Vascular dysfunction in mycobacterial pathogenesis

Summary

This project will investigate the importance of vascular remodelling and leakage in fuelling tuberculosis infection

Supervisor(s)

Dr Stefan Oehlers, Professor Warwick J Britton

Research Location

Camperdown - Centenary Institute

Program Type

Masters/PHD

Synopsis

Tuberculosis is now the deadliest bacterial disease affecting the world. Our research group uses the zebrafish model system to better understand and treat this disease.
Mycobacterial infection results in the formation of complex aggregates of immune cells known as granulomas, and these can be readily visualised in zebrafish. These granulomas behave similarly to tumours in many ways including the way they recruit leaky blood vessels to the site of infection. We have shown that angiogenesis (http://dx.doi.org/10.1038/nature13967),vascular permeability
(http://dx.doi.org/10.1093/infdis/jiw355), and haemostasis (https://doi.org/10.1101/338111) aid mycobacterial growth in zebrafish infection models.
This project expands these findings by determining the effects of vascularisation on host immunity and mycobacterial physiology using a combination of zebrafish, mouse, and in vitro cell culture models of TB.

Additional Information

<html />

Want to find out more?

Contact us to find out what’s involved in applying for a PhD. Domestic students and International students

Contact Research Expert to find out more about participating in this opportunity.

Browse for other opportunities within the Camperdown - Centenary Institute .

Keywords

tuberculosis, Vascular biology, inflammation, Immunology, infection, Cell biology

Opportunity ID

The opportunity ID for this research opportunity is: 2523

Other opportunities with Dr Stefan Oehlers

Other opportunities with Professor Warwick J Britton