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GPCR and IR genes in Schistosoma mansoni miracidia

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 p...

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Autores principales: Liang, Di, Zhao, Min, Wang, Tianfang, McManus, Donald P., Cummins, Scott F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080760/
https://www.ncbi.nlm.nih.gov/pubmed/27784323
http://dx.doi.org/10.1186/s13071-016-1837-2
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author Liang, Di
Zhao, Min
Wang, Tianfang
McManus, Donald P.
Cummins, Scott F.
author_facet Liang, Di
Zhao, Min
Wang, Tianfang
McManus, Donald P.
Cummins, Scott F.
author_sort Liang, Di
collection PubMed
description 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1837-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-50807602016-10-31 GPCR and IR genes in Schistosoma mansoni miracidia Liang, Di Zhao, Min Wang, Tianfang McManus, Donald P. Cummins, Scott F. Parasit Vectors Research 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-016-1837-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-26 /pmc/articles/PMC5080760/ /pubmed/27784323 http://dx.doi.org/10.1186/s13071-016-1837-2 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Liang, Di
Zhao, Min
Wang, Tianfang
McManus, Donald P.
Cummins, Scott F.
GPCR and IR genes in Schistosoma mansoni miracidia
title GPCR and IR genes in Schistosoma mansoni miracidia
title_full GPCR and IR genes in Schistosoma mansoni miracidia
title_fullStr GPCR and IR genes in Schistosoma mansoni miracidia
title_full_unstemmed GPCR and IR genes in Schistosoma mansoni miracidia
title_short GPCR and IR genes in Schistosoma mansoni miracidia
title_sort gpcr and ir genes in schistosoma mansoni miracidia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080760/
https://www.ncbi.nlm.nih.gov/pubmed/27784323
http://dx.doi.org/10.1186/s13071-016-1837-2
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