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Understanding Staphylococcus capitis Skin Colonisation in Atopic Dermatitis

University of Birmingham Department of Microbes, Infections and Microbiomes
✓ Funded (Competition) 🎓 Microbiology 🎓 Molecular Biology staphylococcus capitis atopic dermatitis skin microbiome bacterial adhesion molecular mechanisms microbiome dysbiosis chronic inflammation

Investigate how Staphylococcus capitis colonises skin and its role in atopic dermatitis. Characterise bacterial factors influencing skin adhesion and disease mechanisms to uncover new therapeutic targets for chronic inflammatory skin disease.

AI-generated overview

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Why This Research Matters

This research will improve understanding of microbial influences on atopic dermatitis, a widespread and painful skin condition. By elucidating how Staphylococcus capitis colonises skin and contributes to disease, it may guide innovative treatments that reduce inflammation and improve patient quality of life.

Staphylococcus capitis Atopic Dermatitis Skin Colonisation Microbiome Dysbiosis Bacterial Adhesion Inflammatory Skin Disorder

Project Description

Project Overview

Atopic dermatitis is a chronic inflammatory skin condition marked by painful, itchy lesions and a disrupted skin microbiome. This project focuses on Staphylococcus capitis, found on the skin of 40% of adults with moderate atopic dermatitis, investigating how it colonises the stratum corneum and affects skin biology. Previous work has identified key adhesive proteins mediating Staphylococcus aureus interactions but little is known about S. capitis colonisation strategies.

What You Will Do

The project will explore molecular mechanisms that enable S. capitis to adhere to and colonise the skin's outermost layer, characterising bacterial surface factors and their interactions with skin proteins. Functional assays, microbiological and molecular biology techniques will be employed to elucidate bacterial factors driving colonisation and their role in atopic dermatitis pathology.

Expected Outcomes

The research expects to identify novel bacterial determinants of S. capitis adhesion and colonisation, contributing to better understanding of skin microbiome dysbiosis in atopic dermatitis. This may highlight new targets for therapeutic intervention to modulate skin colonisation and inflammation.

Why This Matters

Understanding how S. capitis colonises skin and influences atopic dermatitis progression addresses a key gap in knowledge about skin microbiota’s role in chronic inflammatory diseases. Insights could inform development of improved treatments for atopic dermatitis, a common and debilitating condition affecting millions worldwide.

Eligibility

UK/Home
EU
International

Supervisor Profile

PJ
Prof Joan Geoghegan
University of Birmingham, Department of Microbes, Infections and Microbiomes
9677 Citations
48 h-index
Google Scholar

Prof Joan Geoghegan is a leading microbiologist at the University of Birmingham specializing in the bacterial surface proteins of Staphylococcus aureus and their roles in infection and immune evasion. Her research combines molecular microbiology and immunology to understand host-pathogen interactions in skin infections. She has a significant impact with numerous highly cited publications in the field.

Key Publications

2023 742 citations
Molecular medical microbiology
2018 618 citations
Staphylococcus aureus and atopic dermatitis: a complex and evolving relationship
2014 345 citations
Protein-based biofilm matrices in Staphylococci
2010 309 citations
Role of Surface Protein SasG in Biofilm Formation by Staphylococcus aureus
2016 247 citations
CRIg functions as a macrophage pattern recognition receptor to directly bind and capture blood-borne gram-positive bacteria

Research Contributions

Characterization of Staphylococcus aureus surface proteins involved in adhesion, invasion, and immune evasion.
Improved understanding of bacterial pathogenesis mechanisms provides targets for therapeutic interventions.
Investigation of biofilm formation by Staphylococcus aureus focusing on the role of surface proteins like SasG.
Insights gained aid in developing strategies to prevent biofilm-related infections.
Study of Staphylococcus aureus interactions with the immune system, including macrophage recognition receptors.
Enhanced knowledge of host-pathogen interactions informs vaccine and treatment development.

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