The long term objective of this lab is to study development in Schistosoma mansoni, especially factors affecting the development of female worms. A central need of these studies is a marker to assess the developmental status of female worms. The enzymes involved in eggshell protein activation and cross linking are only expressed in adult, sexually active female worms. Enzymatic assays and molecular probes will be developed to monitor the expression of these enzymes. These enzymes will therefore serve as markers for female worm development. A parallel objective of this lab is to apply the knowledge gained in fundamental investigations of worm biochemistry and molecular biology to the generation of novel methods of schistosomiasis control. Schistosome eggs are of central importance in the pathology and transmission of schistosomiasis. A better understanding of the biochemical and molecular events involved in the production of eggs in the female schistosome may also lead to the development of novel chemotherapies or a schistosome vaccine. The specific research proposed in this application is to identify the enzymes involved in eggshell formation in female S. mansoni. Our working hypothesis is that eggshell formation is schistosomes uses enzymatic pathways similar to those used for eggshell formation and cuticle hardening by arthropods and mollusks; the enzymes of quinone tanning and Beta-sclerotization. The role that tyrosine hydrolase, phenol oxidase, and peroxidase play in schistosome eggshell production will be investigated. The goals of this project are 1) to determine role of peroxidase in eggshell formation; 2) to determine the role of tyrosine hydroxylase in the hydroxylation of schistosome eggshell proteins; 3) to determine the relationship of schistosome phenol oxidase to the phenol oxidases of other organisms by cloning its gene; 4) to understand the role of phenol oxidase in the hydroxylation and oxidation of schistosome eggshell proteins; and 5) to determine the stage and tissue specific expression phenol oxidase in schistosomes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15AI041197-01A1
Application #
2614898
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1998-03-01
Project End
2002-02-28
Budget Start
1998-03-01
Budget End
2002-02-28
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Illinois State University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
City
Normal
State
IL
Country
United States
Zip Code
61790
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Foulk, Bradley W; Pappas, Gus; Hirai, Yuriko et al. (2002) Adenylosuccinate lyase of Schistosoma mansoni: gene structure, mRNA expression, and analysis of the predicted peptide structure of a potential chemotherapeutic target. Int J Parasitol 32:1487-95
Alger, Heather M; Sayed, Ahmed A; Stadecker, Miguel J et al. (2002) Molecular and enzymatic characterisation of Schistosoma mansoni thioredoxin. Int J Parasitol 32:1285-92
Alger, Heather M; Williams, David L (2002) The disulfide redox system of Schistosoma mansoni and the importance of a multifunctional enzyme, thioredoxin glutathione reductase. Mol Biochem Parasitol 121:129-39
Williams, D L; Asahi, H; Botkin, D J et al. (2001) Schistosome infection stimulates host CD4(+) T helper cell and B-cell responses against a novel egg antigen, thioredoxin peroxidase. Infect Immun 69:1134-41
Kwatia, M A; Botkin, D J; Williams, D L (2000) Molecular and enzymatic characterization of Schistosoma mansoni thioredoxin peroxidase. J Parasitol 86:908-15