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柔嫩艾美耳球虫在细胞培养中第一代裂殖生殖期间细胞质和细胞核变化的超微结构

Ultrastructure of cytoplasmic and nuclear changes in Eimeria tenella during first-generation schizogony in cell culture.

作者信息

Pacheco N D, Vetterling J M, Doran D J

出版信息

J Parasitol. 1975 Feb;61(1):31-42.

PMID:1167908
Abstract

Eimeria tenella sporozoites were inoculated into primary cultures of chick kidney cells. Cells fixed from 1 1/2 to 54 hr later were examined with the electron microscope. At 1 1/2 and 24 hr, most intracellular sporozoites were fusiform and retained organelles typical of extracellular sporozoites. However, at 35 hr, rounded trophozoites were present without these structures; only a refractile body, nucleus, mitochondria, and endoplasmic reticulum remained. Binucleate parasites were also present at that time, but at 48 hr many multinucleate schizonts were present. Nuclei, with adjacent conoids, were at the periphery of these schizonts. Partly developed merozoites, each containing a conoid and a nucleus, protruded into the parasitophorous vacuole. At 54 hr, fully developed merozoites were separated from the residual body. Merozoites resembled sporozoites but lacked the large refractile bodies seen in sporozoites. Linear inclusions were present near the merozoite nucleus and in the residual body. Round vacuoles and ribosomes were also found in the residuum. Nucleoli were first seen in sporozoite nuclei at 1 1/2 hr. They were also present in merozoites but were more prominent in trophozoites and schizonts. Peripheral and scattered nuclear heterochromatins were prominent in intracellular sporozoites and diminished in trophozoites, but increased after several nuclear divisions and were again prominent in the merozoite. Small, distinct interchromatin granules were found in all stages. Intranuclear spindles, centrocones, and centrioles were found in connection with nuclear divisions. Ultrastructure of first-generation schizogony in cell culture was similar to that described for second-generation E. tenella in the chicken and to schizogony of other species of Eimeria.

摘要

将柔嫩艾美耳球虫子孢子接种到鸡肾细胞原代培养物中。在接种后1.5至54小时固定细胞,并用电子显微镜检查。在1.5小时和24小时时,大多数细胞内子孢子呈梭形,并保留细胞外子孢子的典型细胞器。然而,在35小时时,出现了圆形滋养体,这些结构消失;仅留下一个折光体、细胞核、线粒体和内质网。此时也出现了双核寄生虫,但在48小时时出现了许多多核裂殖体。带有相邻类锥体的细胞核位于这些裂殖体的周边。部分发育的裂殖子,每个含有一个类锥体和一个细胞核,突出到寄生泡中。在54小时时,完全发育的裂殖子与残体分离。裂殖子类似于子孢子,但没有子孢子中可见的大折光体。裂殖子细胞核附近和残体中存在线性内含物。残体中还发现了圆形液泡和核糖体。核仁在1.5小时时首次出现在子孢子细胞核中。它们也存在于裂殖子中,但在滋养体和裂殖体中更明显。周边和散在的核异染色质在细胞内子孢子中突出,在滋养体中减少,但在几次核分裂后增加,并在裂殖子中再次突出。在所有阶段都发现了小的、明显的染色质间颗粒。与核分裂相关的核内纺锤体、中心锥和中心粒也被发现。细胞培养中第一代裂体生殖的超微结构与鸡体内第二代柔嫩艾美耳球虫以及其他艾美耳球虫种类的裂体生殖描述相似。

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