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Field
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, such as asthma, non-invasive infections such as chronic pulmonary aspergillosis (CA) or aspergilloma, or life-threatening systemic infections, such as invasive aspergillosis (IA). Late diagnosis, limited
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weapon against bacterial infections. These naturally occurring viruses selectively destroy harmful bacteria, offering hope where antibiotics fail. Yet a major challenge remains: how do we use phage
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Department of Nuclear Medicine and Molecular Imaging, who is one of the partners of PREFERENCE and work on the topic of detection of early-stage infection and inflammation. Your role: You will pursue research
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A PhD studentship is available for commencement October 2026 – January 2027 as part of the first Cohort of a new EPSRC Centre for Doctoral Training in UK Semiconductor Industry Future Skills* led by Swansea University in partnership with the University of Leeds. The PhD studentship will be: 4...
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. The position is part of a newly funded Wellcome Leap Focused Antibiotics project developing nanoparticle-mediated antibiotic delivery systems for site-directed treatment of infection while protecting the gut
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physiological state shapes bacteriophage infection. We aim to determine how dormancy, nutrient limitation, growth transitions and stress generate transient phage resistance or tolerance, identify the underlying
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to modern medicine, and bacteriophage therapy is a promising route to treat drug-resistant infections. Yet phage therapy can fail when bacteria evolve resistance or deploy defence systems that block
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to modern medicine, and bacteriophage therapy is a promising route to treat drug-resistant infections. Yet phage therapy can fail when bacteria evolve resistance or deploy defence systems that block
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immunomodulatory compound, you will determine how it reprograms host lipid pathways to boost immunity and eliminate infection. Using lipidomics, zebrafish models and clinical samples, this research will identify
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infection context from hundreds of thousands scientific publications, with comparative bacterial genomics, to identify molecular signatures of host switches. Integrating these complementary approaches will