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Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve

Bifidobacterium breve represents one of the most abundant bifidobacterial species in the gastro-intestinal tract of breast-fed infants, where their presence is believed to exert beneficial effects. In the present study whole genome sequencing, employing the PacBio Single Molecule, Real-Time (SMRT) s...

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Autores principales: Bottacini, Francesca, Morrissey, Ruth, Roberts, Richard John, James, Kieran, van Breen, Justin, Egan, Muireann, Lambert, Jolanda, van Limpt, Kees, Knol, Jan, Motherway, Mary O’Connell, van Sinderen, Douwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829577/
https://www.ncbi.nlm.nih.gov/pubmed/29294107
http://dx.doi.org/10.1093/nar/gkx1289
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author Bottacini, Francesca
Morrissey, Ruth
Roberts, Richard John
James, Kieran
van Breen, Justin
Egan, Muireann
Lambert, Jolanda
van Limpt, Kees
Knol, Jan
Motherway, Mary O’Connell
van Sinderen, Douwe
author_facet Bottacini, Francesca
Morrissey, Ruth
Roberts, Richard John
James, Kieran
van Breen, Justin
Egan, Muireann
Lambert, Jolanda
van Limpt, Kees
Knol, Jan
Motherway, Mary O’Connell
van Sinderen, Douwe
author_sort Bottacini, Francesca
collection PubMed
description Bifidobacterium breve represents one of the most abundant bifidobacterial species in the gastro-intestinal tract of breast-fed infants, where their presence is believed to exert beneficial effects. In the present study whole genome sequencing, employing the PacBio Single Molecule, Real-Time (SMRT) sequencing platform, combined with comparative genome analysis allowed the most extensive genetic investigation of this taxon. Our findings demonstrate that genes encoding Restriction/Modification (R/M) systems constitute a substantial part of the B. breve variable gene content (or variome). Using the methylome data generated by SMRT sequencing, combined with targeted Illumina bisulfite sequencing (BS-seq) and comparative genome analysis, we were able to detect methylation recognition motifs and assign these to identified B. breve R/M systems, where in several cases such assignments were confirmed by restriction analysis. Furthermore, we show that R/M systems typically impose a very significant barrier to genetic accessibility of B. breve strains, and that cloning of a methyltransferase-encoding gene may overcome such a barrier, thus allowing future functional investigations of members of this species.
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spelling pubmed-58295772018-03-06 Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve Bottacini, Francesca Morrissey, Ruth Roberts, Richard John James, Kieran van Breen, Justin Egan, Muireann Lambert, Jolanda van Limpt, Kees Knol, Jan Motherway, Mary O’Connell van Sinderen, Douwe Nucleic Acids Res Genomics Bifidobacterium breve represents one of the most abundant bifidobacterial species in the gastro-intestinal tract of breast-fed infants, where their presence is believed to exert beneficial effects. In the present study whole genome sequencing, employing the PacBio Single Molecule, Real-Time (SMRT) sequencing platform, combined with comparative genome analysis allowed the most extensive genetic investigation of this taxon. Our findings demonstrate that genes encoding Restriction/Modification (R/M) systems constitute a substantial part of the B. breve variable gene content (or variome). Using the methylome data generated by SMRT sequencing, combined with targeted Illumina bisulfite sequencing (BS-seq) and comparative genome analysis, we were able to detect methylation recognition motifs and assign these to identified B. breve R/M systems, where in several cases such assignments were confirmed by restriction analysis. Furthermore, we show that R/M systems typically impose a very significant barrier to genetic accessibility of B. breve strains, and that cloning of a methyltransferase-encoding gene may overcome such a barrier, thus allowing future functional investigations of members of this species. Oxford University Press 2018-02-28 2017-12-27 /pmc/articles/PMC5829577/ /pubmed/29294107 http://dx.doi.org/10.1093/nar/gkx1289 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Genomics
Bottacini, Francesca
Morrissey, Ruth
Roberts, Richard John
James, Kieran
van Breen, Justin
Egan, Muireann
Lambert, Jolanda
van Limpt, Kees
Knol, Jan
Motherway, Mary O’Connell
van Sinderen, Douwe
Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve
title Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve
title_full Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve
title_fullStr Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve
title_full_unstemmed Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve
title_short Comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal Bifidobacterium breve
title_sort comparative genome and methylome analysis reveals restriction/modification system diversity in the gut commensal bifidobacterium breve
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829577/
https://www.ncbi.nlm.nih.gov/pubmed/29294107
http://dx.doi.org/10.1093/nar/gkx1289
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