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Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung
Aspergillus fumigatus is a ubiquitous opportunistic fungal pathogen that can cause severe infections in immunocompromised patients. Conidia that reach the lower respiratory tract are confronted with alveolar macrophages, which are the resident phagocytic cells, constituting the first line of defense...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370618/ https://www.ncbi.nlm.nih.gov/pubmed/30804941 http://dx.doi.org/10.3389/fimmu.2019.00142 |
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author | Blickensdorf, Marco Timme, Sandra Figge, Marc Thilo |
author_facet | Blickensdorf, Marco Timme, Sandra Figge, Marc Thilo |
author_sort | Blickensdorf, Marco |
collection | PubMed |
description | Aspergillus fumigatus is a ubiquitous opportunistic fungal pathogen that can cause severe infections in immunocompromised patients. Conidia that reach the lower respiratory tract are confronted with alveolar macrophages, which are the resident phagocytic cells, constituting the first line of defense. If not efficiently removed in time, A. fumigatus conidia can germinate causing severe infections associated with high mortality rates. Mice are the most extensively used model organism in research on A. fumigatus infections. However, in addition to structural differences in the lung physiology of mice and the human host, applied infection doses in animal experiments are typically orders of magnitude larger compared to the daily inhalation doses of humans. The influence of these factors, which must be taken into account in a quantitative comparison and knowledge transfer from mice to humans, is difficult to measure since in vivo live cell imaging of the infection dynamics under physiological conditions is currently not possible. In the present study, we compare A. fumigatus infection in mice and humans by virtual infection modeling using a hybrid agent-based model that accounts for the respective lung physiology and the impact of a wide range of infection doses on the spatial infection dynamics. Our computer simulations enable comparative quantification of A. fumigatus infection clearance in the two hosts to elucidate (i) the complex interplay between alveolar morphometry and the fungal burden and (ii) the dynamics of infection clearance, which for realistic fungal burdens is found to be more efficiently realized in mice compared to humans. |
format | Online Article Text |
id | pubmed-6370618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63706182019-02-25 Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung Blickensdorf, Marco Timme, Sandra Figge, Marc Thilo Front Immunol Immunology Aspergillus fumigatus is a ubiquitous opportunistic fungal pathogen that can cause severe infections in immunocompromised patients. Conidia that reach the lower respiratory tract are confronted with alveolar macrophages, which are the resident phagocytic cells, constituting the first line of defense. If not efficiently removed in time, A. fumigatus conidia can germinate causing severe infections associated with high mortality rates. Mice are the most extensively used model organism in research on A. fumigatus infections. However, in addition to structural differences in the lung physiology of mice and the human host, applied infection doses in animal experiments are typically orders of magnitude larger compared to the daily inhalation doses of humans. The influence of these factors, which must be taken into account in a quantitative comparison and knowledge transfer from mice to humans, is difficult to measure since in vivo live cell imaging of the infection dynamics under physiological conditions is currently not possible. In the present study, we compare A. fumigatus infection in mice and humans by virtual infection modeling using a hybrid agent-based model that accounts for the respective lung physiology and the impact of a wide range of infection doses on the spatial infection dynamics. Our computer simulations enable comparative quantification of A. fumigatus infection clearance in the two hosts to elucidate (i) the complex interplay between alveolar morphometry and the fungal burden and (ii) the dynamics of infection clearance, which for realistic fungal burdens is found to be more efficiently realized in mice compared to humans. Frontiers Media S.A. 2019-02-05 /pmc/articles/PMC6370618/ /pubmed/30804941 http://dx.doi.org/10.3389/fimmu.2019.00142 Text en Copyright © 2019 Blickensdorf, Timme and Figge. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Blickensdorf, Marco Timme, Sandra Figge, Marc Thilo Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung |
title | Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung |
title_full | Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung |
title_fullStr | Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung |
title_full_unstemmed | Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung |
title_short | Comparative Assessment of Aspergillosis by Virtual Infection Modeling in Murine and Human Lung |
title_sort | comparative assessment of aspergillosis by virtual infection modeling in murine and human lung |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370618/ https://www.ncbi.nlm.nih.gov/pubmed/30804941 http://dx.doi.org/10.3389/fimmu.2019.00142 |
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