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Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei
Members of the genus Trypanosoma cause African trypanosomiasis in humans and animals in Africa. Infection of mammals by African trypanosomes is characterized by an upregulation of prostaglandin (PG) production in the plasma and cerebrospinal fluid. These metabolites of arachidonic acid (AA) may, in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193354/ https://www.ncbi.nlm.nih.gov/pubmed/11067881 |
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author | Kubata, Bruno Kilunga Duszenko, Michael Kabututu, Zakayi Rawer, Marc Szallies, Alexander Fujimori, Ko Inui, Takashi Nozaki, Tomoyoshi Yamashita, Kouwa Horii, Toshihiro Urade, Yoshihiro Hayaishi, Osamu |
author_facet | Kubata, Bruno Kilunga Duszenko, Michael Kabututu, Zakayi Rawer, Marc Szallies, Alexander Fujimori, Ko Inui, Takashi Nozaki, Tomoyoshi Yamashita, Kouwa Horii, Toshihiro Urade, Yoshihiro Hayaishi, Osamu |
author_sort | Kubata, Bruno Kilunga |
collection | PubMed |
description | Members of the genus Trypanosoma cause African trypanosomiasis in humans and animals in Africa. Infection of mammals by African trypanosomes is characterized by an upregulation of prostaglandin (PG) production in the plasma and cerebrospinal fluid. These metabolites of arachidonic acid (AA) may, in part, be responsible for symptoms such as fever, headache, immunosuppression, deep muscle hyperaesthesia, miscarriage, ovarian dysfunction, sleepiness, and other symptoms observed in patients with chronic African trypanosomiasis. Here, we show that the protozoan parasite T. brucei is involved in PG production and that it produces PGs enzymatically from AA and its metabolite, PGH(2). Among all PGs synthesized, PGF(2α) was the major prostanoid produced by trypanosome lysates. We have purified a novel T. brucei PGF(2α) synthase (TbPGFS) and cloned its cDNA. Phylogenetic analysis and molecular properties revealed that TbPGFS is completely distinct from mammalian PGF synthases. We also found that TbPGFS mRNA expression and TbPGFS activity were high in the early logarithmic growth phase and low during the stationary phase. The characterization of TbPGFS and its gene in T. brucei provides a basis for the molecular analysis of the role of parasite-derived PGF(2α) in the physiology of the parasite and the pathogenesis of African trypanosomiasis. |
format | Text |
id | pubmed-2193354 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21933542008-04-16 Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei Kubata, Bruno Kilunga Duszenko, Michael Kabututu, Zakayi Rawer, Marc Szallies, Alexander Fujimori, Ko Inui, Takashi Nozaki, Tomoyoshi Yamashita, Kouwa Horii, Toshihiro Urade, Yoshihiro Hayaishi, Osamu J Exp Med Original Article Members of the genus Trypanosoma cause African trypanosomiasis in humans and animals in Africa. Infection of mammals by African trypanosomes is characterized by an upregulation of prostaglandin (PG) production in the plasma and cerebrospinal fluid. These metabolites of arachidonic acid (AA) may, in part, be responsible for symptoms such as fever, headache, immunosuppression, deep muscle hyperaesthesia, miscarriage, ovarian dysfunction, sleepiness, and other symptoms observed in patients with chronic African trypanosomiasis. Here, we show that the protozoan parasite T. brucei is involved in PG production and that it produces PGs enzymatically from AA and its metabolite, PGH(2). Among all PGs synthesized, PGF(2α) was the major prostanoid produced by trypanosome lysates. We have purified a novel T. brucei PGF(2α) synthase (TbPGFS) and cloned its cDNA. Phylogenetic analysis and molecular properties revealed that TbPGFS is completely distinct from mammalian PGF synthases. We also found that TbPGFS mRNA expression and TbPGFS activity were high in the early logarithmic growth phase and low during the stationary phase. The characterization of TbPGFS and its gene in T. brucei provides a basis for the molecular analysis of the role of parasite-derived PGF(2α) in the physiology of the parasite and the pathogenesis of African trypanosomiasis. The Rockefeller University Press 2000-11-06 /pmc/articles/PMC2193354/ /pubmed/11067881 Text en © 2000 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Original Article Kubata, Bruno Kilunga Duszenko, Michael Kabututu, Zakayi Rawer, Marc Szallies, Alexander Fujimori, Ko Inui, Takashi Nozaki, Tomoyoshi Yamashita, Kouwa Horii, Toshihiro Urade, Yoshihiro Hayaishi, Osamu Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei |
title | Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei
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title_full | Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei
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title_fullStr | Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei
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title_full_unstemmed | Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei
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title_short | Identification of a Novel Prostaglandin F(2α) Synthase in Trypanosoma brucei
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title_sort | identification of a novel prostaglandin f(2α) synthase in trypanosoma brucei |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193354/ https://www.ncbi.nlm.nih.gov/pubmed/11067881 |
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