Early invasion of the bladder wall by solitary bacteria protects UPEC from antibiotics and neutrophil swarms in an organoid model
Sharma, Kunal; Thacker, Vivek V.; Dhar, Neeraj; Clapés Cabrer, Maria; Dubois, Anaëlle; Signorino-Gelo, François; Mullenders, Jasper; Knott, Graham W.; Clevers, Hans; McKinney, John D.
(2021) Cell Reports, volume 36, issue 3, pp. 1 - 22
(Article)
Abstract
Recurrence of uropathogenic Escherichia coli (UPEC) infections has been attributed to reactivation of quiescent intracellular reservoirs (QIRs) in deep layers of the bladder wall. QIRs are thought to arise late during infection following dispersal of bacteria from intracellular bacterial communities (IBCs) in superficial umbrella cells. Here, we track the formation
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of QIR-like bacteria in a bladder organoid model that recapitulates the stratified uroepithelium within a volume suitable for high-resolution live-cell imaging. Bacteria injected into the organoid lumen enter umbrella-like cells and proliferate to form IBC-like bodies. In parallel, single bacteria penetrate deeper layers of the organoid wall, where they localize within or between uroepithelial cells. These “solitary” bacteria evade killing by antibiotics and neutrophils and are morphologically distinct from bacteria in IBCs. We conclude that bacteria with QIR-like properties may arise at early stages of infection, independent of IBC formation and rupture.
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Keywords: antibiotic persistence, bladder organoids, IBCs, intracellular bacterial colonies, neutrophils, QIRs, quiescent intracellular reservoirs, serial block-face scanning electron microscopy (SBEM), time-lapse microscopy, UPEC, uropathogenic Escherichia coli, General Biochemistry,Genetics and Molecular Biology
ISSN: 2211-1247
Publisher: Cell Press
Note: Funding Information: V.V.T. acknowledges support by Long-Term Fellowships from the Human Frontier Science Program (HFSP; LT000231/2016-L ) and the European Molecular Biology Organization (EMBO; 921-2015 ). This research was supported by grants to J.D.M. from the Swiss National Science Foundation (SNSF) ( 310030B_176397 ) and the National Centre of Competence in Research AntiResist funded by the SNSF ( 51NF40_180541 ). K.S. wishes to thank the members of the EPFL Bioimaging & Optics Core Facility for assistance in confocal live-cell imaging and analysis in Bitplane Imaris, D. Dutta and S. Rosset for help in optimizing the protocol for rupturing infected organoids, J. Sordet-Desimoz and G.-F. Mancini for assistance with paraffin-embedded slicing of organoids, G. Markus for development of the neutrophil isolation protocol, M. Nikolaev for assistance with the collagen gel polymerization protocol, T. Simonet for the UPEC ΔfliC strain, A. Marcos for optimizing the microinjection of bladder organoids, and A. Oates for access to a stereo microscope. The authors credit BioRender.com for the illustrations and schematics used in this manuscript. Publisher Copyright: © 2021 The Authors
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