Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing
Background Metagenomics seeks to understand microbial communities and assemblages by DNA sequencing. Technological advances in next generation sequencing technologies are fuelling a rapid growth in the number and scope of projects aiming to analyze complex microbial environments such as marine, s...
Saved in:
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
2014
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/103644 http://hdl.handle.net/10220/19357 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-103644 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1036442022-02-16T16:29:35Z Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing Mitra, Suparna Förster-Fromme, Karin Damms-Machado, Antje Scheurenbrand, Tim Biskup, Saskia Huson, Daniel H. Bischoff, Stephan C. DRNTU::Engineering::Environmental engineering DRNTU::Science::Biological sciences Background Metagenomics seeks to understand microbial communities and assemblages by DNA sequencing. Technological advances in next generation sequencing technologies are fuelling a rapid growth in the number and scope of projects aiming to analyze complex microbial environments such as marine, soil or the gut. Recent improvements in longer read lengths and paired-sequencing allow better resolution in profiling microbial communities. While both 454 sequencing and Illumina sequencing have been used in numerous metagenomic studies, SOLiD sequencing is not commonly used in this area, as it is believed to be more suitable in the context of reference-guided projects. Results To investigate the performance of SOLiD sequencing in a metagenomic context, we compared taxonomic profiles of SOLiD mate-pair sequencing reads with Sanger paired reads and 454 single reads. All sequences were obtained from the bacterial 16S rRNA gene, which was amplified from microbial DNA extracted from a human fecal sample. Additionally, from the same fecal sample, complete genomic microbial DNA was extracted and shotgun sequenced using SOLiD sequencing to study the composition of the intestinal microbiota and the existing microbial metabolism. We found that the microbiota composition of 16S rRNA gene sequences obtained using Sanger, 454 and SOLiD sequencing provide results comparable to the result based on shotgun sequencing. Moreover, with SOLiD sequences we obtained more resolution down to the species level. In addition, the shotgun data allowed us to determine a functional profile using the databases SEED and KEGG. Conclusions This study shows that SOLiD mate-pair sequencing is a viable and cost-efficient option for analyzing a complex microbiome. To the best of our knowledge, this is the first time that SOLiD sequencing has been used in a human sample. Published version 2014-05-19T01:09:36Z 2019-12-06T21:16:56Z 2014-05-19T01:09:36Z 2019-12-06T21:16:56Z 2013 2013 Journal Article Mitra, S., Förster-Fromme, K., Damms-Machado, A., Scheurenbrand, T., Biskup, S., Huson, D. H., el al. (2013). Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing. BMC Genomics, 14(Suppl 5), S16 . 1471-2164 https://hdl.handle.net/10356/103644 http://hdl.handle.net/10220/19357 10.1186/1471-2164-14-S5-S16 24564472 179162 en BMC genomics © 2013 Mitra et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. application/pdf |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
DRNTU::Engineering::Environmental engineering DRNTU::Science::Biological sciences |
spellingShingle |
DRNTU::Engineering::Environmental engineering DRNTU::Science::Biological sciences Mitra, Suparna Förster-Fromme, Karin Damms-Machado, Antje Scheurenbrand, Tim Biskup, Saskia Huson, Daniel H. Bischoff, Stephan C. Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing |
description |
Background
Metagenomics seeks to understand microbial communities and assemblages by DNA sequencing. Technological advances in next generation sequencing technologies are fuelling a rapid growth in the number and scope of projects aiming to analyze complex microbial environments such as marine, soil or the gut. Recent improvements in longer read lengths and paired-sequencing allow better resolution in profiling microbial communities. While both 454 sequencing and Illumina sequencing have been used in numerous metagenomic studies, SOLiD sequencing is not commonly used in this area, as it is believed to be more suitable in the context of reference-guided projects.
Results
To investigate the performance of SOLiD sequencing in a metagenomic context, we compared taxonomic profiles of SOLiD mate-pair sequencing reads with Sanger paired reads and 454 single reads. All sequences were obtained from the bacterial 16S rRNA gene, which was amplified from microbial DNA extracted from a human fecal sample. Additionally, from the same fecal sample, complete genomic microbial DNA was extracted and shotgun sequenced using SOLiD sequencing to study the composition of the intestinal microbiota and the existing microbial metabolism. We found that the microbiota composition of 16S rRNA gene sequences obtained using Sanger, 454 and SOLiD sequencing provide results comparable to the result based on shotgun sequencing. Moreover, with SOLiD sequences we obtained more resolution down to the species level. In addition, the shotgun data allowed us to determine a functional profile using the databases SEED and KEGG.
Conclusions
This study shows that SOLiD mate-pair sequencing is a viable and cost-efficient option for analyzing a complex microbiome. To the best of our knowledge, this is the first time that SOLiD sequencing has been used in a human sample. |
format |
Article |
author |
Mitra, Suparna Förster-Fromme, Karin Damms-Machado, Antje Scheurenbrand, Tim Biskup, Saskia Huson, Daniel H. Bischoff, Stephan C. |
author_facet |
Mitra, Suparna Förster-Fromme, Karin Damms-Machado, Antje Scheurenbrand, Tim Biskup, Saskia Huson, Daniel H. Bischoff, Stephan C. |
author_sort |
Mitra, Suparna |
title |
Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing |
title_short |
Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing |
title_full |
Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing |
title_fullStr |
Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing |
title_full_unstemmed |
Analysis of the intestinal microbiota using SOLiD 16SrRNA gene sequencing and SOLiD shotgun sequencing |
title_sort |
analysis of the intestinal microbiota using solid 16srrna gene sequencing and solid shotgun sequencing |
publishDate |
2014 |
url |
https://hdl.handle.net/10356/103644 http://hdl.handle.net/10220/19357 |
_version_ |
1725985601651474432 |