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刚地弓形虫缓殖子和裂殖子中的一种新型棒状体蛋白。

A novel rhoptry protein in Toxoplasma gondii bradyzoites and merozoites.

作者信息

Schwarz Jodi A, Fouts Ashley E, Cummings Craig A, Ferguson David J P, Boothroyd John C

机构信息

Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, USA.

出版信息

Mol Biochem Parasitol. 2005 Dec;144(2):159-66. doi: 10.1016/j.molbiopara.2005.08.011. Epub 2005 Sep 8.

Abstract

The secretory organelles of Toxoplasma gondii orchestrate invasion of the host cell and establish the parasitophorous vacuole. Although much has been learned about the roles played by these organelles in invasion by the tachyzoite stage, little is known about the contents or functions of these organelles during bradyzoite development or pathogenesis. We identified a novel protein that localizes to the rhoptries of the bradyzoite stage, but is absent from the tachyzoite stage. This protein, BRP1, first appears in the nascent rhoptries during the first division of bradyzoite stage development. We observed secretion of BRP1 and other rhoptry proteins into the parasitophorous vacuole during bradyzoite development in vitro, but there was no evidence that this occurs in vivo. Brp1 knockout parasites did not appear to have any developmental or growth defects in vitro, and were able to establish infections in mice both as tachyzoites (via intraperitoneal injection of in vitro-derived tachyzoites) or bradyzoites (via oral gavage using cysts harvested from mouse brain). Mice infected using brain cysts from the brp1 knockout or the control strain developed similar numbers and sizes of brain cysts. Thus BRP1 does not appear to play an essential role in development of the bradyzoite stage, development of brain cysts, or oral infection of new hosts, at least in the mouse model used here. Since we also observed that BRP1 is expressed in the merozoite stages in the gut of infected cats, the coccidian phase of the life cycle may be where BRP1 plays its most important role.

摘要

刚地弓形虫的分泌细胞器协调对宿主细胞的侵袭并形成寄生泡。尽管对于这些细胞器在速殖子阶段侵袭过程中所起的作用已了解很多,但对于这些细胞器在缓殖子发育或发病机制中的内容物或功能却知之甚少。我们鉴定出一种新蛋白,它定位于缓殖子阶段的棒状体,但在速殖子阶段不存在。这种蛋白,即BRP1,在缓殖子阶段发育的第一次分裂期间首次出现在新生的棒状体中。我们观察到在体外缓殖子发育过程中BRP1和其他棒状体蛋白分泌到寄生泡中,但没有证据表明这在体内发生。敲除Brp1的寄生虫在体外似乎没有任何发育或生长缺陷,并且能够作为速殖子(通过腹腔注射体外培养的速殖子)或缓殖子(通过口服使用从小鼠脑中收获的包囊)在小鼠中建立感染。使用来自敲除brp1的小鼠或对照菌株的脑包囊感染的小鼠,其脑包囊的数量和大小相似。因此,至少在这里使用的小鼠模型中,BRP1似乎在缓殖子阶段的发育、脑包囊的形成或新宿主的口服感染中不发挥重要作用。由于我们还观察到BRP1在受感染猫肠道中的裂殖子阶段表达,因此生命周期的球虫阶段可能是BRP1发挥其最重要作用的地方。

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