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The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter

Adult schistosomes are intravascular parasites that metabolize imported glucose largely via glycolysis. How the parasites get rid of the large amounts of lactic acid this generates is unknown at the molecular level. Here, we report that worms whose aquaporin gene (SmAQP) has been suppressed using RN...

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Autores principales: Faghiri, Zahra, Camargo, Simone M. R., Huggel, Katja, Forster, Ian C., Ndegwa, David, Verrey, François, Skelly, Patrick J.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862721/
https://www.ncbi.nlm.nih.gov/pubmed/20454673
http://dx.doi.org/10.1371/journal.pone.0010451
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author Faghiri, Zahra
Camargo, Simone M. R.
Huggel, Katja
Forster, Ian C.
Ndegwa, David
Verrey, François
Skelly, Patrick J.
author_facet Faghiri, Zahra
Camargo, Simone M. R.
Huggel, Katja
Forster, Ian C.
Ndegwa, David
Verrey, François
Skelly, Patrick J.
author_sort Faghiri, Zahra
collection PubMed
description Adult schistosomes are intravascular parasites that metabolize imported glucose largely via glycolysis. How the parasites get rid of the large amounts of lactic acid this generates is unknown at the molecular level. Here, we report that worms whose aquaporin gene (SmAQP) has been suppressed using RNAi fail to rapidly acidify their culture medium and excrete less lactate compared to controls. Functional expression of SmAQP in Xenopus oocytes demonstrates that this protein can transport lactate following Michaelis-Menten kinetics with low apparent affinity (Km = 41±5. 8 mM) and with a low energy of activation (E(a) = 7.18±0.7 kcal/mol). Phloretin, a known inhibitor of lactate release from schistosomes, also inhibits lactate movement in SmAQP-expressing oocytes. In keeping with the substrate promiscuity of other aquaporins, SmAQP is shown here to be also capable of transporting water, mannitol, fructose and alanine but not glucose. Using immunofluorescent and immuno-EM, we confirm that SmAQP is localized in the tegument of adult worms. These findings extend the proposed functions of the schistosome tegument beyond its known capacity as an organ of nutrient uptake to include a role in metabolic waste excretion.
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spelling pubmed-28627212010-05-07 The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter Faghiri, Zahra Camargo, Simone M. R. Huggel, Katja Forster, Ian C. Ndegwa, David Verrey, François Skelly, Patrick J. PLoS One Research Article Adult schistosomes are intravascular parasites that metabolize imported glucose largely via glycolysis. How the parasites get rid of the large amounts of lactic acid this generates is unknown at the molecular level. Here, we report that worms whose aquaporin gene (SmAQP) has been suppressed using RNAi fail to rapidly acidify their culture medium and excrete less lactate compared to controls. Functional expression of SmAQP in Xenopus oocytes demonstrates that this protein can transport lactate following Michaelis-Menten kinetics with low apparent affinity (Km = 41±5. 8 mM) and with a low energy of activation (E(a) = 7.18±0.7 kcal/mol). Phloretin, a known inhibitor of lactate release from schistosomes, also inhibits lactate movement in SmAQP-expressing oocytes. In keeping with the substrate promiscuity of other aquaporins, SmAQP is shown here to be also capable of transporting water, mannitol, fructose and alanine but not glucose. Using immunofluorescent and immuno-EM, we confirm that SmAQP is localized in the tegument of adult worms. These findings extend the proposed functions of the schistosome tegument beyond its known capacity as an organ of nutrient uptake to include a role in metabolic waste excretion. Public Library of Science 2010-05-03 /pmc/articles/PMC2862721/ /pubmed/20454673 http://dx.doi.org/10.1371/journal.pone.0010451 Text en Faghiri 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
Faghiri, Zahra
Camargo, Simone M. R.
Huggel, Katja
Forster, Ian C.
Ndegwa, David
Verrey, François
Skelly, Patrick J.
The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter
title The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter
title_full The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter
title_fullStr The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter
title_full_unstemmed The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter
title_short The Tegument of the Human Parasitic Worm Schistosoma mansoni as an Excretory Organ: The Surface Aquaporin SmAQP Is a Lactate Transporter
title_sort tegument of the human parasitic worm schistosoma mansoni as an excretory organ: the surface aquaporin smaqp is a lactate transporter
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862721/
https://www.ncbi.nlm.nih.gov/pubmed/20454673
http://dx.doi.org/10.1371/journal.pone.0010451
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