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球虫中类异戊二烯生物合成的甲基赤藓糖醇磷酸途径:存在及对磷霉素的敏感性

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

作者信息

Clastre Marc, Goubard Armelle, Prel Anne, Mincheva Zoia, Viaud-Massuart Marie-Claude, Bout Daniel, Rideau Marc, Velge-Roussel Florence, Laurent Fabrice

机构信息

EA2106 Biomolécules et Biotechnologies Végétales, UFR Sciences Pharmaceutiques, Université de Tours, 37200 Tours, France.

出版信息

Exp Parasitol. 2007 Aug;116(4):375-84. doi: 10.1016/j.exppara.2007.02.002. Epub 2007 Feb 21.

Abstract

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.

摘要

顶质体是最近发现的一种存在于大多数顶复门原虫中的类似质体的细胞器。参与类异戊二烯生物合成的甲基赤藓糖醇磷酸(MEP)途径是与顶质体相关的代谢途径之一,也是恶性疟原虫中一个新的有前景的治疗靶点。在此,我们根据基因组数据库搜索来检查四种球虫寄生虫中类异戊二烯基因的存在情况。没有质体基因组的微小隐孢子虫和人隐孢子虫缺乏MEP途径。相比之下,基因表达研究表明,该代谢途径存在于柔嫩艾美耳球虫的几个发育阶段以及刚地弓形虫的速殖子中。我们研究了一种阻断MEP途径的抗疟药物磷霉素抑制柔嫩艾美耳球虫和刚地弓形虫体外生长的潜力。即使在高浓度下,该药物的效果也很差。因此,磷霉素敏感性和类异戊二烯代谢在顶复门物种之间存在很大差异。

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