Architecture and function of human uromodulin filaments in urinary tract infections.


Journal

Science (New York, N.Y.)
ISSN: 1095-9203
Titre abrégé: Science
Pays: United States
ID NLM: 0404511

Informations de publication

Date de publication:
21 08 2020
Historique:
received: 25 10 2019
revised: 22 04 2020
accepted: 18 06 2020
pubmed: 4 7 2020
medline: 22 9 2020
entrez: 4 7 2020
Statut: ppublish

Résumé

Uromodulin is the most abundant protein in human urine, and it forms filaments that antagonize the adhesion of uropathogens; however, the filament structure and mechanism of protection remain poorly understood. We used cryo-electron tomography to show that the uromodulin filament consists of a zigzag-shaped backbone with laterally protruding arms. N-glycosylation mapping and biophysical assays revealed that uromodulin acts as a multivalent ligand for the bacterial type 1 pilus adhesin, presenting specific epitopes on the regularly spaced arms. Imaging of uromodulin-uropathogen interactions in vitro and in patient urine showed that uromodulin filaments associate with uropathogens and mediate bacterial aggregation, which likely prevents adhesion and allows clearance by micturition. These results provide a framework for understanding uromodulin in urinary tract infections and in its more enigmatic roles in physiology and disease.

Identifiants

pubmed: 32616672
pii: science.aaz9866
doi: 10.1126/science.aaz9866
doi:

Substances chimiques

Adhesins, Bacterial 0
Ligands 0
Uromodulin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1005-1010

Subventions

Organisme : Swiss National Science Foundation
Pays : Switzerland
Organisme : European Research Council
Pays : International

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

Auteurs

Gregor L Weiss (GL)

Institute of Molecular Biology and Biophysics, ETH Zürich, Otto-Stern-Weg 5, CH-8093 Zürich, Switzerland.

Jessica J Stanisich (JJ)

Institute of Molecular Biology and Biophysics, ETH Zürich, Otto-Stern-Weg 5, CH-8093 Zürich, Switzerland.

Maximilian M Sauer (MM)

Institute of Molecular Biology and Biophysics, ETH Zürich, Otto-Stern-Weg 5, CH-8093 Zürich, Switzerland.

Chia-Wei Lin (CW)

Institute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 1-5/10, CH-8093 Zürich, Switzerland.

Jonathan Eras (J)

Institute of Molecular Biology and Biophysics, ETH Zürich, Otto-Stern-Weg 5, CH-8093 Zürich, Switzerland.

Dawid S Zyla (DS)

Institute of Molecular Biology and Biophysics, ETH Zürich, Otto-Stern-Weg 5, CH-8093 Zürich, Switzerland.

Johannes Trück (J)

University Children's Hospital Zürich, Steinwiesstrasse 75, CH-8032 Zürich, Switzerland.

Olivier Devuyst (O)

Institute of Physiology, Mechanisms of Inherited Kidney Disorders, University of Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.
Division of Nephrology, UCLouvain Medical School, Brussels, Belgium.

Markus Aebi (M)

Institute of Microbiology, ETH Zürich, Vladimir-Prelog-Weg 1-5/10, CH-8093 Zürich, Switzerland.

Martin Pilhofer (M)

Institute of Molecular Biology and Biophysics, ETH Zürich, Otto-Stern-Weg 5, CH-8093 Zürich, Switzerland. pilhofer@biol.ethz.ch.

Rudi Glockshuber (R)

Institute of Molecular Biology and Biophysics, ETH Zürich, Otto-Stern-Weg 5, CH-8093 Zürich, Switzerland.

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Classifications MeSH