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Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations

BACKGROUND: Inanimate surfaces within a hospital serve as a reservoir of microbial life that may colonize patients and ultimately result in healthcare associated infections (HAIs). Critically ill patients in intensive care units (ICUs) are particularly vulnerable to HAIs. Little is known about how t...

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Autores principales: Chopyk, Jessica, Akrami, Kevan, Bavly, Tovia, Shin, Ji H., Schwanemann, Leila K., Ly, Melissa, Kalia, Richa, Xu, Ying, Kelley, Scott T., Malhotra, Atul, Torriani, Francesca J., Sweeney, Daniel A., Pride, David T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278141/
https://www.ncbi.nlm.nih.gov/pubmed/32513256
http://dx.doi.org/10.1186/s40168-020-00852-7
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author Chopyk, Jessica
Akrami, Kevan
Bavly, Tovia
Shin, Ji H.
Schwanemann, Leila K.
Ly, Melissa
Kalia, Richa
Xu, Ying
Kelley, Scott T.
Malhotra, Atul
Torriani, Francesca J.
Sweeney, Daniel A.
Pride, David T.
author_facet Chopyk, Jessica
Akrami, Kevan
Bavly, Tovia
Shin, Ji H.
Schwanemann, Leila K.
Ly, Melissa
Kalia, Richa
Xu, Ying
Kelley, Scott T.
Malhotra, Atul
Torriani, Francesca J.
Sweeney, Daniel A.
Pride, David T.
author_sort Chopyk, Jessica
collection PubMed
description BACKGROUND: Inanimate surfaces within a hospital serve as a reservoir of microbial life that may colonize patients and ultimately result in healthcare associated infections (HAIs). Critically ill patients in intensive care units (ICUs) are particularly vulnerable to HAIs. Little is known about how the microbiome of the ICU is established or what factors influence its evolution over time. A unique opportunity to bridge the knowledge gap into how the ICU microbiome evolves emerged in our health system, where we were able to characterize microbial communities in an established hospital ICU prior to closing for renovations, during renovations, and then after re-opening. RESULTS: We collected swab specimens from ICU bedrails, computer keyboards, and sinks longitudinally at each renovation stage, and analyzed the bacterial compositions on these surfaces by 16S rRNA gene sequencing. Specimens collected before ICU closure had the greatest alpha diversity, while specimens collected after the ICU had been closed for over 300 days had the least. We sampled the ICU during the 45 days after re-opening; however, within that time frame, the alpha diversity never reached pre-closure levels. There were clear and significant differences in microbiota compositions at each renovation stage, which was driven by environmental bacteria after closure and human-associated bacteria after re-opening and before closure. CONCLUSIONS: Overall, we identified significant differences in microbiota diversity and community composition at each renovation stage. These data help to decipher the evolution of the microbiome in the most critical part of the hospital and demonstrate the significant impacts that microbiota from patients and staff have on the evolution of ICU surfaces.
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spelling pubmed-72781412020-06-09 Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations Chopyk, Jessica Akrami, Kevan Bavly, Tovia Shin, Ji H. Schwanemann, Leila K. Ly, Melissa Kalia, Richa Xu, Ying Kelley, Scott T. Malhotra, Atul Torriani, Francesca J. Sweeney, Daniel A. Pride, David T. Microbiome Research BACKGROUND: Inanimate surfaces within a hospital serve as a reservoir of microbial life that may colonize patients and ultimately result in healthcare associated infections (HAIs). Critically ill patients in intensive care units (ICUs) are particularly vulnerable to HAIs. Little is known about how the microbiome of the ICU is established or what factors influence its evolution over time. A unique opportunity to bridge the knowledge gap into how the ICU microbiome evolves emerged in our health system, where we were able to characterize microbial communities in an established hospital ICU prior to closing for renovations, during renovations, and then after re-opening. RESULTS: We collected swab specimens from ICU bedrails, computer keyboards, and sinks longitudinally at each renovation stage, and analyzed the bacterial compositions on these surfaces by 16S rRNA gene sequencing. Specimens collected before ICU closure had the greatest alpha diversity, while specimens collected after the ICU had been closed for over 300 days had the least. We sampled the ICU during the 45 days after re-opening; however, within that time frame, the alpha diversity never reached pre-closure levels. There were clear and significant differences in microbiota compositions at each renovation stage, which was driven by environmental bacteria after closure and human-associated bacteria after re-opening and before closure. CONCLUSIONS: Overall, we identified significant differences in microbiota diversity and community composition at each renovation stage. These data help to decipher the evolution of the microbiome in the most critical part of the hospital and demonstrate the significant impacts that microbiota from patients and staff have on the evolution of ICU surfaces. BioMed Central 2020-06-08 /pmc/articles/PMC7278141/ /pubmed/32513256 http://dx.doi.org/10.1186/s40168-020-00852-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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
Chopyk, Jessica
Akrami, Kevan
Bavly, Tovia
Shin, Ji H.
Schwanemann, Leila K.
Ly, Melissa
Kalia, Richa
Xu, Ying
Kelley, Scott T.
Malhotra, Atul
Torriani, Francesca J.
Sweeney, Daniel A.
Pride, David T.
Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations
title Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations
title_full Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations
title_fullStr Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations
title_full_unstemmed Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations
title_short Temporal variations in bacterial community diversity and composition throughout intensive care unit renovations
title_sort temporal variations in bacterial community diversity and composition throughout intensive care unit renovations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278141/
https://www.ncbi.nlm.nih.gov/pubmed/32513256
http://dx.doi.org/10.1186/s40168-020-00852-7
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