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Within-host microevolution of Streptococcus pneumoniae is rapid and adaptive during natural colonisation

Chaguza, C; Senghore, M; Bojang, E; Gladstone, RA; Lo, SW; Tientcheu, P-E; Bancroft, RE; ... Kwambana-Adams, BA; + view all (2020) Within-host microevolution of Streptococcus pneumoniae is rapid and adaptive during natural colonisation. Nature Communications , 11 , Article 3442. 10.1038/s41467-020-17327-w. Green open access

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Abstract

Genomic evolution, transmission and pathogenesis of Streptococcus pneumoniae, an opportunistic human-adapted pathogen, is driven principally by nasopharyngeal carriage. However, little is known about genomic changes during natural colonisation. Here, we use whole-genome sequencing to investigate within-host microevolution of naturally carried pneumococci in ninety-eight infants intensively sampled sequentially from birth until twelve months in a high-carriage African setting. We show that neutral evolution and nucleotide substitution rates up to forty-fold faster than observed over longer timescales in S. pneumoniae and other bacteria drives high within-host pneumococcal genetic diversity. Highly divergent co-existing strain variants emerge during colonisation episodes through real-time intra-host homologous recombination while the rest are co-transmitted or acquired independently during multiple colonisation episodes. Genic and intergenic parallel evolution occur particularly in antibiotic resistance, immune evasion and epithelial adhesion genes. Our findings suggest that within-host microevolution is rapid and adaptive during natural colonisation.

Type: Article
Title: Within-host microevolution of Streptococcus pneumoniae is rapid and adaptive during natural colonisation
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1038/s41467-020-17327-w
Publisher version: https://doi.org/10.1038/s41467-020-17327-w
Language: English
Additional information: This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Keywords: Bacterial genetics, Clinical microbiology, Genome evolution, Paediatric research
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Infection and Immunity
URI: https://discovery.ucl.ac.uk/id/eprint/10120477
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