pakistani surfaces, respectively, include common nosocomial pathogens, rare opportunistic pathogens, and novel taxa. Common nosocomial isolates are dominated by single lineages of different clones, are phenotypically MDR, and have high resistance gene burdens. Many resistance genes (e.g., bla(NDM), bla(OXA) carbapenamases), are shared by multiple species and flanked by mobilization elements. We identify Acinetobacter baumannii and Enterococcus faecium co-association on multiple surfaces, and demonstrate these species establish synergistic biofilms in vitro. Our results highlight substantial MDR pathogen burdens in hospital built-environments, provide evidence for spatiotemporal-dependent transmission, and demonstrate potential mechanisms for multi-species surface persistence. Nature Publishing Group UK 2019-10-08 /pmc/articles/PMC6783542/ /pubmed/31594927 http://dx.doi.org/10.1038/s41467-019-12563-1 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
D’Souza, Alaric W.
Potter, Robert F.
Wallace, Meghan
Shupe, Angela
Patel, Sanket
Sun, Xiaoqing
Gul, Danish
Kwon, Jennie H.
Andleeb, Saadia
Burnham, Carey-Ann D.
Dantas, Gautam
Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces
title Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces
title_full Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces
title_fullStr Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces
title_full_unstemmed Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces
title_short Spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces
title_sort spatiotemporal dynamics of multidrug resistant bacteria on intensive care unit surfaces
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783542/
https://www.ncbi.nlm.nih.gov/pubmed/31594927
http://dx.doi.org/10.1038/s41467-019-12563-1
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