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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...

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Detalles Bibliográficos
Autores principales: Fisch, Daniel, Yakimovich, Artur, Clough, Barbara, Wright, Joseph, Bunyan, Monique, Howell, Michael, Mercer, Jason, Frickel, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
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).
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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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