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Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis

Naturally drying bacterial droplets on inanimate surfaces representing fomites are the most consequential mode for transmitting infection through oro-fecal route. We provide a multiscale holistic approach to understand flow dynamics induced bacterial pattern formation on fomites leading to pathogene...

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Autores principales: Majee, Sreeparna, Chowdhury, Atish Roy, Pinto, Roven, Chattopadhyay, Ankur, Agharkar, Amey Nitin, Chakravortty, Dipshikha, Basu, Saptarshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501104/
https://www.ncbi.nlm.nih.gov/pubmed/34625643
http://dx.doi.org/10.1038/s42003-021-02711-z
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author Majee, Sreeparna
Chowdhury, Atish Roy
Pinto, Roven
Chattopadhyay, Ankur
Agharkar, Amey Nitin
Chakravortty, Dipshikha
Basu, Saptarshi
author_facet Majee, Sreeparna
Chowdhury, Atish Roy
Pinto, Roven
Chattopadhyay, Ankur
Agharkar, Amey Nitin
Chakravortty, Dipshikha
Basu, Saptarshi
author_sort Majee, Sreeparna
collection PubMed
description Naturally drying bacterial droplets on inanimate surfaces representing fomites are the most consequential mode for transmitting infection through oro-fecal route. We provide a multiscale holistic approach to understand flow dynamics induced bacterial pattern formation on fomites leading to pathogenesis. The most virulent gut pathogen, Salmonella Typhimurium (STM), typically found in contaminated food and water, is used as model system in the current study. Evaporation-induced flow in sessile droplets facilitates the transport of STM, forming spatio-temporally varying bacterial deposition patterns based on droplet medium’s nutrient scale. Mechanical and low moisture stress in the drying process reduced bacterial viability but interestingly induced hyper-proliferation of STM in macrophages, thereby augmenting virulence in fomites. In vivo studies of fomites in mice confirm that STM maintains enhanced virulence. This work demonstrates that stressed bacterial deposit morphologies formed over small timescale (minutes) on organic and inorganic surfaces, plays a significant role in enhancing fomite’s pathogenesis over hours and days.
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spelling pubmed-85011042021-10-22 Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis Majee, Sreeparna Chowdhury, Atish Roy Pinto, Roven Chattopadhyay, Ankur Agharkar, Amey Nitin Chakravortty, Dipshikha Basu, Saptarshi Commun Biol Article Naturally drying bacterial droplets on inanimate surfaces representing fomites are the most consequential mode for transmitting infection through oro-fecal route. We provide a multiscale holistic approach to understand flow dynamics induced bacterial pattern formation on fomites leading to pathogenesis. The most virulent gut pathogen, Salmonella Typhimurium (STM), typically found in contaminated food and water, is used as model system in the current study. Evaporation-induced flow in sessile droplets facilitates the transport of STM, forming spatio-temporally varying bacterial deposition patterns based on droplet medium’s nutrient scale. Mechanical and low moisture stress in the drying process reduced bacterial viability but interestingly induced hyper-proliferation of STM in macrophages, thereby augmenting virulence in fomites. In vivo studies of fomites in mice confirm that STM maintains enhanced virulence. This work demonstrates that stressed bacterial deposit morphologies formed over small timescale (minutes) on organic and inorganic surfaces, plays a significant role in enhancing fomite’s pathogenesis over hours and days. Nature Publishing Group UK 2021-10-08 /pmc/articles/PMC8501104/ /pubmed/34625643 http://dx.doi.org/10.1038/s42003-021-02711-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Majee, Sreeparna
Chowdhury, Atish Roy
Pinto, Roven
Chattopadhyay, Ankur
Agharkar, Amey Nitin
Chakravortty, Dipshikha
Basu, Saptarshi
Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis
title Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis
title_full Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis
title_fullStr Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis
title_full_unstemmed Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis
title_short Spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis
title_sort spatiotemporal evaporating droplet dynamics on fomites enhances long term bacterial pathogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501104/
https://www.ncbi.nlm.nih.gov/pubmed/34625643
http://dx.doi.org/10.1038/s42003-021-02711-z
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