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Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome

The analysis of microbiome compositions in the human gut has gained increasing interest due to the broader availability of data and functional databases and substantial progress in data analysis methods, but also due to the high relevance of the microbiome in human health and disease. While most ana...

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Autores principales: Claussen, Jens Christian, Skiecevičienė, Jurgita, Wang, Jun, Rausch, Philipp, Karlsen, Tom H., Lieb, Wolfgang, Baines, John F., Franke, Andre, Hütt, Marc-Thorsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480827/
https://www.ncbi.nlm.nih.gov/pubmed/28640804
http://dx.doi.org/10.1371/journal.pcbi.1005361
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author Claussen, Jens Christian
Skiecevičienė, Jurgita
Wang, Jun
Rausch, Philipp
Karlsen, Tom H.
Lieb, Wolfgang
Baines, John F.
Franke, Andre
Hütt, Marc-Thorsten
author_facet Claussen, Jens Christian
Skiecevičienė, Jurgita
Wang, Jun
Rausch, Philipp
Karlsen, Tom H.
Lieb, Wolfgang
Baines, John F.
Franke, Andre
Hütt, Marc-Thorsten
author_sort Claussen, Jens Christian
collection PubMed
description The analysis of microbiome compositions in the human gut has gained increasing interest due to the broader availability of data and functional databases and substantial progress in data analysis methods, but also due to the high relevance of the microbiome in human health and disease. While most analyses infer interactions among highly abundant species, the large number of low-abundance species has received less attention. Here we present a novel analysis method based on Boolean operations applied to microbial co-occurrence patterns. We calibrate our approach with simulated data based on a dynamical Boolean network model from which we interpret the statistics of attractor states as a theoretical proxy for microbiome composition. We show that for given fractions of synergistic and competitive interactions in the model our Boolean abundance analysis can reliably detect these interactions. Analyzing a novel data set of 822 microbiome compositions of the human gut, we find a large number of highly significant synergistic interactions among these low-abundance species, forming a connected network, and a few isolated competitive interactions.
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spelling pubmed-54808272017-07-05 Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome Claussen, Jens Christian Skiecevičienė, Jurgita Wang, Jun Rausch, Philipp Karlsen, Tom H. Lieb, Wolfgang Baines, John F. Franke, Andre Hütt, Marc-Thorsten PLoS Comput Biol Research Article The analysis of microbiome compositions in the human gut has gained increasing interest due to the broader availability of data and functional databases and substantial progress in data analysis methods, but also due to the high relevance of the microbiome in human health and disease. While most analyses infer interactions among highly abundant species, the large number of low-abundance species has received less attention. Here we present a novel analysis method based on Boolean operations applied to microbial co-occurrence patterns. We calibrate our approach with simulated data based on a dynamical Boolean network model from which we interpret the statistics of attractor states as a theoretical proxy for microbiome composition. We show that for given fractions of synergistic and competitive interactions in the model our Boolean abundance analysis can reliably detect these interactions. Analyzing a novel data set of 822 microbiome compositions of the human gut, we find a large number of highly significant synergistic interactions among these low-abundance species, forming a connected network, and a few isolated competitive interactions. Public Library of Science 2017-06-22 /pmc/articles/PMC5480827/ /pubmed/28640804 http://dx.doi.org/10.1371/journal.pcbi.1005361 Text en © 2017 Claussen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Claussen, Jens Christian
Skiecevičienė, Jurgita
Wang, Jun
Rausch, Philipp
Karlsen, Tom H.
Lieb, Wolfgang
Baines, John F.
Franke, Andre
Hütt, Marc-Thorsten
Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome
title Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome
title_full Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome
title_fullStr Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome
title_full_unstemmed Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome
title_short Boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome
title_sort boolean analysis reveals systematic interactions among low-abundance species in the human gut microbiome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480827/
https://www.ncbi.nlm.nih.gov/pubmed/28640804
http://dx.doi.org/10.1371/journal.pcbi.1005361
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