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Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes

The colonization of the human gut microbiome begins at birth, and over time, these microbial communities become increasingly complex. Most of what we currently know about the human microbiome, especially in early stages of development, was described using culture-independent sequencing methods that...

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Autores principales: Peterson, Danielle, Bonham, Kevin S., Rowland, Sophie, Pattanayak, Cassandra W., Klepac-Ceraj, Vanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320171/
https://www.ncbi.nlm.nih.gov/pubmed/34335499
http://dx.doi.org/10.3389/fmicb.2021.670336
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author Peterson, Danielle
Bonham, Kevin S.
Rowland, Sophie
Pattanayak, Cassandra W.
Klepac-Ceraj, Vanja
author_facet Peterson, Danielle
Bonham, Kevin S.
Rowland, Sophie
Pattanayak, Cassandra W.
Klepac-Ceraj, Vanja
author_sort Peterson, Danielle
collection PubMed
description The colonization of the human gut microbiome begins at birth, and over time, these microbial communities become increasingly complex. Most of what we currently know about the human microbiome, especially in early stages of development, was described using culture-independent sequencing methods that allow us to identify the taxonomic composition of microbial communities using genomic techniques, such as amplicon or shotgun metagenomic sequencing. Each method has distinct tradeoffs, but there has not been a direct comparison of the utility of these methods in stool samples from very young children, which have different features than those of adults. We compared the effects of profiling the human infant gut microbiome with 16S rRNA amplicon vs. shotgun metagenomic sequencing techniques in 338 fecal samples; younger than 15, 15–30, and older than 30 months of age. We demonstrate that observed changes in alpha-diversity and beta-diversity with age occur to similar extents using both profiling methods. We also show that 16S rRNA profiling identified a larger number of genera and we find several genera that are missed or underrepresented by each profiling method. We present the link between alpha diversity and shotgun metagenomic sequencing depth for children of different ages. These findings provide a guide for selecting an appropriate method and sequencing depth for the three studied age groups.
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spelling pubmed-83201712021-07-30 Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes Peterson, Danielle Bonham, Kevin S. Rowland, Sophie Pattanayak, Cassandra W. Klepac-Ceraj, Vanja Front Microbiol Microbiology The colonization of the human gut microbiome begins at birth, and over time, these microbial communities become increasingly complex. Most of what we currently know about the human microbiome, especially in early stages of development, was described using culture-independent sequencing methods that allow us to identify the taxonomic composition of microbial communities using genomic techniques, such as amplicon or shotgun metagenomic sequencing. Each method has distinct tradeoffs, but there has not been a direct comparison of the utility of these methods in stool samples from very young children, which have different features than those of adults. We compared the effects of profiling the human infant gut microbiome with 16S rRNA amplicon vs. shotgun metagenomic sequencing techniques in 338 fecal samples; younger than 15, 15–30, and older than 30 months of age. We demonstrate that observed changes in alpha-diversity and beta-diversity with age occur to similar extents using both profiling methods. We also show that 16S rRNA profiling identified a larger number of genera and we find several genera that are missed or underrepresented by each profiling method. We present the link between alpha diversity and shotgun metagenomic sequencing depth for children of different ages. These findings provide a guide for selecting an appropriate method and sequencing depth for the three studied age groups. Frontiers Media S.A. 2021-07-15 /pmc/articles/PMC8320171/ /pubmed/34335499 http://dx.doi.org/10.3389/fmicb.2021.670336 Text en Copyright © 2021 Peterson, Bonham, Rowland, Pattanayak, RESONANCE Consortium and Klepac-Ceraj. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Peterson, Danielle
Bonham, Kevin S.
Rowland, Sophie
Pattanayak, Cassandra W.
Klepac-Ceraj, Vanja
Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes
title Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes
title_full Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes
title_fullStr Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes
title_full_unstemmed Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes
title_short Comparative Analysis of 16S rRNA Gene and Metagenome Sequencing in Pediatric Gut Microbiomes
title_sort comparative analysis of 16s rrna gene and metagenome sequencing in pediatric gut microbiomes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8320171/
https://www.ncbi.nlm.nih.gov/pubmed/34335499
http://dx.doi.org/10.3389/fmicb.2021.670336
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