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Competitive behaviors in Serratia marcescens are coordinately regulated by a lifestyle switch frequently inactivated in the clinical environment
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dc.contributor.author | Williams, David J | |
dc.contributor.author | Hawkins, Alexandra | |
dc.contributor.author | Hernandez, Ruth E | |
dc.contributor.author | Mariano, Giuseppina | |
dc.contributor.author | Mathers, Katharine | |
dc.contributor.author | Buchanan, Grant | |
dc.contributor.author | Stonier, Barnaby J | |
dc.contributor.author | Inkster, Teresa | |
dc.contributor.author | Leanord, Alistair | |
dc.contributor.author | Chalmers, James D | |
dc.contributor.author | Thomson, Nicholas R. | |
dc.contributor.author | Holden, Matthew T. G. | |
dc.contributor.author | Coulthurst, Sarah J. | |
dc.date.accessioned | 2025-02-17T12:30:16Z | |
dc.date.available | 2025-02-17T12:30:16Z | |
dc.date.issued | 2025-02-12 | |
dc.identifier | 314281039 | |
dc.identifier | 8696d4bb-e2bf-43c0-a6d3-1158d5197b90 | |
dc.identifier | 39884275 | |
dc.identifier.citation | Williams , D J , Hawkins , A , Hernandez , R E , Mariano , G , Mathers , K , Buchanan , G , Stonier , B J , Inkster , T , Leanord , A , Chalmers , J D , Thomson , N R , Holden , M T G & Coulthurst , S J 2025 , ' Competitive behaviors in Serratia marcescens are coordinately regulated by a lifestyle switch frequently inactivated in the clinical environment ' , Cell Host & Microbe , vol. 33 , no. 2 , pp. 252-266.E5 . https://doi.org/10.1016/j.chom.2025.01.001 | en |
dc.identifier.issn | 1931-3128 | |
dc.identifier.other | ORCID: /0000-0002-4958-2166/work/177673944 | |
dc.identifier.uri | https://hdl.handle.net/10023/31401 | |
dc.description | Funding: This work was supported by Wellcome (104556/Z/14/Z, 220321/Z/20/Z, 109118/Z/15/Z, 218520/Z/19/Z, and 206194), NIHR (NIHR200639), and Chief Scientist Office (Scotland) Scottish Healthcare Associated Infection Prevention Institute (SIRN/10). | en |
dc.description.abstract | Opportunistic bacterial pathogens must compete with other bacteria and switch between host- and environment-adapted states. Type VI secretion systems (T6SSs) occur widely in gram-negative bacteria and can efficiently kill neighboring competitors. We determined the distribution of T6SSs across the genus Serratia and observed that a highly conserved antibacterial T6SS is differentially active between closely related clinical isolates of Serratia marcescens. By combining genomic and experimental approaches, we identified a genus-core two-component system, BetR-Reg1-Reg2, that controls T6SS activity and exhibits frequent inactivating mutations, exclusively in S. marcescens isolates of clinical origin. This regulatory system controls a number of lifestyle-related traits at transcriptional and post-translational levels, including T6SS activity, antibiotic production, motility, and adhesion, with loss of BetR increasing virulence in an in vivo infection model. Our data support a model whereby this system represents a conserved, modular switch from sessile to pioneering and aggressive behavior, which is subject to selection pressure in clinical environments. | |
dc.format.extent | 20 | |
dc.format.extent | 6527196 | |
dc.language.iso | eng | |
dc.relation.ispartof | Cell Host & Microbe | en |
dc.rights | © 2025 The Authors. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/). | en |
dc.subject | Inter-bacterial competition | en |
dc.subject | Type VI secretion system | en |
dc.subject | Bacterial genomics and evolution | en |
dc.subject | Clinical adaptation | en |
dc.subject | Serratia marcescens | en |
dc.subject | Opportunistic bacterial pathogens | en |
dc.subject | DAS | en |
dc.subject | MCC | en |
dc.title | Competitive behaviors in Serratia marcescens are coordinately regulated by a lifestyle switch frequently inactivated in the clinical environment | en |
dc.type | Journal article | en |
dc.contributor.institution | University of St Andrews.School of Medicine | en |
dc.contributor.institution | University of St Andrews.St Andrews Bioinformatics Unit | en |
dc.contributor.institution | University of St Andrews.Infection and Global Health Division | en |
dc.contributor.institution | University of St Andrews.Biomedical Sciences Research Complex | en |
dc.identifier.doi | 10.1016/j.chom.2025.01.001 | |
dc.description.status | Peer reviewed | en |
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