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TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni
Over 200 million people have, and another 600 million are at risk of contracting, schistosomiasis, one of the major neglected tropical diseases. Transmission of this infection, which is caused by helminth parasites of the genus Schistosoma, depends upon the release of parasite eggs from the human ho...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847691/ https://www.ncbi.nlm.nih.gov/pubmed/17411340 http://dx.doi.org/10.1371/journal.ppat.0030052 |
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author | Freitas, Tori C Jung, Euihye Pearce, Edward J |
author_facet | Freitas, Tori C Jung, Euihye Pearce, Edward J |
author_sort | Freitas, Tori C |
collection | PubMed |
description | Over 200 million people have, and another 600 million are at risk of contracting, schistosomiasis, one of the major neglected tropical diseases. Transmission of this infection, which is caused by helminth parasites of the genus Schistosoma, depends upon the release of parasite eggs from the human host. However, approximately 50% of eggs produced by schistosomes fail to reach the external environment, but instead become trapped in host tissues where pathological changes caused by the immune responses to secreted egg antigens precipitate disease. Despite the central importance of egg production in transmission and disease, relatively little is understood of the molecular processes underlying the development of this key life stage in schistosomes. Here, we describe a novel parasite-encoded TGF-β superfamily member, Schistosoma mansoni Inhibin/Activin (SmInAct), which is key to this process. In situ hybridization localizes SmInAct expression to the reproductive tissues of the adult female, and real-time RT-PCR analyses indicate that SmInAct is abundantly expressed in ovipositing females and the eggs they produce. Based on real-time RT-PCR analyses, SmInAct transcription continues, albeit at a reduced level, both in adult worms isolated from single-sex infections, where reproduction is absent, and in parasites from IL-7R(−/−) mice, in which viable egg production is severely compromised. Nevertheless, Western analyses demonstrate that SmInAct protein is undetectable in parasites from single-sex infections and from infections of IL-7R(−/−) mice, suggesting that SmInAct expression is tightly linked to the reproductive potential of the worms. A crucial role for SmInAct in successful embryogenesis is indicated by the finding that RNA interference–mediated knockdown of SmInAct expression in eggs aborts their development. Our results demonstrate that TGF-β signaling plays a major role in the embryogenesis of a metazoan parasite, and have implications for the development of new strategies for the treatment and prevention of an important and neglected human disease. |
format | Text |
id | pubmed-1847691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-18476912007-04-06 TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni Freitas, Tori C Jung, Euihye Pearce, Edward J PLoS Pathog Research Article Over 200 million people have, and another 600 million are at risk of contracting, schistosomiasis, one of the major neglected tropical diseases. Transmission of this infection, which is caused by helminth parasites of the genus Schistosoma, depends upon the release of parasite eggs from the human host. However, approximately 50% of eggs produced by schistosomes fail to reach the external environment, but instead become trapped in host tissues where pathological changes caused by the immune responses to secreted egg antigens precipitate disease. Despite the central importance of egg production in transmission and disease, relatively little is understood of the molecular processes underlying the development of this key life stage in schistosomes. Here, we describe a novel parasite-encoded TGF-β superfamily member, Schistosoma mansoni Inhibin/Activin (SmInAct), which is key to this process. In situ hybridization localizes SmInAct expression to the reproductive tissues of the adult female, and real-time RT-PCR analyses indicate that SmInAct is abundantly expressed in ovipositing females and the eggs they produce. Based on real-time RT-PCR analyses, SmInAct transcription continues, albeit at a reduced level, both in adult worms isolated from single-sex infections, where reproduction is absent, and in parasites from IL-7R(−/−) mice, in which viable egg production is severely compromised. Nevertheless, Western analyses demonstrate that SmInAct protein is undetectable in parasites from single-sex infections and from infections of IL-7R(−/−) mice, suggesting that SmInAct expression is tightly linked to the reproductive potential of the worms. A crucial role for SmInAct in successful embryogenesis is indicated by the finding that RNA interference–mediated knockdown of SmInAct expression in eggs aborts their development. Our results demonstrate that TGF-β signaling plays a major role in the embryogenesis of a metazoan parasite, and have implications for the development of new strategies for the treatment and prevention of an important and neglected human disease. Public Library of Science 2007-04 2007-04-06 /pmc/articles/PMC1847691/ /pubmed/17411340 http://dx.doi.org/10.1371/journal.ppat.0030052 Text en © 2007 Freitas et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Freitas, Tori C Jung, Euihye Pearce, Edward J TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni |
title | TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni
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title_full | TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni
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title_fullStr | TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni
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title_full_unstemmed | TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni
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title_short | TGF-β Signaling Controls Embryo Development in the Parasitic Flatworm Schistosoma mansoni
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title_sort | tgf-β signaling controls embryo development in the parasitic flatworm schistosoma mansoni |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1847691/ https://www.ncbi.nlm.nih.gov/pubmed/17411340 http://dx.doi.org/10.1371/journal.ppat.0030052 |
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