Tim J. Sloan
Timing is everything – impact of naturally occurring Staphylococcus aureus AgrC cytoplasmic domain adaptive mutations on auto-induction
Sloan, Tim J.; Murray, Ewan; Yokoyama, Maho; Massey, Ruth C.; Chan, Weng C.; Bonev, Boyan; Williams, Paul
Authors
EWAN MURRAY EWAN.MURRAY@NOTTINGHAM.AC.UK
Teaching Fellow
Maho Yokoyama
Ruth C. Massey
Prof WENG CHAN WENG.CHAN@NOTTINGHAM.AC.UK
Professor of Chemical Biology
BOYAN BONEV boyan.bonev@nottingham.ac.uk
Professor of Biophysics
PAUL WILLIAMS PAUL.WILLIAMS@NOTTINGHAM.AC.UK
Professor of Molecular Microbiology
Abstract
Mutations in the polymorphic Staphylococcus aureus agr locus responsible for quorum sensing (QS) dependent virulence gene regulation occur frequently during host adaptation. In two genomically closely related S. aureus clinical isolates exhibiting marked differences in Pantone-Valentine leukocidin production, a mutation conferring an N267I substitution was identified in the cytoplasmic domain of the QS sensor kinase, AgrC. This natural mutation delayed the onset and accumulation of auto-inducing peptide (AIP) and showed reduced responsiveness to exogenous AIPs. Other S. aureus strains harbouring naturally occurring AgrC cytoplasmic domain mutations were identified including T247I, I311T, A343T, L245S and F264C. These mutations were associated with reduced cytotoxicity, delayed/reduced AIP production and impaired sensitivity to exogenous AIP. Molecular dynamics simulations were used to model the AgrC cytoplasmic domain conformational changes arising. While mutations were localised in different parts of the C-terminal domain, their impact on molecular structure was manifested by twisting of the leading helical hairpin α1-α2, accompanied by repositioning of the H-box and G-box along with closure of the flexible loop connecting the two and occlusion of the ATP-binding site. Such conformational rearrangements of key functional subdomains in these mutants highlight the cooperative response of molecular structure involving dimerization, ATP binding and phosphorylation, as well as the binding site for the downstream response element AgrA. These appear to increase the threshold for agr activation via AIP-dependent autoinduction so reducing virulence and maintaining S. aureus in an agr-down-regulated ‘colonization’ mode.
Citation
Sloan, T. J., Murray, E., Yokoyama, M., Massey, R. C., Chan, W. C., Bonev, B., & Williams, P. (2019). Timing is everything – impact of naturally occurring Staphylococcus aureus AgrC cytoplasmic domain adaptive mutations on auto-induction. Journal of Bacteriology, 201(20), Article e00409-19. https://doi.org/10.1128/jb.00409-19
Journal Article Type | Article |
---|---|
Acceptance Date | Jul 22, 2019 |
Online Publication Date | Jul 29, 2019 |
Publication Date | Jul 29, 2019 |
Deposit Date | Aug 5, 2019 |
Publicly Available Date | Aug 5, 2019 |
Journal | Journal of Bacteriology |
Print ISSN | 0021-9193 |
Electronic ISSN | 1098-5530 |
Publisher | American Society for Microbiology |
Peer Reviewed | Peer Reviewed |
Volume | 201 |
Issue | 20 |
Article Number | e00409-19 |
DOI | https://doi.org/10.1128/jb.00409-19 |
Keywords | Molecular Biology; Microbiology |
Public URL | https://nottingham-repository.worktribe.com/output/2358316 |
Publisher URL | https://jb.asm.org/content/early/2019/07/23/JB.00409-19 |
Files
Journal of Bacteriology-2019-Sloan-e00409-19.full
(2.6 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
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