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微小隐孢子虫一个编码血小板反应蛋白家族新成员的基因的分子克隆与表达分析

Molecular cloning and expression analysis of a Cryptosporidium parvum gene encoding a new member of the thrombospondin family.

作者信息

Spano F, Putignani L, Naitza S, Puri C, Wright S, Crisanti A

机构信息

Istituto di Parassitologia, Università di Roma La Sapienza, Italy.

出版信息

Mol Biochem Parasitol. 1998 Apr 1;92(1):147-62. doi: 10.1016/s0166-6851(97)00243-0.

Abstract

The apicomplexan parasite Cryptosporidium parvum invades and multiplies primarily in the brush border cells of the intestinal mucosa causing in AIDS patients a severe diarrhoea that represents a significant contributing factor leading to death. Morphological analysis indicates that the invasion machinery of C. parvum is similar to the apical complex of other parasites of the phylum Apicomplexa. We provide here evidence indicating that C. parvum also shares with these parasites a molecule crucial for the invasion of host cells. We have cloned a 3894 bp-long C. parvum cDNA encoding a protein characterised by sequence and structural similarities with members of the thrombospondin (TSP) family previously described in apicomplexan parasites of the genera Toxoplasma, Eimeria and Plasmodium. This novel C. partum molecule, the TSP-related adhesive protein of Cryptosporidium-1 (TRAP-C1), is encoded by a single copy gene containing no introns. TRAP-C1 is localised in the apical end of C. parvum sporozoites and is structurally related to the micronemal proteins MIC2 of Toxoplasma and Etp100 of Eimeria, which are involved in host-cell attachment and/or invasion. The identification of TRAP-C1 sheds new light on the molecules possibly involved in the invasion process of intestinal cells by C. parvum. We have also analysed the sequence variation of TRAP-C1 among C. parvum isolates and in the closely related species C. wrairi.

摘要

顶复门寄生虫微小隐孢子虫主要在肠道黏膜的刷状缘细胞中侵入并繁殖,在艾滋病患者中引发严重腹泻,这是导致死亡的一个重要因素。形态学分析表明,微小隐孢子虫的侵入机制与顶复门其他寄生虫的顶端复合体相似。我们在此提供证据表明,微小隐孢子虫与这些寄生虫还共享一种对宿主细胞侵入至关重要的分子。我们克隆了一段3894 bp长的微小隐孢子虫cDNA,其编码的蛋白质在序列和结构上与先前在弓形虫属、艾美耳球虫属和疟原虫属的顶复门寄生虫中描述的血小板反应蛋白(TSP)家族成员相似。这种新的微小隐孢子虫分子,即隐孢子虫-1的TSP相关黏附蛋白(TRAP-C1),由一个无内含子的单拷贝基因编码。TRAP-C1定位于微小隐孢子虫子孢子的顶端,在结构上与弓形虫的微线体蛋白MIC2和艾美耳球虫的Etp100相关,它们参与宿主细胞的黏附和/或侵入。TRAP-C1的鉴定为可能参与微小隐孢子虫侵入肠道细胞过程的分子提供了新的线索。我们还分析了TRAP-C1在微小隐孢子虫分离株以及密切相关物种怀氏隐孢子虫中的序列变异。

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