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Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone

Many antibiotic resistant uropathogenic Escherichia coli (UPEC) strains belong to clones defined by their multilocus sequence type (ST), with ST131 being the most dominant. Although we have a good understanding of resistance development to fluoroquinolones and third-generation cephalosporins by ST13...

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Autores principales: Alvarez-Fraga, Laura, Phan, Minh-Duy, Goh, Kelvin G. K., Nhu, Nguyen Thi Khanh, Hancock, Steven J., Allsopp, Luke P., Peters, Kate M., Forde, Brian M., Roberts, Leah W., Sullivan, Matthew J., Totsika, Makrina, Beatson, Scott A., Ulett, Glen C., Schembri, Mark A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764528/
https://www.ncbi.nlm.nih.gov/pubmed/35038925
http://dx.doi.org/10.1128/mbio.03519-21
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author Alvarez-Fraga, Laura
Phan, Minh-Duy
Goh, Kelvin G. K.
Nhu, Nguyen Thi Khanh
Hancock, Steven J.
Allsopp, Luke P.
Peters, Kate M.
Forde, Brian M.
Roberts, Leah W.
Sullivan, Matthew J.
Totsika, Makrina
Beatson, Scott A.
Ulett, Glen C.
Schembri, Mark A.
author_facet Alvarez-Fraga, Laura
Phan, Minh-Duy
Goh, Kelvin G. K.
Nhu, Nguyen Thi Khanh
Hancock, Steven J.
Allsopp, Luke P.
Peters, Kate M.
Forde, Brian M.
Roberts, Leah W.
Sullivan, Matthew J.
Totsika, Makrina
Beatson, Scott A.
Ulett, Glen C.
Schembri, Mark A.
author_sort Alvarez-Fraga, Laura
collection PubMed
description Many antibiotic resistant uropathogenic Escherichia coli (UPEC) strains belong to clones defined by their multilocus sequence type (ST), with ST131 being the most dominant. Although we have a good understanding of resistance development to fluoroquinolones and third-generation cephalosporins by ST131, our understanding of the virulence repertoire that has contributed to its global dissemination is limited. Here we show that the genes encoding Afa/Dr fimbriae, a group of adhesins strongly associated with UPEC that cause gestational pyelonephritis and recurrent cystitis, are found in approximately one third of all ST131 strains. Sequence comparison of the AfaE adhesin protein revealed a unique allelic variant carried by 82.9% of afa-positive ST131 strains. We identify the afa regulatory region as a hotspot for the integration of insertion sequence (IS) elements, all but one of which alter afa transcription. Close investigation demonstrated that the integration of an IS1 element in the afa regulatory region leads to increased expression of Afa/Dr fimbriae, promoting enhanced adhesion to kidney epithelial cells and suggesting a mechanism for altered virulence. Finally, we provide evidence for a more widespread impact of IS1 on ST131 genome evolution, suggesting that IS dynamics contribute to strain level microevolution that impacts ST131 fitness.
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spelling pubmed-87645282022-01-24 Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone Alvarez-Fraga, Laura Phan, Minh-Duy Goh, Kelvin G. K. Nhu, Nguyen Thi Khanh Hancock, Steven J. Allsopp, Luke P. Peters, Kate M. Forde, Brian M. Roberts, Leah W. Sullivan, Matthew J. Totsika, Makrina Beatson, Scott A. Ulett, Glen C. Schembri, Mark A. mBio Research Article Many antibiotic resistant uropathogenic Escherichia coli (UPEC) strains belong to clones defined by their multilocus sequence type (ST), with ST131 being the most dominant. Although we have a good understanding of resistance development to fluoroquinolones and third-generation cephalosporins by ST131, our understanding of the virulence repertoire that has contributed to its global dissemination is limited. Here we show that the genes encoding Afa/Dr fimbriae, a group of adhesins strongly associated with UPEC that cause gestational pyelonephritis and recurrent cystitis, are found in approximately one third of all ST131 strains. Sequence comparison of the AfaE adhesin protein revealed a unique allelic variant carried by 82.9% of afa-positive ST131 strains. We identify the afa regulatory region as a hotspot for the integration of insertion sequence (IS) elements, all but one of which alter afa transcription. Close investigation demonstrated that the integration of an IS1 element in the afa regulatory region leads to increased expression of Afa/Dr fimbriae, promoting enhanced adhesion to kidney epithelial cells and suggesting a mechanism for altered virulence. Finally, we provide evidence for a more widespread impact of IS1 on ST131 genome evolution, suggesting that IS dynamics contribute to strain level microevolution that impacts ST131 fitness. American Society for Microbiology 2022-01-18 /pmc/articles/PMC8764528/ /pubmed/35038925 http://dx.doi.org/10.1128/mbio.03519-21 Text en Copyright © 2022 Alvarez-Fraga et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Alvarez-Fraga, Laura
Phan, Minh-Duy
Goh, Kelvin G. K.
Nhu, Nguyen Thi Khanh
Hancock, Steven J.
Allsopp, Luke P.
Peters, Kate M.
Forde, Brian M.
Roberts, Leah W.
Sullivan, Matthew J.
Totsika, Makrina
Beatson, Scott A.
Ulett, Glen C.
Schembri, Mark A.
Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone
title Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone
title_full Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone
title_fullStr Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone
title_full_unstemmed Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone
title_short Differential Afa/Dr Fimbriae Expression in the Multidrug-Resistant Escherichia coli ST131 Clone
title_sort differential afa/dr fimbriae expression in the multidrug-resistant escherichia coli st131 clone
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764528/
https://www.ncbi.nlm.nih.gov/pubmed/35038925
http://dx.doi.org/10.1128/mbio.03519-21
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