Author
Listed:
- Ana Sousa Manso
(University of Leicester
Università di Siena)
- Melissa H. Chai
(Research Centre for Infectious Diseases, School of Molecular and Biomedical Science, University of Adelaide)
- John M. Atack
(Institute for Glycomics, Griffith University)
- Leonardo Furi
(University of Leicester
Università di Siena)
- Megan De Ste Croix
(University of Leicester)
- Richard Haigh
(University of Leicester)
- Claudia Trappetti
(Research Centre for Infectious Diseases, School of Molecular and Biomedical Science, University of Adelaide)
- Abiodun D. Ogunniyi
(Research Centre for Infectious Diseases, School of Molecular and Biomedical Science, University of Adelaide)
- Lucy K. Shewell
(Institute for Glycomics, Griffith University)
- Matthew Boitano
(Pacific Biosciences)
- Tyson A. Clark
(Pacific Biosciences)
- Jonas Korlach
(Pacific Biosciences)
- Matthew Blades
(Bioinformatics and Biostatistics Analysis Support Hub, University of Leicester)
- Evgeny Mirkes
(University of Leicester)
- Alexander N. Gorban
(University of Leicester)
- James C. Paton
(Research Centre for Infectious Diseases, School of Molecular and Biomedical Science, University of Adelaide)
- Michael P. Jennings
(Institute for Glycomics, Griffith University)
- Marco R. Oggioni
(University of Leicester
Università di Siena)
Abstract
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.
Suggested Citation
Ana Sousa Manso & Melissa H. Chai & John M. Atack & Leonardo Furi & Megan De Ste Croix & Richard Haigh & Claudia Trappetti & Abiodun D. Ogunniyi & Lucy K. Shewell & Matthew Boitano & Tyson A. Clark & , 2014.
"A random six-phase switch regulates pneumococcal virulence via global epigenetic changes,"
Nature Communications, Nature, vol. 5(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6055
DOI: 10.1038/ncomms6055
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