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Pneumococcal prophages are diverse, but not without structure or history

Abstract:
Bacteriophages (phages) infect many bacterial species, but little is known about the diversity of phages among the pneumococcus, a leading global pathogen. The objectives of this study were to determine the prevalence, diversity and molecular epidemiology of prophages (phage DNA integrated within the bacterial genome) among pneumococci isolatedover the past 90 years. Nearly 500 pneumococcal genomes were investigated and RNA sequencing was used to explore prophage gene expression. We revealed that every pneumococcal genome contained prophage DNA. 286 full-length/putatively full-length pneumococcal prophages were identified, of which 163 have not previously been reported. Full-length prophages clustered into four major groups and every group dated from the 1930-40s onward. There was limited evidence for genes shared between prophage clusters. Prophages typically integrated in one of five different sites within the pneumococcal genome. 72% of prophages possessed the virulence genes pblAand/or pblB. Individual prophages and the host pneumococcal genetic lineage were strongly associated and some prophages persisted for many decades. RNA sequencing provided clear evidence of prophage gene expression. Overall, pneumococcal prophages were highly prevalent, demonstrated a structured population, possessed genes associated with virulence, and were expressed under experimental conditions. Pneumococcal prophages are likely to play a more important role in pneumococcal biology and evolution than previously recognised.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/srep42976

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Doctoral Training Centre - MPLS
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
NDM Experimental Medicine
Role:
Author


More from this funder
Funding agency for:
Brueggemann, A
Grant:
123/734
More from this funder
Funding agency for:
Brueggemann, A
Grant:
123/734
090532/Z/09/Z


Publisher:
Nature Publishing Group
Journal:
Scientific Reports More from this journal
Volume:
7
Pages:
42976
Publication date:
2017-01-01
Acceptance date:
2017-01-17
DOI:
ISSN:
2045-2322


Pubs id:
pubs:671579
UUID:
uuid:7ea55cd5-86cf-4c16-b4cc-cac538d30f7c
Local pid:
pubs:671579
Deposit date:
2017-01-18

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