Green, Angharad 
ORCID: 0000-0002-8683-8191, Howarth, Deborah, Chaguza, Chrispin ORCID: 0000-0002-2108-1757, Echlin, Haley, Langendonk, Frèdi, Munro, Connor, Barton, Thomas, Hinton, Jay CD, Bentley, Stephen ORCID: 0000-0001-8094-3751, Rosch, Jason ORCID: 0000-0002-1798-1760 et al (show 1 more authors)
(2020)
Identification of colonisation and virulence determinants of <i>Streptococcus pneumoniae</i> via experimental evolution in mouse infection models.
2020.09.08.287698-.
Abstract
Streptococcus pneumoniae is a commensal of the human nasopharynx and a major cause of respiratory and invasive disease. Pneumococcus stimulates upper respiratory tract inflammation that promotes shedding from mucosal surfaces and transmission to new hosts. Colonisation and transmission are partially antagonistic processes. Adhesion to surfaces and evasion of host responses favours the former, whilst detachment, promoted by inflammation, is necessary for the latter. We sought to determine how adaptation and evolution of pneumococcus within its nasopharyngeal niche might progress when selective pressures associated with transmission were removed. This was achieved by serial passage of pneumococci in mouse models of nasopharyngeal carriage, manually transferring bacteria between mice. To assess the role of host environmental factors on pneumococcal evolution, we also performed analogous experimental evolution in a mouse pneumonia model, passaging pneumococci through lungs. Nasopharynx-passaged pneumococci became more effective colonisers, whilst those evolved within lungs showed reduced virulence. We observed selection of mutations in genes associated with cell wall biogenesis and metabolism in both nasopharynx and lung lineages, but identified prominent examples of parallel evolution that were niche specific. We focussed on gpsA , a gene in which the same single nucleotide polymorphism arose in two independently evolved nasopharynx-passaged lineages. We identified a single nucleotide change conferring resistance to oxidative stress and enhanced nasopharyngeal colonisation potential. We show that gpsA is also a frequent target of mutation during human colonisation. These findings highlight the role played by the host environment in determining trajectories of bacterial evolution and the potential of experimental evolution in animal infection models for identification of novel pathogen virulence and colonisation factors.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Biotechnology, Pneumonia & Influenza, Lung, Pneumonia, Infectious Diseases, 2.2 Factors relating to the physical environment, 2 Aetiology, 2.1 Biological and endogenous factors, Infection |
| Divisions: | Faculty of Health and Life Sciences Faculty of Health and Life Sciences > Institute of Infection, Veterinary and Ecological Sciences |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 04 Oct 2021 13:57 |
| Last Modified: | 14 Mar 2024 20:36 |
| DOI: | 10.1101/2020.09.08.287698 |
| Open Access URL: | https://doi.org/10.1101/2020.09.08.287698 |
| Related URLs: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3139266 |
Dimensions
Dimensions
