Description
The gastrointestinal bacterial pathogens enteropathogenic E. coli (EPEC) and Shigella translocate virulence proteins, termed "effector proteins", into host cells via specialised protein secretion systems. Many of the effectors interfere with host innate immune signalling pathways that lead to inflammation and cell death. In diseases such as inflammatory bowel disease (IBD), these pathways are often dysregulated leading to chronic inflammation. In this way, pathogens can be used as tools to understand the mucosal innate immune response. The aim of this project is to utilise patient-derived gut organoid models to study infection induced mechanisms of mucosal damage and to understand the processes leading to epithelial barrier repair. This work has relevance to chronic intestinal disorders such as Crohn's disease and may inform the development of therapeutics to treat a range of intestinal conditions.
Essential criteria:
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords
microbiology, inflammation, cellular biology, innate immunity, bacterial diseases
School
School of Clinical Sciences at Monash Health / Hudson Institute of Medical Research » Molecular and Translational Sciences
Available options
PhD/Doctorate
Masters by research
Honours
Time commitment
Full-time
Top-up scholarship funding available
No
Physical location
Monash Health Translation Precinct (Monash Medical Centre)
Research webpage
Co-supervisors
Dr
Cristina Giogha
(External)
Dr
Eva Chan
(External)