100% of home tuition fees paid and annual stipend (living expenses) of £19,237. International candidates will be required to fund the difference between home fees and international fees.
Cystic fibrosis (CF) is a genetic condition affecting 1 in 2500 babies in the UK. Disruption in chloride secretion results in build-up of thick mucus in the lungs, trapping bacteria and promoting their growth. Staphylococcus aureus (Sa) is one of the earliest infections in the lungs of children with CF. Sa persists for many years in the CF lung environment.
Sa uses the type VII secretion system (T7SS) to secrete antibacterial toxins that target competitor bacteria. The T7SS and its toxins are strongly linked with colonisation. We hypothesise that the CF lung environment, and co-infecting bacteria, modulate activity of the Sa T7SS.
You will engineer GFP promoter fusions to assess T7SS ‘switching on’ in response to the CF environment, clinically relevant antibiotics and presence of other bacteria. You will assess ability of Sa wild type, T7SS mutants and secreted toxin mutants to form biofilms with other CF pathogens, in particular Pseudomonas aeruginosa (Pa), looking at spatial localisation and survival in the biofilm. You will determine how Sa interacts with airway commensals and whether/how they modulate Sa/Pa interactions.
Number of awards
1
Start date
15th September 2025
Award duration
The funding covers a three-year PhD
Application closing date
17th January 2025
Sponsor
LifeArc/CF Trust
Name of supervisor/s
Professor Tracy Palmer
You must have, or expect to achieve, at least a 2:1 honours degree or international equivalent, in a subject relating to biomedical sciences, including biochemistry/microbiology. Further qualification such as an MRes is advantageous.
You must apply through the University’s Apply to Newcastle Portal.
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You must submit one application per studentship, you cannot apply for multiple studentships on one application.
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