Müller B E
Z Parasitenkd. 1975 Sep 12;47(2):91-101. doi: 10.1007/BF00382632.
The development of first-generation merozoites to second-generation schizonts and merozoites of Eimeria contorta in one of its natural hosts, the mouse, was investigated with the electron microscope. Merozoites inside a host cell show a marked U-shape and a degeneration of the inner-pellicular membrane complex prior to transformation into schizonts. These processes closely resemble those seen in transforming sporozoites. In young schizonts with about 3-5 nuclei, the Golgi-adjuncts (structures of unknown function) form a large interconnected network. Nuclear divisions in growing schizonts involve the formation of a centrocône, which develops in a pocket-like indentation of the nuclear envelope. At least one centriole is present immediately adjacent to this indentation. In a later stage, the centrocône forms a conical nuclear protrusion directed towards a merozoite-anlage. This developing merozoite contains anlagen of a conoid, of rhoptries, and of micronemes and a refractile body in addition to the nucleus, centrioles, and a Golgi-adjunct. The merozoite-anlage is limited by a triple unit membrane complex. Schizonts give rise to 8-15 second-generation merozoites. Interesting features of these merozoites are the high number of micronemes, the finding of one single large mitochondrion per merozoite, and the occurrence of 26 subpellicular microtubules, i.e. the same number as in sporozoites of E. contorta. At the end of their development, merozoites come into direct contact with the host cell cytoplasm as the parasitophorous vacuole breaks down.
利用电子显微镜研究了艾美耳球虫在其天然宿主之一小鼠体内第一代裂殖子发育为第二代裂殖体和裂殖子的过程。宿主细胞内的裂殖子在转化为裂殖体之前呈明显的U形,内膜复合体退化。这些过程与转化中的子孢子所见的过程极为相似。在含有约3 - 5个细胞核的年轻裂殖体内,高尔基体附属物(功能不明的结构)形成一个大的相互连接的网络。生长中的裂殖体的核分裂涉及中心锥的形成,中心锥在核膜的袋状凹陷中发育。至少有一个中心粒紧邻这个凹陷。在后期,中心锥形成一个指向裂殖子原基的锥形核突出物。这个正在发育的裂殖子除了细胞核、中心粒和高尔基体附属物外,还含有类锥体、棒状体和微线体的原基以及一个折光体。裂殖子原基由三层单位膜复合体界定。裂殖体产生8 - 15个第二代裂殖子。这些裂殖子的有趣特征包括微线体数量众多、每个裂殖子发现单个大线粒体以及出现26根表膜下微管,即与艾美耳球虫子孢子中的数量相同。在发育末期,随着寄生泡破裂,裂殖子与宿主细胞质直接接触。