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WHAT WE FUND

Cystic Fibrosis

Respiratory diseases

At a glance

Exploiting novel technologies to identify respiratory pathogens and characterise bacterial interactions in patients with cystic fibrosis

Lead researcher

Dr Jo Fothergill

Institution

University of Liverpool

Status

Completed

Amount awarded

£309,696.00

Last updated

08/01/24

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A fellowship to determine if new technology can be used to identify bacteria in the nasal passageway by analysing respiratory samples from the lungs of patients with cystic fibrosis (CF). Dr Fothergill will also look at how these infecting bacteria interact and look for genes that might make them resistant to antibiotics. We hope that this could lead to better, earlier and more targeted treatments to improve long-term outcomes for people living with CF.

Lung infections in patients with CF have been shown to have lots of different bugs that can survive despite antibiotics. We don’t know, however, how the different bugs interact with one another, how they survive antibiotics and what impact this has on patients with CF.

If infection is detected early, aggressive antimicrobial treatment can clear it, but any later, treatments are only able to keep infection at bay. It is thought that bacteria may initially live in the nose and sinuses before they move into the lungs and cause infection. Dr Jo Fothergill from the University of Liverpool was awarded a fellowship to determine if new technology can be used to identify bacteria in the nasal passageway by analysing respiratory samples from the lungs of patients with CF. She will also look at how these infecting bacteria interact and look for genes that might make them resistant to antibiotics – a devastating complication for CF patients. We hope that developing new diagnostic approaches for the earlier detection of infection and the rapid identification of antibiotic resistant bacteria could lead to better, earlier and more targeted treatments which will improve long-term outcomes for people living with CF.

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Respiratory Diseases - ​Cystic Fibrosis

  • Why there is a need to fund new research

    Cystic Fibrosis (CF) is a  rare lung disease with a poor prognosis. Its incidence varies across the globe and in the European Union 1 in 2,000-3,000 new-borns are affected. CF is a genetic disorder caused by mutations in a gene that leads to the build-up of abnormally thick mucus in the bodies’ passageways, in particular in the lining of the lungs. The mucus provides a favourable environment for bacteria to grow and increases the susceptibility of CF patients to fatal lung infections.

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