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The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei

Despite the large interest in the human microbiome in recent years, there are no reports of bacterial DNA methylation in the microbiome. Here metagenomic sequencing using the Pacific Biosciences platform allowed for rapid identification of bacterial GATC methylation status of a bacterial species in...

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Autores principales: Leonard, Michael T., Davis-Richardson, Austin G., Ardissone, Alexandria N., Kemppainen, Kaisa M., Drew, Jennifer C., Ilonen, Jorma, Knip, Mikael, Simell, Olli, Toppari, Jorma, Veijola, Riitta, Hyöty, Heikki, Triplett, Eric W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101878/
https://www.ncbi.nlm.nih.gov/pubmed/25101067
http://dx.doi.org/10.3389/fmicb.2014.00361
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author Leonard, Michael T.
Davis-Richardson, Austin G.
Ardissone, Alexandria N.
Kemppainen, Kaisa M.
Drew, Jennifer C.
Ilonen, Jorma
Knip, Mikael
Simell, Olli
Toppari, Jorma
Veijola, Riitta
Hyöty, Heikki
Triplett, Eric W.
author_facet Leonard, Michael T.
Davis-Richardson, Austin G.
Ardissone, Alexandria N.
Kemppainen, Kaisa M.
Drew, Jennifer C.
Ilonen, Jorma
Knip, Mikael
Simell, Olli
Toppari, Jorma
Veijola, Riitta
Hyöty, Heikki
Triplett, Eric W.
author_sort Leonard, Michael T.
collection PubMed
description Despite the large interest in the human microbiome in recent years, there are no reports of bacterial DNA methylation in the microbiome. Here metagenomic sequencing using the Pacific Biosciences platform allowed for rapid identification of bacterial GATC methylation status of a bacterial species in human stool samples. For this work, two stool samples were chosen that were dominated by a single species, Bacteroides dorei. Based on 16S rRNA analysis, this species represented over 45% of the bacteria present in these two samples. The B. dorei genome sequence from these samples was determined and the GATC methylation sites mapped. The Bacteroides dorei genome from one subject lacked any GATC methylation and lacked the DNA adenine methyltransferase genes. In contrast, B. dorei from another subject contained 20,551 methylated GATC sites. Of the 4970 open reading frames identified in the GATC methylated B. dorei genome, 3184 genes were methylated as well as 1735 GATC methylations in intergenic regions. These results suggest that DNA methylation patterns are important to consider in multi-omic analyses of microbiome samples seeking to discover the diversity of bacterial functions and may differ between disease states.
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spelling pubmed-41018782014-08-06 The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei Leonard, Michael T. Davis-Richardson, Austin G. Ardissone, Alexandria N. Kemppainen, Kaisa M. Drew, Jennifer C. Ilonen, Jorma Knip, Mikael Simell, Olli Toppari, Jorma Veijola, Riitta Hyöty, Heikki Triplett, Eric W. Front Microbiol Microbiology Despite the large interest in the human microbiome in recent years, there are no reports of bacterial DNA methylation in the microbiome. Here metagenomic sequencing using the Pacific Biosciences platform allowed for rapid identification of bacterial GATC methylation status of a bacterial species in human stool samples. For this work, two stool samples were chosen that were dominated by a single species, Bacteroides dorei. Based on 16S rRNA analysis, this species represented over 45% of the bacteria present in these two samples. The B. dorei genome sequence from these samples was determined and the GATC methylation sites mapped. The Bacteroides dorei genome from one subject lacked any GATC methylation and lacked the DNA adenine methyltransferase genes. In contrast, B. dorei from another subject contained 20,551 methylated GATC sites. Of the 4970 open reading frames identified in the GATC methylated B. dorei genome, 3184 genes were methylated as well as 1735 GATC methylations in intergenic regions. These results suggest that DNA methylation patterns are important to consider in multi-omic analyses of microbiome samples seeking to discover the diversity of bacterial functions and may differ between disease states. Frontiers Media S.A. 2014-07-17 /pmc/articles/PMC4101878/ /pubmed/25101067 http://dx.doi.org/10.3389/fmicb.2014.00361 Text en Copyright © 2014 Leonard, Davis-Richardson, Ardissone, Kemppainen, Drew, Ilonen, Knip, Simell, Toppari, Veijola, Hyöty and Triplett. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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
Leonard, Michael T.
Davis-Richardson, Austin G.
Ardissone, Alexandria N.
Kemppainen, Kaisa M.
Drew, Jennifer C.
Ilonen, Jorma
Knip, Mikael
Simell, Olli
Toppari, Jorma
Veijola, Riitta
Hyöty, Heikki
Triplett, Eric W.
The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei
title The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei
title_full The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei
title_fullStr The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei
title_full_unstemmed The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei
title_short The methylome of the gut microbiome: disparate Dam methylation patterns in intestinal Bacteroides dorei
title_sort methylome of the gut microbiome: disparate dam methylation patterns in intestinal bacteroides dorei
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4101878/
https://www.ncbi.nlm.nih.gov/pubmed/25101067
http://dx.doi.org/10.3389/fmicb.2014.00361
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