The methylerythritol phosphate pathway for isoprenoid biosynthesis in coccidia: Presence and sensitivity to fosmidomycin

被引:34
作者
Clastre, Marc
Goubard, Armelle
Prel, Anne
Mincheva, Zoia
Viaud-Massuart, Marie-Claude
Bout, Daniel
Rideau, Marc
Velge-Roussel, Florence
Laurent, Fabrice [1 ]
机构
[1] INRA, UR1282, IASP, Equipe Controle & Immunol Malad Enter Nouveau NE, F-37380 Nouzilly, France
[2] Univ Tours, UFR Sci Pharmaceut, EA2106 Biomol & Biotechnol Vegetales, F-37200 Tours, France
[3] Univ Tours, INRA, UFR Sci Pharmaceut, UMR 483 Immunol Parasitaire & Vaccinol, F-37200 Tours, France
[4] Univ Tours, UFR Sci Pharmaceut, EA3857, Lab Synth & Physicochim Organ & Therapeut, F-37200 Tours, France
关键词
Apicomplexa; Coccidia; Cryptosporidium parutan; Cryptosporiditan hominis; Euneria tenella; Plasmoditunfialcipartun; Toxoplasina gondii; fosmidomycin; soprenoid biosynthesis;
D O I
10.1016/j.exppara.2007.02.002
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The apicoplast is a recently discovered, plastid-like organelle present in most apicomplexa. The methylerythritol phosphate (MEP) pathway involved in isoprenoid biosynthesis is one of the metabolic pathways associated with the apicoplast, and is a new promising therapeutic target in Plasmodium falciparum. Here, we check the presence of isoprenoid genes in four coccidian parasites according to genome database searches. Cryptosporidium parvum and C hominis, which have no plastid genome, lack the MEP pathway. In contrast, gene expression studies suggest that this metabolic pathway is present in several development stages of Eimeria tenella and in tachyzoites of Toxoplasma gondii. We studied the potential of fosmidomycin, an antimalarial drug blocking the MEP pathway, to inhibit E. tenella and T gondii growth in vitro. The drug was poorly effective even at high concentrations. Thus, both fosmidomycin sensitivity and isoprenoid metabolism differs substantially between apicomplexan species. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:375 / 384
页数:10
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