首页> 美国卫生研究院文献>Infection and Immunity >Toxoplasma gondii sporozoites form a transient parasitophorous vacuole that is impermeable and contains only a subset of dense-granule proteins.
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Toxoplasma gondii sporozoites form a transient parasitophorous vacuole that is impermeable and contains only a subset of dense-granule proteins.

机译:弓形虫子孢子形成暂时的寄生虫液泡该液泡不可渗透并且仅包含致密颗粒蛋白的一个子集。

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摘要

Toxoplasma gondii sporozoites form two parasitophorous vacuoles during development within host cells, the first (PV1) during host cell invasion and the second (PV2) 18 to 24 h postinoculation. PV1 is structurally distinctive due to its large size, yet it lacks a tubulovesicular network (C. A. Speer, M. Tilley, M. Temple, J. A. Blixt, J. P. Dubey, and M. W. White, Mol. Biochem. Parasitol. 75:75-86, 1995). Confirming the finding that sporozoites have a different electron-dense-granule composition, we have now found that sporozoites within oocysts lack the mRNAs encoding the 5' nucleoside triphosphate hydrolases (NTPase). NTPase first appears 12 h postinfection. Other tachyzoite dense-granule proteins, GRA1, GRA2, GRA4, GRA5, and GRA6, were detected in oocyst extracts, and antibodies against these proteins stained granules in the sporozoite cytoplasm. In contrast to tachyzoite invasion of host cells, however, sporozoites did not exocytose the dense-granule proteins GRA1, GRA2, or GRA4 during PV1 formation. Even after NTPase induction, these proteins were retained within cytoplasmic granules rather than being secreted into PV1. Only GRA5 was secreted by the sporozoite during host cell invasion, becoming associated with the membrane surrounding PV1. Microinjection of sporozoite-infected cells with fluorescent dyes showed that PV1 is impermeable to fluorescent dyes with molecular masses as small as 330 Da, indicating that PV1 lacks channels through which molecules can pass from the host cytoplasm into the vacuole. By contrast, lucifer yellow rapidly diffused into PV2, demonstrating the presence of molecular channels. These studies indicate that PV1 and PV2 are morphologically, immunologically, and functionally distinct, and that PV2 appears to be identical to the tachyzoite vacuole. The inaccessibility of PV1 to host cell nutrients may explain why parasite replication does not occur in this vacuole.
机译:弓形虫子孢子在宿主细胞内发育期间形成两个寄生虫液泡,接种后18至24 h,第一个(PV1)和第二个(PV2)。 PV1因其尺寸大而在结构上与众不同,但缺少微管网状结构(CA Speer,M。Tilley,M。Temple,JA Blixt,JP Dubey和MW White,Mol。Biochem。Parasitol。75:75-86, 1995)。证实子孢子具有不同的电子致密颗粒组成的发现,我们现在发现卵囊内的子孢子缺乏编码5'核苷三磷酸水解酶(NTPase)的mRNA。 NTPase首先在感染后12小时出现。在卵囊提取物中还检测到其他速殖子致密颗粒蛋白GRA1,GRA2,GRA4,GRA5和GRA6,针对这些蛋白的抗体将子孢子细胞质中的颗粒染色。然而,与速殖子侵入宿主细胞相反,子孢子在PV1形成过程中并未胞吐致密颗粒蛋白GRA1,GRA2或GRA4。即使在NTPase诱导后,这些蛋白质仍保留在细胞质颗粒中,而不是分泌到PV1中。在宿主细胞侵袭过程中,子孢子仅分泌GRA5,与周围的PV1膜相关。用荧光染料显微注射子孢子感染的细胞表明,PV1对分子量小至330 Da的荧光染料是不可渗透的,这表明PV1缺少分子可以从宿主细胞质进入液泡的通道。相比之下,萤光黄迅速扩散到PV2中,表明存在分子通道。这些研究表明PV1和PV2在形态,免疫学和功能上是不同的,并且PV2似乎与速殖子液泡相同。 PV1无法吸收宿主细胞的营养素可能解释了为什么在此液泡中不会发生寄生虫复制。

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