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A random six-phase switch regulates pneumococcal virulence via global epigenetic changes
Streptococcus pneumoniae (the pneumococcus) is the world’s foremost bacterial pathogen in both morbidity and mortality. Switching between phenotypic forms (or ‘phases’) that favour asymptomatic carriage or invasive disease was first reported in 1933. Here, we show that the underlying mechanism for s...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190663/ https://www.ncbi.nlm.nih.gov/pubmed/25268848 http://dx.doi.org/10.1038/ncomms6055 |
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author | Manso, Ana Sousa Chai, Melissa H. Atack, John M. Furi, Leonardo De Ste Croix, Megan Haigh, Richard Trappetti, Claudia Ogunniyi, Abiodun D. Shewell, Lucy K. Boitano, Matthew Clark, Tyson A. Korlach, Jonas Blades, Matthew Mirkes, Evgeny Gorban, Alexander N. Paton, James C. Jennings, Michael P. Oggioni, Marco R. |
author_facet | Manso, Ana Sousa Chai, Melissa H. Atack, John M. Furi, Leonardo De Ste Croix, Megan Haigh, Richard Trappetti, Claudia Ogunniyi, Abiodun D. Shewell, Lucy K. Boitano, Matthew Clark, Tyson A. Korlach, Jonas Blades, Matthew Mirkes, Evgeny Gorban, Alexander N. Paton, James C. Jennings, Michael P. Oggioni, Marco R. |
author_sort | Manso, Ana Sousa |
collection | PubMed |
description | Streptococcus pneumoniae (the pneumococcus) is the world’s foremost bacterial pathogen in both morbidity and mortality. Switching between phenotypic forms (or ‘phases’) that favour asymptomatic carriage or invasive disease was first reported in 1933. Here, we show that the underlying mechanism for such phase variation consists of genetic rearrangements in a Type I restriction-modification system (SpnD39III). The rearrangements generate six alternative specificities with distinct methylation patterns, as defined by single-molecule, real-time (SMRT) methylomics. The SpnD39III variants have distinct gene expression profiles. We demonstrate distinct virulence in experimental infection and in vivo selection for switching between SpnD39III variants. SpnD39III is ubiquitous in pneumococci, indicating an essential role in its biology. Future studies must recognize the potential for switching between these heretofore undetectable, differentiated pneumococcal subpopulations in vitro and in vivo. Similar systems exist in other bacterial genera, indicating the potential for broad exploitation of epigenetic gene regulation. |
format | Online Article Text |
id | pubmed-4190663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-41906632014-10-21 A random six-phase switch regulates pneumococcal virulence via global epigenetic changes Manso, Ana Sousa Chai, Melissa H. Atack, John M. Furi, Leonardo De Ste Croix, Megan Haigh, Richard Trappetti, Claudia Ogunniyi, Abiodun D. Shewell, Lucy K. Boitano, Matthew Clark, Tyson A. Korlach, Jonas Blades, Matthew Mirkes, Evgeny Gorban, Alexander N. Paton, James C. Jennings, Michael P. Oggioni, Marco R. Nat Commun Article Streptococcus pneumoniae (the pneumococcus) is the world’s foremost bacterial pathogen in both morbidity and mortality. Switching between phenotypic forms (or ‘phases’) that favour asymptomatic carriage or invasive disease was first reported in 1933. Here, we show that the underlying mechanism for such phase variation consists of genetic rearrangements in a Type I restriction-modification system (SpnD39III). The rearrangements generate six alternative specificities with distinct methylation patterns, as defined by single-molecule, real-time (SMRT) methylomics. The SpnD39III variants have distinct gene expression profiles. We demonstrate distinct virulence in experimental infection and in vivo selection for switching between SpnD39III variants. SpnD39III is ubiquitous in pneumococci, indicating an essential role in its biology. Future studies must recognize the potential for switching between these heretofore undetectable, differentiated pneumococcal subpopulations in vitro and in vivo. Similar systems exist in other bacterial genera, indicating the potential for broad exploitation of epigenetic gene regulation. Nature Pub. Group 2014-09-30 /pmc/articles/PMC4190663/ /pubmed/25268848 http://dx.doi.org/10.1038/ncomms6055 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Manso, Ana Sousa Chai, Melissa H. Atack, John M. Furi, Leonardo De Ste Croix, Megan Haigh, Richard Trappetti, Claudia Ogunniyi, Abiodun D. Shewell, Lucy K. Boitano, Matthew Clark, Tyson A. Korlach, Jonas Blades, Matthew Mirkes, Evgeny Gorban, Alexander N. Paton, James C. Jennings, Michael P. Oggioni, Marco R. A random six-phase switch regulates pneumococcal virulence via global epigenetic changes |
title | A random six-phase switch regulates pneumococcal virulence via global epigenetic changes |
title_full | A random six-phase switch regulates pneumococcal virulence via global epigenetic changes |
title_fullStr | A random six-phase switch regulates pneumococcal virulence via global epigenetic changes |
title_full_unstemmed | A random six-phase switch regulates pneumococcal virulence via global epigenetic changes |
title_short | A random six-phase switch regulates pneumococcal virulence via global epigenetic changes |
title_sort | random six-phase switch regulates pneumococcal virulence via global epigenetic changes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190663/ https://www.ncbi.nlm.nih.gov/pubmed/25268848 http://dx.doi.org/10.1038/ncomms6055 |
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