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Defining host–pathogen interactions employing an artificial intelligence workflow
For image-based infection biology, accurate unbiased quantification of host–pathogen interactions is essential, yet often performed manually or using limited enumeration employing simple image analysis algorithms based on image segmentation. Host protein recruitment to pathogens is often refractory...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372283/ https://www.ncbi.nlm.nih.gov/pubmed/30744806 http://dx.doi.org/10.7554/eLife.40560 |
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author | Fisch, Daniel Yakimovich, Artur Clough, Barbara Wright, Joseph Bunyan, Monique Howell, Michael Mercer, Jason Frickel, Eva |
author_facet | Fisch, Daniel Yakimovich, Artur Clough, Barbara Wright, Joseph Bunyan, Monique Howell, Michael Mercer, Jason Frickel, Eva |
author_sort | Fisch, Daniel |
collection | PubMed |
description | For image-based infection biology, accurate unbiased quantification of host–pathogen interactions is essential, yet often performed manually or using limited enumeration employing simple image analysis algorithms based on image segmentation. Host protein recruitment to pathogens is often refractory to accurate automated assessment due to its heterogeneous nature. An intuitive intelligent image analysis program to assess host protein recruitment within general cellular pathogen defense is lacking. We present HRMAn (Host Response to Microbe Analysis), an open-source image analysis platform based on machine learning algorithms and deep learning. We show that HRMAn has the capacity to learn phenotypes from the data, without relying on researcher-based assumptions. Using Toxoplasma gondii and Salmonella enterica Typhimurium we demonstrate HRMAn’s capacity to recognize, classify and quantify pathogen killing, replication and cellular defense responses. HRMAn thus presents the only intelligent solution operating at human capacity suitable for both single image and high content image analysis. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). |
format | Online Article Text |
id | pubmed-6372283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-63722832019-02-15 Defining host–pathogen interactions employing an artificial intelligence workflow Fisch, Daniel Yakimovich, Artur Clough, Barbara Wright, Joseph Bunyan, Monique Howell, Michael Mercer, Jason Frickel, Eva eLife Computational and Systems Biology For image-based infection biology, accurate unbiased quantification of host–pathogen interactions is essential, yet often performed manually or using limited enumeration employing simple image analysis algorithms based on image segmentation. Host protein recruitment to pathogens is often refractory to accurate automated assessment due to its heterogeneous nature. An intuitive intelligent image analysis program to assess host protein recruitment within general cellular pathogen defense is lacking. We present HRMAn (Host Response to Microbe Analysis), an open-source image analysis platform based on machine learning algorithms and deep learning. We show that HRMAn has the capacity to learn phenotypes from the data, without relying on researcher-based assumptions. Using Toxoplasma gondii and Salmonella enterica Typhimurium we demonstrate HRMAn’s capacity to recognize, classify and quantify pathogen killing, replication and cellular defense responses. HRMAn thus presents the only intelligent solution operating at human capacity suitable for both single image and high content image analysis. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter). eLife Sciences Publications, Ltd 2019-02-12 /pmc/articles/PMC6372283/ /pubmed/30744806 http://dx.doi.org/10.7554/eLife.40560 Text en © 2019, Fisch et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Fisch, Daniel Yakimovich, Artur Clough, Barbara Wright, Joseph Bunyan, Monique Howell, Michael Mercer, Jason Frickel, Eva Defining host–pathogen interactions employing an artificial intelligence workflow |
title | Defining host–pathogen interactions employing an artificial intelligence workflow |
title_full | Defining host–pathogen interactions employing an artificial intelligence workflow |
title_fullStr | Defining host–pathogen interactions employing an artificial intelligence workflow |
title_full_unstemmed | Defining host–pathogen interactions employing an artificial intelligence workflow |
title_short | Defining host–pathogen interactions employing an artificial intelligence workflow |
title_sort | defining host–pathogen interactions employing an artificial intelligence workflow |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6372283/ https://www.ncbi.nlm.nih.gov/pubmed/30744806 http://dx.doi.org/10.7554/eLife.40560 |
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