Comprehensive analysis of type 1 fimbriae regulation in fimB-null strains from the multidrug resistant Escherichia coli ST131 clone
Sarkar, Sohinee, Roberts, Leah, Phan, Minh-Duy, Tan, Lendl, Lo, Alvin, Peters, Kate, Paterson, David, Upton, Mathew, Ulett, Glen, Beatson, Scott, Totsika, Makrina, & Schembri, Mark (2016) Comprehensive analysis of type 1 fimbriae regulation in fimB-null strains from the multidrug resistant Escherichia coli ST131 clone. Molecular Microbiology, 101(6), pp. 1069-1087.
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Description
Summary Uropathogenic Escherichia coli (UPEC) of sequence type 131 (ST131) are a pandemic multidrug resistant clone associated with urinary tract and bloodstream infections. Type 1 fimbriae, a major UPEC virulence factor, are essential for ST131 bladder colonization. The globally dominant sub-lineage of ST131 strains, clade C/H30-R, possess an ISEc55 insertion in the fimB gene that controls phase-variable type 1 fimbriae expression via the invertible fimS promoter. We report that inactivation of fimB in these strains causes altered regulation of type 1 fimbriae expression. Using a novel read-mapping approach based on Illumina sequencing, we demonstrate that ‘off’ to ‘on’ fimS inversion is reduced in these strains and controlled by recombinases encoded by the fimE and fimX genes. Unlike typical UPEC strains, the nucleoid-associated H-NS protein does not strongly repress fimE transcription in clade C ST131 strains. Using a genetic screen to identify novel regulators of fimE and fimX in the clade C ST131 strain EC958, we defined a new role for the guaB gene in the regulation of type 1 fimbriae and in colonisation of the mouse bladder. Our results provide a comprehensive analysis of type 1 fimbriae regulation in ST131, and highlight important differences in its control compared to non-ST131 UPEC.
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| ID Code: | 221944 | ||||
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| Item Type: | Contribution to Journal (Journal Article) | ||||
| Refereed: | Yes | ||||
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| Additional Information: | The authors thank Barbara Arnts and Kendall Hepple for technical assistance with the mouse UTI model. This work was supported by grants from the National Health and Medical Research Council (NHMRC) of Australia (APP1069370 and APP1067455). MAS is supported by an NHMRC Senior Research Fellowship (APP1106930), SAB is supported by an NHMRC Career Development Fellowship (APP1090456), MT is supported by an Australian Research Council (ARC) Discovery Early Career Researcher Award (DE130101169) and GCU is supported by an ARC Future Fellowship (FT110101048). | ||||
| Measurements or Duration: | 19 pages | ||||
| DOI: | 10.1111/mmi.13442 | ||||
| ISSN: | 0950-382X | ||||
| Pure ID: | 33067414 | ||||
| Divisions: | Past > QUT Faculties & Divisions > Faculty of Health Past > Institutes > Institute of Health and Biomedical Innovation |
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| Copyright Owner: | 2016 John Wiley & Sons Ltd | ||||
| Copyright Statement: | This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au | ||||
| Deposited On: | 07 Nov 2021 01:36 | ||||
| Last Modified: | 30 Apr 2026 09:51 |
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