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Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential

To further investigate the importance of insulin signaling in the growth, development, sexual maturation and egg production of adult schistosomes, we have focused attention on the insulin receptors (SjIRs) of Schistosoma japonicum, which we have previously cloned and partially characterised. We now...

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Autores principales: You, Hong, Gobert, Geoffrey N., Cai, Pengfei, Mou, Rong, Nawaratna, Sujeevi, Fang, Guofu, Villinger, Francois, McManus, Donald P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427307/
https://www.ncbi.nlm.nih.gov/pubmed/25961574
http://dx.doi.org/10.1371/journal.pntd.0003730
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author You, Hong
Gobert, Geoffrey N.
Cai, Pengfei
Mou, Rong
Nawaratna, Sujeevi
Fang, Guofu
Villinger, Francois
McManus, Donald P.
author_facet You, Hong
Gobert, Geoffrey N.
Cai, Pengfei
Mou, Rong
Nawaratna, Sujeevi
Fang, Guofu
Villinger, Francois
McManus, Donald P.
author_sort You, Hong
collection PubMed
description To further investigate the importance of insulin signaling in the growth, development, sexual maturation and egg production of adult schistosomes, we have focused attention on the insulin receptors (SjIRs) of Schistosoma japonicum, which we have previously cloned and partially characterised. We now show, by Biolayer Interferometry, that human insulin can bind the L1 subdomain (insulin binding domain) of recombinant (r)SjIR1 and rSjIR2 (designated SjLD1 and SjLD2) produced using the Drosophila S2 protein expression system. We have then used RNA interference (RNAi) to knock down the expression of the SjIRs in adult S. japonicum in vitro and show that, in addition to their reduced transcription, the transcript levels of other important downstream genes within the insulin pathway, associated with glucose metabolism and schistosome fecundity, were also impacted substantially. Further, a significant decrease in glucose uptake was observed in the SjIR-knockdown worms compared with luciferase controls. In vaccine/challenge experiments, we found that rSjLD1 and rSjLD2 depressed female growth, intestinal granuloma density and faecal egg production in S. japonicum in mice presented with a low dose challenge infection. These data re-emphasize the potential of the SjIRs as veterinary transmission blocking vaccine candidates against zoonotic schistosomiasis japonica in China and the Philippines.
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spelling pubmed-44273072015-05-21 Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential You, Hong Gobert, Geoffrey N. Cai, Pengfei Mou, Rong Nawaratna, Sujeevi Fang, Guofu Villinger, Francois McManus, Donald P. PLoS Negl Trop Dis Research Article To further investigate the importance of insulin signaling in the growth, development, sexual maturation and egg production of adult schistosomes, we have focused attention on the insulin receptors (SjIRs) of Schistosoma japonicum, which we have previously cloned and partially characterised. We now show, by Biolayer Interferometry, that human insulin can bind the L1 subdomain (insulin binding domain) of recombinant (r)SjIR1 and rSjIR2 (designated SjLD1 and SjLD2) produced using the Drosophila S2 protein expression system. We have then used RNA interference (RNAi) to knock down the expression of the SjIRs in adult S. japonicum in vitro and show that, in addition to their reduced transcription, the transcript levels of other important downstream genes within the insulin pathway, associated with glucose metabolism and schistosome fecundity, were also impacted substantially. Further, a significant decrease in glucose uptake was observed in the SjIR-knockdown worms compared with luciferase controls. In vaccine/challenge experiments, we found that rSjLD1 and rSjLD2 depressed female growth, intestinal granuloma density and faecal egg production in S. japonicum in mice presented with a low dose challenge infection. These data re-emphasize the potential of the SjIRs as veterinary transmission blocking vaccine candidates against zoonotic schistosomiasis japonica in China and the Philippines. Public Library of Science 2015-05-11 /pmc/articles/PMC4427307/ /pubmed/25961574 http://dx.doi.org/10.1371/journal.pntd.0003730 Text en © 2015 You 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
You, Hong
Gobert, Geoffrey N.
Cai, Pengfei
Mou, Rong
Nawaratna, Sujeevi
Fang, Guofu
Villinger, Francois
McManus, Donald P.
Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential
title Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential
title_full Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential
title_fullStr Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential
title_full_unstemmed Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential
title_short Suppression of the Insulin Receptors in Adult Schistosoma japonicum Impacts on Parasite Growth and Development: Further Evidence of Vaccine Potential
title_sort suppression of the insulin receptors in adult schistosoma japonicum impacts on parasite growth and development: further evidence of vaccine potential
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427307/
https://www.ncbi.nlm.nih.gov/pubmed/25961574
http://dx.doi.org/10.1371/journal.pntd.0003730
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