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Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections
Colony expansion is an essential feature of fungal infections. Although mechanisms that regulate hyphal forces on the substrate during expansion have been reported previously, there is a critical need of a methodology that can compute the pressure profiles exerted by fungi on substrates during expan...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531784/ https://www.ncbi.nlm.nih.gov/pubmed/26262897 http://dx.doi.org/10.1038/srep12928 |
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author | Patra, Subir Banerjee, Sourav Terejanu, Gabriel Chanda, Anindya |
author_facet | Patra, Subir Banerjee, Sourav Terejanu, Gabriel Chanda, Anindya |
author_sort | Patra, Subir |
collection | PubMed |
description | Colony expansion is an essential feature of fungal infections. Although mechanisms that regulate hyphal forces on the substrate during expansion have been reported previously, there is a critical need of a methodology that can compute the pressure profiles exerted by fungi on substrates during expansion; this will facilitate the validation of therapeutic efficacy of novel antifungals. Here, we introduce an analytical decoding method based on Biot’s incremental stress model, which was used to map the pressure distribution from an expanding mycelium of a popular plant pathogen, Aspergillus parasiticus. Using our recently developed Quantitative acoustic contrast tomography (Q-ACT) we detected that the mycelial growth on the solid agar created multiple surface and subsurface wrinkles with varying wavelengths across the depth of substrate that were computable with acousto-ultrasonic waves between 50 MHz–175 MHz. We derive here the fundamental correlation between these wrinkle wavelengths and the pressure distribution on the colony subsurface. Using our correlation we show that A. parasiticus can exert pressure as high as 300 KPa on the surface of a standard agar growth medium. The study provides a novel mathematical foundation for quantifying fungal pressures on substrate during hyphal invasions under normal and pathophysiological growth conditions. |
format | Online Article Text |
id | pubmed-4531784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45317842015-08-12 Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections Patra, Subir Banerjee, Sourav Terejanu, Gabriel Chanda, Anindya Sci Rep Article Colony expansion is an essential feature of fungal infections. Although mechanisms that regulate hyphal forces on the substrate during expansion have been reported previously, there is a critical need of a methodology that can compute the pressure profiles exerted by fungi on substrates during expansion; this will facilitate the validation of therapeutic efficacy of novel antifungals. Here, we introduce an analytical decoding method based on Biot’s incremental stress model, which was used to map the pressure distribution from an expanding mycelium of a popular plant pathogen, Aspergillus parasiticus. Using our recently developed Quantitative acoustic contrast tomography (Q-ACT) we detected that the mycelial growth on the solid agar created multiple surface and subsurface wrinkles with varying wavelengths across the depth of substrate that were computable with acousto-ultrasonic waves between 50 MHz–175 MHz. We derive here the fundamental correlation between these wrinkle wavelengths and the pressure distribution on the colony subsurface. Using our correlation we show that A. parasiticus can exert pressure as high as 300 KPa on the surface of a standard agar growth medium. The study provides a novel mathematical foundation for quantifying fungal pressures on substrate during hyphal invasions under normal and pathophysiological growth conditions. Nature Publishing Group 2015-08-11 /pmc/articles/PMC4531784/ /pubmed/26262897 http://dx.doi.org/10.1038/srep12928 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Patra, Subir Banerjee, Sourav Terejanu, Gabriel Chanda, Anindya Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections |
title | Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections |
title_full | Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections |
title_fullStr | Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections |
title_full_unstemmed | Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections |
title_short | Subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections |
title_sort | subsurface pressure profiling: a novel mathematical paradigm for computing colony pressures on substrate during fungal infections |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531784/ https://www.ncbi.nlm.nih.gov/pubmed/26262897 http://dx.doi.org/10.1038/srep12928 |
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