The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.

Evaluating the composition of the human gut microbiota greatly facilitates studies on its role in human pathophysiology, and is heavily reliant on culture-independent molecular methods. A microarray designated the Human Gut Chip (HuGChip) was developed to analyze and compare human gut microbiota sam...

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Main Authors: William Tottey, Jeremie Denonfoux, Faouzi Jaziri, Nicolas Parisot, Mohiedine Missaoui, David Hill, Guillaume Borrel, Eric Peyretaillade, Monique Alric, Hugh M B Harris, Ian B Jeffery, Marcus J Claesson, Paul W O'Toole, Pierre Peyret, Jean-François Brugère
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3656878?pdf=render
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spelling doaj-cadaaf2ae73649d7a5b42e2602ade7e82020-11-24T21:41:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0185e6254410.1371/journal.pone.0062544The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.William TotteyJeremie DenonfouxFaouzi JaziriNicolas ParisotMohiedine MissaouiDavid HillGuillaume BorrelEric PeyretailladeMonique AlricHugh M B HarrisIan B JefferyMarcus J ClaessonPaul W O'ToolePierre PeyretJean-François BrugèreEvaluating the composition of the human gut microbiota greatly facilitates studies on its role in human pathophysiology, and is heavily reliant on culture-independent molecular methods. A microarray designated the Human Gut Chip (HuGChip) was developed to analyze and compare human gut microbiota samples. The PhylArray software was used to design specific and sensitive probes. The DNA chip was composed of 4,441 probes (2,442 specific and 1,919 explorative probes) targeting 66 bacterial families. A mock community composed of 16S rRNA gene sequences from intestinal species was used to define the threshold criteria to be used to analyze complex samples. This was then experimentally verified with three human faecal samples and results were compared (i) with pyrosequencing of the V4 hypervariable region of the 16S rRNA gene, (ii) metagenomic data, and (iii) qPCR analysis of three phyla. When compared at both the phylum and the family level, high Pearson's correlation coefficients were obtained between data from all methods. The HuGChip development and validation showed that it is not only able to assess the known human gut microbiota but could also detect unknown species with the explorative probes to reveal the large number of bacterial sequences not yet described in the human gut microbiota, overcoming the main inconvenience encountered when developing microarrays.http://europepmc.org/articles/PMC3656878?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author William Tottey
Jeremie Denonfoux
Faouzi Jaziri
Nicolas Parisot
Mohiedine Missaoui
David Hill
Guillaume Borrel
Eric Peyretaillade
Monique Alric
Hugh M B Harris
Ian B Jeffery
Marcus J Claesson
Paul W O'Toole
Pierre Peyret
Jean-François Brugère
spellingShingle William Tottey
Jeremie Denonfoux
Faouzi Jaziri
Nicolas Parisot
Mohiedine Missaoui
David Hill
Guillaume Borrel
Eric Peyretaillade
Monique Alric
Hugh M B Harris
Ian B Jeffery
Marcus J Claesson
Paul W O'Toole
Pierre Peyret
Jean-François Brugère
The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.
PLoS ONE
author_facet William Tottey
Jeremie Denonfoux
Faouzi Jaziri
Nicolas Parisot
Mohiedine Missaoui
David Hill
Guillaume Borrel
Eric Peyretaillade
Monique Alric
Hugh M B Harris
Ian B Jeffery
Marcus J Claesson
Paul W O'Toole
Pierre Peyret
Jean-François Brugère
author_sort William Tottey
title The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.
title_short The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.
title_full The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.
title_fullStr The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.
title_full_unstemmed The human gut chip "HuGChip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.
title_sort human gut chip "hugchip", an explorative phylogenetic microarray for determining gut microbiome diversity at family level.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Evaluating the composition of the human gut microbiota greatly facilitates studies on its role in human pathophysiology, and is heavily reliant on culture-independent molecular methods. A microarray designated the Human Gut Chip (HuGChip) was developed to analyze and compare human gut microbiota samples. The PhylArray software was used to design specific and sensitive probes. The DNA chip was composed of 4,441 probes (2,442 specific and 1,919 explorative probes) targeting 66 bacterial families. A mock community composed of 16S rRNA gene sequences from intestinal species was used to define the threshold criteria to be used to analyze complex samples. This was then experimentally verified with three human faecal samples and results were compared (i) with pyrosequencing of the V4 hypervariable region of the 16S rRNA gene, (ii) metagenomic data, and (iii) qPCR analysis of three phyla. When compared at both the phylum and the family level, high Pearson's correlation coefficients were obtained between data from all methods. The HuGChip development and validation showed that it is not only able to assess the known human gut microbiota but could also detect unknown species with the explorative probes to reveal the large number of bacterial sequences not yet described in the human gut microbiota, overcoming the main inconvenience encountered when developing microarrays.
url http://europepmc.org/articles/PMC3656878?pdf=render
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