A new model for NTHi middle ear infection in the Junbo mutant mouse

Author:

Hood Derek1,Moxon Richard2,Purnell Tom1,Richter Caroline1,Williams Debbie1,Azar Ali3,Crompton Michael1,Wells Sara4,Fray Martin4,Brown Steve D.M.1,Cheeseman Michael T.143

Affiliation:

1. MRC Mammalian Genetics Unit, MRC Harwell, UK

2. Department of Paediatrics, University of Oxford Medical Sciences Division. John Radcliffe Hospital, Oxford , UK

3. The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh EH8 9YL, UK

4. Mary Lyon Centre, MRC Harwell, UK

Abstract

Acute otitis media, inflammation of the middle ear, is the most common bacterial infection in children and as a consequence is the most common reason for antimicrobial prescription to this age group. There is currently no effective vaccine for the principal pathogen involved, non-typeable Haemophilus influenzae (NTHi). The most frequently used and widely accepted experimental animal model of middle ear infection is in chinchillas, but mice and gerbils have also been used. We have established a robust model of middle ear infection by NTHi in the Junbo mouse, a mutant mouse line that spontaneously develops chronic middle ear inflammation under specific pathogen free conditions. The heterozygote Junbo mouse (Jbo/+) bears a mutation in a gene (Evi1, also known as Mecom) that plays a role in host innate immune regulation; pre-existing middle ear inflammation promotes NTHi middle ear infection. A single intranasal inoculation with NTHi produces high rates (up to 90%) of middle ear infection and bacterial titers (104 to 105 CFU/μl) in bulla fluids. Bacteria are cleared from the majority of middle ears between day 21 and 35 post-inoculation but remain in approximately 20% of middle ears at least up to day 56 post-infection. The expression of TLR-dependent response cytokine genes is elevated in the middle ear of the Jbo/+ mouse following NTHi infection. The translational potential of the Junbo model for studying antimicrobial intervention regimens was shown using a 3-day course of Azithromycin to clear NTHi infection, and its potential use in vaccine development studies by demonstrating protection in mice immunized with killed homologous, but not heterologous, NTHi bacteria.

Publisher

The Company of Biologists

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)

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