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刚地弓形虫的子孢子缺乏致密颗粒蛋白GRA3,并形成独特的寄生泡。

Sporozoites of Toxoplasma gondii lack dense-granule protein GRA3 and form a unique parasitophorous vacuole.

作者信息

Speer C A, Tilley M, Temple M E, Blixt J A, Dubey J P, White M W

机构信息

Department of Veterinary Molecular Biology, Montana State University, Bozeman 59717, USA.

出版信息

Mol Biochem Parasitol. 1995 Dec;75(1):75-86. doi: 10.1016/0166-6851(95)02515-4.

Abstract

The invasion of host cells by sporozoites of Toxoplasma gondii leads to the formation of parasitophorous vacuoles that are distinctly different from those surrounding tachyzoites. In sporozoite-infected cells, the fluid-filled space surrounding the sporozoite is many times larger in volume than the sporozoite, essentially lacks granular or tubular structures, and has no detectable continuous parasitophorous vacuolar membrane when prepared by conventional electron microscopic methods. Consistent with the ultrastructural differences, dense-granule protein GRA3, which associates with the parasitophorous vacuolar membrane of tachyzoites, was not detected by indirect immunofluorescence in sporozoite-infected cells 2-12 h post-inoculation or by Western blot analysis of sporozoite extracts. Western blots incubated with the alpha ROP/DG antiserum, which recognizes tachyzoite rhoptry and dense-granule proteins, revealed numerous other antigenic differences between sporozoites and tachyzoites. Cell cultures inoculated with sporozoites were monitored at various intervals for the expression of GRA3 and the developmentally-regulated tachyzoite surface protein SAG1. Expression of SAG1 and GRA3 was first observed in 30% of the sporozoite-infected cells at 12 and 15 h post-inoculation, respectively, and in all intracellular parasites at 24 h. Parasite replication was only observed in sporozoite-infected cells that were positive for GRA3 and SAG1. Thus, these data indicate that sporozoites and their interaction with host cells differ substantially from tachyzoites and the expression of tachyzoite-specific proteins is likely required for parasite replication.

摘要

刚地弓形虫的子孢子侵入宿主细胞会导致形成与速殖子周围的空泡明显不同的纳虫空泡。在子孢子感染的细胞中,围绕子孢子的充满液体的空间体积比子孢子大许多倍,基本上没有颗粒状或管状结构,并且用传统电子显微镜方法制备时未检测到连续的纳虫空泡膜。与超微结构差异一致,与速殖子的纳虫空泡膜相关的致密颗粒蛋白GRA3,在接种后2 - 12小时的子孢子感染细胞中通过间接免疫荧光未检测到,在子孢子提取物的蛋白质免疫印迹分析中也未检测到。用识别速殖子棒状体和致密颗粒蛋白的αROP/DG抗血清孵育的蛋白质免疫印迹显示,子孢子和速殖子之间存在许多其他抗原差异。对接种子孢子的细胞培养物在不同时间间隔监测GRA3和发育调控的速殖子表面蛋白SAG1的表达。SAG1和GRA3的表达分别在接种后12小时和15小时首次在30%的子孢子感染细胞中观察到,在24小时时在所有细胞内寄生虫中观察到。仅在GRA3和SAG1呈阳性的子孢子感染细胞中观察到寄生虫复制。因此,这些数据表明,子孢子及其与宿主细胞的相互作用与速殖子有很大不同,寄生虫复制可能需要速殖子特异性蛋白的表达。

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