Functional Genomic Analysis of Exported DNA J Molecules in the Malaria Parasite Plasmodium falciparum [ 2007 - 2010 ]

Research Grant

Researchers: A/Pr Alexander Maier (Principal investigator) ,  Dr Melanie Rug

Brief description Every day 3500 people die of malaria and more than 40% of the world s population is at risk. Malaria is one of the biggest scourges of mankind. This project aims to translate the available genomic data into functional insights using frontier technology to identify new intervention targets for P. falciparum infection. Developing novel targets against malaria is important from a humanitarian point of view, and also to safeguard Australia and its neighbouring regions against the social and economical implication of this disease. The malaria parasite seeks shelter from the host immune system by hiding in red blood cells, but at the same time it has to stay in contact with the blood environment. This is achieved by export of virulence factors onto the surface of malaria parasite-infected red blood cells, which are essential for the maintenance of malaria infection. Without these virulence factors the body's immune system can get rid of the malaria parasites by itself. For display on the surface the proteins have to pass several membranes and are transferred through the red blood cell. The whole transport and assembly process of the virulence factors into functional units is very complex and requires several helper and co-helper molecules. With the deciphering of the malarial genetic code it became obvious that the parasite displays an unusual large number of co-helper molecules, which are putatively exported into the red blood cell. We will generate transgenic parasites deficient in the expression of these exported co-helper proteins and assess their role on the pathogenesis of this debilitating infectious disease.

Funding Amount $AUD 529,698.29

Funding Scheme NHMRC Project Grants

Notes New Investigator Grant