Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples

Large-scale and in-depth characterization of the intestinal microbiota necessitates application of high-throughput 16S rRNA gene-based technologies, such as barcoded pyrosequencing and phylogenetic microarray analysis. In this study, the two techniques were compared and contrasted for analysis of the bacterial composition in three fecal and three small intestinal samples from human individuals. As PCR remains a crucial step in sample preparation for both techniques, different forward primers were used for amplification to assess their impact on microbial profiling results. An average of 7,944 pyrosequences, spanning the V1 and V2 region of 16S rRNA genes, was obtained per sample. Although primer choice in barcoded pyrosequencing did not affect species richness and diversity estimates, detection of Actinobacteria strongly depended on the selected primer. Microbial profiles obtained by pyrosequencing and phylogenetic microarray analysis (HITChip) correlated strongly for fecal and ileal lumen samples but were less concordant for ileostomy effluent. Quantitative PCR was employed to investigate the deviations in profiling between pyrosequencing and HITChip analysis. Since cloning and sequencing of random 16S rRNA genes from ileostomy effluent confirmed the presence of novel intestinal phylotypes detected by pyrosequencing, especially those belonging to the Veillonella group, the divergence between pyrosequencing and the HITChip is likely due to the relatively low number of available 16S rRNA gene sequences of small intestinal origin in the DNA databases that were used for HITChip probe design. Overall, this study demonstrated that equivalent biological conclusions are obtained by high-throughput profiling of microbial communities, independent of technology or primer choice

Saved in:
Bibliographic Details
Main Authors: van den Bogert, B., de Vos, W.M., Zoetendal, E.G., Kleerebezem, M.
Format: Article/Letter to editor biblioteca
Language:English
Subjects:bacterial community, extensive set, fecal samples, gastrointestinal-tract microbiota, gut microbiome, phylogenetic microarray, quantitative-analysis, real-time pcr, ribosomal-rna genes, sequence data,
Online Access:https://research.wur.nl/en/publications/microarray-analysis-and-barcoded-pyrosequencing-provide-consisten
Tags: Add Tag
No Tags, Be the first to tag this record!
id dig-wur-nl-wurpubs-405092
record_format koha
spelling dig-wur-nl-wurpubs-4050922024-12-04 van den Bogert, B. de Vos, W.M. Zoetendal, E.G. Kleerebezem, M. Article/Letter to editor Applied and Environmental Microbiology 77 (2011) 6 ISSN: 0099-2240 Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples 2011 Large-scale and in-depth characterization of the intestinal microbiota necessitates application of high-throughput 16S rRNA gene-based technologies, such as barcoded pyrosequencing and phylogenetic microarray analysis. In this study, the two techniques were compared and contrasted for analysis of the bacterial composition in three fecal and three small intestinal samples from human individuals. As PCR remains a crucial step in sample preparation for both techniques, different forward primers were used for amplification to assess their impact on microbial profiling results. An average of 7,944 pyrosequences, spanning the V1 and V2 region of 16S rRNA genes, was obtained per sample. Although primer choice in barcoded pyrosequencing did not affect species richness and diversity estimates, detection of Actinobacteria strongly depended on the selected primer. Microbial profiles obtained by pyrosequencing and phylogenetic microarray analysis (HITChip) correlated strongly for fecal and ileal lumen samples but were less concordant for ileostomy effluent. Quantitative PCR was employed to investigate the deviations in profiling between pyrosequencing and HITChip analysis. Since cloning and sequencing of random 16S rRNA genes from ileostomy effluent confirmed the presence of novel intestinal phylotypes detected by pyrosequencing, especially those belonging to the Veillonella group, the divergence between pyrosequencing and the HITChip is likely due to the relatively low number of available 16S rRNA gene sequences of small intestinal origin in the DNA databases that were used for HITChip probe design. Overall, this study demonstrated that equivalent biological conclusions are obtained by high-throughput profiling of microbial communities, independent of technology or primer choice en application/pdf https://research.wur.nl/en/publications/microarray-analysis-and-barcoded-pyrosequencing-provide-consisten 10.1128/AEM.02477-10 https://edepot.wur.nl/165705 bacterial community extensive set fecal samples gastrointestinal-tract microbiota gut microbiome phylogenetic microarray quantitative-analysis real-time pcr ribosomal-rna genes sequence data Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic bacterial community
extensive set
fecal samples
gastrointestinal-tract microbiota
gut microbiome
phylogenetic microarray
quantitative-analysis
real-time pcr
ribosomal-rna genes
sequence data
bacterial community
extensive set
fecal samples
gastrointestinal-tract microbiota
gut microbiome
phylogenetic microarray
quantitative-analysis
real-time pcr
ribosomal-rna genes
sequence data
spellingShingle bacterial community
extensive set
fecal samples
gastrointestinal-tract microbiota
gut microbiome
phylogenetic microarray
quantitative-analysis
real-time pcr
ribosomal-rna genes
sequence data
bacterial community
extensive set
fecal samples
gastrointestinal-tract microbiota
gut microbiome
phylogenetic microarray
quantitative-analysis
real-time pcr
ribosomal-rna genes
sequence data
van den Bogert, B.
de Vos, W.M.
Zoetendal, E.G.
Kleerebezem, M.
Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples
description Large-scale and in-depth characterization of the intestinal microbiota necessitates application of high-throughput 16S rRNA gene-based technologies, such as barcoded pyrosequencing and phylogenetic microarray analysis. In this study, the two techniques were compared and contrasted for analysis of the bacterial composition in three fecal and three small intestinal samples from human individuals. As PCR remains a crucial step in sample preparation for both techniques, different forward primers were used for amplification to assess their impact on microbial profiling results. An average of 7,944 pyrosequences, spanning the V1 and V2 region of 16S rRNA genes, was obtained per sample. Although primer choice in barcoded pyrosequencing did not affect species richness and diversity estimates, detection of Actinobacteria strongly depended on the selected primer. Microbial profiles obtained by pyrosequencing and phylogenetic microarray analysis (HITChip) correlated strongly for fecal and ileal lumen samples but were less concordant for ileostomy effluent. Quantitative PCR was employed to investigate the deviations in profiling between pyrosequencing and HITChip analysis. Since cloning and sequencing of random 16S rRNA genes from ileostomy effluent confirmed the presence of novel intestinal phylotypes detected by pyrosequencing, especially those belonging to the Veillonella group, the divergence between pyrosequencing and the HITChip is likely due to the relatively low number of available 16S rRNA gene sequences of small intestinal origin in the DNA databases that were used for HITChip probe design. Overall, this study demonstrated that equivalent biological conclusions are obtained by high-throughput profiling of microbial communities, independent of technology or primer choice
format Article/Letter to editor
topic_facet bacterial community
extensive set
fecal samples
gastrointestinal-tract microbiota
gut microbiome
phylogenetic microarray
quantitative-analysis
real-time pcr
ribosomal-rna genes
sequence data
author van den Bogert, B.
de Vos, W.M.
Zoetendal, E.G.
Kleerebezem, M.
author_facet van den Bogert, B.
de Vos, W.M.
Zoetendal, E.G.
Kleerebezem, M.
author_sort van den Bogert, B.
title Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples
title_short Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples
title_full Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples
title_fullStr Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples
title_full_unstemmed Microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples
title_sort microarray analysis and barcoded pyrosequencing provide consistent microbial profiles depending on the source of human intestinal samples
url https://research.wur.nl/en/publications/microarray-analysis-and-barcoded-pyrosequencing-provide-consisten
work_keys_str_mv AT vandenbogertb microarrayanalysisandbarcodedpyrosequencingprovideconsistentmicrobialprofilesdependingonthesourceofhumanintestinalsamples
AT devoswm microarrayanalysisandbarcodedpyrosequencingprovideconsistentmicrobialprofilesdependingonthesourceofhumanintestinalsamples
AT zoetendaleg microarrayanalysisandbarcodedpyrosequencingprovideconsistentmicrobialprofilesdependingonthesourceofhumanintestinalsamples
AT kleerebezemm microarrayanalysisandbarcodedpyrosequencingprovideconsistentmicrobialprofilesdependingonthesourceofhumanintestinalsamples
_version_ 1819149504958431232