Schistosomes and other snail-transmitted parasites persist as significant public health problems, particularly in children and women, across much of the developing world. The use by these parasites of freshwater snails as intermediate hosts makes control very difficult. We need to develop a broader base of knowledge regarding these parasites, particularly in light of recent concerns about the potential evolution among schistosomes of resistance to praziquantel. This proposal focuses on the interactions between two trematodes, Schistosoma mansoni and Echinostoma paraensei, and their molluscan host Biomphalaria glabrata, with the goal of obtaining a deeper understanding of how these parasites establish infections in snails, and more importantly, how the snail can overcome these infections. Capitalizing on discoveries made during our previous funding period, we intend to further characterize the structure, diversity and genomic organization of members of a family of B. glabrata blood proteins termed fibrinogen-related proteins or FREPs, that have several attributes that make them likely candidates as non-self recognition molecules in B. glabrata. As such, they may be key regulators of the molluscan response to trematode infection and become particularly useful in future attempts to develop transgenic snails resistant to schistosome infection. Because FREPs exist in a multigene family and are invertebrate members of the immunoglobulin superfamily, they also provide a unique model to study the evolution of invertebrate immune responses. Also outlined are experiments to characterize the molecules used by trematode larvae in affecting host defense cells (hemocytes) and to identify hemocyte molecules that are targeted for attack. Finally, we propose to examine a model system in which snails can be provoked to develop acquired resistance to trematode infection. We will apply the tools and insights developed in recent years to this model to reveal the factors most closely linked to the resistant state. These studies will provide novel insights pertaining to both basic and applied aspects of schistosome (trematode) biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI024340-17
Application #
6627975
Study Section
Special Emphasis Panel (ZRG1-TMP (02))
Program Officer
Aultman, Kathryn S
Project Start
1986-12-01
Project End
2005-01-31
Budget Start
2003-02-01
Budget End
2004-01-31
Support Year
17
Fiscal Year
2003
Total Cost
$245,211
Indirect Cost
Name
University of New Mexico
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
868853094
City
Albuquerque
State
NM
Country
United States
Zip Code
87131
Hanington, Patrick C; Forys, Michelle A; Loker, Eric S (2012) A somatically diversified defense factor, FREP3, is a determinant of snail resistance to schistosome infection. PLoS Negl Trop Dis 6:e1591
Loker, Eric S (2012) Macroevolutionary Immunology: A Role for Immunity in the Diversification of Animal life. Front Immunol 3:25
Hanington, Patrick C; Zhang, Si-Ming (2011) The primary role of fibrinogen-related proteins in invertebrates is defense, not coagulation. J Innate Immun 3:17-27
Hanington, Patrick C; Lun, Cheng-Man; Adema, Coen M et al. (2010) Time series analysis of the transcriptional responses of Biomphalaria glabrata throughout the course of intramolluscan development of Schistosoma mansoni and Echinostoma paraensei. Int J Parasitol 40:819-31
Hanington, Patrick C; Forys, Michelle A; Dragoo, Jerry W et al. (2010) Role for a somatically diversified lectin in resistance of an invertebrate to parasite infection. Proc Natl Acad Sci U S A 107:21087-92
Hathaway, Jennifer J M; Adema, Coen M; Stout, Barbara A et al. (2010) Identification of protein components of egg masses indicates parental investment in immunoprotection of offspring by Biomphalaria glabrata (gastropoda, mollusca). Dev Comp Immunol 34:425-35
Adema, Coen M; Hanington, Patrick C; Lun, Cheng-Man et al. (2010) Differential transcriptomic responses of Biomphalaria glabrata (Gastropoda, Mollusca) to bacteria and metazoan parasites, Schistosoma mansoni and Echinostoma paraensei (Digenea, Platyhelminthes). Mol Immunol 47:849-60
Loker, Eric S (2010) Gastropod immunobiology. Adv Exp Med Biol 708:17-43
Zhang, Si-Ming; Nian, Hong; Wang, Bo et al. (2009) Schistosomin from the snail Biomphalaria glabrata: expression studies suggest no involvement in trematode-mediated castration. Mol Biochem Parasitol 165:79-86
Adema, Coen M; Luo, Mei-Zhong; Hanelt, Ben et al. (2006) A bacterial artificial chromosome library for Biomphalaria glabrata, intermediate snail host of Schistosoma mansoni. Mem Inst Oswaldo Cruz 101 Suppl 1:167-77

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