Image: RNA transfection of mother Schistosoma Mansoni sporocysts
About
FUGI /ˈfuːɡɪ/ noun: Flatworm Functional Genomics Initiative
Parasitic flatworms cause some of the most chronic infectious diseases on our planet. While existing control is primarily based on chemotherapy, there is a real risk that this strategy is unsustainable as parasites become increasingly resistant to the limited drug classes available.
To counter the risk of increasing resistance, flatworm genome sequencing projects are paving the way for the identification of novel drug targets and vaccines. However, the challenge facing researchers mining this genomic information is the lack of suitable tools to effectively characterise the function of flatworm gene products and translate them into urgently needed products.
FUGI will develop transformative functional genomics reagents and make them readily available to the academic research community by deposition in well-curated North American and European repositories. This will drawn on the team's expertise in molecular biology, cell biology and parasitology to create transgenic lines of parasitic flatworms, as well as primary and immortal cell lines, derived from the pathogens.
The new reagents developed by FUGI will enable helminthologists to keep pace with other more tractable areas of infectious disease biology and make a significant contribution to the control of parasites responsible for chronic human and animal diseases.
Partners

Karl Hoffmann
Aberystwyth University

Matthew Berriman
WT Sanger Institute

Paul Brindley
George Washington University

Klaus Brehm
University of Wuerzburg

Christoph Grevelding
Justus-Liebig University Giessen

Christoph Grunau
CNRS University of Perpignan

James Collins
UT Southwestern Medical Center

Ludovic Vallier
Cambridge University
Collaborators
External advisory boards
Contact Us
Tel: +44 (0) 1970 621830
Mon - Fri: 0900 - 1330
UK Local Time
Edward Llwyd, Penglais Campus
Aberystwyth Wales UK SY23 3DA