A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach

Abstract The microbiota of the human gut is a complex and rich community where bacteria and their viruses, the bacteriophages, are dominant. There are few studies on the phage community and no clear standard for isolating them, sequencing and analysing their genomes. Since this makes comparisons bet...

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Autores principales: Camille d’Humières, Marie Touchon, Sara Dion, Jean Cury, Amine Ghozlane, Marc Garcia-Garcera, Christiane Bouchier, Laurence Ma, Erick Denamur, Eduardo P.C.Rocha
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Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/625625c4a5b3443fb1772a7064b052ec
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spelling oai:doaj.org-article:625625c4a5b3443fb1772a7064b052ec2021-12-02T15:08:09ZA simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach10.1038/s41598-019-47656-w2045-2322https://doaj.org/article/625625c4a5b3443fb1772a7064b052ec2019-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-019-47656-whttps://doaj.org/toc/2045-2322Abstract The microbiota of the human gut is a complex and rich community where bacteria and their viruses, the bacteriophages, are dominant. There are few studies on the phage community and no clear standard for isolating them, sequencing and analysing their genomes. Since this makes comparisons between studies difficult, we aimed at defining an easy, low-cost, and reproducible methodology. We analysed five different techniques to isolate phages from human adult faeces and developed an approach to analyse their genomes in order to quantify contamination and classify phage contigs in terms of taxonomy and lifestyle. We chose the polyethylene glycol concentration method to isolate phages because of its simplicity, low cost, reproducibility, and of the high number and diversity of phage sequences that we obtained. We also tested the reproducibility of this method with multiple displacement amplification (MDA) and showed that MDA severely decreases the phage genetic diversity of the samples and the reproducibility of the method. Lastly, we studied the influence of sequencing depth on the analysis of phage diversity and observed the beginning of a plateau for phage contigs at 20,000,000 reads. This work contributes to the development of methods for the isolation of phages in faeces and for their comparative analysis.Camille d’HumièresMarie TouchonSara DionJean CuryAmine GhozlaneMarc Garcia-GarceraChristiane BouchierLaurence MaErick DenamurEduardo P.C.RochaNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Camille d’Humières
Marie Touchon
Sara Dion
Jean Cury
Amine Ghozlane
Marc Garcia-Garcera
Christiane Bouchier
Laurence Ma
Erick Denamur
Eduardo P.C.Rocha
A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
description Abstract The microbiota of the human gut is a complex and rich community where bacteria and their viruses, the bacteriophages, are dominant. There are few studies on the phage community and no clear standard for isolating them, sequencing and analysing their genomes. Since this makes comparisons between studies difficult, we aimed at defining an easy, low-cost, and reproducible methodology. We analysed five different techniques to isolate phages from human adult faeces and developed an approach to analyse their genomes in order to quantify contamination and classify phage contigs in terms of taxonomy and lifestyle. We chose the polyethylene glycol concentration method to isolate phages because of its simplicity, low cost, reproducibility, and of the high number and diversity of phage sequences that we obtained. We also tested the reproducibility of this method with multiple displacement amplification (MDA) and showed that MDA severely decreases the phage genetic diversity of the samples and the reproducibility of the method. Lastly, we studied the influence of sequencing depth on the analysis of phage diversity and observed the beginning of a plateau for phage contigs at 20,000,000 reads. This work contributes to the development of methods for the isolation of phages in faeces and for their comparative analysis.
format article
author Camille d’Humières
Marie Touchon
Sara Dion
Jean Cury
Amine Ghozlane
Marc Garcia-Garcera
Christiane Bouchier
Laurence Ma
Erick Denamur
Eduardo P.C.Rocha
author_facet Camille d’Humières
Marie Touchon
Sara Dion
Jean Cury
Amine Ghozlane
Marc Garcia-Garcera
Christiane Bouchier
Laurence Ma
Erick Denamur
Eduardo P.C.Rocha
author_sort Camille d’Humières
title A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
title_short A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
title_full A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
title_fullStr A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
title_full_unstemmed A simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
title_sort simple, reproducible and cost-effective procedure to analyse gut phageome: from phage isolation to bioinformatic approach
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/625625c4a5b3443fb1772a7064b052ec
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