Tilley M, Fichera M E, Jerome M E, Roos D S, White M W
Department of Veterinary Molecular Biology, Montana State University, Bozeman 59717, USA.
Infect Immun. 1997 Nov;65(11):4598-605. doi: 10.1128/iai.65.11.4598-4605.1997.
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.
刚地弓形虫子孢子在宿主细胞内发育过程中形成两个寄生泡,第一个(PV1)在宿主细胞入侵时形成,第二个(PV2)在接种后18至24小时形成。PV1因其体积大而在结构上具有独特性,但它缺乏管状囊泡网络(C.A.斯皮尔、M.蒂利、M.坦普尔、J.A.布利克斯、J.P.杜比和M.W.怀特,《分子生物化学寄生虫学》75:75 - 86,1995年)。为证实子孢子具有不同的电子致密颗粒组成这一发现,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在感染后12小时首次出现。其他速殖子致密颗粒蛋白,GRA1、GRA2、GRA4、GRA5和GRA6,在卵囊提取物中被检测到,并且针对这些蛋白的抗体对子孢子细胞质中的颗粒进行了染色。然而,与速殖子入侵宿主细胞不同,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,这些蛋白仍保留在细胞质颗粒中,而不是分泌到PV1中。只有GRA5在宿主细胞入侵期间被子孢子分泌,与围绕PV1的膜结合。用荧光染料对感染子孢子的细胞进行显微注射表明,PV1对分子量低至330 Da的荧光染料是不可渗透的,这表明PV1缺乏分子可从宿主细胞质进入泡囊的通道。相比之下,荧光黄迅速扩散到PV2中,证明存在分子通道。这些研究表明PV1和PV2在形态、免疫和功能上是不同的,并且PV2似乎与速殖子泡囊相同。PV1对宿主细胞营养物质的不可接近性可能解释了为什么寄生虫复制不在这个泡囊中发生。