Hildebrand H F
Z Parasitenkd. 1976 Jun 10;49(3):193-215. doi: 10.1007/BF00380590.
The fine structure of the epimerite and the protomerite of D. gigantea was investigated following the different stages of the evolution of the trophozoite. The first stage is mononucleate and very poor of cytoplasmic structures (Fig. 1). All following stages are polynucleate (Fig. 3). The septum between protomerite and deutomerite appears at the third stage (Fig. 22). The body of the gregarine is in all stages surrounded by a thick cell-wall constituted of three membranes. The limit between epimerite and protomerite is indicated by the existence of an osmiophilic basal ring just under the parasite's cell-wall. This basal ring has a transverse substructure with a periodical distance of 450 A (Fig. 12). The two inner membranes join together just beneath the basal ring, whereas the outer membrane continues and forms the single cell membrane of the epimerite (Fig.9). The epimerite displays a large number of microvillosities and evaginations of the membrane which increase considerably its surface (Figs. 11-14). The epimerite essentially contains ribosomes and mitochondria (Fig.6). The protomerite contains in addition to the usual cell organites cytoplasmic agglomerations consisting of endoplasmic reticulum, ribonucleoprotein and peripheric mitochondria. During evolution from stage IV to V, these agglomerations produce osmiophilic granula of different form and size, most of which are surrounded by an elementary membrane (Fig. 18). Beside these granula one can observe sometimes small spherical or lamellar structures (Fig. 21). Large bundles of microtubules run from the protomerite into the epimerite where they generally branch off and penetrate into the mitochondrial layer (Figs. 6, 19, 20). Between the parasite and the host-cell exists a space, the periparasitic space, without any cytoplasmic inclusions. The cell membrane of the host-cell has in the periparasitic space an outer cell-coat with a ripped pattern (Fig. 13). The microvillosities of the cell membrane disappear at this place. The host-cell cytoplasm displays a large number of microtubules and a fibrillar network (Figs. 13, 14). The importance of these structures for the relationship between parasite and host-cell is discussed.
随着巨型双核变形虫滋养体进化的不同阶段,对其附着器和原虫体的精细结构进行了研究。第一阶段为单核,细胞质结构非常少(图1)。所有后续阶段均为多核(图3)。原虫体和后虫体之间的隔膜出现在第三阶段(图22)。在所有阶段,簇虫的身体都被由三层膜构成的厚细胞壁包围。附着器和原虫体之间的界限由寄生虫细胞壁正下方存在的嗜锇基环表明。这个基环具有横向亚结构,周期距离为450埃(图12)。两层内膜在基环正下方连接在一起,而外膜继续延伸并形成附着器的单细胞膜(图9)。附着器显示出大量的微绒毛和膜的外翻,这大大增加了其表面积(图11 - 14)。附着器主要含有核糖体和线粒体(图6)。原虫体除了通常的细胞器外,还含有由内质网、核糖核蛋白和周边线粒体组成的细胞质团聚物。在从第四阶段到第五阶段的进化过程中,这些团聚物产生了不同形状和大小的嗜锇颗粒,其中大部分被一层基本膜包围(图18)。除了这些颗粒外,有时还可以观察到小球形或层状结构(图21)。大量微管束从原虫体延伸到附着器,在那里它们通常分支并穿透线粒体层(图6、19、20)。在寄生虫和宿主细胞之间存在一个空间,即寄生虫周围空间,没有任何细胞质内含物。宿主细胞膜在寄生虫周围空间有一个呈撕裂图案的外细胞被(图13)。细胞膜的微绒毛在这个位置消失。宿主细胞细胞质显示出大量微管和纤维网络(图13、14)。讨论了这些结构对寄生虫与宿主细胞关系的重要性。