GPCR and IR genes in Schistosoma mansoni miracidia

Parasites & Vectors

Scott F. Cummins¹  Min Zhao¹  Di Liang¹  Tianfang Wang¹  Donald P. McManus² 

[1] Faculty of Science, Health and Education, University of the Sunshine Coast;Molecular Parasitology Laboratory, QIMR Berghofer Medical Research Institute;

关键词: Schistosoma mansoni;    G protein-coupled receptor;    Ionotropic receptor;    Biomphalaria glabrata;   

DOI  :  10.1186/s13071-016-1837-2

来源: DOAJ

【 摘 要 】

Abstract Background Schistosoma species are responsible for the disease schistosomiasis, a highly prevalent helminthic disease that requires a freshwater snail as intermediate host. The S. mansoni free-living miracidium must utilize olfaction to find a suitable snail host, and certain types of rhodopsin G protein-coupled receptors (GPCRs) and ionotropic receptors (IRs) have been identified as olfactory receptors in other animal phyla. The Schistosoma genome project, together with the recent availability of proteomic databases, allowed for studies to explore receptors within S. mansoni, some of which may contribute to host finding. Results We have identified 17 rhodopsin-type GPCR sequences in S. mansoni belonging to four subclasses, including ligand-specific GPCRs (i.e. neuropeptide and opsin). RT-PCR demonstrated the expression of nine out of the 17 GPCRs in the free-living miracidia, each of which have been characterized for homology to S. haematobium. Among the nine GPCRs, two are predicted as Gq-opsins. We also describe the characterization of a Schistosoma-encoded IR based on similarity with other species IR and conservation of IR-like domains. Schistosoma mansoni IR is expressed in miracidia at 3 and 6 h post-hatch. Conclusions The identification of receptors in S. mansoni miracidia, presented here, contributes not only to further understanding of Schistosoma biology and signal transduction but also provides a basis for approaches that may modify parasite behaviour.

【 授权许可】

Unknown