Rapid Bladder Interleukin-10 Synthesis in Response to Uropathogenic Escherichia coli Is Part of a Defense Strategy Triggered by the Major Bacterial Flagellar Filament FliC and Contingent on TLR5

Author:

Acharya Dhruba1,Sullivan Matthew J.1ORCID,Duell Benjamin L.1,Goh Kelvin G. K.1ORCID,Katupitiya Lahiru1,Gosling Dean1,Chamoun Michelle N.1,Kakkanat Asha2,Chattopadhyay Debasish3,Crowley Michael4,Crossman David K.4,Schembri Mark A.2ORCID,Ulett Glen C.13ORCID

Affiliation:

1. School of Medical Sciences and Menzies Health Institute Queensland, Griffith University, Parklands, Australia

2. School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Australia

3. School of Medicine, Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, Alabama, USA

4. Heflin Center for Genomic Sciences, University of Alabama at Birmingham, Birmingham, Alabama, USA

Abstract

Interleukin-10 is part of the immune response to urinary tract infection (UTI) due to E. coli , and it is important in the early control of infection in the bladder. Defining the mechanism of engagement of the immune system by the bacteria that enables the protective IL-10 response is critical to exploring how we might exploit this mechanism for new infection control strategies. In this study, we reveal part of the bacterial flagellar apparatus (FliC) is an important component that is sensed by and responsible for induction of IL-10 in the response to UPEC. We show this response occurs in a TLR5-dependent manner. Using infection prevention and control trials in mice infected with E. coli , this study also provides evidence that purified FliC might be of value in novel approaches for the treatment of UTI or in preventing infection by exploiting the FliC-triggered bladder transcriptome.

Funder

Department of Health | National Health and Medical Research Council

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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