Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus
The virulence and fitness in vivo of the major human pathogen Staphylococcus aureus are associated with a cell-to-cell signaling mechanism known as quorum sensing (QS). QS coordinates the production of virulence factors via the production and sensing of autoinducing peptide (AIP) signal molecules by...
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| Format: | Article |
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ASM Press
2014
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| Online Access: | https://eprints.nottingham.ac.uk/2991/ |
| _version_ | 1848790925737721856 |
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| author | Pollitt, Eric J.G. West, Stuart A. Crusz, Shanika A. Burton-Chellew, Maxwell N. Diggle, Stephen P. |
| author_facet | Pollitt, Eric J.G. West, Stuart A. Crusz, Shanika A. Burton-Chellew, Maxwell N. Diggle, Stephen P. |
| author_sort | Pollitt, Eric J.G. |
| building | Nottingham Research Data Repository |
| collection | Online Access |
| description | The virulence and fitness in vivo of the major human pathogen Staphylococcus aureus are associated with a cell-to-cell signaling mechanism known as quorum sensing (QS). QS coordinates the production of virulence factors via the production and sensing of autoinducing peptide (AIP) signal molecules by the agr locus. Here we show, in a wax moth larva virulence model, that (i) QS in S. aureus is a cooperative social trait that provides a benefit to the local population of cells, (ii) agr mutants, which do not pro- duce or respond to QS signal, are able to exploit the benefits provided by the QS of others (“cheat”), allowing them to increase in frequency when in mixed populations with cooperators, (iii) these social interactions between cells determine virulence, with the host mortality rate being negatively correlated to the percentage of agr mutants (“cheats”) in a population, and (iv) a higher within-host relatedness (lower strain diversity) selects for QS and hence higher virulence. Our results provide an explanation for why agr mutants show reduced virulence in animal models but can be isolated from infections of humans. More generally, by providing the first evidence that QS is a cooperative social behavior in a Gram-positive bacterium, our results suggest conver- gent, and potentially widespread, evolution for signaling to coordinate cooperation in bacteria. |
| first_indexed | 2025-11-14T18:20:22Z |
| format | Article |
| id | nottingham-2991 |
| institution | University of Nottingham Malaysia Campus |
| institution_category | Local University |
| last_indexed | 2025-11-14T18:20:22Z |
| publishDate | 2014 |
| publisher | ASM Press |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | nottingham-29912020-05-04T20:17:36Z https://eprints.nottingham.ac.uk/2991/ Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus Pollitt, Eric J.G. West, Stuart A. Crusz, Shanika A. Burton-Chellew, Maxwell N. Diggle, Stephen P. The virulence and fitness in vivo of the major human pathogen Staphylococcus aureus are associated with a cell-to-cell signaling mechanism known as quorum sensing (QS). QS coordinates the production of virulence factors via the production and sensing of autoinducing peptide (AIP) signal molecules by the agr locus. Here we show, in a wax moth larva virulence model, that (i) QS in S. aureus is a cooperative social trait that provides a benefit to the local population of cells, (ii) agr mutants, which do not pro- duce or respond to QS signal, are able to exploit the benefits provided by the QS of others (“cheat”), allowing them to increase in frequency when in mixed populations with cooperators, (iii) these social interactions between cells determine virulence, with the host mortality rate being negatively correlated to the percentage of agr mutants (“cheats”) in a population, and (iv) a higher within-host relatedness (lower strain diversity) selects for QS and hence higher virulence. Our results provide an explanation for why agr mutants show reduced virulence in animal models but can be isolated from infections of humans. More generally, by providing the first evidence that QS is a cooperative social behavior in a Gram-positive bacterium, our results suggest conver- gent, and potentially widespread, evolution for signaling to coordinate cooperation in bacteria. ASM Press 2014 Article PeerReviewed Pollitt, Eric J.G., West, Stuart A., Crusz, Shanika A., Burton-Chellew, Maxwell N. and Diggle, Stephen P. (2014) Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus. Infection and Immunity, 82 (3). pp. 1045-1051. ISSN 1098-5522 http://iai.asm.org/content/82/3/1045 doi:10.1128/IAI.01216-13 doi:10.1128/IAI.01216-13 |
| spellingShingle | Pollitt, Eric J.G. West, Stuart A. Crusz, Shanika A. Burton-Chellew, Maxwell N. Diggle, Stephen P. Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus |
| title | Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus |
| title_full | Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus |
| title_fullStr | Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus |
| title_full_unstemmed | Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus |
| title_short | Cooperation, quorum sensing, and evolution of virulence in Staphylococcus aureus |
| title_sort | cooperation, quorum sensing, and evolution of virulence in staphylococcus aureus |
| url | https://eprints.nottingham.ac.uk/2991/ https://eprints.nottingham.ac.uk/2991/ https://eprints.nottingham.ac.uk/2991/ |