Schistosomiasis, a disease that afflicts 200 million people, is caused by helminth parasites of the genus Schistosoma. Schistosomes are complex metazoan pathogens that belong to an early diverging branch of the Bilateria, the Lophotrochozoans. Little is known of the molecular basis of cell to cell communication in animals in this group, but targeted studies and genome sequencing efforts have revealed that, not surprisingly, schistosomes contain some of the intercellular signaling systems that are found in higher order metazoa. Amongst these, we are particularly interested in the transforming growth factor beta (TGF beta) pathways. Elucidating the role(s) of this pathway in schistosome biology will be the goal of this proposal. Central to our view of what the TGF beta pathway might be doing in schistosomes has been our failure to identify a gene for a TGF beta ligand in these organisms, which led us to hypothesize that the TGF beta signaling pathway in schistosomes evolved to receive signals from host TGF beta ligands, a concept that was given credence by findings that schistosome TGF beta receptors can respond to human TGF beta ligands. Recently however, we made a breakthrough by identifying two schistosome TGF beta family members, SmInAct, which is a TGF beta homologue, and SmBMP, a member of the Bone Morphogenetic Protein subfamily of TGF beta ligands. Based on these published reports and our preliminary data we hypothesize that the TGF beta signaling pathway plays two distinct roles in schistosomes: 1) in embryogenesis, and 2) in the maintenance of the surface tegument. To address these hypotheses we will: 1) Explore the role of SmInAct in female reproductive potential and in embryogenesis;2) Explore the role of TGF beta ligands in schistosome tegument biology, and 3) Explore the regulation of expression of TGF beta ligands. Our ability to address these issues has improved dramatically recently through the development of techniques for inhibiting endogenous gene expression and expressing transgenes in schistosomes, and we intend to make full use of these technologies in this proposal. We believe that our proposal addresses new and novel areas of schistosome biology and has the potential to identify new targets for chemotherapy. This is important since we currently have broad access to only one drug, praziquantel, for the treatment of schistosomiasis and consequently the potential for the development of resistance to this drug must be considered high.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
7R01AI075266-06
Application #
8197242
Study Section
Special Emphasis Panel (ZRG1-IDM-H (02))
Program Officer
Mcgugan, Glen C
Project Start
2007-12-15
Project End
2013-11-30
Budget Start
2011-12-01
Budget End
2013-11-30
Support Year
6
Fiscal Year
2012
Total Cost
$372,438
Indirect Cost
$127,413
Name
Washington University
Department
Pathology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Galanti, Sarah E; Huang, Stanley Ching-Cheng; Pearce, Edward J (2012) Cell death and reproductive regression in female Schistosoma mansoni. PLoS Negl Trop Dis 6:e1509
Tran, Mai H; Freitas, Tori C; Cooper, Leanne et al. (2010) Suppression of mRNAs encoding tegument tetraspanins from Schistosoma mansoni results in impaired tegument turnover. PLoS Pathog 6:e1000840
Freitas, Tori C; Jung, Euihye; Pearce, Edward J (2009) A bone morphogenetic protein homologue in the parasitic flatworm, Schistosoma mansoni. Int J Parasitol 39:281-7