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Glyceroneogenesis: An unexpected metabolic pathway for glutamine in Schistosoma mansoni sporocysts

Authors :
Christine Coustau
Carine Zitoun
Colette Dissous
Naji Khayath
Aloysius G.M. Tielens
Jérôme Vicogne
Gilles Mithieux
Source :
Molecular and Biochemical Parasitology. 147:145-153
Publication Year :
2006
Publisher :
Elsevier BV, 2006.

Abstract

To date, glyceroneogenesis has only been described in mammals but we demonstrate in this paper that it could exist in the invertebrate Schistosoma mansoni, the parasitic helminth transmitted by fresh water molluscs and responsible for the major human endemic disease, schistosomiasis. Glyceroneogenesis is a phosphoenolpyruvate carboxykinase (PEPCK)-dependent process by which glycerol can be produced from precursors like glutamine and therefore represents a truncated gluconeogenic pathway. We have previously demonstrated the possible central role of glutamine in mollusc-schistosome interactions. In this work, we show that glutamine effectively promotes in vitro survival and protein synthesis in sporocysts, the intramolluscan larval stages of S. mansoni, possibly through its role as an energy source. However, the demonstration that PEPCK is massively expressed in these larval forms as compared to adult parasites, together with the observation that 3-mercaptopicolinate, a specific inhibitor of PEPCK, significantly reduces the effect of glutamine on sporocyst growth, suggest that glutamine could also be used for glucose or glycerol production. Results of [14C] glutamine incorporation confirmed that neosynthesis of glucose and mainly of glycerol occurred in sporocysts and was dependent on PEPCK activity. Therefore, our results strongly indicate that glyceroneogenesis could exist in schistosomes. Several hypotheses can be proposed concerning the importance of glycerol for the adaptation of this helminth to its host osmotic and energetic environment.

Details

ISSN :
01666851
Volume :
147
Database :
OpenAIRE
Journal :
Molecular and Biochemical Parasitology
Accession number :
edsair.doi.dedup.....bd14285f6d4700f8bbe66b36fa487fe2
Full Text :
https://doi.org/10.1016/j.molbiopara.2006.02.002