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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8501104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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