To aid in the development of prevention and control measures for schistosomiasis (caused by blood flukes Schistosoma mansoni and Schistosoma haematobium, which are major causes of hepatic and urinary tract disease in Africa and the Middle East), a serologic test of human exposure to the infectious larvae of the parasite will be developed based on a protease antigen released at the initial stage of human infection by cercaria. Recently isolated cDNAs coding for both the S. mansoni and S. haematobium protease antigens will be expressed in E. coli or yeast to provide a standardized source of antigen protein for an ELISA-based test. The antigens from each individual species, as well as a combination of the two, will be evaluated to optimize detection. Once the optimal antigen preparation is identified, a longitudinal field study will be carried out to evaluate the efficacy of the ELISA-based assay. This work will be a collaboration between laboratories at the University of California, San Francisco, and Ain Shams University in Cairo, Egypt. The field trials will be carried out in the Nile Delta region, where both infections are highly endemic. Development of this assay will provide a necessary tool to identify foci of drug resistance, evaluate therapeutic efficacy, identify new outbreaks of disease, and evaluate potential anti-schistosomal vaccines.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Research Grants (R03)
Project #
5R03AI041466-02
Application #
2673020
Study Section
Microbiology and Infectious Diseases B Subcommittee (MID)
Project Start
1997-09-30
Project End
1999-08-31
Budget Start
1998-09-01
Budget End
1999-08-31
Support Year
2
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Pathology
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Newcomb, William W; Homa, Fred L; Brown, Jay C (2005) Involvement of the portal at an early step in herpes simplex virus capsid assembly. J Virol 79:10540-6